OsWRKY80-OsWRKY4 Module as a Positive Regulatory Circuit in Rice Resistance Against Rhizoctonia solani
© The Author(s). 2016
Received: 4 October 2016
Accepted: 19 November 2016
Published: 25 November 2016
Plant WRKY transcription factors play pivotal roles in diverse biological processes but most notably in plant defense response to pathogens. Sheath blight represents one of the predominant diseases in rice. However, our knowledge about the functions of WRKY proteins in rice defense against sheath blight is rather limited.
Here we demonstrate that the expression of Oryza sativa WRKY80 gene (OsWRKY80) is rapidly and strongly induced upon infection of Rhizoctonia solani, the causal agent of rice sheath blight disease. OsWRKY80 expression is also induced by exogenous jasmonic acid (JA) and ethylene (ET), but not by salicylic acid (SA). OsWRKY80-GFP is localized in the nuclei of onion epidermal cells in a transient expression assay. Consistently, OsWRKY80 exhibits transcriptional activation activity in a GAL4 assay in yeast cells. Overexpression of OsWRKY80 in rice plants significantly enhanced disease resistance to R. solani, concomitant with elevated expression of OsWRKY4, another positive regulator in rice defense against R. solani. Suppression of OsWRKY80 by RNA interference (RNAi), on the other hand, compromised disease resistance to R. solani. Results of yeast one-hybrid assay and transient expression assay in tobacco cells have revealed that OsWRKY80 specifically binds to the promoter regions of OsWRKY4, which contain W-box (TTGAC[C/T]) or W-box like (TGAC[C/T]) cis-elements.
We propose that OsWRKY80 functions upstream of OsWRKY4 as an important positive regulatory circuit that is implicated in rice defense response to sheath blight pathogen R. solani.
In the natural environment, plants are frequently confronted with diverse biotic and abiotic stresses that detrimentally affect their growth and development. Among them, pathogen attack is one of the most limiting factors of crop productivity and quality, and consequently poses a serious threat to agricultural industry worldwide. To ensure survival, plants have evolved intricate and robust mechanisms to respond to pathogen invasion through their innate immune system. Plant innate immune system is comprised of two interconnected branches. The first branch is pathogen-associated molecular pattern (PAMP)-triggered immunity (PTI), initiated by the recognition of molecular signatures of certain pathogens (e.g., bacterial flagellin and fungal chitin oligosaccharide). PTI often activates downstream mitogen-activated protein kinase (MPK) cascades and defense response genes. The second branch is effector-triggered immunity (ETI), which is a more accelerated defense response than PTI and is triggered by host-resistance (R) protein-mediated recognition of pathogen effectors (Jones and Dangl 2006). PTI- and ETI-mediated defense responses in plants are modulated mainly by three signaling hormone molecules, salicylic acid (SA), jasmonic acid (JA), and ethylene (ET) (Tsuda et al. 2009). There are both synergistic and antagonistic interactions between SA and JA/ET signaling pathways during plant immune progression (Kunkel and Brooks 2002; Mur et al. 2006). This apparent discrepancy reflects the complexity of plant defense mechanisms (Kim et al. 2006). Moreover, the expression of downstream defense-related genes is crucial for the establishment of plant immune responses. The interaction between plants and pathogens eventually leads to extensive transcriptional reprogramming of plant defense-responsive genes (Eulgem 2005), indicating that transcription factors play a pivotal role in plant disease resistance.
The transcription factor families involved in plant defense responses include TGA family of basic domain-leucine zipper (bZIP), ethylene response factor (ERF), MYB, WRKY and Whirly family proteins (Eulgem 2005). WRKY proteins are one of the largest families of transcription factors in plants with 72-74 members in Arabidopsis (Ülker and Somssich 2004; Dong et al. 2003) and over 100 members in rice (Wu et al. 2005; Ross et al. 2007). The WRKY factors are characterized by their conserved DNA-binding WRKY domains consisting of a highly conserved WRKYGQK stretch in N-termini, and a zinc-finger motif (C-X4-5-C-X22-23-H-X1-H or C-X7-C-X23-H-X1-C) in C-termini (Eulgem et al. 2000). The WRKY domain generally binds to the W-box (C/T)TGAC(C/T) or W-box like cis-elements in the promoters of target genes (Eulgem et al. 2000; Maleck et al. 2000). According to the number of WRKY domains and the features of zinc-finger motifs, the WRKY protein family is categorized into three distinct groups (I, II and III). Group II is further divided into five subgroups (IIa to IIe) based on the presence of additional short conserved structural motifs outside of the WRKY domain (Eulgem et al. 2000).
