Correction
23 May 2016: Qin P, Wang Y, Li Y, Ma B, Li S, et al. (2016) Correction: Analysis of Cytoplasmic Effects and Fine-Mapping of a Genic Male Sterile Line in Rice. PLOS ONE 11(5): e0156470. https://doi.org/10.1371/journal.pone.0156470 View correction
Figures
Abstract
Cytoplasm has substantial genetic effects on progeny and is important for yield improvement in rice breeding. Studies on the cytoplasmic effects of cytoplasmic male sterility (CMS) show that most types of CMS have negative effects on yield-related traits and that these negative effects vary among CMS. Some types of genic male sterility (GMS), including photo-thermo sensitive male sterility (PTMS), have been widely used in rice breeding, but the cytoplasmic effects of GMS remain unknown. Here, we identified a GMS mutant line, h2s, which exhibited small, white anthers and failed to produce mature pollen. Unlike CMS, the h2s had significant positive cytoplasmic effects on the seed set rate, weight per panicle, yield, and general combining ability (GCA) for plant height, seed set rate, weight per panicle, and yield. These effects indicated that h2s cytoplasm may show promise for the improvement of rice yield. Genetic analysis suggested that the phenotype of h2s was controlled by a single recessive locus. We mapped h2s to a 152 kb region on chromosome 6, where 22 candidate genes were predicted. None of the 22 genes had previously been reported to be responsible for the phenotypes of h2s. Sequencing analysis showed a 12 bp deletion in the sixth exon of Loc_Os06g40550 in h2s in comparison to wild type, suggesting that Loc_Os06g40550 is the best candidate gene. These results lay a strong foundation for cloning of the H2S gene to elucidate the molecular mechanism of male reproduction.
Citation: Qin P, Wang Y, Li Y, Ma B, Li S (2013) Analysis of Cytoplasmic Effects and Fine-Mapping of a Genic Male Sterile Line in Rice. PLoS ONE 8(4): e61719. https://doi.org/10.1371/journal.pone.0061719
Editor: Tongming Yin, Nanjing Forestry University, China
Received: August 17, 2012; Accepted: March 16, 2013; Published: April 16, 2013
Copyright: © 2013 Qin et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This work was supported by the National Natural Science Foundation of China (31025017 and 30971763). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Cytoplasmic male sterility (CMS) is essential to the exploitation of heterosis in three-line hybrid rice breeding programs. CMS cytoplasm has been reported to have substantial genetic effects on various traits of hybrid rice [1], [2], [3]. Studies of the cytoplasmic effects of CMS show that the effects within a type of cytoplasm vary across different agronomic traits in hybrid rice and that the effects on one agronomic trait vary among different types of cytoplasm. For example, the male sterile cytoplasm of IR19661-283-3-2 has a significant negative effect on both yield and days to flowering but does not affect plant height. The male sterile cytoplasms of IR46828, IR46831, IR48483, IR54752, IR17492-18-10-2-2-3, IR54753, IR19661-283-1-3-2, IR54758, and IR54756 have been found to have different effects on grain yield [4]. Most CMS cytoplasms have been reported to have negative effects on yield-related traits, and these effects vary among different sources of cytoplasm [5]. These studies provide practical information for breeding CMS lines and for selecting appropriate CMS line to mate with certain restorers to improve rice yield.
In the three-line system of hybrid rice, male sterility (MS) and its restoration are governed by genetic interaction between male sterile cytoplasm and the nucleus. The interaction maintains the MS, allows the regeneration of the MS line, and restores MS for enjoyment of yield advantage in the F1 hybrid. Genetic interaction limits the flexibility of germplasm selection and increases production costs [6]. Genic male sterility (GMS) is solely determined by the nucleus, thus has a wider spectrum of restorers than CMS and facilitates the widespread use of hybrid vigor. GMS can also be used to simplify rice breeding by creating a two-line breeding system. This is because the male sterility caused by recessive GMS can be maintained and restored by introducing a hemizygotic construct into the male sterile plant. This construct comprises a gene whose product is exclusively fatal to pollen and a corresponding restoration gene [7]. Although GMS is useful in rice breeding, the cytoplasmic effects of GMS have not received as much attention as those of CMS. Here, we used a GMS mutant line (h2s) identified in our breeding program to evaluate cytoplasmic effects on plant height, yield-related traits, and general combining ability (GCA) for these traits.
