- Original article
- Open Access
Overexpression of OsAGO1b Induces Adaxially Rolled Leaves by Affecting Leaf Abaxial Sclerenchymatous Cell Development in Rice
Ricevolume 12, Article number: 60 (2019)
ARGONAUTE 1 (AGO1) proteins can recruit small RNAs to regulate gene expression, involving several growth and development processes in Arabidopsis. Rice genome contains four AGO1 genes, OsAGO1a to OsAGO1d. However, the regulatory functions to rice growth and development of each AGO1 gene are still unknown.
We obtained overexpression and RNAi transgenic lines of each OsAGO1 gene. However, only up- and down-regulation of OsAGO1b caused multiple abnormal phenotypic changes in rice, indicating that OsAGO1b is the key player in rice growth and organ development compared with other three OsAGO1s. qRT-PCR assays showed that OsAGO1b was almost unanimously expressed in leaves at different developmental stages, and strongly expressed in spikelets at S1 to S3 stages. OsAGO1b is a typical AGO protein, and co-localized in both the nucleus and cytoplasm simultaneously. Overexpression of OsAGO1b caused adaxially rolled leaves and a series of abnormal phenotypes, such as the reduced tiller number and plant height. Knockdown lines of OsAGO1b showed almost normal leaves, but the seed setting percentage was significantly reduced accompanied by the disturbed anther patterning and reduced pollen fertility. Further anatomical observation revealed that OsAGO1b overexpression plants showed the partially defective development of sclerenchymatous cells on the abaxial side of leaves. In situ hybridization showed OsAGO1b mRNA was uniformly accumulated in P1 to P3 primordia without polarity property, suggesting OsAGO1b did not regulate the adaxial-abaxial polarity development directly. The expression levels of several genes related to leaf polarity development and vascular bundle differentiation were observably changed. Notably, the accumulation of miR166 and TAS3-siRNA was decreased, and their targeted OSHBs and OsARFs were significantly up-regulated. The mRNA distribution patterns of OSHB3 and OsARF4 in leaves remained almost unchanged between ZH11 and OsAGO1b overexpression lines, but their expression levels were enhanced at the regions of vascular bundles and sclerenchymatous cell differentiation.
In summary, we demonstrated OsAGO1b is the leading player among four OsAGO1s in rice growth and development. We propose that OsAGO1b may regulate the abaxial sclerenchymatous cell differentiation by affecting the expression of OSHBs in rice.
The leaf is a type of lateral organ of seed plants, formed from the flanks of the shoot apical meristem (SAM) (Bowman et al. 2002). In order to improve the biomass and grain yield of crops, the plants should have more net photosynthesis. Leaf is the main organ to process photosynthesis in rice, and it is necessary to increase the photosynthetic rates at leaf level (Horton 2000). It is widely accepted that the most important leaf morphological features of high-yielding rice should be long, erect, narrow, V-type (rolled leaves) and thick (Yuan 1997). Rice plants with suitable inwardly rolled leaves can improve light transmission and increase the light capture of lower leaves for photosynthesis and nitrogen storage for grain filling (Sinclair and Sheehy 1999; Sakamoto et al. 2006).
At the initiation stage of leaf formation, three polarity axes, i.e. adaxial-abaxial, medial-lateral and proximal-distal, of the leaf primordia are established on the flanks of SAM (Bowman et al. 2002; Kidner and Timmermans 2007; Braybrook and Kuhlemeier 2010; Moon and Hake 2011). Generally, plants show two types of transversely rolled leaves: inward/adaxial and outward/abaxial rolling. The rolled leaf formation is principally regulated by adaxial-abaxial polarity development (Yamaguchi et al. 2012). The molecular mechanism of leaf polarity establishment has been extensively studied in Arabidopsis thaliana. PHABULOSA (PHB), PHAVOLUTA (PHV), and REVOLUTE (REV) belong to the HD-ZIP III gene family, encoding class III homeodomain-leucine zipper transcription factors that regulate adaxial cell development in leaves (McConnell et al. 2001; Prigge et al. 2005; Otsuga et al. 2008). KANADI (KAN) encodes a GARP transcription factor regulating leaf abaxial identity (Kerstetter et al. 2001). YABBY2 and YABBY3, encoding YABBY transcription factors, are expressed on the abaxial side of leaf primordia and have been proposed to specify the abaxial cell fate of leaves (Siegfried et al. 1999). A few small RNAs have also been proved to regulate leaf polarity development. HD-ZIP III genes, such as PHB and PHV, are the targets of miR165/166 that can affect leaf adaxial-abaxial polarity development by repressing HD-ZIP III genes (Reinhart et al. 2002; Williams et al. 2005b). TAS3 trans-acting small interference RNAs (tasiRNAs) can bind to AUXIN RESPONSE FACTOR 3/ETTIN (ARF3/ETT) that determines the abaxial cell fate to regulate leaf polarity identity (Garcia et al. 2006).
In rice, a number of genes regulating leaf rolling have been cloned and characterized. Among them, several genes regulate leaf rolling through affecting bulliform cell development (Zou et al. 2011; Xiang et al. 2012; Chen et al. 2015; Yang et al. 2016; Liang et al. 2018) or cell wall component (Li et al. 2009; Hu et al. 2010; Yang et al. 2014b; Ye et al. 2015). Moreover, SHALLOT-LIKE 1 (SLL1) and Semi-Rolled Leaf 2 (SRL2)/NARROW AND ROLLED LEAF 2 (NRL2) can promote abaxial sclerenchymatous cell formation to regulate leaf development. SLL1 encodes a SHAQKYF class MYB transcription factor, homologous to KAN in Arabidopsis. Its knock-out mutant sll1 exhibits adaxially rolled leaves with defective sclerenchymatous cell formation caused by deficient programmed cell death (PCD) of abaxial mesophyll cells; SLL1 overexpression inhibited the development of bulliform cells and sclerenchymatous cells on the adaxial side of leaves (Zhang et al. 2009). SRL2/NRL2 encodes a novel plant-specific protein with an unknown function, and its deficient mutant srl2 also exhibits adaxially rolled leaves with defective sclerenchymatous cells on the abaxial side; phenotypic observation and gene expression analyses of the sll1 srl2 double mutant suggested that SLL1 and SRL2 might regulate abaxial cell development in distinct pathways (Liu et al. 2016; Zhao et al. 2016).
ARGONAUTE (AGO) protein members are central components of the RNA-induced silencing complex (RISC) and the key players in the small RNA-mediated gene-silencing pathway (Mallory and Vaucheret 2010; Fang and Qi 2016). Generally, small RNAs are recruited by AGO, and then RISC is guided by small RNA to bind to its target, causing mRNA degradation, translational repression or epigenetic modifications (Baulcombe 2004). It is well known that AGO proteins are involved in many biological processes and participate in the regulation of plant growth and development. The rice genome contains 19 AGO members that can be divided into four groups: MEL1, AGO1, AGO4 and AGO7 (Wu et al. 2009). The biological function of a few rice AGO members were well studied. For instance, MEL1 can bind to the phased small interfering RNAs (phasiRNAs) and is also involved in histone H3 modification of meiotic chromosomes to regulate cell division of the premeiotic germ cells (Nonomura et al. 2007; Komiya et al. 2014; Liu and Nonomura 2016). OsPNH1 is homologous to Arabidopsis PINHEAD/ZWILLE (PNH/ZLL)/AGO10 that plays essential roles in SAM formation and leaf adaxial cell specification (Nishimura et al. 2002). OsAGO7/SHOOTLESS 4 (SHL4)/SHOOT ORGANIZATION2 (SHO2) involves in tasiRNA biosynthesis, coordinating leaf polarity development (Nagasaki et al. 2007; Itoh et al. 2008b), and OsAGO7 overexpression causes erect and adaxially rolled leaves (Shi et al. 2007). OsAGO2 participates in the regulation of rice pollen development by epigenetically regulating OsHXK1 expression (Zheng et al. 2019). OsAGO18 can confer broad-spectrum virus resistance in rice (Du et al. 2011; Wu et al. 2015; Wu et al. 2017). The rice AGO1 family contains four members: OsAGO1a, OsAGO1b, OsAGO1c and OsAGO1d. Transgenic plants with decreased expression of four AGO1s simultaneously displayed pleiotropic developmental changes accompanying increased expression of miRNA targets (Wu et al. 2009). In addition, the subset of miRNAs recruited by OsAGO1a, OsAGO1b, and OsAGO1c is different, although most of the miRNAs are almost evenly distributed in the three AGO1 complexes, which suggests that rice AGO1 members might be functionally redundant yet distinct (Wu et al. 2009).
To characterize the biological function of individual AGO1 in rice, we generated RNAi lines and overexpression lines for each AGO1 gene. We found that OsAGO1b knockdown plants mainly showed severe development defects in anthers, accompanying with the decreased rates of pollen fertility and seed setting. OsAGO1b-overexpression lines (OE-AGO1b) displayed pleiotropic phenotypes, such as adaxially rolled leaves and significantly decreased tiller numbers, which are distinct from other transgenic lines of OsAGO1 genes. Further investigation showed that the abaxial sclerenchymatous cells were partially defective in OE-AGO1b leaves. The expression levels of some genes and small RNAs related to leaf development such as OSHBs and OsARF genes were significantly changed in OE-AGO1b plants, suggesting a regulatory role of OsAGO1b in leaf development in rice.
Plant Materials and Phenotypic Statistics
Rice (Oryza sativa L.) japonica variety Zhonghua11 (ZH11) was used as the wild type (WT) control. Two japonica rice varieties, Nipponbare (Nip) and Songgeng (Sg), and two indica rice varieties, Huanghuazhan (HHZ) and Annong (AN), were also used for rice transformation. WT and transgenic rice lines were grown in the greenhouse at South China Agricultural University, Guangzhou, China. The leaf rolling index (LRI) and leaf erect index (LEI) of the top three leaves were determined at the grain-filling stage as described previously (Shi et al. 2007; Zhang et al. 2009). For testing the LRI, the leaf greatest width of natural state (Lnw) and flat state (Lfw) were measured at the same position. For testing the LEI, the leaf length (from the lamina joint to leaf tip) of natural state (Lnl) and straighten state (Lsl) were measured. The LEI and LRI were calculated as following formulas: LRI (%) = (Lfw-Lnw)/Lfw × 100% and LEI (%) = Lnl/Lsl × 100%, respectively. All the phenotypic data shown in this study were measured using ZH11 and two or three independent transgenic lines, and ten individual plants per line were used for the measurement. The information of primers used in this study was listed in Additional file 1: Table S1.