Loss- and gain-of-function studies have revealed that WRKYs act in a complex signaling network as both positive and negative regulators of various biological processes, but most notably in biotic stress responses (Pandey and Somssich 2009). To date, at least 13 Oryza sativa WRKY (OsWRKY) genes are known to positively regulate rice resistance against pathogens, such as Magnaporthe oryzae, Rhizoctonia solani and Xanthomonas oryzae pv oryzae (Xoo) (Cheng et al. 2015; Wang et al. 2015; Choi et al. 2015; Hwang et al. 2016). For instance, OsWRKY13 activates SA-dependent defense response whereas suppresses JA-dependent response, in mediating rice defense response to bacterial blight and fungal blast pathogens (Qiu et al. 2007). OsWRKY45 positively regulates systemic acquired resistance (SAR) in an SA-dependent manner (Shimono et al. 2007; Shimono et al. 2012). More recently, it has been reported that OsWRKY51 functions as a positive transcriptional regulator in defense signaling against Xoo by direct binding to the promoter of defense related gene, OsPR10a (Hwang et al. 2016). By contrast, although the transcription of OsWRKY28, 62, and 76 is upregulated upon pathogen infection, their protein products act to repress plant defense response against rice fungal blast or bacterial blight pathogens (Peng et al. 2008; Delteil et al. 2012; Chujo et al. 2013; Yokotani et al. 2013). More intriguingly, OsWRKY45-1 derived from subspecies japonica acts as a negative regulator, whereas its allele OsWRKY45-2 derived from subspecies indica as a positive regulator in the interactions between rice and bacterial pathogens such as Xoo and X. oryzae pv oryzicola. Nevertheless, both OsWRKY45 alleles function as positive regulators in the defense against fungal pathogen M. oryzae (Tao et al. 2009). WRKYs often work in concert in plant defense response to pathogens. OsWRKY42 has been characterized as a negative regulator functioning downstream of OsWRKY13. OsWRKY42-OsWRKY13 together with OsWRKY45-2 form a WRKY transcriptional regulatory cascade in the rice- M. oryzae interaction (Cheng et al. 2015). The multiple roles of WRKYs suggest that the complex signaling and transcriptional networks of biotic stress responses require concerted regulation. Coordinated modulation of WRKY proteins as positive and negative regulators could also enable the proper amplitude and duration of plant response to minimize detrimental effects on plant growth and development during pathogen attack (Pandey and Somssich 2009).
Blast, caused by M. oryzae, bacterial blight, caused by Xoo, and sheath blight, caused by R. solani are considered to be three major diseases in rice. Among those characterized OsWRKY genes, at least 12 and 10 genes have been shown to function as either positive or negative regulators in rice resistance against M. oryzae and Xoo, respectively. However, only 2 OsWRKY genes (OsWRKY30 and OsWRKY4) have been shown to mediate the defense responses against R. solani (Peng et al. 2012; Wang et al. 2015). Additionally, rice sheath blight is a necrotrophic disease (Zhao et al. 2008). The strategies of resistance to necrotrophs are distinct from those against biotrophs, and likely involved in defense mechanisms mediated by JA/ET-dependent signaling routes (Bari and Jones 2009). To elucidate the regulatory roles of rice WRKY factors in defense response to the sheath blight fungus, we have analyzed the expression profiles of rice WRKY family under R. solani infection and methyl jasmonate (MeJA) treatment. We have identified several pathogen- and JA-inducible WRKY genes, including OsWRKY30 and OsWRKY4, which are positive regulators in rice resistance to R. solani (Peng et al. 2012; Wang et al. 2015). In this report, we investigate the expression pattern of OsWRKY80 gene in response to exogenous defense-related phytohormones JA, ET and SA and R. solani challenge. We have found that OsWRKY80 is a nuclear-localized transcriptional activator. Compared to wild-type plants, the OsWRKY80 overexpression rice plants are more resistant whereas knockdown (RNAi) lines are more susceptible to R. solani attack. In addition, we have found opposing expression pattern of OsWRKY4 in gain- and loss-of function OsWRKY80 plants, respectively. We have further demonstrated that OsWRKY80 specifically binds to the W-box, or W-box like cis-elements in the promoter of the OsWRKY4 gene. Our findings suggest that OsWRKY80 functions upstream of OsWRKY4 and together this module acts as a positive regulatory circuit in the rice defense response against sheath blight disease.
