Tetrapyrroles play indispensable roles in various biological processes. In higher plants, glutamate 1-semialdehyde 2,1-aminomutase (GSAM) converts glutamate 1-semialdehyde (GSA) to 5-aminolevulinic acid (ALA), which is the rate-limiting step of tetrapyrrole biosynthesis. Up to now, GSAM genes have been successively identified from many species. Besides, it was found that GSAM could form a dimeric protein with itself by x-ray crystallography. However, no mutant of GSAM has been identified in monocotyledonous plants, and no experiment on interaction of GSAM protein with itself has been reported so far.
We isolated a yellow leaf mutant, ys53, in rice (Oryza sativa). The mutant showed decreased photosynthetic pigment contents, suppressed chloroplast development, and reduced photosynthetic capacity. In consequence, its major agronomic traits were significantly affected. Map-based cloning revealed that the candidate gene was LOC_Os08g41990 encoding GSAM protein. In ys53 mutant, a single nucleotide substitution in this gene caused an amino acid change in the encoded protein, so its ALA-synthesis ability was significantly reduced and GSA was massively accumulated. Complementation assays suggested the mutant phenotype of ys53 could be rescued by introducing wild-type OsGSAM gene, confirming that the point mutation in OsGSAM is the cause of the mutant phenotype. OsGSAM is mainly expressed in green tissues, and its encoded protein is localized to chloroplast. qRT-PCR analysis indicated that the mutation of OsGSAM not only affected the expressions of tetrapyrrole biosynthetic genes, but also influenced those of photosynthetic genes in rice. In addition, the yeast two-hybrid experiment showed that OsGSAM protein could interact with itself, which could largely depend on the two specific regions containing the 81th–160th and the 321th–400th amino acid residues at its N- and C-terminals, respectively.
We successfully characterized rice GSAM gene by a yellow leaf mutant and map-based cloning approach. Meanwhile, we verified that OsGSAM protein could interact with itself mainly by means of the two specific regions of amino acid residues at its N- and C-terminals, respectively.
Tetrapyrroles play vital roles in various key biological processes, including photosynthesis and respiration (Ilag et al. 1994; Mochizuki et al. 2010). There are four classes of tetrapyrroles in higher plants, namely, chlorophyll (Chl), heme, siroheme, and phytochromobilin (Tanaka et al. 2011). All of these tetrapyrroles are derived from a common biosynthetic pathway that resides in the plastid, in which eight molecules of 5-aminolevulinic acid (δ-aminolevulinic acid, ALA) are assembled into the tetrapyrrole core structure (Ge et al. 2010).
The synthesis of ALA in animals, fungi and some bacteria was a condensation of glycine and succinyl-coenzyme A by ALA synthase (Tanaka and Tanaka 2007). However, in plants, algae and some photosynthetic bacteria, ALA is usually derived from the glutamate, which is called the five-carbon pathway (Grimm et al. 1991). In higher plants, ALA is the universal precursor of all tetrapyrroles, and its synthesis process is the rate-limiting step of tetrapyrroles biosynthesis (Lytovchenko et al. 2011). ALA was formed by transferance of the amino group of glutamate 1-semialdehyde (GSA) from C2 to C1, which was catalyzed by glutamate 1-semialdehyde 2,1-aminomutase (GSA aminotransferase, GSAM) (Grimm et al. 1991).
GSAM belongs to class-III pyridoxal-phosphate-dependent aminotransferase family (https://www.uniprot.org/uniprot/Q6YZE2), which was widely found in photosynthetic algae and plants (Song et al. 2016). In higher plants, the GSAM protein was first purified from the de-etiolated barley (Hordeum vulgare) seedings (Grimm et al. 1989), and GSAM genes have been successively identified from many species, such as soybean (Glycine max, Sangwan and O'Brian 1993), Arabidopsis (Song et al. 2016), tobacco (Nicotiana tabacum, Höfgen et al. 1994; PöRs et al. 2001), tomato (Lycopersicon esculentum, Polking et al. 1995; Lytovchenko et al. 2011), and Brassica napus (Tsang et al. 2003a). However, no mutant of GSAM has been identified in monocotyledonous plants. On the other hand, it was found that the GSAM could form a dimeric protein with itself (Grimm et al. 1989; Stetefeld et al. 2006; Ge et al. 2010), and different subunit states could show negative synergy when working (Hennig et al. 1997). Nonetheless, almost all researches on the dimeric structures of GSAM were conducted by x-ray crystallography, and no experiment on interaction of GSAM protein with itself has been reported so far.
In our research, we isolated a yellow leaf mutant, ys53, in rice (Oryza sativa). The mutant showed yellow phenotype throughout the whole growth period. Its photosynthetic pigment contents were decreased, and the chloroplasts showed obvious developmental impairment. In consequence, its major agronomic traits were significantly affected. Map-based cloning, intermediate product detection and complementation assays suggested that a single nucleotide mutation in OsGSAM (LOC_Os08g41990) is the reason for the mutant phenotype. OsGSAM is mainly expressed in green tissues and its encoded protein is localized to chloroplast. In addition, the yeast two-hybrid experiment showed that OsGSAM protein could interact with itself mainly by means of the two specific regions of amino acid residues at its N- and C-terminals, respectively.