Construction of Vectors, Rice Transformation and Southern Blot
The cloning vector pBluescript II SK (+) (pSK) and binary vectors pCAMBIA1380, pCAMBIA1390, pRNAi-Ubi and pOx were used to generate overexpression and RNAi constructs of rice four AGO1s. The pOx vector was modified from pRNAi-Ubi and can be used to generate the overexpression construct driven by the maize Ubiqutin (Ubi) promoter (Hu and Liu 2006). A 1986-bp fragment of the miaze Ubi promoter (NCBI accession number: S94464) was amplified from maize genomic DNA and then inserted into pSK, and the resulting construct pSK-Ubi was used to provide the Ubi constitutive promoter. For OsAGO1b overexpression vector construction, the Ubi promoter was cut from pSK-Ubi and then inserted into pCAMBIA1380, and the resulting construct was named pCAMBIA1380-Ubi. A 3399-bp fragment of OsAGO1b was amplified from ZH11 cDNA by RT-PCR and was then inserted into pCAMBIA1380-Ubi to generate the overexpression construct. For OsAGO1b RNAi vector construction, a 191-bp fragment was amplified from ZH11 cDNA by RT-PCR and cloned into pRNAi-Ubi by two orientations. The detailed information for all overexpression and RNAi vector construction of rice four AGO1s was listed in Additional file 2: Table S2. Each construct was transformed into rice calli via the Agrobacterium-mediated protocol (Hiei et al. 1994). To determine the copy number of T-DNA insertion in transgenic plants, Southern hybridization was performed by using a DIG High Prime DNA Labeling and Detection Starter Kit II (Roche). A 750-bp fragment of the selectable marker gene hygromycin phosphotransferase (Hyg) was used as the probe. Approximate 7 μg genomic DNA of each sample was digested by Hind III, and the following electrophoresis, blotting, hybridization and signal detection were performed according to the manufacturer’s protocol.
The protein sequences of 18 AGO1 proteins from different plant species were obtained through searching the GenBank database (https://www.ncbi.nlm.nih.gov/genbank/) of NCBI (https://www.ncbi.nlm.nih.gov/) through blastp using OsAGO1b (Q7XSA2) as a query. The detailed information of protein names, accession numbers and plant species was listed in Additional file 3: Table S3. The multiple alignments of the sequences were performed by ClustalW (Thompson et al. 1994). A phylogenetic tree was constructed using the neighbor-joining method (Saitou and Nei 1987) with 1000 replicates in MEGA 7.0 software (Felsenstein 1985; Kumar et al. 2016).
Nucleic Acid Extraction and Quantitative Real-Time RT-PCR (qRT-PCR)
Genomic DNA was extracted from expanded leaves by CTAB method. Total RNAs were extracted from different rice tissues using TRIzol Regeant (Life Technologies). Spikelets at different developmental stages were collected according to Zhang and Wilson (2009). RNA samples were treated with DNaseI (New England Biolabs) before reverse transcription, and then single-stranded cDNA was synthesized from 500 ng of total RNA using HiScript II Q RT SuperMix for qPCR (Vazyme Biotech, China). For miRNA and siRNA quantitative expression analysis, stem-loop reverse transcription was performed using stem-loop primers for different small RNAs (Shen et al. 2010). The OsActin1 (XM_015774830) and the 5S ribosomal RNA gene rrn5 (NC_011033.1, 282,532..282653, complement) were used as internal standards to normalize the expression levels of detected genes and small RNAs respectively. qRT-PCR was performed using Bio-Rad CFX96 and the 2 × RealStar Power SYBR Mixture (GeneStar, China). The amplification conditions were as follows: 95 °C for 3 min, following 39 cycles of 95 °C for 10 s, 58–60 °C for 10 s, and 72 °C for 10 s. Relative expression levels of genes were measured using the 2−ΔΔCT method (Livak and Schmittgen 2001).
Subcellular Localization of OsAGO1b
The cauliflower mosaic virus (CaMV) 35S promoter, the yellow florescence protein (YFP) fragment, and the nopaline synthase (NOS) terminator of Agrobacterium tumefaciens were successively cloned into pUC18 to construct the transient expression vector p35S-YFP as described previously (Yang et al. 2014a). The fragment containing the entire OsAGO1b coding region without a start codon was amplified by RT-PCR and then inserted into p35S-YFP, downstream of YFP, to form the p35S-YFP-OsAGO1b fusion. The resultant vector was transformed into rice protoplasts prepared from leaf sheaths of 14-day-old seedlings, and transient expression was analyzed as described (Yang et al. 2014a).
Western Blot Analysis
The amino acid sequence of OsAGO1b (Q7XSA2) was used for epitope design. Seven peptide-affinity polyclonal antibodies against OsAGO1b (amino acids 6–15, 31–40, 48–57, 112–121, 133–142, 164–173, 194–203) were raised in rabbits by Abmart (Shanghai, China). The specificity of the purified antibodies was confirmed by Western blot analysis. For OsAGO1b detection, flag leaves of ZH11 and the transgenic plants at the heading stage were used. Protein extraction, SDS-PAGE and Western blotting were carried out as described previously (Li et al. 2011). Coomassie blue staining was used as a loading control. For OsAGO1b subcellular localization, total, nuclear, and cytoplasmic proteins were extracted from 14-day-old seedlings of ZH11 and fractionated as described previously (Roccaro and Somssich 2011; Wang et al. 2011b). As quality controls for the fractionation, RNase Z (Os02g0214300) was used as the cytoplasmic marker (Zhou et al. 2014), and histone H3 (Millipore) was used as the nuclear marker (Ye et al. 2012). Western blot analysis was performed as described previously (Li et al. 2011).
Anatomical Observation of Leaves
Free-hand and semi-thin transverse sections of leaves were used for anatomical observation. For semi-thin sections, fully expanded leaves of 30-day-old seedlings were harvested and fixed in paraformaldehyde buffer containing 4% (w/v) paraformaldehyde, 0.1 mmol/L sodium phosphate (pH 7.0), 0.25% (v/v) glutaraldehyde and 0.1% (v/v) Tween-20. After fixation, the samples were dehydrated in a series of increasing concentrations of ethanol and were then infiltrated and embedded in Epon-812 resin. The polymerization reaction was performed at 60 °C overnight. Semi-thin sections with a thickness of 2 μm were prepared using a Leica UCT ultramicrotome. The sample sections were stained with toluidine blue O, and then examined and photographed with a ZEISS microscope (Axio Observer D1). For autofluorescence analysis, fully expanded leaves of 30-day-old seedlings were fixed with FAA solution overnight, and were then dehydrated through a series of graded ethanol solutions. After dehydration, the samples were embedded in paraffin, and sectioned at a thickness of 8 μm. For observation of spontaneous fluorescence, the sections were examined and photographed under the excitation light for green florescence protein (GFP) on a ZEISS microscope (Axio Observer D1).
In Situ Hybridization
The shoot base about 1 cm in length including SAM of 14-day-old seedlings of ZH11 and two OsAGO1b overexpression lines were collected and then fixed in FAA overnight. After dehydration by a series of graded ethanol solutions, the samples were embedded in paraffin. Before hybridization, sections with a thickness of 8 μm were prepared. The 522-bp, 738-bp, and 705-bp fragments of the OsAGO1b, OSHB3 and OsARF4 cDNA respectively were used as probe sequences. The probe sequences were amplified by RT-PCR and then cloned into the pGEM™-T Easy vector (Promega). The resulting recombinant clones were used as templates to amplify the sense and antisense probe sequences followed by in vitro transcription. Probe labeling was performed using the DIG RNA Labeling Kit (Roche), and the hybridization was performed as described previously (Itoh et al. 2008a; Chen et al. 2010).
Overexpression of OsAGO1b Causes Adaxially Rolled Leaves and Multiple Developmental Defects
Plant AGO proteins play important roles in the small RNA pathway, as well as in the regulation of various aspects of plant growth and development (Fang and Qi 2016). In the process of characterizing the biological function of individual rice AGO1 member, transgenic plants overexpressing OsAGO1b (OE-AGO1b) were obtained. Phenotypic observation showed that most of the T0 transgenic seedlings displayed adaxially rolled leaves compared with the seedlings from a control transformation of the empty vector (Additional file 4: Figure S1A). The homozygotes of the three lines (25, 40, and 365) with a single T-DNA insertion confirmed by Southern blot analysis were obtained by planting and hygromycin-resistant selection, and were used for further studies (Additional file 4: Figure S1B). Further observation showed that OE-AGO1b plants displayed adaxially rolled leaves from the fourth-leaf stage throughout the whole growth period compared with the wild type ZH11 plants (Fig. 1 a-d; Additional file 5: Figure S2). The expression levels of OsAGO1b detected by qRT-PCR were increased by approximately 12- to 15-fold in the three OE-AGO1b lines (Fig. 1e), and the accumulation of OsAGO1b protein was also significantly increased (Fig. 1f). At the grain-filling period, the top three leaves of ZH11 were flat, and the LRIs and LEIs of the top three leaves of OE-AGO1b plants were significantly increased (Fig. 2 a and b). In addition, the width and length of OE-AGO1b leaves were significantly decreased (Fig. 2c and d), and the reduced numbers of veins may have accounted for the narrow leaves of the OE-AGO1b plants (Fig. 2e).
OE-AGO1b plants also exhibited other phenotypic changes, including significantly decreased tiller numbers, primary and secondary branch numbers of the inflorescence, plant height, inflorescence length, grain numbers and seed setting percentages (Additional file 6: Figure S3). Furthermore, to verify the conservation of OsAGO1b regulatory function between japonica and indica rice, we introduced the OE-AGO1b construct into two other japonica rice varieties, Nipponbare and Songgeng, as well as into two indica rice varieties, Huanghuazhan and Annong. The obtained homozygous plants with increased OsAGO1b expression showed almost the same phenotypic changes such as adaxially rolled leaves and reduced tiller numbers as in the ZH11 OE-AGO1b lines (Additional file 7: Figure S4). The results mentioned above showed that overexpression of OsAGO1b could cause adaxially rolled leaves and accompanied by a series of growth and development defects in rice. Furthermore, the regulatory function of OsAGO1b was conserved in indica and japonica rice.
OsAGO1b Encodes a Typical AGO Protein Which Co-localized in Both the Nucleus and Cytoplasm Simultaneously
According to the information in NCBI, OsAGO1b is located on rice chromosome 4. There are two transcript variants for OsAGO1b in rice, i.e. transcript X1 (XM_015780805, 3785 bp) and transcript X2 (XM_015780806, 3825 bp) encoding OsAGO1b isoform X1 (XP_015636291, 1118 aa) and isoform X2 (XP_015636292, 1101 aa) respectively. The amino acids 1–17 of isoform X1 are missing in isoform X2 according to the UniProt record (http://www.uniprot.org/uniprot/Q7XSA2). All the data presented in this study used the OsAGO1b transcript variant X2 and the OsAGO1 isoform X2 as in the previous studies (Kapoor et al. 2008; Wu et al. 2009). The annotated genomic sequence of OsAGO1b (AL662954.2) contains 22 exons and 21 introns for isoform X2 (Fig. 3a). The intact coding sequence of the OsAGO1b transcript variant X2 is 3306 bp, encoding a peptide with a molecular weight of 121.6 kD and a theoretical PI of 9.55 predicted by the ProtParam program (http://web.expasy.org/protparam/). The annotation of the functional domains of OsAGO1b based on a search of the Conserved Domain Database of NCBI (https://www.ncbi.nlm.nih.gov/cdd) indicated that OsAGO1b has a Glycine-rich domain, PAZ domain, and Piwi domain that has significant similarity with RNaseH and possesses the DDH (Asp-Asp-His) catalytic motif required for endonucleolytic cleavage of the target RNA (Fig. 3b; Additional file 8: Figure S5; Rivas et al. 2005). The conserved PAZ and PIWI domains shared by AtAGO1 and three other OsAGO1s suggest that OsAGO1s may recruit small RNAs and possess endonuclease activity. Although the PAZ domain is highly conserved among four OsAGO1s, some polymorphic amino acids exist (Additional file 8: Figure S5), suggesting the small RNAs recruited by each AGO1 might be partially different, as presented for OsAGO1a, OsAGO1b, and OsAGO1c in a previous study (Wu et al. 2009).