Cloning and Sequence Analysis of OsWRKY80 cDNA
Several nomenclature systems of rice WRKY genes were proposed in the past by independent research groups (Zhang et al. 2004; Wu et al. 2005; Zhang and Wang 2005). To avoid the conflicts and confusion, the rice WRKY-working group has redefined the WRKY gene nomenclature based on the CGSNL (Committee on Gene Symbolization, Nomenclature and Linkage, Rice Genetics Cooperative) rules (Rice WRKY Working Group 2012). In the present study, we isolated a full-length cDNA of OsWRKY80 gene. The OsWRKY80 gene is located on chromosome 3 and designated with the locus number Loc_Os03g63810. This OsWRKY80 is not to be confused with a previously reported OsWRKY80 gene by Li et al. (2009) and Ricachenevsky et al. (2010), which is now designated as OsWRKY90 (LOC _Os09g30400) according to the new CGSNL nomenclature. The obtained cDNA sequence of OsWRKY80 was 1392 bp in length, containing an ORF of 1164 bp, encoding a polypeptide of 387 amino acid residues. Structure analysis revealed that the deduced OsWRKY80 consisted of one classic conserved WRKY domain with a zinc finger motif of C-X5-C-X23-H-X1-H, indicating that it belongs to the WRKY group II-e family (Eulgem et al. 2000). BLAST analysis revealed that OsWRKY80 shared the highest homology with previously uncharacterized OsWRKY37 (54.8%, LOC_Os04g50920) and AtWRKY14 (50.7%, At1g30650), respectively.
Expression of OsWRKY80 is Induced by JA, ET and R. Solani
To determine the possible involvement of OsWRKY80 in hormone-mediated defense signaling pathways, we also monitored the expression of OsWRKY80 following treatment with exogenously applied SA, JA and ET. As shown in Fig. 1, the expression of OsWRKY80 was rapidly induced by JA within 1 h, peaked at 12 h, and sharply declined to basal levels at 24 h. The OsWRKY80 transcripts were also noticeably induced by an ethylene precursor ethephon during 6–12 h before returning to basal levels at 24 h. However, exogenous SA application exerted no effects on the expression of OsWRKY80.
The strong induction of OsWRKY80 expression by JA, ET and pathogen suggests that this gene may be involved in JA/ET-dependent defense signaling pathways.
OsWRKY80 is Localized in the Nucleus
OsWRKY80 Acts as a Transcriptional Activator in Yeast Cells
Modulation of Rice Resistance to Sheath Blight Fungus by OsWRKY80
OsWRKY80 Positively Regulates OsWRKY4 Expression
Emerging evidence has highlighted the importance of WRKY factors as positive or negative regulators in rice disease resistance networks (Pandey and Somssich 2009). Global gene expression profiling has revealed a large number of WRKY genes that are rapidly induced or repressed upon pathogen infection, suggesting that these WRKY genes may contribute to the regulation of rice response to pathogen infection (Ryu et al. 2006; Bagnaresi et al. 2012; Wei et al. 2013). Moreover, some rice WRKY factors have been characterized to be involved in plant defense responses (Pandey and Somssich 2009; Jimmy and Babu 2015; Phukan et al. 2016). However, the roles of WRKY transcription factors in rice denfense against sheath blight is quite limited. Overexpression of OsWRKY30 enhanced resistance to R. solani and M. oryzae possibly by activating several downstream genes, including JA biosynthesis-related genes (Peng et al. 2012). OsWRKY4 acts as a transcriptional activator in modulating defense response against R. solani (Wang et al. 2015). Both OsWRKY4 and OsWRKY30 belong to group I family. Here, we have added a novel OsWRKY80 gene to the list of WRKY defense regulators in rice- R. solani interaction. Our results demonstrate that overexpression of OsWRKY80 significantly enhanced, whereas suppression of OsWRKY80 by RNAi markedly compromised sheath blight resistance. Furthermore, we show that OsWRKY80 acts upstream of the previously characterized OsWRKY4 in defense signaling pathway against R. solani. On the basis of these results, we conclude that OsWRKY80-OsWRKY4 regulatory circuit plays a positive role in rice defense response to sheath blight infection.