Isolation and Characterization of the ys53 Mutant
The ys53 mutant was obtained from japonica rice variety Nipponbare by ethyl methanesulfonate (EMS) mutagenesis. It exhibited a yellow leaf phenotype throughout the whole growth period, and grew at a slow rate (Fig. 1a, b), which caused its heading period to be delayed by 7 days (Fig. 1c). At maturity, except 1000-grain weight, major agronomic traits of ys53 were significantly affected. For instance, its plant height, number of productive panicles per plant, number of spikelets per panicle and seed-setting rate were significantly reduced by 18.5%, 21.0%, 20.4% and 8.9%, respectively, compared with those of the wild type (Fig. 1d-h). In addition, because plant height of ys53 was significantly lower than that of the wild type, we measured its internode and panicle length. The results showed that each internode of ys53 was shortened proportionally, but its panicle length was not changed significantly (Additional file 2: Supplementary Fig. S1).
In order to further clarify the yellow phenotype of ys53, we determined photosynthetic pigment contents of the mutant and its wild type at different stages. At the seedling stage, contents of total chlorophyll (Chl), Chl a, Chl b and carotenoids (Caro) in leaves of ys53 were significantly reduced by 61.0%, 59.5%, 66.1%, and 30.0% respectively, compared with those in the wild-type leaves (Fig. 2a). At the booting stage, total Chl, Chl a, Chl b and Caro contents in the mutant leaves were also significantly decreased by 55.7%, 58.0%, 46.5% and 28.3%, respectively (Fig. 2b). These data suggested that the yellow leaf phenotype of ys53 was due to the defect in photosynthetic pigments.
To explore effect of the decreased pigment levels on the chloroplast structure of ys53, the ultrastructure of chloroplasts was observed under a transmission electron microscope. In wild type, chloroplasts had intact thylakoid and granum structure, with dense and ordered grana stacks. In contrast, ys53 mutant chloroplasts had no intact thylakoid and granum structure, and exhibited obvious vacuolation (Fig. 2c-f). The result indicated that the development of chloroplast was suppressed in the ys53 mutant.
Next, we investigated the photosynthetic capacity of ys53. As shown in Fig. 2g, net photosynthetic rate of the ys53 flag leaves at the grain-filling stage was significantly lower than that of the wild type, suggesting that decreased level of pigments and suppressed development of chloroplasts significantly affected the photosynthetic capacity of the ys53 mutant.
In addition, to explore whether the yellow leaf phenotype of ys53 was affected by temperature, we treated ys53 and wild-type seedlings grown in the growth chamber using two different temperature conditions (constant 23 °C and 30 °C), respectively. As a result, the ys53 mutant grown under different temperature conditions exhibited similar leaf-color phenotype and decrease degree of photosynthetic pigment contents (Additional file 2: Supplementary Fig. S2), which indicated that the yellow phenotype of ys53 was independent upon temperature.
Map-Based Cloning of the ys53 Mutant Gene
For genetic analysis of the mutant, ys53 was crossed with normal indica restorer line Minghui 63. The resulting F1 plants exhibited a normal green phenotype, and leaf-color phenotypes of the F2 population segregated with a ratio of 3:1 (χ2 < χ20.05 = 3.84, P > 0.05, Additional file 1: Supplementary Table S1). The result suggested that the yellow leaf phenotype of the mutant was controlled by a single recessive nuclear gene. Then, SSR and InDel markers and the (ys53/Minghui 63) F2 population were used to map the mutant gene. The initial mapping result with 352 F2 yellow-leaf individuals showed that the target gene ys53 was linked to the SSR marker RM80 located on the long arm of Chromosome 8 (Fig. 3a). After that, the 852 F2 yellow-leaf plants and the seven InDel and SSR markers with polymorphism between the two parents were used to fine map the ys53 locus (Table 1). Finally, the target locus was narrowed to 102.5-kb region between SSR marker RM502 and InDel marker YS6, at genetic distance of 0.6 cM and 0.2 cM, respectively (Fig. 3b).