Phylogenetic analysis showed the 18 plant AGO1s are classified into three clades. OsAGO1b is closely related to ZmAGO1b, ZmAGO1c, SiAGO1b, and is also closely related to OsAGO1a, ZmAGO1a and TaAGO1; thus, they form Clade I specific to monocot crops. The AGO1s from dicotyledonous plants are clustered together to form Clade II including AtAGO1, GmAGO1, MtAGO1, SlAGO1b, SlAGO1a, and NtAGO1. Clade I is closely related to Clade II, implying OsAGO1b may have similar functions to AtAGO1. OsAGO1c and OsAGO1d belong to Clade III that is also specific to monocotyledons and is more diverged from Clade I and Clade II, suggesting their function might be distinct from that of AtAGO1 (Fig. 3c).
To investigate the subcellular localization of OsAGO1b, the p35S-YFP-OsAGO1b transient expression vector was constructed and transformed into rice leaf sheath protoplasts as described previously (Yang et al. 2014a). The fluorescence signal of the fusion protein was observed in both the nucleus and the cytoplasm (Fig. 3d). To verify the above result, total, nuclear and cytoplasmic proteins were isolated, fractionalized, and used for Western blot analysis. As shown in Fig. 3e, the nuclear-located histone H3 was detected in total and nuclear proteins, and cytoplasm-located RNase Z (Zhou et al. 2014) was detected in total and cytoplasmic proteins. As expected, OsAGO1b was detected in total, nuclear and cytoplasmic proteins. Thus, we propose that OsAGO1b may function in both the nucleus and the cytoplasm to regulate gene expression, similar to AtAGO1 (Bologna et al. 2018; Liu et al. 2018).
OsAGO1b is the Key Regulator for Rice Growth and Development Among Four OsAGO1s
It is noteworthy that transgenic plants with increased or decreased expression of the three other rice AGO1s, i.e. OsAGO1a, OsAGO1c, and OsAGO1d, did not exhibit dramatic phenotypic alterations, especially in leaves and tiller numbers at the mature stage (Additional file 9: Figure S6). Except the remarkable phenotypic changes of OE-AGO1b lines, it is worth noting that the OsAGO1b RNAi lines showed no obviously phenotypes in young leaves and mature plant height, however, the seed setting rates were significantly decreased (Additional file 10: Figure S7; Additional file 11: Figure S8A). To investigate the reasons of lower seed setting rates of OsAGO1b RNAi lines, the anatomical observation of spikelets was further performed. In contrast to the six erect anthers in one spikelet of ZH11, most anthers of the OsAGO1b RNAi spikelet were extremely curved due to the defective development of some pollen sacs accompanied by the reduced pollen fertility, which indicated that anther patterning was disturbed in OsAGO1b RNAi lines (Additional file 11: Figure S8B-D). These results suggested that OsAGO1b is the key regulator for the normal growth and development of rice among four rice OsAGO1 genes.
qRT-PCR assay showed that down-regulation/overexpression of one OsAGO1 gene often caused the increased/decreased expression of another/other AGO1 member (s) (Fig. 4). For example, OsAGO1b overexpression was accompanied by the decreased expression of OsAGO1a, and down-regulation of OsAGO1b caused an increased expression of OsAGO1c and OsAGO1d (Fig. 4c and d). Multiple phenotypic changes of the transgenic plants with altered OsAGO1b expression suggested that abnormal OsAGO1b expression has pleiotropic effects on rice growth and development. It suggested that the complex regulatory loop might exist among rice AGO1 members.
To analyze the expression patterns of four OsAGO1 genes, total RNAs were extracted from various tissues and organs at different developmental stages of ZH11. qRT-PCR assays showed that four OsAGO1 transcripts were detected in almost all tissues and organs examined; however, different expression patterns were observed (Fig. 5). Notably, OsAGO1b showed much higher expression than other OsAGO1 genes, and the highest expression of OsAGO1b was observed in young spikelets at stage 1–3 (S1–3). In 5-day-old seedlings and roots, OsAGO1b was expressed at a rather low level and was almost undetectable. In leaves at different developmental stages, OsAGO1b was almost unanimously expressed (Fig. 5b). These expression profiles also suggested that the four OsAGO1s may share overlapping and distinct functions in rice.
The Sclerenchymatous Cells are Defective on the Abaxial Side of OE-AGO1b Leaves
To determine the cytological cause of adaxially rolled leaves of OE-AGO1b plants, the freehand and semi-thin cross-sections of 30-day-old seedlings were observed, and the results revealed that leaf veins had sclerenchymatous cells on the adaxial and abaxial sides of leaves in ZH11, whereas the sclerenchymatous cells on the abaxial side of some small veins were replaced by mesophyll cells in the region where the leaf was curved in OE-AGO1b (Fig. 6a-f). Sclerenchymatous cells are generated from mesophyll cells through PCD and are located on the adaxial and abaxial sides of leaf veins. Mesophyll cells undergo secondary cell wall thickening and become dead cells which have thick lignified secondary walls with high amounts of lignin and fiber deposited and provide structural support to a plant (Zhong and Ye 2007). The phenolic compounds of lignin, such as p-coumaric acid and ferulic acid, can generate autofluorescence; thus, the autofluorescence intensity can reflect the thickness of the cell wall (Willemse and Den Outer 1988). We then detected the autofluorescence of the leaves from 30-day-old seedling of ZH11 and OE-AGO1b. The sclerenchymatous cells of ZH11 leaves showed conspicuous green fluorescence signals on the both sides of the leaf veins. However, no fluorescence signals were detected on the abaxial side of some leaf veins in OE-AGO1b (Fig. 6g-i), indicating the abaxial sclerenchymatous cells were developmentally impaired. Our results suggested that OsAGO1b might be involved in leaf adaxial-abaxial polarity development or abaxial side cell differentiation, and it is possible that the defect in sclerenchyma formation in OE-AGO1b could be due to more upstream defects such as mis-specification of cellular identity.
OsAGO1b Transcripts do not Show Adaxial-Abaxial Polarity Distribution During Rice Leaf Development
Previous studies have shown that the transcripts of some genes involved in leaf polarity development displayed adaxial-abaxial polarity distribution in leaves (Juarez et al. 2004; Fahlgren et al. 2006; Hunter et al. 2006; Zhou et al. 2013). To determine whether OsAGO1b mRNAs show polarity distribution, in situ hybridization was performed to detect the expression pattern of OsAGO1b in the vegetative shoot apex of ZH11. During leaf development OsAGO1b transcripts were visibly accumulating in P1 to P3 primordia without obviously abaxial-adaxial polarity distribution, and it was weakly expressed in SAM. In P4 primordum, OsAGO1b mRNAs were detected around vascular bundles (Fig. 7a and c). No visible signal was detected by the sense probe (Fig. 7b and d). These results indicated that the expression of OsAGO1b did not show polarity distribution during leaf development, and OsAGO1b may be involved in the abaxial side cell differentiation indirectly or directly. Meanwhile, OsAGO1b may be participating in the differentiation of vascular tissue.
SLL1 and SRL2 are Not Directly Involved in the Defective Development of Sclerenchymatous Cells of OE-AGO1b Leaves
SLL1 and SRL2 have been proved to play important roles in regulating abaxial sclerenchymatous cell formation through distinct pathways in rice leaves (Zhang et al. 2009; Liu et al. 2016). The phenotype of the adaxially rolled leaves caused by defective sclerenchymatous cell formation of OE-AGO1b was very similar to that observed in the sll1 and srl2 mutants, suggesting SLL1 and SRL2 might be involved in the rolled leaf formation of OE-AGO1b plants. We then checked the expression levels of SLL1 and SRL2 in ZH11 and OE-AGO1b. The results showed that the expression levels of SLL1 and SRL2 were increased in OE-AGO1b compared with those in ZH11 (Fig. 8a), suggesting SLL1 and SRL2 may not directly influence the adaxial sclerenchymatous cell formation in OE-AGO1b leaves. Sclerenchymatous cells are transdifferentiated from mesophyll cells in three stages, i.e. dedifferentiation (stage I), conversion of mesophyll cells into tracheary element (TE element) precursor cells (stage II), and TE-specific secondary wall thickening followed by lignification and PCD (stage III) (Fukuda 2000). SLL1 participates in the TE-PCD process by regulating the expression of TE-PCD related genes (Zhang et al. 2009). We then checked the expression of five TE-PCD related genes, i.e. C4H (cinnamate 4-hydroxylase), 4CL (4-coumarate-CoA ligase), CP (Cys protease), TED2 (tracheary element dehydrogenase 2), and PI (protease inhibitor) (Zhang et al. 2009). The expression levels of 4CL, TED2 and PI were significantly increased in OE-AGO1b, whereas the expression changes of C4H and CP were relatively small (Fig. 8b), which suggested that overexpression of OsAGO1b might affect the TE-PCD process of abaxial mesophyll cells through regulating the expression of TE-PCD related genes.
In rice, it has been demonstrated that YABBYs are not involved in the regulation of leaf polarity formation like in Arabidopsis, but participate in cell growth and differentiation, as well as vascular/TE element development of leaves (Liu et al. 2007b; Toriba et al. 2007). Rice contains eight YABBYs, named OsYABBY1 to OsYABBY7, and DROOPING LEAF (Yamaguchi et al. 2004; Toriba et al. 2007). In the srl2 mutant, the expression of several YABBY genes was decreased significantly (Liu et al. 2016). We then analyzed the expression of OsYABBY1 to OsYABBY7. In contrast to srl2, the expression of OsYABBY5 was almost undetectable in the leaves of 30-day-old seedlings. And the expression levels of OsYABBY1, OsYABBY2, OsYABBY3 and OsYABBY7 were significantly increased in OE-AGO1b leaves (Fig. 8c). In general, these results suggested that SLL1 and SRL2 may not directly influence the adaxial sclerenchymatous cell formation in OE-AGO1b leaves.
Overexpression of OsAGO1b Affects the Abundance of Small RNAs and their Target Genes Related to Leaf Polarity Development
Some miRNAs have been shown to be involved in the regulation of leaf polarity development, such as miR166 (Reinhart et al. 2002; Williams et al. 2005b), miR319 (Schommer et al. 2008; Yang et al. 2013), miR390 (Douglas et al. 2010) and miR396 (Wang et al. 2011a; Mecchia et al. 2013). To see whether small RNAs may be involved in the development of rolled leaves in OE-AGO1b plants, we detected the accumulation changes of four miRNAs, i.e. miRNA166f, miR319b, miR390, and miR396a. The results showed that the accumulation of miR166f and miR319b was significantly reduced, whereas miR390 and miR396a did not show obviously altered accumulation in at least one OE-AGO1b line compared with those in ZH11 (Fig. 8d).
HD-ZIP III family genes are the targets of miR165/166, and miR165/166 can regulate leaf adaxial-abaxial polarity development by suppressing the expression of HD-ZIP III genes on the abaxial side of the leaf (Reinhart et al. 2002; Bowman 2004; Kidner and Martienssen 2004; Byrne 2006). In rice, there are five HD-ZIP III genes named OSHB1 to OSHB5, and overexpression of OSHB1, OSHB3, OSHB5 respectively caused adaxially rolled leaves with defective sclerenchymatous cells on the abaxial side (Itoh et al. 2008a), which is similar to OE-AGO1b plants. We then detected the expression of OSHB genes. The results showed that, except for OSHB4, the four other genes exhibited significantly increased expression in OE-AGO1b leaves (Fig. 8e). Accordingly, we propose that the increased expression of some OSHB genes might be the key reason for the adaxially rolled leaves of OE-AGO1b plants.