Compared to other groups, a higher percentage of rice WRKY Group II proteins are involved in plant defense responses to pathogens. A systematic expression analysis of OsWRKY genes revealed that the expression of one-third of tested genes was upregulated in response to an incompatible interaction between rice and M. grisea. Among the inducible OsWRKY genes, 8 genes belong to the members of Group II subfamily (Ryu et al. 2006). Moreover, 10 out of 16 OsWRKY genes, which have been characterized to mediate plant innate or induced immunity in rice, belong to Group II. For instance, OsWRKY13 positively mediates rice defense responses against both Xoo and M. grisea (Qiu et al. 2007). OsWRKY6, 13/03, 51 and 71 also positively mediate rice resistance to Xoo (Choi et al. 2015; Liu et al. 2005; Hwang et al. 2016; Liu et al. 2007). On the other hand, some Group IIa proteins, such as OsWRKY28, 62 and 76 are transcriptional repressors, and they act as negative regulators in rice response to M. grisea or Xoo (Chujo et al. 2013; Peng et al. 2008; Yokotani et al. 2013). In the present study, OsWRKY80, a member of the IIe subgroup protein, has also been identified as a positive modulator of rice resistance to sheath blight. Together these results suggest that Group II WRKY proteins represent a major force in mediating plant defense responses against various pathogens. In support of this notion, Arabidopsis Group IIe AtWRKY22 and 29 have been shown as important downstream components of a MAPK pathway that confers resistance to both bacterial and fungal pathogens (Asai et al. 2002). Conversely, AtWRKY27 negatively modulates symptom development caused by Ralstonia solanacearum infection (Mukhtar et al. 2008).
To date, only a few investigations have revealed regulatory cascades amongst different WRKYs. OsWRKY45-2, functioning as a transcriptional activator, directly activates WRKY13. OsWRKY13 functioning as a transcriptional repressor, in turn suppresses OsWRKY42. The three WRKYs form a transcriptional regulatory cascade in the defense signaling pathway against M. oryzae. In the present study, we have identified a new OsWRKY80-OsWRKY4 regulatory circuit in the rice defense signaling pathway to R. solani. First, OsWRKY80 and OsWRKY4 control the same subset of defense-related genes such as PR1a, PR1b, PR5 and PR10/PBZ1, suggesting that the two regulators may be located in the same pathway. Second, the transcript levels of OsWRKY4 were activated by OsWRKY80-overexpression, whereas suppressed by OsWRKY80 RNAi, suggesting that OsWRKY4 may be a target gene of OsWRKY80. By contrast, no changes in the expression of OsWRKY80 were observed in OsWRKY4-overexpressing or -RNAi transgenic rice plants. Finally, the promoter region of the OsWRKY4 gene contains 9 W-box or W-box like elements. Yeast one-hybrid assay and transient expression analysis in tobacco cells results showed that OsWRKY80 could specifically bind to the OsWRKY4 promoter, and the 5’ promoter region containing W-box, or W-box like elements is responsible for the binding activity. Together these lines of evidence clearly suggest that OsWRKY80 acts upstream of OsWRKY4 by regulating its expression.
Functional studies have suggested an intricate regulatory network involved in both WRKY transcription factors and phytohormone signaling pathways. WRKY proteins frequently act as key components and interact with diverse partners related to hormone signaling pathways (Jiang and Yu 2015). In plants, pathogen attack often triggers multiple defense-response signaling pathways mediated by SA, JA and ET. Multiple lines of evidence have also revealed the roles of WRKY factors in modulating the balance between SA- and JA/ET-mediated signaling pathways. For instance, AtWRKY33, a positive regulator of JA/ET-mediated defense response signaling and a negative regulator of SA-mediated defense response signaling, plays an important role in plant defense against necrotrophic pathogens (Zheng et al. 2006). By contrast, OsWRKY13 appears to promote SA-dependent and suppress JA-dependent defense responses, acting in a convergent point of the two defense signal pathways (Qiu et al. 2007). Recently, we have identified OsWRKY4 as a crucial positive regulator in JA/ET-mediated defense signaling pathway (Wang et al. 2015). In this study, OsWRKY80 and WRKY4 gene exhibited similar expression pattern induced by JA, ET and R. solani, bu not by SA (Fig. 1; Wang et al. 2015). More importantly, OsWRKY80 directly binds the promoter of the OsWRKY4 gene, suggesting that OsWRKY4 acts downstream of OsWRKY80 in the defense signaling pathway. These findings strongly suggest that OsWRKY80 may affect defense responses through JA/ET-mediated signaling pathway.