Within the above-mentioned 102.5-kb region, 14 putative genes are annotated by Rice Genome Annotation Project (http://rice.plantbiology.msu.edu) (Fig. 3c, Additional file 1: Supplementary Table S2). Among these genes, only one gene (LOC_Os08g41990) contains a chloroplast transit peptide according to the analysis result using ChloroP and TargetP (http://www.cbs.dtu.dk/services/ChloroP/; http://www.cbs.dtu.dk/services/TargetP/). Meanwhile, 9 genes locating on the middle of this region were first amplified from ys53 genomic DNA and sequenced one by one (Additional file 1: Supplementary Table S3), and only one mutation was found and furthermore, occurred in the LOC_Os08g41990 gene in ys53 mutant. Then, we sequenced cDNA of this gene from ys53 mutant and its wild-type parent Nipponbare using reverse transcription (RT)-PCR, and confirmed the point mutation mentioned above. This gene encodes an aminotransferase with 78.9% and 75.7% identities to Arabidopsis GSA1 and GSA2 respectively, which participate in tetrapyrrole biosynthetic pathway in higher plants. In the ys53 mutant, a single nucleotide G to A substitution occurred at position 1453 of LOC_Os08g41990 genome sequence (corresponding to position 511 of its cDNA) (Fig. 3d), causing an amino acid change in its encoded protein. Therefore, LOC_Os08g41990 was considered as the candidate gene of ys53 mutant, and designated tentatively as OsGSAM.
Database searching showed that the OsGSAM gene is a single copy gene in rice genome. Sequencing revealed that this gene contains three exons and two introns. The full length of its genomic sequence is 2379 bp and the cDNA length is 1437 bp. The protein encoded by OsGSAM consists of 478 amino acids and is predicted to have approximately 50 kDa molecular weight. The OsGSAM protein contains two domains, a chloroplast transit peptide of 40 amino acid residues at N-terminus and an aminotransferase class-III of 397 amino acid residues at C-terminus (Additional file 2: Supplementary Fig. S3) (http://smart.embl-heidelberg.de/). Meanwhile, it has 20 α-helixes and 21 β-sheets, and the mutation site in ys53 mutant was located on a conserved site of the 8th α-helix (Additional file 2: Supplementary Fig. S3) (https://swissmodel.expasy.org/interactive).
According to the multiple sequence alignment of OsGSAM and its homologues in different species, OsGSAM has a high similarity to its homologues in monocotyledonous plants, maize (Zea mays), and barley (Hordeum vulgare) and dicotyledonous plants, Arabidopsis thaliana (GSA2, GSA1), tobaco (Nicotiana attenuate) and cucumber (Cucumis satvus), with 92.2%, 90.7%, 78.9%, 75.7%, 78.3%, 76.6% respectively. OsGSAM also has 76.6% and 73.4% similarity to its homologues in single-celled algaes Chlamydomonas reinhardtii and Synechococcus, respectively. In addition, phylogenetic analysis showed that OsGSAM is more closely related to GSAM homologues from maize and barley than those from other species (Additional file 2: Supplementary Fig. S4).
GSA Accumulation and ALA-Synthesis Ability in ys53 Mutant
GSAM converts GSA to ALA by transferance of the amino group of GSA from C2 to C1 in higher plants (Tanaka and Tanaka 2007). If the ys53 mutant indeed has a defective GSAM, its ALA-synthesising capacity should be decreased, resulting in massive accumulation of GSA in the mutant plants. So we should first examine GSA content in ys53. However, GSA is an isomer of its product ALA, and both GSA and ALA can react with acetylacetone to form a pyrrole that further reacts with Ehrlich’s reagent to form a colored compound. Then, we compared total content of GSA and ALA between ys53 and its wild type using the method of Mauzerall and Granick (1955) with slight optimization. The results showed that total content of GSA and ALA in ys53 mutant reached to 103.3 μg/g·FW, but that in the wild type was only 3.9 μg/g·FW under natural condition (Fig. 4a). Generally, GSA is stable in dilute solution at acidic pH (such as the acidic condition in the present study) (Houen et al. 1983; Kannangara and Schouboe 1985). On the other hand, ALA is undetectable because it is very quickly converted to porphobilinogen by ALA dehydratase in normal plants (Richter et al. 2010). So the overwhelming majority of total content of GSA and ALA should actually be GSA content in ys53 mutant. Therefore, the data suggested that GSA massively accumulated in the mutant.
On the other hand, LA (levulinic acid) has a similar molecular structure to ALA and can compete with ALA to bind to ALA dehydratase, so excess LA can block the conversion of ALA to porphobilinogen. Therefore, we cultivated yellow seedlings of ys53 and its wild type under light and excess LA conditions to compare ALA-synthesis capacity of them. As shown in Fig. 4b, the ALA-synthesis capacity of ys53 was 22.6 μg/g·FW·h, while that of wild type was 39.4 μg/g·FW·h, which showed that ALA-synthesis ability of the mutant was significantly reduced by 42.6% compared with that of the wild type.
Taken together, we concluded that GSAM protein should be defective in the ys53 mutant.