On the other hand, TAS3-tasiRNAs are involved in leaf polarity development by suppressing the expression of their target genes, i.e. ARF2, ETT/ARF3, and ARF4, on the abaxial leaf side of Arabidopsis (Williams et al. 2005a; Hunter et al. 2006; Husbands et al. 2015). In rice, TAS3-tasiRNA 5′-D6 (+) and TAS3-tasiRNA 5′-D7 (+) are generated from OsTAS3 loci (Liu et al. 2007a), and there are five orthologous genes of Arabidopsis ARF2, ARF3, and ARF4, i.e. OsARF2/ARF3-like 2/OsETTIN2, OsARF3/ARF3-like B, OsARF4/OsARF2/ARF2-like, OsARF14/ARF3-like A, and OsARF15/ARF3-like 1/OsETTIN1 (Sato et al. 2001; Williams et al. 2005a; Liu et al. 2007a; Wang et al. 2007). To investigate whether the TAS3-tasiRNA-ARF pathway is involved in the leaf developmental defects of OE-AGO1b plants, the expression levels of two TAS3-tasiRNAs and five OsARF genes were detected. The results showed that two TAS3-tasiRNAs exhibited reduced accumulation, and all five OsARFs displayed increased expression in OE-AGO1b leaves (Fig. 8f). In plants, miR390 guides the generation of tasiRNAs from TAS3 transcripts to regulate the expression of ARF genes (Xia et al. 2017); however, the accumulation of miR390 did not change in OE-AGO1b leaves compared with that in ZH11, implying other factors might exist to regulate TAS3-tasiRNA generation.
In rice, miR319 was predicted to target five TCP genes, i.e. OsPCF5, OsPCF6, OsPCF7, OsPCF8 and OsTCP21 (Wang et al. 2014). In OE-AGO1b lines, the expression levels of OsPCF6, OsPCF7, OsPCF8 and OsTCP21 were significantly increased, whereas OsPCF5 was slightly decreased (Fig. 8g). The changed accumulation of miR319 and its target genes might account for the reduced vein numbers and leaf width of OE-AGO1b, as found in a previous study (Wang et al. 2014). Two AGO members, OsAGO7 (Nagasaki et al. 2007; Shi et al. 2007; Itoh et al. 2008b) and OsPNH1 (Nishimura et al. 2002) are proved to be involved in leaf development in rice. To investigate whether OsAGO7 and OsPNH1 are involved in the abnormal leaf development of OE-AGO1b plants, we analyzed the expression levels of OsAGO7 and OsPNH1. OsAGO7 expression was slightly increased in OE-AGO1b, implying that OsAGO7 may not be involved in the phenotypic changes of OE-AGO1b leaves; however, OsPNH1 showed significantly decreased expression in OE-AGO1b leaves, suggesting that OsPNH1 might participate in the altered leaf development in OE-AGO1b plants (Fig. 8h).
OsAGO1b-RNAi seedlings showed normal leaves similar to that in ZH11 (Additional file 10: Figure S7A and B), we then detected the expression of the OSHBs and OsARFs in the young leaves of OsAGO1b-RNAi lines. And the qRT-PCR results showed that most of the genes showed similar expression levels to ZH11, including OSHB3, OSHB4, OSHB5, ARF2, and ARF5. And only OSHB1 showed increased expression in both RNAi lines. The accumulation of OSHB3 and OsARF4 were only significantly changed in one RNAi lines (Additional file 12: Figure S9). These results suggested that OsAGO1b knockdown may not affect the expression of OSHBs and ARFs during leaf development. In addition, to see whether OSHBs were specifically up-regulated in OE-AGO1b, we detected the expression of OSHBs in young leaves of OsAGO1a, OsAGO1c and OsAGO1d overexpression lines which showed normal leaf phenotypes (Additional file 13: Figure S10A-C). In contrast to OE-AGO1b lines, the expression levels of OSHBs did not show the uniformly changing trends in OsAGO1a, OsAGO1c and OsAGO1d overexpression lines (Additional file 13: Figure S10D). For instance, the expression of OSHB1 and OSHB2 was significantly decreased and OSHB3 was obviously increased in OE-AGO1a lines; OSHB1 was significantly increased and OSHB3 to OSHB5 were decreased in OE-AGO1c lines; OSHB1 to OSHB4 were somewhat decreased in OE-AGO1d. These results indicated OSHBs were specifically up-regulated in rolled leaves of OE-AGO1b, distinguished from the overexpression lines of other three OsAGO1s.
Overexpression of OsAGO1b does not Affect the Distribution of OSHB3 and OsARF4 Transcripts
The expression levels of some genes related to leaf adaxial-abaxial polarity development, such as OSHBs and OsARFs, were significant increased in OE-AGO1b lines as mentioned above. However, whether the distribution of the transcripts of OSHBs and OsARFs had changed was not clear. To answer this question, we compared the expression patterns of OSHB3 and OsARF4 in ZH11 and OE-AGO1b lines using in situ hybridization. During the leaf development, the OSHB3 mRNA was limited to the adaxial sides of P1 to P3 primordia and accumulated in the region where the xylem would develop in ZH11 (Fig. 9a and e; Additional file 14: Figure S11A; Additional file 15: Figure S12A), as previously described (Itoh et al. 2008a). Similarly, in OE-AGO1b lines, OSHB3 mRNA was accumulated in almost the same region compared with ZH11, but the expression was significantly enhanced, consistent with the qRT-PCR results (Fig. 9b and f; Additional file 14: Figure S11B; Additional file 15: Figure S12B). OsARF4 were weakly expressed in the primary cambiums (protoxylem and protophloem) of vascular bundles from P4 primordium in ZH11 (Fig. 9c and g; Additional file 14: Figure S11C; Additional file 15: Figure S12C). In OE-AGO1b lines, the OsARF4 mRNAs were obviously accumulated on the abaxial sides of leaf primordia as expected, and expressed in the regions of primary cambiums similar to ZH11 (Fig. 9d and h; Additional file 14: Figure S11D; Additional file 15: Figure S12D). However, the OsARF4 transcripts were mainly first detected in vascular bundles in P3 primordium of OE-AGO1b lines (Fig. 9d and h; Additional file 14: Figure S11D; Additional file 15: Figure S12D). In summary, overexpression of OsAGO1b may not change the mRNA polarity distributions of OSHBs and OsARFs during leaf development, but enhanced their expression at the regions of vascular bundles or sclerenchymatous cell differentiation.
OsAGO1b has the Most Important Regulatory Function Among Four Rice AGO1 Genes
AGO proteins play important roles in plant growth and development through gene regulation mediated by small RNAs, such as miRNAs and siRNAs (Hutvagner and Simard 2008). The Arabidopsis ago1 mutant displayed a dwarf stem, reduced inflorescence branching, small rosette leaves, and filamentous cauline leaves without adaxial-abaxial differentiation, indicating that AtAGO1 is involved in the regulation of many processes of plant growth and development (Bohmert et al. 1998). Rice contains four AGO1 members orthologous to AtAGO1. A previous work showed simultaneously knockdown four rice AGO1s led to pleiotropic developmental defects and the impaired miRNA pathway (Wu et al. 2009). Deep sequencing of small RNAs showed the subset of miRNAs recruited by OsAGO1a, OsAGO1b, and OsAGO1c is different, although most of the miRNAs are almost evenly distributed in the three AGO1 complexes (Wu et al. 2009). In this study, we found that the expression patterns and levels of each OsAGO1 gene were different in several tissues of different growth stages (Fig. 5), and OsAGO1c and OsAGO1d constitutes a particular clade specific to monocotyledon plants (Fig. 3c). These results suggested although the biological functions of four OsAGO1s may be redundant, it is likely that they have some differences of regulatory functions during rice development. Our study indicated that the expression levels of OsAGO1b was higher than other three AGO1 members and its spatio-temporal expression pattern showed more tissue specific, especially in spikelets of different developmental stages (Fig. 5b). Intriguingly, OsAGO1b RNAi lines showed the disturbed anther patterning, decreased pollen fertility and seed setting rates (Additional file 11: Figure S8). A previous study showed that tasiRNA pathway may be involved in regulating adaxial-abaxial polarity in rice stamen development, and the disturbed anther patterning of the rol mutant was conferred by a weak mutation in SHOOTLESS2 encoding an RNA-dependent RNA polymerase (Toriba et al. 2010). The disturbed anther patterning of our OsAGO1b RNAi lines was similar to rol mutant. Thus, we hypothesize OsAGO1b may be involved in anther patterning and development by regulating tasiRNA pathway, which need to be studied further. In addition, the RNAi lines for each OsAGO1 gene did not exhibit severe adaxial-abaxial polarity defects on leaves as described in Arabidopsis ago1 mutants (Bohmert et al. 1998; Vaucheret et al. 2004; Yang et al. 2006), verifying the redundant regulatory functions among four rice AGO1s.
Among the overexpression lines of four OsAGO1s, only OsAGO1b overexpression plants displayed pleiotropic abnormal phenotypes, especially in T0 generation lines, such as dark green, severely rolled leaves and decreased root system (Additional file 4: Figure S1A). The phenotypic defects of OE-AGO1b seedlings were reminiscent of the phenotypes of the OsDCL1 RNAi transformants with weak loss of function (Liu et al. 2005) and the RNAi lines with decreased expression of four OsAGO1 genes simultaneously, and the above OsDCL1- and OsAGO1- RNAi transformants were both accompanied with the impaired miRNA pathway (Liu et al. 2005; Wu et al. 2009). Moreover, overexpressed miR168-resistant AGO1 in Arabidopsis exhibited impaired miRNA pathway and elevated miRNA targets as well (Vaucheret et al. 2004). Taken together, we propose that ectopic expression of OsAGO1b may impair the miRNA pathway and lead to upregulated miRNA targets although other three OsAGO1s may have overlapping functions in miRNA pathway. The reduced accumulation of miR166 and miR319 and their up-regulated targets in OE-AGO1b leaves supported the speculation above (Fig. 8).
In Arabidopsis, different AGO members showed functional diversification and redundancy, such as AGO1 and AGO10, which might be dependent or independent on their slicing activity. Arabidopsis AGO10/PHN/ZLL exhibits overlapping function with AGO1 in some developmental processes, such as SAM maintenance and leaf polarity establishment, possibly by competing miR166/165 with AGO1 and repressing miR166/165 (Moussian et al. 1998; Lynn et al. 1999; Fagard et al. 2000; Mallory et al. 2009; Liu et al. 2010; Ji et al. 2011; Zhu et al. 2011; Zhou et al. 2015). Furthermore, protein domain swapping experiments showed that only AGO1 protein with replaced PAZ domain from AGO10 could rescue the developmental defects in ago1 mutant, but not the AGO1 protein with the replaced AGO10 Piwi domain, suggesting AGO1 and AGO10 could recruit similar miRNAs to regulate SAM and leaf formation, and Piwi domain may contribute to maintain their specific regulatory functions (Mallory et al. 2009). In our study, we found that there were several conserved motifs in the PAZ domains of four OsAGO1s and AtAGO1, however they also had a few diverse amino acid residues between each other, such as three mis-matched residues S-L-S in OsAGO1b (Additional file 8: Figure S5), implying the binding affinity of miRNAs among different OsAGO1s may be different. Similarly, differences in the Piwi domains of each OsAGO1s may cause some different regulatory functions for each OsAGO1 (Additional file 8: Figure S5), similar to AGO1 and AGO10 in Arabidopsis, which might partially account for the unique function of OsAGO1b. In addition, the expression of OSHBs in four OE-AGO1s plants was quite different (Fig. 8e; Additional file 13: Figure S10), implying the distinct regulatory roles of AGO1-miR166-HD-ZIP III pathway during leaf morphology formation in rice. Taken together, we propose that OsAGO1b plays the most important regulatory roles in the growth and development of rice among four OsAGO1s, and complex regulatory networks may exist among different AGO proteins in rice.