SA and JA/ET signaling pathways mediate resistance against different types of microbial pathogens. SA is usually involved in resistance against biotrophic pathogens (Hammond-Kosack and Parker 2003). On the other hand, the synergistic action of JA and ET is usually induced by necrotrophic pathogens and insects (Bari and Jones 2009). AtWRKY33 is a positive regulator of JA responses. Ectopic overexpression of AtWRKY33 increases resistance to necrotrophic fungal pathogens Botrytis cinerea and Alternaria brassicicola, concomitant with reduced expression of JA-regulated gene PDF1.2 (Zheng et al. 2006). Shimono et al. (2007) reported that overexpression of OsWRKY45, a positive regulator in BTH-induced disease resistance by mediating SA signaling, enhanced resistance against hemibiotrophic M. oryzae and biotrophic Xoo, but not against necrotic R. solani (Shimono et al. 2012). The results presented here showed that OsWRKY80 plays a positive role in the resistance to a necrotic fungal pathogen (Fig. 5). These findings are consistent with the facts that OsWRKY80 activates OsWRKY4 expression, and subsequently activates JA/ET-dependent defense responses, thus protecting rice plants from the necrotic fungus. Thus, both dicots and monocots may share similar defense mechanisms to diverse pathogens through discrete phytohormone-mediated signal pathways.
This study provides data on the role of OsWRKY80 in defense responses. Our results clearly demonstrated that OsWRKY80 contributes to activating defense responses to the rice sheath blight fungus by directly controlling OsWRKY4 via JA/ET-mediated signal pathway. To gain more insights into the integral regulatory network mediated by OsWRKY80 and OsWRKY4, further investigations are needed to explore additional functional linkages with MPK cascades and other novel components.
Plant Material, Growth Conditions and Chemical Treatments
Rice plants (Oryza sativa L. japonica cv. Xiushui 11) were grown in a greenhouse with day/night cycle of 14/10 h, 28°C/25°C, photosynthetically active radiation (PAR) of 100 μmol m-2 s-1, and relative humidity around 85% in hydroponic culture, as previously described by Peng et al. (2012).
Three-week-old rice seedlings were sprayed with 1 mM SA, 100 μM MeJA and 1 mM ethephon (an ethylene generator) until liquid dripped off the leaves. Control plants were treated in the same way with diluted water or 0.1% methanol (for MeJA only). Leaf samples were harvested at given time points after treatments for total RNA extraction.
Pathogen Inoculation and Disease Investigation
Isolation of OsWRKY80 cDNA
The full-length cDNA of OsWRKY80 was amplified from the total RNA extracted from MeJA-infected rice seedlings by RT-PCR using specific primer pairs: forward primer, 5’- AATACTGAATAGGCAGCAGCAACA -3’ and reverse primer, 5’- GCACAGGCGACCATCATATCATAT -3’. The primers were designed according to the annotated OsWRKY80 gene (Loc_Os03g63810) including its longest open reading frame (ORF). The PCR products were cloned to a pUCmT vector and sequenced for verification.
Gene Expression Analysis
Total RNA was extracted using PureYield™ RNA Midiprep System (Promega). Reverse transcription was performed using 2 μg of total RNA treated with DNase I (Invitrogen) and SuperScript reverse transcriptase II (Invitrogen) according to the manual. qRT-PCR was performed as previously described (Peng et al. 2011). Each experiment was repeated independently three times. Rice Actin1 (AK071586) was used as internal reference (Qiu et al. 2008). Northern blot analysis was carried out as described by Sambrook et al. (1989). The GenBank accession numbers of the defense-related genes examined in the qRT-PCR analysis are as follows: PR1a (AJ278436), PR1b (AK107926), PR3 (D16221), PR5 (OSU77657), PR10/PBZ1 (D38170), LOX (D14000), AOS2 (AY062258), CHS (NM_001058538) and PAL/ZB8 (KF556681). The gene-specific primers for gene expression analysis are listed in Additional file 1: Table S1.
The coding sequence of OsWRKY80 was fused in frame to the N-terminus of an enhanced green fluorescent protein gene (eGFP) in p35S: eGFP (Wang et al. 2007) to generate p35S: WRKY80-eGFP construct. The primers are as follows: 5’-TTGGATCC ATGGATATGATGGAGGAGGA-3’ and 5’-TCACTCGAGGAACTTGTGCCACTGATGATCA-3’ with an underlined BamH I site and Sal I site, respectively. The empty p35S: eGFP vector was used as control. The fusion and the control constructs were transformed into onion (Allium cepa) epidermis cells by particle bombardment using PDS-1000/He (BIO-RAD) (Xie et al. 2003). The transformed cells were incubated on 1/2 MS medium at 28°C for 2 d, and GFP signals were detected by a confocal fluorescence microscope (Bio-Rad MRC 1024).