Complementation of the ys53 Mutant
In order to further confirm that the yellow leaf phenotype of ys53 was caused by the mutation in the OsGSAM gene, we constructed complementary vector and carried out transgenic experiment. First, the full-length cDNA of the wild-type OsGSAM gene was amplified, and inserted into the pCAMBIA2300 vector containing the Actin 1 promoter. Then, the fusion vector pCAMBIA2300-OsGSAM was introduced into the ys53 mutant by Agrobacterium-mediated transformation. As a result, a total of 13 positive transgenic lines were obtained through identification with PCR (Fig. 5a). These transgenic lines all showed normal leaf-color phenotype as the wild type (Fig. 5b, c). Meanwhile, we measured pigment contents in the positive transgenic lines at seedling stage and booting stage, respectively. As shown in Fig. 5d and e, pigment contents of transgenic lines TP-1, TP-2 and TP-3 were not significantly different from those of the wild type. In addition, we tested GSA accumulation and ALA-synthesis ability of TP-1, TP-2 and TP-3. The results showed that the three positive transgenic lines had significant increase of ALA-synthesis ability compared with ys53 mutant (Fig. 5f), and they had no obvious accumulation of GSA as the wild type (Fig. 5g). In a word, these data suggested that the OsGSAM gene rescued the yellow leaf phenotype of ys53, confirming that the mutant phenotype was a consequent of the single-base mutation of OsGSAM gene.
Subcellular Localization of OsGSAM Protein
OsGSAM was predicted to be located in chloroplast because it contains a chloroplast transit peptide with 30 amino acid residues at its N-terminus. To verify this prediction, we made pCAMBIA2300-35S-OsGSAM-GFP vector, a construct expressing the OsGSAM-GFP (green fluorescent protein) fusion protein, and transformed rice protoplast using the resulting construct and the empty vector pCAMBIA2300-35S-GFP (as control) respectively. Then, the transformed protoplasts were observed by laser-scanning confocal microscopy. As expected, the green fluorescence of OsGSAM-GFP fusion protein exactly overlapped with the red autofluorescence of chlorophyll in chloroplasts (Fig. 6a). Meanwhile, the green fluorescence of empty vector was diffusely distributed in the protoplast (Fig. 6b). This result suggested that OsGSAM is indeed located in chloroplast.
Expression Pattern of OsGSAM Gene
In order to explore the expression pattern of OsGSAM, its transcriptional levels in different tissues of the wild type were measured by qRT-PCR at the seedling stage and the booting stage, respectively. The data showed that OsGSAM was expressed in wide range of tissues, including roots, stems, leaf sheaths, leaf blades and young panicles. Nonetheless, OsGSAM was differentially expressed in different tissues. Specifically, leaf blades had the highest expression, followed by young panicles and leaf sheaths, while stems and roots had lower levels of expression (Fig. 7a).
Expression Analysis of the Genes for Tetrapyrrole Biosynthesis and Photosynthesis
Due to the contents of photosynthetic pigments and their precursor ALA in the ys53 mutant were significantly reduced, we examined transcription levels of the 14 genes involved in tetrapyrrole biosynthesis by qRT-PCR at seedling stage. Among them, three genes encode the enzymes for the common steps of tetrapyrrole biosynthetic pathway, including glutamyl-tRNA reductase (GluTR, HEMA) (Apitz et al. 2016), GSAM, and 5-aminolevulinate dehydratase (HEMB) (Tang et al. 2012); nine genes encode the enzymes for chlorophyll biosynthesis, including magnesium chelatase D subunit (CHLD), chelatase H subunit (CHLH), magnesium chelatase I subunit (CHLI), magnesium chelatase M subunit (CHLM), Mg-protoporphyrin IX monomethylester cyclase (CHL27), 3,8-divinyl protochlorophyllide a 8-vinyl reductase (DVR), protochlorophyllide oxidoreductase A (PORA), Chl synthase (YGL1) and chlorophyllide a oxygenase (CAO1) (Inagaki et al. 2015; Li et al. 2019; Kong et al. 2016; Wang et al. 2010; Sakuraba et al. 2013; Wu et al. 2007; Lee et al. 2005); and two genes encode ferrochelatase1 and 2 (FC1 and FC2) for the heme branch (Inagaki et al. 2015). As shown in Fig. 7b, all the three genes (HEMA, GSAM and HEMB) for the common steps were significantly down-regulated in the ys53 mutant, compared with the wild type. In the 11 genes for chlorophyll and heme branches, only CHLH, CHL27 and YGL1 did not significantly change in expression level, and the other eight genes, including CHLD, CHLI, CHLM, DVR, PORA, CAO1, FC1 and FC2, were all significantly up-regulated in the mutant.
Besides, the chloroplast development of ys53 mutant was suppressed, and its net photosynthetic rate was significantly decreased, so we also performed qRT-PCR to explore expression levels of the eight genes associated with photosynthesis at seedling stage. The proteins encoded by these genes were as follows: rubisco small/large subunit (rbcS and rbcL), two reaction center polypeptides (psaA and psbA)), reaction center subunit of PSI (psaN), thylakoid luminal subunit of PSII (psbP), and light-harvesting Chl a/b-binding protein of PSII (CAB1R and CAB2R) (Li et al. 2015; Su et al. 2012; Amunts et al. 2010; Ifuku et al. 2008; Ma et al. 2017). The result showed that expression level of psbP did not significantly change, but those of the other seven genes were all significantly decreased in the mutant relative to those in the wild type (Fig. 7c).