Excess of OsAGO1b Induces Elevated miRNA Targets
In plants, miRNAs and siRNAs are important regulators for SAM formation and maintenance, leaf morphogenesis, and leaf polarity formation (Liu et al. 2005; Hunter et al. 2006; Abe et al. 2010; Kidner 2010; Pulido and Laufs 2010; Yang et al. 2018). In this study, we detected the reduced accumulation of miR166, miR319, and two TAS3-tasiRNAs, but no changes were found for miR390 and miR396 in OE-AGO1b leaves (Fig. 8d). The reduced accumulation of miR166, miR319 and two TAS3-tasiRNAs possibly caused the abnormal leaf development in OE-AGO1b plants by regulating the expression of their target genes (Fig. 8d, f, and g). The reduced accumulation of miR166 may cause the increased expression of OSHB genes, which may result in the adaxially rolled leaves of OE-AGO1b plants (Fig. 8e). The excess of OsAGO1b might impair the accumulation of small RNAs by interfering with miRNA stabilization, RISC formation and function, similar to overexpression line of the miR168-resistant AGO1 in Arabidopsis (Vaucheret et al. 2004), suggesting that the excess of AGO1 protein can reduce miRNA accumulation and elevate miRNA targets in both Arabidopsis and rice.
A recent study showed that, in addition to binding miRNAs to repress their target genes in cytoplasm, Arabidopsis AGO1 can also bind the chromatin of active genes, such as IAA induced genes to promote gene transcription in the nucleus in response to hormones and stresses, suggesting that AGO1 can participate in the regulation of diverse signaling pathways and the corresponding biological processes (Liu et al. 2018). ARFs are transcription factors involved in auxin pathway, and the expression of OSHBs could be induced by auxin treatment (Itoh et al. 2008a), thus we speculate excess of OsAGO1b in nucleus may promote the expression of some auxin-induced genes and then stimulate the expression of ARFs and OSHBs. This may be another reason for the up-regulated expression of ARFs and OSHBs.
The Arabidopsis miR168-resistant AGO1 plants with a strong increase in AGO1 accumulation (12.9-fold to 21.7-fold increase) displayed more severe developmental defects, and most of the plants died before flowering (Vaucheret et al. 2004). However, OE-AGO1b plants with a 15-fold increase approximately in OsAGO1b expression can complete a normal life cycle with almost normal fertility (Fig. 1b). Functional redundancy among different OsAGO1 members may explain this difference.
OsAGO1b Might Participate in a New Pathway to Control Sclerenchymatous Cell Development
In OE-AGO1b plants, the abaxial sclerenchymatous cells of some small leaf veins were developmentally deficient, and a set of genes and small RNAs involved in leaf polarity development showed changed expression (Fig. 6 and Fig. 8), suggesting OsAGO1b may participate in regulating the abaxial sclerenchymatous cell development by affecting the accumulation of downstream genes dependent or independent of the small RNA pathway. SLL1 and SRL2 are involved in regulating the abaxial sclerenchymatous cell development of leaves through different pathways in rice, and down-regulation of SLL1 or SRL2 resulted in the adaxially rolled leaves with defective abaxial sclerenchymatous cells (Zhang et al. 2009; Liu et al. 2016). In OE-AGO1b plants, the expression of SLL1 and SRL2 were both up-regulated, and SLL1 overexpression caused twisted and inner rolled leaves with enhanced phloem development on the abaxial side and suppressed sclerenchymatous cell development on the adaxial side of the leaf blade (Zhang et al. 2009), which is different from that of OE-AGO1b, suggesting that OsAGO1b might affect the sclerenchymatous cell development in a pathway different from those related to SLL1 and SRL2. In the sll1 mutant, TE-related genes CP, PI and 4CL showed decreased expression, and no obvious expression changes were detected for TED2 and C4H (Zhang et al. 2009). The increased expression of CP, PI and 4CL in OE-AGO1b plants may be caused by the increased expression of SLL1. Notably, TED2 expression was greatly increased in OE-AGO1b, suggesting that OsAGO1b can promote TED2 expression directly or indirectly (Fig. 8b). TED2 is the only identified marker gene of stage II of TE-PCD process, and the increased expression of TED2 suggested that OsAGO1b might affect the initiation of stage III events of TE-PCD during sclerenchymatous cell formation (Fukuda 2000). C4H and 4CL are both involved in lignin monomer biosynthesis (Baucher et al. 2003), and the increased 4CL expression in OE-AGO1b suggested that OsAGO1b might affect lignin synthesis.
The Up-Regulated OSHB May Account for Leaf Rolling in OsAGO1b Overexpressed Rice Plants
HD-ZIP III family genes are involved in SAM maintenance, leaf adaxial cell development, and vascular cell fate determination in Arabidopsis (McConnell and Barton 1998; McConnell et al. 2001; Prigge et al. 2005; Ramachandran et al. 2017). Maize Rld1 encodes a HD-ZIP III protein, and Rld1 overexpression resulted in upwardly rolled, thread-like leaves (Juarez et al. 2004). Transgenic rice plants with increased expression of OSHB1 or OSHB3 exhibited narrow and adaxially rolled, or filamentous leaves and ectopic ligules, and enhanced expression of OSHB5 led to adaxially rolled leaves with a normal blade-sheath boundary (Itoh et al. 2008a). OSHB1 overexpression also caused bulliform-like cells on the abaxial side of leaves, and part of the abaxial sclerenchymatous cells exhibited defective development (Itoh et al. 2008a ). OSHB4/OsHox32 overexpression also produced narrow and upwardly rolled leaves with a deceased number of bulliform cells (Li et al. 2016). The above studies indicate that the suppression of HD-ZIP III genes is crucial for the normal development of leaf adaxial-abaxial polarity. In OE-AGO1b plants, the expression levels of the five OSHB genes were increased overall, and the expression of OSHB1 and OSHB2 increased by 2-fold (Fig. 8e), and OE-AGO1b showed adaxially rolled leaves with defective abaxial sclerenchymatous cells, similar to the rice plants overexpressing OSHB genes (Fig. 6e and f). Notably, the increased expression levels of OSHBs in our chosen OE-AGO1b lines were much lower than those in the previous study (Itoh et al. 2008a), which might account for the less severe phenotypes of OE-AGO1b leaves. One of the possibilities is that some T0 plants with severe phenotypes, such as shallot-like rolled leaves, were dead during planting or could not produce seeds (Additional file 4: Figure S1A), indicating the dosage-dependent effect of OsAGO1b on the phenotypic changes, which has been proved by the less severe phenotype of the heterozygous OE-AGO1b lines (data not shown).
A recent study showed that down-regulation of miR166 generated rice plants with adaxially rolled leaves with abnormal sclerenchymatous cells, accompanied by the increased expression of five OSHB genes, and OSHB4 was proved to be the major target of miR166; OSHB4 overexpression caused leaf rolling similar to miR166 down-regulated plants, indicating a correlation between the miR166-OSHB regulatory pathway and leaf adaxial-abaxial polarity development in rice, similar to Arabidopsis (Zhang et al. 2018). In this study, OsAGO1b overexpression also resulted in the increased accumulation of OSHBs and the decreased accumulation of miR166, suggesting an OsAGO1b-miR166-HD-ZIP III regulatory pathway in leaf adaxial-abaxial patterning in rice. How the regulatory pathways related to SLL, SRL2, and OsAGO1b respectively coordinate and interact in the regulation of sclerenchymatous cell development needs further study. In addition, OsHox32/OSHB4 overexpression caused significantly decreased or increased expression of different YABBY genes, suggesting that OSHB4 might participate in leaf development by regulating YABBY genes (Li et al. 2016). In OE-AGO1b plants, the expression of some YABBY genes was also changed; however, OSHB4 showed a very similar expression to that in the wild type, suggesting the regulation of YABBY genes is complicated (Fig. 8c). ATHB4 and HAT3, two HD-ZIP II transcription factors, were also proved to control leaf adaxial/abaxial patterning in Arabidopsis (Bou-Torrent et al. 2012; Turchi et al. 2013). And a further study showed that HD-ZIP III and HD-ZIP II protein can act together to directly repress the expression of MIR165/166 genes, indicating a complex regulation circuit between these regulators (Merelo et al. 2016). From our in situ hybridization results, OsAGO1b, OSHB3 and OsARF4 were all expressed in the regions of vascular tissue formation in this study. Considering that OSHB3 and OsARF4 are both auxin inducing genes, our results suggest that OsAGO1b may afftect the sclerenchymatous cell formation of the leaf abaxial side through the auxin pathway.
In summary, our work demonstrated that overexpression of OsAGO1b resulted in narrow and adaxially rolled leaves with reduced leaf vein number and defective sclerenchymatous cells, accompanying with the reduced small RNA levels and increased expression of their target genes. This study provided a new perspective to the understanding of the molecular mechanisms governing the sclerenchymatous cell development in rice. We analyzed and compared the protein motifs, expression patterns, transgenic plant phenotypes and related genes expression of four rice AGO1s, and our results showed that OsAGO1b is the main regulator in rice organ development among four rice AGO1s.
Availability of Data and Materials
All data supporting the conclusions of this article are provided with the article and its supplementary information files.