Transactivation Activity Assay in Yeast
The coding region of OsWRKY80 and its truncated fragments were amplified by PCR and fused to the GAL4 DNA binding-domain (BD) vector pGBKT7 (Clontech) to generate pBD-WRKY80, -dN1 (61-387), -dN2 (201-387), -dC1 (1-301), -dC2 (1-285) and -dN1C1 (61-301) constructs. The PCR primers are listed in Additional file 2: Table S2. The empty vector pGBKT7 was used as negative control. The yeast strain AH109 was transformed with different constructs and grown on SD-Trp-Ade-His selective medium at 30°C for 3 d. The α-galactosidase activity assay was performed with the transformed cell lines grown in liquid SD-Trp medium using p-nitrophenyl α-D-galactopyranoside as a substrate according to the manual.
Generation of Transgenic Plants
The full-length coding sequence of OsWRKY80 was digested with BamH I and Sac I and inserted into a modified pCambia1301 vector under the control of the constitutive maize (Zea mays) ubiquitin promoter (Wang et al. 2007). To construct a plasmid for OsWRKY80 RNAi, part of the WRKY80 cDNA (302 bp, nucleotides 775 to 1076) was amplified by PCR and used to construct self-complementary hairpin vector pCo-Ubi: dsWRKY80 after several steps of enzyme digestions and ligations. The hairpin structure, which is composed of the sense and antisense of OsWRKY80 cDNA fragments seperated by a catalase intron, was put under the control of constitutive maize ubiquitin promoter. The resulting constructs were introduced into rice calli of cultivar Xiushui 11 by the Agrobacterium-mediated transformation method (Hiei et al. 1994).
Promoter Fragments-Binding in Yeast one-Hybrid System
For analysis of the putative W-box (TTGAC[C/T]) or W-box like (TGAC[C/T]) cis-elements in promoters, the 1500 nucleotide sequences upstream of the transcription initiation sites of genes were used to search the PLACE (Plant Cis-acting Regulatory DNA Elements) database available online (http://tenor.dna.affrc.go.jp/).
OsWRKY80 coding region was amplified and in frame fused with the GAL4 activation domain of pGADT7-rec2 prey vector (Clontech), forming pGAD-WRKY80. Construction of pHIS2 vector, yeast cotransformation and growth were performed as previously described (Wang et al. 2015).
Transient Expression Assay in Tobacco (Nicotiana Benthamiana)
The construct for generation of transgenic plants described above was used as the effector vector for transient expression assay. The intact (about 1500 bp) and 5′-deleted promoters of OsWRKY4 were amplified and constructed into the reporter vector pGreenII0800-LUC (Hellens et al. 2005). The recombinant reporter and effector plasmids, or reporter plasmids alone, were transferred into the Agrobacterium GV3101 lines, and infiltrated into the N. benthamiana leaves as described previously by Yang et al. (2000). The Firefly and Renilla luciferase activities were measured using a Dual Luciferase assay kit (Promega) according to the manufacturer’s instructions. The primers used are listed in Additional file 3: Table S3.
Data are represented as mean values ± standard error (SE) for three replicates. Analysis of variance (one-way ANOVA) and multiple comparisons of differences between treatments (Duncan’s multiple range test, p < 0.05, 0.01) were performed using SPSS for Windows version 11.5 (SPSS Inc.).
This research was funded by National Natural Science Foundation of China (No. 31301617), Project of Hunan Provincial Natural Science Foundation (No. 2016JJ3060), Project of Scientific Research Fund of Hunan Provincial Education Department (No. 15K045), and Project of China Scholarship Council (No. 201608430089).
XP performed the experiments of gene cloning and phenotype assays of transgenic plants. HW and XP designed the experiments. XT and HH generated T0, T1 and T2 generations of transgenic rice lines and performed the experiments of molecular analyses. DJ and XT performed analyzed the biochemical characteristics of OsWRKY80. HW and JCJ discussed the research and wrote the manuscript. All authors read and approved the final version of the manuscript.
The authors declare that they have no competing interests.
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