The above data indicated that the mutation of OsGSAM not only affected the expressions of tetrapyrrole biosynthetic genes, but also influenced those of photosynthetic genes in rice.
Protein Interaction of OsGSAM with Itself
GSAM protein was first found to exist as dimer in barley and Synechococcus (Grimm et al. 1989). To date, the dimers of GSAM were usually identified by x-ray crystallography in many species, such as Escherichia coli, Synechococcus and Arabidopsis (Ilag et al. 1991; Hennig et al. 1997; Zhao et al. 2014). Here we carried out a series of yeast two-hybrid experiment to explore whether rice GSAM exists in the same form of dimer and where the dimeric protein was formed by interaction.
First, the full-length cDNA sequence of OsGSAM (FL-cDNA) was fused to GAL4 AD and GAL4 BD vectors respectively, and the resulting constructs were co-transformed into Y2H Gold yeast cells. The result showed that OsGSAM could interact with itself (Fig. 8b), which was consistent with the phenomenon of GSAM dimer in the previous reports.
Next, the FL-cDNA was divided into four different fragments encoding R1, R2, R3 and R4 peptide sequences, respectively (Fig. 8a). The four fragments were fused to GAL4 AD, and the resulting constructs were co-transferred with the GAL4 BD construct containing FL-cDNA into Y2H GOLD cells, respectively. The data showed that R1, R2 and R3 could interact with the full-length GSAM protein, but R4 could not (Fig. 8c), implying that OsGSAM might contain two different interaction regions at its N- and C-ends, respectively.
After that, the FL-cDNA was again divided into six different fragments encoding R5, R6, R7, R8, R9 and R10 peptide sequences, respectively (Fig. 8a). The six fragments were fused to GAL4 AD, and the resulting constructs were co-transferred with the GAL4 BD construct containing FL-cDNA into Y2H GOLD cells, respectively. As shown in Fig. 8d, R5, R6, R8 and R9 could interact with the full-length GSAM protein, but R7 and R10 could not. These results indicated that the interaction of OsGSAM with itself could largely depend on the two specific regions R8 and R9 which contain the 81th–160th and the 321th–400th amino acid residues at the N- and C-terminals of OsGSAM, respectively.
GSAM protein was first purified from barley and cyanobacteria Synechococcus using affinity chromatography and polyacrylamide gel electrophoresis under non-denaturing conditions (Grimm et al. 1989). So far, GSAM genes have only been identified via homology cloning strategy or RNA interference in many plant species, such as soybean (Sangwan and O'Brian 1993), tobacco (Höfgen et al. 1994; PöRs et al. 2001), tomato (Polking et al. 1995; Lytovchenko et al. 2011), and Brassica napus (Tsang et al. 2003a). However, no mutant of GSAM has been reported in monocotyledonous plants. In this study, a rice yellow-leaf mutant ys53 was isolated, which showed a yellow phenotype, reduced contents of pigments, and impaired development of chloroplasts. Then, we cloned the OsGSAM gene by means of the ys53 mutant and map-based cloning approach, and found that a single nucleotide substitution occurred in the mutated gene of ys53, causing an amino acid change in its encoded protein. Furthermore, the yellow leaf phenotype of the mutant could be rescued by introducing the wild-type OsGSAM (Fig. 5). Therefore, we confirmed that the point mutation of OsGSAM was the cause of the yellow phenotype of this mutant, and successfully identified a GSAM gene in monocotyledonous plants through map-based cloning.
Up to now, a few of GSAM RNAi plants have been reported in higher plants. Among them, the GSAM RNAi plants of tabaco showed different degrees of chlorophyll reduction and variegation patterns (Höfgen et al. 1994). Brassica napus plants expressing a GSAM antisense gene directed by a Brassica napin promoter exhibited yellow cotyledons and a range of chlorophyll reduction in the seeds, but the seed growth and development were not affected (Tsang et al. 2003b). The tomato plants expressing antisense GSAM gene directed by TFM5 green fruit-specific promoter displayed lower chlorophyll levels and photosynthetic activity, but almost no differences in fruit size, weight, or ripening capacity (Lytovchenko et al. 2011). In this study, a single-base mutation of OsGSAM led to an amino acid substitution of the encoded protein, and finally caused yellow leaf phenotype throughout the whole growth period in ys53 mutant (Fig. 1a, b). Meanwhile, its pigment contents were reduced (Fig. 2a, b), chloroplast development was suppressed (Fig. 2c-f), and the net photosynthetic rate declined (Fig. 2g). In consequence, its plant height, number of productive panicles per plant, number of grains per panicle and seed setting rate were significantly reduced, but its grain weight was almost unchanged (Fig. 1d-g). The above phenotypes of ys53 were not completely consistent with the phenotypes of RNAi lines of tabaco, Brassica napus and tomato as previously reports, which could be due to the differences between a point mutation and RNA interferences and among the different plant species.