- 4CL :
- ARF3/ETT :
AUXIN RESPONSE FACTOR 3/ETTIN
- C4H :
cauliflower mosaic virus
- CP :
hexadecy ltrimethyl ammonium bromide
- DCL1 :
- HD-ZIP III/OSHB :
Class III homeodomain-leucine zipper
- HEN1 :
HUA ENHANCER 1
- Hyg :
- HYL1 :
HYPONASTIC LEAVES 1
- KAN :
Leaf erect index
Leaf greatest width of flat state
Leaf length of natural state
Leaf greatest width of natural state
Leaf rolling index
Leaf length of straighten state
- MEL1 :
MEIOSIS ARRESTED AT LEPTOTENE1
- NOS :
- OE-AGO1 :
Polyacrylamide gel electrophoresis
Programmed cell death
Phased small interfering RNA
- PHB :
- PHV :
- PI :
- PNH/ZLL :
pBluescript II SK (+)
Quantitative reverse transcription-PCR
- REV :
RNA-induced silencing complex
Shoot apical meristem
Sodium dodecyl sulfate
- SHL4 :
- SHO2 :
- SLL1 :
- SRL1 :
- SRL2 :
Semi-Rolled Leaf 2
Trans-acting small interference RNA
Teosinte branched1/Cincinnata/proliferating cell factor
- TED2 :
tracheary element dehydrogenase 2
- Ubi :
- YFP :
Yellow florescence protein
Abe M, Yoshikawa T, Nosaka M, Sakakibara H, Sato Y, Nagato Y, Itoh J (2010) WAVY LEAF1, an ortholog of Arabidopsis HEN1, regulates shoot development by maintaining microRNA and trans-acting small interfering RNA accumulation in rice. Plant Physiol 154:1335–1346
Baucher M, Halpin C, Petit-Conil M, Boerjan W (2003) Lignin: genetic engineering and impact on pulping. Crit Rev Biochem Mol Biol 38:305–350
Baulcombe D (2004) RNA silencing in plants. Nature 431:356–363
Bohmert K, Camus I, Bellini C, Bouchez D, Caboche M, Benning C (1998) AGO1 defines a novel locus of Arabidopsis controlling leaf development. EMBO J 17:170–180
Bologna NG, Iselin R, Abriata LA, Sarazin A, Pumplin N, Jay F, Grentzinger T, Dal Peraro M, Voinnet O (2018) Nucleo-cytosolic shuttling of ARGONAUTE1 prompts a revised model of the plant microRNA pathway. Mol Cell 69:709–719
Bou-Torrent J, Salla-Martret M, Brandt R, Musielak T, Palauqui JC, Martínez-García JF, Wenkel S (2012) ATHB4 and HAT3, two class II HD-ZIP transcription factors, control leaf development in Arabidopsis. Plant Signal Behav 7:1382–1387
Bowman JL (2004) Class III HD-zip gene regulation, the golden fleece of ARGONAUTE activity? Bioessays 26:938–942
Bowman JL, Eshed Y, Baum SF (2002) Establishment of polarity in angiosperm lateral organs. Trends Genet 18:134–141
Braybrook SA, Kuhlemeier C (2010) How a plant builds leaves. Plant Cell 22:1006–1018
Byrne ME (2006) Shoot meristem function and leaf polarity: the role of class III HD-ZIP genes. PLoS Genet 2:e89
Chen J, Yu J, Ge L, Wang H, Berbel A, Liu Y, Chen Y, Li G, Tadege M, Wen J, Cosson V, Mysore KS, Ratet P, Madueño F, Bai G, Chen R (2010) Control of dissected leaf morphology by a Cys (2)his(2) zinc finger transcription factor in the model legume Medicago truncatula. Proc Natl Acad Sci U S A 107:10754–10759
Chen Q, Xie Q, Gao J, Wang W, Sun B, Liu B, Zhu H, Peng H, Zhao H, Liu C, Wang J, Zhang J, Zhang G, Zhang Z (2015) Characterization of rolled and erect leaf 1 in regulating leave morphology in rice. J Exp Bot 66:6047–6058
Douglas RN, Wiley D, Sarkar A, Springer N, Timmermans MC, Scanlon MJ (2010) ragged seedling2 encodes an ARGONAUTE7-like protein required for mediolateral expansion, but not dorsiventrality of maize leaves. Plant Cell 22:1441–1451
Du P, Wu J, Zhang J, Zhao S, Zheng H, Gao G, Wei L, Li Y (2011) Viral infection induces expression of novel phased microRNAs from conserved cellular microRNA precursors. PLoS Pathog 7:e1002176
Fagard M, Boutet S, Morel JB, Bellini C, Vaucheret H (2000) AGO1, QDE-2, and RDE-1 are related proteins required for post-transcriptional gene silencing in plants, quelling in fungi, and RNA interference in animals. Proc Natl Acad Sci U S A 97:11650–11654
Fahlgren N, Montgomery TA, Howell MD, Allen E, Dvorak SK, Alexander AL, Carrington JC (2006) Regulation of AUXIN RESPONSE FACTOR3 by TAS3 ta-siRNA affects developmental timing and patterning in Arabidopsis. Curr Biol 16:939–944
Fang X, Qi Y (2016) RNAi in plants: an Argonaute-centered view. Plant Cell 28:272–285
Felsenstein J (1985) Confidence limits on phylogenies: an approach using the bootstrap. Evolution 39:783–791
Fukuda H (2000) Programmed cell death of tracheary elements as a paradigm in plants. Plant Mol Biol 44:245–253
Garcia D, Collier SA, Byrne ME, Martienssen RA (2006) Specification of leaf polarity in Arabidopsis via the trans-acting siRNA pathway. Curr Biol 16:933–938
Hiei Y, Ohta S, Komari T, Kumashiro T (1994) Efficient transformation of rice (Oryza sativa L.) mediated by Agrobacterium and sequence analysis of the boundaries of the T-DNA. Plant J 6:271–282
Horton P (2000) Prospects for crop improvement through the genetic manipulation of photosynthesis: morphological and biochemical aspects of light capture. J Exp Bot 51:475–485
Hu J, Zhu L, Zeng D, Gao Z, Guo L, Fang Y, Zhang G, Dong G, Yan M, Liu J, Qian Q (2010) Identification and characterization of NARROW AND ROLLED LEAF 1, a novel gene regulating leaf morphology and plant architecture in rice. Plant Mol Biol 73:283–292
Hu X, Liu Y-G (2006) The construction of RNAi vectors and the use for gene silencing in rice. Mol Plant Breeding 4:621–626 (in Chinese)
Hunter C, Willmann MR, Wu G, Yoshikawa M, de la Luz Gutierrez-Nava M, Poethig SR (2006) Trans-acting siRNA-mediated repression of ETTIN and ARF4 regulates heteroblasty in Arabidopsis. Development 133:2973–2981
Husbands AY, Benkovics AH, Nogueira FT, Lodha M, Timmermans MC (2015) The ASYMMETRIC LEAVES complex employs multiple modes of regulation to affect adaxial-abaxial patterning and leaf complexity. Plant Cell 27:3321–3335
Hutvagner G, Simard MJ (2008) Argonaute proteins: key players in RNA silencing. Nat Rev Mol Cell Bio 9:22–32
Itoh J, Hibara K, Sato Y, Nagato Y (2008a) Developmental role and auxin responsiveness of class III homeodomain leucine zipper gene family members in rice. Plant Physiol 147:1960–1975
Itoh J, Sato Y, Nagato Y (2008b) The SHOOT ORGANIZATION2 gene coordinates leaf domain development along the central-marginal axis in rice. Plant Cell Physiol 49:1226–1236
Ji L, Liu X, Yan J, Wang W, Yumul RE, Kim YJ, Dinh TT, Liu J, Cui X, Zheng B, Agarwal M, Liu C, Cao X, Tang G, Chen X (2011) ARGONAUTE10 and ARGONAUTE1 regulate the termination of floral stem cells through two microRNA in Arabidopsis. PLoS Genet 7:e1001358
Juarez MT, Twigg RW, Timmermans MC (2004) Specification of adaxial cell fate during maize leaf development. Development 131:4533–4544
Kapoor M, Arora R, Lama T, Nijhawan A, Khurana JP, Tyagi AK, Kapoor S (2008) Genome-wide identification, organization and phylogenetic analysis of dicer-like, Argonaute and RNA-dependent RNA polymerase gene families and their expression analysis during reproductive development and stress in rice. BMC Genomics 9:451
Kerstetter RA, Bollman K, Taylor RA, Bomblies K, Poethig RS (2001) KANADI regulates organ polarity in Arabidopsis. Nature 411:706–709
Kidner CA (2010) The many roles of small RNAs in leaf development. J Genet Genomics 37:13–21
Kidner CA, Martienssen RA (2004) Spatially restricted microRNA directs leaf polarity through ARGONAUTE1. Nature 428:81–84
Kidner CA, Timmermans MC (2007) Mixing and matching pathways in leaf polarity. Curr Opin Plant Biol 10:13–20
Komiya R, Ohyanagi H, Niihama M, Watanabe T, Nakano M, Kurata N, Nonomura K (2014) Rice germline-specific Argonaute MEL1 protein binds to phasiRNAs generated from more than 700 lincRNAs. Plant J 78:385–397
Kumar S, Stecher G, Tamura K (2016) MEGA7: molecular evolutionary genetics analysis version 7.0 for bigger datasets. Mol Biol Evol 33:1870–1874
Li J, Jiang D, Zhou H, Li F, Yang J, Hong L, Fu X, Li Z, Liu Z, Li J, Zhuang C (2011) Expression of RNA interference/antisense transgenes by the cognate promoters of target genes is a better gene-silencing strategy to study gene functions in rice. PLoS One 6:e17444
Li M, Xiong G, Li R, Cui J, Tang D, Zhang B, Pauly M, Cheng Z, Zhou Y (2009) Rice cellulose synthase-like D4 is essential for normal cell-wall biosynthesis and plant growth. Plant J 60:1055–1069
Li YY, Shen A, Xiong W, Sun QL, Luo Q, Song T, Li ZL, Luan WJ (2016) Overexpression of OsHox32 results in pleiotropic effects on plant type architecture and leaf development in rice. Rice 9:46
Liang J, Guo S, Sun B, Liu Q, Chen X, Peng H, Zhang Z, Xie Q (2018) Constitutive expression of REL1 confers the rice response to drought stress and abscisic acid. Rice (N Y) 11:59
Liu B, Chen Z, Song X, Liu C, Cui X, Zhao X, Fang J, Xu W, Zhang H, Wang X, Chu C, Deng X, Xue Y, Cao X (2007a) Oryza sativa dicer-like4 reveals a key role for small interfering RNA silencing in plant development. Plant Cell 19:2705–2718
Liu B, Li P, Li X, Liu C, Cao S, Chu C (2005) Loss of function of OsDCL1 affects microRNA accumulation and causes developmental defects in rice. Plant Physiol 139:296–305
Liu C, Xin Y, Xu L, Cai Z, Xue Y, Liu Y, Xie D, Liu Y, Qi Y (2018) Arabidopsis ARGONAUTE1 binds chromatin to promote gene transcription in response to hormones and stresses. Dev Cell 44:348–361
Liu H, Nonomura KI (2016) A wide reprogramming of histone H3 modifications during male meiosis I in rice is dependent on the Argonaute protein MEL1. J Cell Sci 129:3553–3561
Liu H, Xu Y, Xu Z, Chong K (2007b) A rice YABBY gene, OsYABBY4, preferentially expresses in developing vascular tissue. Dev Genes Evol 217:629–637
Liu Q, Yao X, Pi L, Wang H, Cui X, Huang H (2010) The ARGONAUTE10 gene modulates shoot apical meristem maintenance and establishment of leaf polarity by repressing miR165/166 in Arabidopsis. Plant J 58:27–40