Structure investigations revealed that the Synechococcus GSAM protein contains four clusters of invariant residues, including (i) substrate binding residues (Ser-29–Arg-32 and Glu-406), (ii) interface helix residues (Ser-122–Ala-126, Arg-132, and Arg-135), (iii) residues within the gating loop (Tyr-150–His-153, Leu-158, Ser-163, and Thr-167), and (iv) residues fixing the phosphate group of cofactor of the opposite subunit (Tyr-301*–Thr-305*) (Stetefeld et al. 2006). Each of the four clusters is conservative in different species, and involved in substrate binding, cofactor fixation, formation of the interface helix, or recruiting of the gating loop (Stetefeld et al. 2006). In the present study, the mutation site (the 171th amino acid residue) of ys53 is located on cluster (ii) of invariant residues (the interface helix residues), corresponding to Ala-126 of Synechococcus GSAM (Additional file 2: Supplementary Fig. S3). Therefore, we speculated that the mutation of Ala-171 to Thr could affect biological function of OsGSAM, resulting in significant reduction of ALA-synthesising capacity and the yellow leaf phenotype of the ys53 mutant.
GSAM protein was first found to exist as a dimer in barley and Synechococcus (Grimm et al. 1989). However, almost all studies on the dimers and structures of GSAM were performed by x-ray crystallography, for example, in E. coli (Ilag et al. 1991), cyanobacteria Synechococcus (Hennig et al. 1997; Stetefeld et al. 2006) and Arabidopsis (Zhao et al. 2014). So far, no other form of experimental evidence confirmed the dimeric phenomenon of this protein, and which region drives the formation of this dimer has not been reported. In the present study, we found that OsGSAM protein can interact with itself through yeast two-hybrid experiment (Fig. 8b), which is consistent with the phenomenon of GSAM dimer in the previous reports (Grimm 1990; Hennig et al. 1997; Contestabile et al. 2000; Stetefeld et al. 2006). Meanwhile, our further research indicated that the interaction of OsGSAM with itself could largely depend on the two specific regions R8 and R9 containing the 81th–160th and the 321th–400th amino acid residues at the N- and C-terminals of OsGSAM, respectively (Fig. 8c, d), which might be one aspect of the foundation leading to the formation of GSAM dimer.
YS53 encodes glutamate-1-semialdehyde 2,1-aminomutase (GSAM) participating in tetrapyrrole biosynthesis. In ys53 mutant, a single nucleotide substitution of YS53 gene causes massive accumulation of glutamate 1-semialdehyde, leading to yellow leaf phenotype in rice. In addition, yeast two-hybrid experiment suggested that rice GSAM protein could interact with itself mainly by means of the two specific regions of amino acid residues at its N- and C-terminals, respectively.
Materials and Methods
Plant Materials and Growth Conditions
A yellow leaf mutant, ys53, was obtained from japonica cultivar Nipponbare through ethyl methanesulfonate (EMS) mutagenesis. The mutant was crossed with normal indica restorer line Minghui 63 to construct the F1 and F2 populations for genetic analysis and gene mapping. Rice materials were grown in a paddy field under the local growing environment in Wenjiang District (latitude 30°42′N, longitude 103°50′E and altitude 539.3 m), Chengdu, Sichuan, China (Wang et al. 2010; Wang et al. 2014). In addition, to investigate effect of temperature on the phenotype of ys53, rice seedlings were grown in the growth chamber under 12 h of light (80–100 μmol m− 2 s− 1)/12 h of dark at constant 23 °C (low temperature) or 30 °C (high temperature) (Huang et al. 2017; Chen et al. 2013).
Measurement of Photosynthetic Pigments
Leaf samples were collected from ys53 and its wild type at seedling stage and booting stage respectively. 0.2 g leaf was used to extract pigments with 80% acetone at 4 °C for 48 h under dark condition. Then, contents of chlorophylls (Chl) and carotenoids (Caro) were measured using a BIOMATE 35 UV-Visible Spectrophotometer (Thermo Scientific) at 470 nm, 646 nm and 663 nm, and were calculated according to the method of Lichtenthaler and Wellburn (1983). The pigment data of each sample were measured for three independent experiment repeats.
Measurement of Net Photosynthetic Rate
Net photosynthetic rate (Pn) was measured under 400 ppm of CO2 concentration and sunny weather condition, during 09:30–10:30 a.m. when the solar radiation was approximately 1200 μmol m− 2 s− 1. During grain-filling stage, the flag leaves of wild type and ys53 mutant was selected to measure the photosynthetic capability with a portable photosynthetic apparatus (Li-6400, Li-COR Inc., USA) (Sun et al. 2012).
Map-Based Cloning and Marker Development
Eight hundred fifty-two recessive plants which showed yellow-leaf phenotype were selected from the (ys53/Minghui 63) F2 segregating population. The whole genome DNA of ys53, Minghui 63 and these recessive plants were separately extracted for the linkage mapping analysis based on simple sequence repeat (SSR) markers. The SSR markers used were filtered from the Gramene database (http://archive.gramene.org/markers/microsat/) of the SSR linkage map constructed by McCouch et al. (2002). For fine mapping, the insertion/deletion (InDel) markers were selected, which were based on the flanking sequence that contains natural difference of 25–75 bp of gap between japonica rice cv Nipponbare and indica rice cv 9311 in the multiple sequence alignment, and designed by Primer 5.0. All BLAST searches of the markers were performed by using National Center for Biotechnology Information database (http://www.ncbi.nlm.nih.gov/BLAST/).
Transmission Electron Microscopy Analysis
The fully expanding leaves were harvested from the ys53 mutant and its wild type Nipponbare at the three-leaf stage. The selected leaf tissues were fixed by soaking in a phosphate buffer containing 3% glutaraldehyde and then fixed again with 1% osmium dioxide. Next, the sample was gradually dehydrated, embedded, sectioned, and stained. Finally, submicroscopic structure of the sample was observed by transmission electron microscopy (H-600IV, Hitachi) (Wang et al. 2010).
The full-length cDNA and amino acid sequences of OsGSAM and its homologues were acquired from GeneBank (http://www.ncbi.nlm.nih.gov). The chloroplast signal peptide was predicted according to http://www.cbs.dtu.dk/services/TargetP (Emanuelsson et al. 2007). Multiple sequence alignment was performed using DNAMAN version 6.0 (Lynnon Biosoft). The phylogenetic tree was constructed using the program MEGA 7.0 (Mega Limited) and the maximum likelihood algorithm.
Determination of ALA and GSA Contents and ALA-Synthesis Ability
In order to measure total contents of ALA and GSA under natural condition, the fresh leaves of rice were collected from normal growing plants at seedling stage in the paddy field on sunny afternoons, and immediately stored in liquid nitrogen environment. The detection of ALA and GSA contents was performed according to the protocol of Mauzerall and Granick (1955) with slight optimization. First, the leaf tissues were homogenated adequately in 5 ml of 4% trichloroacetic acid (TCA, PH 1.0). After centrifugation for 5 min at 8000 r/min and 4 °C, 1 mL of the extraction solution was taken into a new tube, and 500 μL 1 M NaAc and 50 μL acetylacetone were added into this tube. Then, the mixed reaction solution in the tube was cooled to room temperature after 10 min in a boiling water bath and centrifuged at 8000 r/min for 5 min. Subsequently, 1.0 ml of the supernatant was taken in another new tube, and an equal volume of Ehrlich’s reagent was added into this tube for reaction under dark condition for 10 min. Finally, the absorbance of the sample was measured at 553 nm, and the ALA and GSA concentration can be obtained according to the standard curve.
For the determination of ALA-synthesising activity, the four steps, including acquisition of yellow seedlings, accumulation, extraction and determination of ALA, were successively carried out. First, the acquisition of yellow seedlings and accumulation of ALA were performed according to the method described previously (Beale 1970; Aarti et al. 2007) with a slight modification. Seeds of ys53 and its wild type were cultivated for 1 week in the dark, and 0.4 g young leaf tissues were harvested and immersed into 100 ml of 20 mM LA (levulinic acid) solution under 7 h of light (100 μmol m− 2 s− 1) for ALA accumulation. Then, the leaf tissues were homogenated adequately in 5 ml of 50 mM phosphate buffer (pH 6.8). Subsequently, extraction and determination of ALA are performed using the above-mentioned method.
For complementation of ys53, the full-length cDNA sequence (1437 bp) of OsGSAM (LOC_Os08g41990) was amplified from the wild-type Nipponbare using a pair of primers 5′-GAGTCTAGAATGGCCGGAGCAGCAGCC-3′ and 5′-TCGCTGCAGCTATATCCGGCGAAGAAC-3′, which have a XbaI site at 5′-end and a PstI site at 3′-end of this gene respectively. After digested with enzymes XbaI and PstI, the PCR product was ligated into the binary vector pCAMBIA2300. The constructed pCAMBIA2300-OsGSAM vector, which contained the target OsGSAM gene driven by the Actin 1 promoter, was transferred into the ys53 mutant by Agrobacterium tumefaciens-mediated transformation. Transgenic plants were detected by a pair of primers 5′-CTTATGGTGGGGCTCAAG-3′ and 5′-GCGATCATAGGCGTCTCG-3′ which located on the OsGSAM gene and the pCAMBIA2300 vector respectively (Additional file 1: Supplementary Table S5).