Liu X, Li M, Liu K, Tang D, Sun M, Li Y, Shen Y, Du G, Cheng Z (2016) Semi-Rolled Leaf2 modulates rice leaf rolling by regulating abaxial side cell differentiation. J Exp Bot 67:2139–2150
Livak KJ, Schmittgen TD (2001) Analysis of relative gene expression data using real-time quantitative PCR and the 2−ΔΔC T method. Methods 25:402–408
Lynn K, Fernandez A, Aida M, Sedbrook J, Tasaka M, Masson P, Barton MK (1999) The PINHEAD/ZWILLE gene acts pleiotropically in Arabidopsis development and has overlapping functions with the ARGONAUTE1 gene. Development 126:469–481
Mallory A, Hinze A, Tucker MR, Bouché N, Gasciolli V, Elmayan T, Lauressergues D, Jauvion V, Vaucheret H, Laux T (2009) Redundant and specific roles of the ARGONAUTE proteins AGO1 and ZLL in development and small RNA-directed gene silencing. PLoS Genet 5:e1000646
Mallory A, Vaucheret H (2010) Form, function, and regulation of ARGONAUTE proteins. Plant Cell 22:3879–3889
McConnell JR, Barton MK (1998) Leaf polarity and meristem formation in Arabidopsis. Development 125:2935–2942
McConnell JR, Emery J, Eshed Y, Bao N, Bowman J, Barton MK (2001) Role of PHABULOSA and PHAVOLUTA in determining radial patterning in shoots. Nature 411:709–713
Mecchia MA, Debernardi JM, Rodriguez RE, Schommer C, Palatnik JF (2013) MicroRNA miR396 and RDR6 synergistically regulate leaf development. Mech Dev 130:2–13
Merelo P, Ram H, Pia Caggiano M, Ohno C, Ott F, Straub D, Graeff M, Cho SK, Yang SW, Wenkel S, Heisler MG (2016) Regulation of MIR165/166 by class II and class III homeodomain leucine zipper proteins establishes leaf polarity. Proc Natl Acad Sci U S A 113:11973–11978
Moon J, Hake S (2011) How a leaf gets its shape. Curr Opin Plant Biol 14:24–30
Moussian B, Schoof H, Haecker A, Jürgens G, Laux T (1998) Role of the ZWILLE gene in the regulation of central shoot meristem cell fate during Arabidopsis embryogenesis. EMBO J 17:1799–1809
Nagasaki H, Itoh J, Hayashi K, Hibara K, Satoh-Nagasawa N, Nosaka M, MukouhataM AM, Kitano H, Matsuoka M, Nagato Y, Sato Y (2007) The small interfering RNA production pathway is required for shoot meristem initiation in rice. Proc Natl Acad Sci U S A 104:14867–14871
Nishimura A, Ito M, Kamiya N, Sato Y, Matsuoka M (2002) OsPNH1 regulates leaf development and maintenance of the shoot apical meristem in rice. Plant J 30:189–201
Nonomura K, Morohoshi A, Nakano M, Eiguchi M, Miyao A, Hirochika H (2007) A germ cell specific gene of the ARGONAUTE family is essential for the progression of premeiotic mitosis and meiosis during sporogenesis in rice. Plant Cell 19:2583–2594
Otsuga D, DeGuzman B, Prigge MJ, Drews GN, Clark SE (2008) REVOLUTA regulates meristem initiation at lateral positions. Plant J 25:223–236
Prigge MJ, Otsuga D, Alonso JM, Ecker JR, Drews GN, Clark SE (2005) Class III homeodomain-leucine zipper gene family members have overlapping, antagonistic, and distinct roles in Arabidopsis development. Plant Cell 17:61–76
Pulido A, Laufs P (2010) Co-ordination of developmental processes by small RNAs during leaf development. J Exp Bot 61:1277–1291
Ramachandran P, Carlsbecker A, Etchells JP (2017) Class III HD-ZIPs govern vascular cell fate: an HD view on patterning and differentiation. J Exp Bot 68:55–69
Reinhart BJ, Weinstein EG, Rhoades MW, Bartel B, Bartel DP (2002) MicroRNAs in plants. Genes Dev 16:1616–1626
Rivas FV, Tolia NH, Song JJ, Aragon JP, Liu J, Hannon GJ, Joshua-Tor L (2005) Purified Argonaute2 and an siRNA form recombinant human RISC. Nat Struct Mol Biol 12:340–349
Roccaro M, Somssich IE (2011) Chromatin immunoprecipitation to identify global targets of WRKY transcription factor family members involved in plant immunity. Methods Mol Biol 712:45–58
Saitou N, Nei M (1987) The neighbor-joining method: a new method for reconstructing phylogenetic trees. Mol Biol Evol 4:406–425
Sakamoto T, Morinaka Y, Ohnishi T, Sunohara H, Fujioka S, Ueguchi-Tanaka M, Mizutani M, Sakata K, Takatsuto S, Yoshida S, Tanaka H, Kitano H, Matsuoka M (2006) Erect leaves caused by brassinosteroid deficiency increase biomass production and grain yield in rice. Nat Biotechnol 24:105–109
Sato Y, Nishimura A, Ito M, Ashikari M, Hirano HY, Matsuoka M (2001) Auxin response factor family in rice. Genes Genet Syst 76:373–380
Schommer C, Palatnik JF, Aggarwal P, Chételat A, Cubas P, Farmer EE, Nath U, Weigel D (2008) Control of jasmonate biosynthesis and senescence by miR319 targets. PLoS Biol 6:e230
Shen J, Xie K, Xiong L (2010) Global expression profiling of rice microRNAs by one-tube stem-loop reverse transcription quantitative PCR revealed important roles of microRNAs in abiotic stress responses. Mol Gen Genomics 284:477–488
Shi Z, Wang J, Wan X, Shen G, Wang X, Zhang J (2007) Over-expression of rice OsAGO7 gene induces upward curling of the leaf blade that enhanced erect-leaf habit. Planta 226:99–108
Siegfried KR, Eshed Y, Baum SF, Otsuga D, Drews GN, Bowman JL (1999) Members of the YABBY gene family specify abaxial cell fate in Arabidopsis. Development 126:4117–4128
Sinclair TR, Sheehy JE (1999) Erect leaves and photosynthesis in rice. Science 283:1455–1455
Thompson JD, Higgins DG, Gibson TJ (1994) Clustal W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. Nucleic Acids Res 22:4673–4680
Toriba T, Harada K, Takamura A, Nakamura H, Ichikawa H, Suzaki T, Hirano HY (2007) Molecular characterization the YABBY gene family in Oryza sativa and expression analysis of OsYABBY1. Mol Gen Genomics 277:457–468
Toriba T, Suzaki T, Yamaguchi T, Ohmori Y, Tsukaya H, Hirano HY (2010) Distinct regulation of adaxial-abaxial polarity in anther patterning in rice. Plant Cell 22:1452–1462
Turchi L, Carabelli M, Ruzza V, Possenti M, Sassi M, Peñalosa A, Sessa G, Salvi S, Forte V, Morelli G, Ruberti I (2013) Arabidopsis HD-zip II transcription factors control apical embryo development and meristem function. Development 140:2118–2129
Vaucheret H, Vazquez F, Crete P, Bartel DP (2004) The action of ARGONAUTE1 in the miRNA pathway and its regulation by the miRNA pathway are crucial for plant development. Genes Dev 18:1187–1197
Wang D, Pei K, Fu Y, Sun Z, Li S, Liu H, Tang K, Han B, Tao Y (2007) Genome-wide analysis of the auxin response factors (ARF) gene family in rice (Oryza sativa). Gene 394:13–24
Wang L, Gu X, Xu D, Wang W, Wang H, Zeng M, Chang Z, Huang H, Cui X (2011a) miR396-targeted AtGRF transcription factors are required for coordination of cell division and differentiation during leaf development in Arabidopsis. J Exp Bot 62:761–773
Wang ST, Sun XL, Hoshino Y, Yu Y, Jia B, Sun ZW, Sun MZ, Duan XB, Zhu YM (2014) MicroRNA319 positively regulates cold tolerance by targeting OsPCF6 and OsTCP21 in rice (Oryza sativa L.). PLoS One 9:e91357
Wang W, Ye R, Xin Y, Fang X, Li C, Shi H, Zhou X, Qi Y (2011b) An importin β protein negatively regulates microRNA activity in Arabidopsis. Plant Cell 23:3565–3576
Willemse MTM, Den Outer RW (1988) Stem anatomy and cell wall autofluorescence during growth of three maize (Zea mays L.) cultivars. Plant Biol 37:39–47
Williams L, Carles CC, Osmont KS, Fletcher JC (2005a) A database analysis method identifies an endogenous trans-acting short-interfering RNA that targets the Arabidopsis ARF2, ARF3, and ARF4 genes. Proc Natl Acad Sci U S A 102:9703–9708
Williams L, Grigg SP, Xie M, Christensen S, Fletcher JC (2005b) Regulation of Arabidopsis shoot apical meristem and lateral organ formation by microRNA miR166g and its AtHD-ZIP target genes. Development 132:3657–3668
Wu J, Yang R, Yang Z, Yao S, Zhao S, Wang Y, Li P, Song X, Jin L, Zhou T, Lan Y, Xie L, Zhou X, Chu C, Qi Y, Cao X, Li Y (2017) ROS accumulation and antiviral defence control by microRNA528 in rice. Nat Plants 3:16203
Wu J, Yang Z, Wang Y, Zheng L, Ye R, Ji Y, Zhao S, Ji S, Liu R, Xu L, Zheng H, Zhou Y, Zhang X, Cao X, Xie L, Wu Z, Qi Y, Li Y (2015) Viral-inducible Argonaute18 confers broad-spectrum virus resistance in rice by sequestering a host microRNA. ELife 4:e05733
Wu L, Zhang Q, Zhou H, Ni F, Wu X, Qi Y (2009) Rice microRNA effector complexes and targets. Plant Cell 21:3421–3435
Xia R, Xu J, Meyers BC (2017) The emergence, evolution, and diversification of the miR390-TAS3-ARF pathway in land plants. Plant Cell 29:1232–1247
Xiang J, Zhang G, Qian Q, Xue H (2012) SEMI-ROLLED LEAF1 encodes a putative glycosylphosphatidylinositol-anchored protein and modulates rice leaf rolling by regulating the formation of bulliform cells. Plant Physiol 159:1488–1500
Yamaguchi T, Nagasawa N, Kawasaki S, Matsuoka M, Nagato Y, Hirano HY (2004) The YABBY gene DROOPING LEAF regulates carpel specification and midrib development in Oryza sativa. Plant Cell 16:500–509
Yamaguchi T, Nukazuka A, Tsukaya H (2012) Leaf adaxial-abaxial polarity specification and lamina outgrowth: evolution and development. Plant Cell Physiol 53:1180–1194
Yang C, Li D, Liu X, Ji C, Hao L, Zhao X, Li X, Chen C, Cheng Z, Zhu L (2014b) OsMYB103L, an R2R3-MYB transcription factor, influences leaf rolling and mechanical strength in rice (Oryza sativa L.). BMC Plant Biol 14:158
Yang C, Li D, Mao D, Liu X, Ji C, Li X, Zhao X, Cheng Z, Chen C, Zhu L (2013) Overexpression of microRNA319 impacts leaf morphogenesis and leads to enhanced cold tolerance in rice (Oryza sativa L.). Plant Cell Environ 36:2207–2218
Yang JW, Fu JX, Li J, Cheng XL, Li F, Dong JF, Liu ZL, Zhuang CX (2014a) A novel co-immunoprecipitation protocol based on protoplast transient gene expression for studying protein-protein interactions in rice. Plant Mol Biol Rep 32:153–161
Yang L, Huang W, Wang H, Cai R, Xu Y, Huang H (2006) Characterizations of a hypomorphic argonaute1 mutant reveal novel AGO1 functions in Arabidopsis lateral organ development. Plant Mol Biol 61:63–78