The full-length cDNA fragment of OsGSAM was amplified from the wild type and inserted into pCAMBIA2300-35S-eGFP vector. The PCR primers were 5′-GAGGGATCCATGGCCGGAGCAGCAGCC-3′ and 5′-TCGTCTAGACTCTATCCGGCGAAGAAC-3′, which contained a BamHI site at the 5′-end and a XbaI site at the 3′-end of the cDNA fragment respectively (Additional file 1: Supplementary Table S5). The constructed fusion vector pCAMBIA2300-35S-OsGSAM-eGFP and the empty vector pCAMBIA2300-35S-eGFP (negative control) were transformed into the rice protoplasts respectively, following the method as previously described (Zhang et al. 2011). Finally, the GFP fluorescence in the transformed protoplasts was examined under a laser-scanning confocal microscopy (Nikon A1).
The roots, stems, leaf sheaths, leaf blades and young panicles of rice in different stages were harvested from the naturally growing plants of ys53 and its wild type in the field at early morning, and the total RNA was extracted with RNA extraction kit (Vazyme). The first strand of cDNA is reversed-transcribed from total RNA (2 μg) using a reverse transcription kit (Vazyme) according to the manufacturer’s instructions. The primer pair qGSAM-1F (5′-TGGACGTAAGGACATCAT-3′) and qGSAM-1R (5′-GTCCAAGTAATCGTAGGT-3′) were used to quantify the OsGSAM expression levels of the various samples to describe the expression pattern of the gene. To measure the relative expression of the genes associated with tetrapyrrole biosynthesis and photosynthesis, 22 pairs of primers were developed. Real-time quantitative PCR (qRT-PCR) was performed in a total volume of 10 μL containing 0.2 μM of each primer pairs and 1 × SYBR green PCR master mix (Vazyme) by using the CFX96 real-time PCR system (Bio-Rad). All reaction conditions were as follows: 95 °C for 5 min, then 40 cycles of 95 °C for 10 s and 58 °C for 30 s. For each experimental group, qRT-PCR was operated with three technical replicates for each of three biological replicates. The 2-△△CT method was applied to calculate the quantitative expression of each genes relative to the internal control. The Actin 1 gene was used for normalization as an internal control. All qRT-PCR primers were listed in Additional file 1: Supplementary Table S4.
Yeast Two Hybrid Assay
The Matchmaker GAL4 two-hybrid system 3 of Clontech (Clontech, USA) was used. The full-length cDNA and a series of truncated cDNA sequences of OsGSAM gene were amplified and inserted into pGADT7 and pGBKT7 vectors respectively, and the BamHI site in the vectors was chosen as the insertion site for all sequences. The self-activation was tested by the bait construct fused with BD. The combination containing the self-activating fusion vector was supplemented with 30 mM 3-AT (3-amino-1,2,4-triazole) in its corresponding medium. The above recombinant vectors were combined according to experimental needs, and then co-transformed into the yeast strain Y2HGold cells. Each transformant was spotted on non-selective (−Leu/−Trp) plates for 3 d at 28 °C, and tested for the protein interaction by observing their growth situation on selective (−Ade/−His/−Leu/−Trp) plates. The saturated culture solution of each transformant was diluted to concentrations of 1, 0.1 and 0.01, and dripped onto its corresponding plates. Interaction between pGADT7-T and pGBKT7-Lam was used as a negative control, and interaction between pGADT7-T and pGBKT7–53 was used as a positive control. The pGBKT7 vector fused with full-length cDNA sequence was combined with empty pGADAD vecter as internal control. Primer sets used for generating constructs were listed in Additional file 1: Supplementary Table S6.
Availability of Data and Materials
All data generated or analyzed during this study are included in this article (and its supplementary information files).
Glutamate 1-semialdehyde 2,1-aminomutase
Green fluorescent protein
Yeast two hybrid
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QW and BZ performed most of the research. YL and SW assisted in the determination of intermediate products. JG and XY carried out subcellular localization assays, CC, ZY, QL and BY assisted in some field experiments, and CS provided technical assistance. QW and XD analyzed the experimental data and drafted the manuscript. PW and XD designed the experiments, supervised the study and revised the manuscript. All authors read and approved the manuscript.
Table S1. Segregation of F2 population from the cross between ys53 and normal green leaf variety. Table S2. Putative genes within the 102.5-kb region. Table S3. The sequenced genes and corresponding PCR amplification primers in the fine mapping region. Table S4. Primers used in qRT-PCR. Table S5. Primers used in vector construction for complementation and subcellular localization. Table S6. Primers used in OsGSAM truncation experiment.
Fig. S1. Internode length of ys53 and its wild type. Fig. S2. Temperature treatment of the ys53 mutant and its wild type. Fig. S3. Sequence alignment of OsGSAM and its homologues. Fig. S4. Phylogenetic analysis of OsGSAM and its homologs. Fig. S5. Tetrapyrrole biosynthetic pathway in higher plants.
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Wang, Q., Zhu, B., Chen, C. et al. A Single Nucleotide Substitution of GSAM Gene Causes Massive Accumulation of Glutamate 1-Semialdehyde and Yellow Leaf Phenotype in Rice.
Rice14, 50 (2021). https://doi.org/10.1186/s12284-021-00492-x