Yang SQ, Li WQ, Miao H, Gan PF, Qiao L, Chang YL, Shi CH, Chen KM (2016) REL2, a gene encoding an unknown function protein which contains DUF630 and DUF632 domains controls leaf rolling in rice. Rice 9:37
Yang T, Wang Y, Teotia S, Zhang Z, Tang G (2018) The making of leaves: how small RNA networks modulate leaf development. Front Plant Sci 9:824
Ye R, Wang W, Iki T, Liu C, Wu Y, Ishikawa M, Zhou X, Qi Y (2012) Cytoplasmic assembly and selective nuclear import of Arabidopsis ARGONAUTE4/siRNA complexes. Mol Cell 46:859–870
Ye Y, Liu B, Zhao M, Wu K, Cheng W, Chen X, Liu Q, Liu Z, Fu X, Wu Y (2015) CEF1/OsMYB103L is involved in GA-mediated regulation of secondary wall biosynthesis in rice. Plant Mol Biol 89:385–401
Yuan LP (1997) Hybrid rice breeding for super high yield. Hybrid Rice 12:1–6
Zhang DB, Wilson ZA (2009) Stamen specification and anther development in rice. Chin Sci Bull 54:2342–2353
Zhang G, Xu Q, Zhu X, Qian Q, Xue H (2009) SHALLOT-LIKE1 is a KANADI transcription factor that modulates rice leaf rolling by regulating leaf abaxial cell development. Plant Cell 21:719–735
Zhang J, Zhang H, Srivastava AK, Pan Y, Bai J, Fang J, Shi H, Zhu JK (2018) Knockdown of rice microRNA166 confers drought resistance by causing leaf rolling and altering stem xylem development. Plant Physiol 176:2082–2094
Zhao S, Zhao L, Liu F, Wu Y, Zhu Z, Sun C, Tan L (2016) NARROW AND ROLLED LEAF 2 regulates leaf shape, male fertility, and seed size in rice. J Integr Plant Biol 58:983–996
Zheng S, Li J, Ma L, Wang H, Zhou H, Ni E, Jiang D, Liu Z, Zhuang C (2019) OsAGO2 controls ROS production and the initiation of tapetal PCD by epigenetically regulating OsHXK1 expression in rice anthers. Proc Natl Acad Sci U S A 116:7549–7558
Zhong R, Ye Z (2007) Regulation of cell wall biosynthesis. Curr Opin Plant Biol 10:564–572
Zhou C, Han L, Fu C, Wen J, Cheng X, Nakashima J, Ma J, Tang Y, Tan Y, Tadege M, Mysore KS, Xia G, Wang ZY (2013) The trans-acting short interfering RNA3 pathway and NO APICAL MERISTEM antagonistically regulate leaf margin development and lateral organ separation, as revealed by analysis of an argonaute7/lobed leaflet1 mutant in Medicago truncatula. Plant Cell 25:4845–4862
Zhou H, Zhou M, Yang Y, Li J, Zhu L, Jiang D, Dong J, Liu Q, Gu L, Zhou L, Feng M, Qin P, Hu X, Song C, Shi J, Song X, Ni E, Wu X, Deng Q, Liu Z, Chen M, Liu YG, Cao X, Zhuang C (2014) RNase ZS1 processes Ub L40 mRNAs and controls thermosensitive genic male sterility in rice. Nat Commun 5:4884
Zhou Y, Honda M, Zhu H, Zhang Z, Guo X, Li T, Li Z, Peng X, Nakajima K, Duan L, Zhang X (2015) Spatiotemporal sequestration of mir165/166 by Arabidopsis Argonaute10 promotes shoot apical meristem maintenance. Cell Rep 10:1819–1827
Zhu H, Hu F, Wang R, Zhou X, Sze SH, Liou LW, Barefoot A, Dickman M, Zhang X (2011) Arabidopsis Argonaute10 specifically sequesters miR166/165 to regulate shoot apical meristem development. Cell 145:242–256
Zou LP, Sun XH, Zhang ZG, Liu P, Wu JX, Tian CJ, Qiu JL, Lu TG (2011) Leaf rolling controlled by the homeodomain leucine zipper class IV gene Roc5 in rice. Plant Physiol 156:1589–1602
We thank Dr. Yao-Guang Liu at South China Agricultural University for providing rice transformation vectors pRNAi-Ubi and pOx. We thank Dr. Xiuyun Lin at Rice Research Institute, Jilin Academy of Agricultural Sciences for providing the japonica rice variety Songgeng seeds.
This work was supported by the grants from the National Key Research and Development Program of China (grant number 2016YFD0100400), Genetically Modified Organisms Breeding Major Project of China (grant number 2016ZX08001–004–001-003), Guangzhou Science and Technology Program of China (grant number 201504010004), and the National Science Foundation of China (grant number 30800596).
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Table S1. Primers used in this study. (DOCX 27 kb)
Table S2. Information of the construction of overexpression and RNAi vectors for rice four AGO1 genes. (DOCX 15 kb)
Table S3. Information of plant AGO1 proteins used for phylogenetic analysis. (DOCX 12 kb)
Figure S1. Characterization of T0 transgenic plants of the OE-AGO1b lines. (A) Regenerated seedlings for the control empty vector pCAMBIA1380 (left) and OsAGO1b-overexpression construct (right). Scale bar = 1 cm. (B) Detection of T-DNA insertion numbers of OsAGO1b-overexpression lines using Southern blot analysis. Transgenic lines 25, 40, 365 containing a single copy T-DNA were chosen for further study. OE-AGO1b, OsAGO1b-overexpression line. (TIF 5135 kb)
Figure S2. Young leaf development of the OE-AGO1b line and ZH11. (A-D) indicates 7-day-old, 14-day-old, 21-day-old, and 28-day-old seedlings after germination. Scale bars = 2 cm for (A) and (B). Scale bars = 10 cm for (C) and (D). The OsAGO1b-overexpression line displayed adaxially rolled leaves from the fourth leaf stage. OE-AGO1b, OsAGO1b-overexpression line; ZH11, wild type Zhonghua 11. (TIF 9073 kb)
Figure S3. Agronomic traits of ZH11 and OE-AGO1b lines. (A-F) Tiller number, inflorescence branch number, plant height, inflorescence length, grain number per panicle, and seed setting percentage of ZH11 (WT) and OE-AGO1b (line 25, line 40, line 365), respectively. Results are shown as the mean ± SD in (A)-(F) (n = 10). ** P < 0.01 (one-way ANOVA). OE-AGO1b, OsAGO1b-overexpression line; ZH11, wild type Zhonghua 11. (TIF 1467 kb)
Figure S4. Phenotypes of OE-AGO1b lines for different rice varieties. (A-D) Wild type and OE-AGO1b plants at the booting stage or heading stage for Nipponbare, Songgeng, Huanghuazhan and Annong. All the plants were geminated and planted at the same time under the same conditions. Scale bars = 15 cm. (E-H) Relative expression of OsAGO1b in OE-AGO1b plants of Nipponbare (Nip), Songgeng (Sg), Huanghuazhan (HHZ) and Annong (AN) backgrounds. Flag leaves at the booting stage were used for RNA extraction and qRT-PCR analysis. Means ± SD are presented in (E-H) (n = 3). * P < 0.05, ** P < 0.01 (one-way ANOVA). OE-AGO1b, OsAGO1b-overexpression; WT, wild type. (TIF 8027 kb)
Figure S5. Amino acid sequences of the PAZ and Piwi domains of OsAGO1s and AtAGO1. Alignment of amino acid sequences of the PAZ domain (A) the Piwi domains (B) of OsAGO1s and AtAGO1. “*” indicated the polymorphic amino acid residues specific to OsAGO1b. (TIF 3570 kb)
Figure S6. Phenotypes of four rice AGO1-overexpression and RNAi transgenic plants. (A, C, E, G) Morphologies of lines overexpressing OsAGO1a, OsAGO1b, OsAGO1c and OsAGO1d at the mature stage. (B, D, F, H) Morphologies of RNAi lines for OsAGO1a, OsAGO1b, OsAGO1c and OsAGO1d at the mature stage. Scale bars = 15 cm. WT, wild type Zhonghua 11; OE, overexpression. (TIF 23721 kb)
Figure S7. Phenotypes and agronomic traits of ZH11 and OsAGO1b RNAi lines. (A) Phenotypes of 30-day-old seedlings of ZH11 and OsAGO1b RNAi lines, scale bar = 10 cm. (B) The leaves of 30-day-old seedlings of ZH11 and OsAGO1b RNAi lines, scale bar = 3 cm. (C and D) Plant heights and seed setting rates of ZH11 (WT) and OsAGO1b RNAi lines. Results are shown as the mean ± SD in (C)-(D) (n = 10). * P < 0.05, ** P < 0.01 (one-way ANOVA). (TIF 5956 kb)
Figure S8. Phenotypes of spikelets and anthers of ZH11 and OsAGO1b RNAi lines. (A) The panicles of ripeness stage, scale bar = 4 cm. (B) Dissection of mature spikelets, the white arrows indicated the curly anthers, scale bar = 1 mm. (C) I2-KI staining of pollens. (D) Phenotypes of anthers, the white arrows indicated the aberrant anther sacs, scale bar = 0.5 mm. (TIF 14943 kb)
Figure S9. Relative expression of OSHB and OsARF genes in WT and OsAGO1b RNAi lines. The fourth leaves of 30-day-old seedlings from wild-type Zhonghua 11 (WT) and OsAGO1b RNAi line 56 and line 63 were used. The expression level of each gene was normalized to 1 in WT. OsActin1 (XM_015774830) was used as an internal standard to normalize the expression levels of detected genes. Error bars represent standard deviations among replicates (n = 3). * P < 0.05, ** P < 0.01 (one-way ANOVA). (TIF 1542 kb)
Figure S10. The phenotypes of OsAGO1a, OsAGO1c and OsAGO1d overexpression lines and their expression levels of OSHBs. (A-C) Phenotypes of 30-day-old seedlings of ZH11 and OsAGO1a, OsAGO1c and OsAGO1d overexpression lines, scale bars = 10 cm. (D) Relative expression of OSHBs. The fourth leaves of 30-day-old seedlings from wild-type Zhonghua 11 (ZH11) and each transgenic line were used for RNA extration. The expression level of each gene was normalized to 1 in WT. OsActin1 (XM_015774830) was used as an internal standard to normalize the expression levels of detected genes. OE-AGO1 indicated AGO1 overexprssion lines. Error bars represent standard deviations among replicates (n = 3). * P < 0.05 (one-way ANOVA). (TIF 7387 kb)
Figure S11. In situ hybridization of OSHB3 and OsARF4 in the vegetative shoot apex of ZH11 and OE-AGO1b-365 (longitudinal sections). (A and C) In situ hybridization of OSHB3 and OsARF4 in ZH11 using sense probe. (B and D) In situ hybridization of OSHB3 and OsARF4 in OE-AGO1b-365 using anti-sense probe. Shoot base cuttings about 1 cm in length including SAM of 14-day-old seedlings were used. Scale bars = 50 μm. (TIF 12330 kb)
Figure S12. In situ hybridization of OSHB3 and OsARF4 in the vegetative shoot apex of ZH11 and OE-AGO1b-365 (cross sections). (A and C) In situ hybridization of OSHB3 and OsARF4 in ZH11 using sense probe. (B and D) In situ hybridization of OSHB3 and OsARF4 in OE-AGO1b-365 using anti-sense probe. Shoot base cuttings about 1 cm in length including SAM of 14-day-old seedlings were used. Black arrows indicate the developing vasculars. Scale bars = 50 μm. (TIF 16952 kb)