GMS includes photoperiod-sensitive male sterility (PMS), temperature-sensitive male sterility (TMS), photo-thermo-sensitive male sterility (PTMS), and non-photo-thermo-sensitive genic male sterility. The MS in PMS, TMS, and PTMS can be maintained and reproduced under certain light and temperature conditions. PMS and PTMS have been successfully applied to the production of hybrid seeds, such as Nongken58s, Peiai64s and Y58s [6]. A spontaneous point mutation in PMS3 (photoperiod-sensitive male sterility3) [8] (also called P/TMS12-1 (Photoperiod-and-thermosensitive genic male sterility) [9]) causes PMS in japonica background and TMS in indica background. Recently, a number of non-photo-thermo-sensitive genic MS genes have been identified in rice, including WDA1 (wax-deficient anther1) [10], CYP704B2 [11], TDR (tapetum degeneration retardation) [12], GAMYB [13], [14], DPW (defective pollen wall) [15], and PTC1 (persistent tapetal cell1) [16]. All these genes were found to be related to lipid metabolism and to be critical to anther and pollen exine development. The corresponding mutants show defective anthers and/or pollen development, causing MS in rice. However, the molecular mechanism of anther and pollen development in rice remains unknown. In this study, we identified a male sterile mutant and fine mapped the mutation to a 152 kb region on chromosome 6. Our results lay the groundwork for cloning the H2S gene and for elucidating the molecular mechanism of anther and pollen development.
Materials and Methods
Plant Materials
The h2s mutant (a spontaneous mutant identified from an indica maintainer Chuannong H2S) and F2 mapping populations generated by respectively crossing h2s as female with Zhenshan97B and Nipponbare were planted in a paddy field at Sichuan Agricultural University (Chengdu, Sichuan, China) and at the Hainan rice station (Lingshui, Hainan, China). Five isonuclear alloplasmic lines were generated by crossing heterozygote (h2s+/−) as male with Zhenshan97A, D702A, G46A, K18A and XieqingzaoA and then backcrossing 8 times using h2s+/− as the recurrent parent to substitute the nuclei of Zhenshan97A, D702A, G46A, K18A, and XieqingzaoA with the h2s nucleus. The h2s mutant was named A1, and the resultant isonuclear alloplasmic lines were A2, A3, A4, A5, and A6, respectively (Table S1). The nuclear background in A1–A6 was checked using 30 ISSR (inter-simple sequence repeat) and 371 SSR markers were used to check the nuclear background of each isonuclear alloplasmic line (A1–A6). A1, A2, A3, A4, A5, and A6 were respectively crossed as female parents with five major restorer lines (Shuhui527 (R1), Minghui63 (R2), Guanghui128 (R3), CDR22 (R4), and Mianhui725 (R5)) to generate 30 F1s. For convenience, we defined A1–A6 as parent 1 (P1) and R1–R5 as parent 2 (P2).
Cytological Characterization of h2s
The wild type and the h2s mutant were cytologically examined for anthers at the meiosis, post-meiosis, young microspore, and vacuolated pollen stages. The preparation for chromosome spreads followed the method described in Chen et al. [17]. Anthers at various stages were fixed overnight in Carnoy’s solution (ethanol:glacial acetic acid = 3∶1) and then rinsed twice with water and twice with 10 mmol/L citrate buffer (pH 4.5), and finally washed with citrate buffer. Treated anthers were placed on a slide with 60% acetic acid and gently pressed with cover glass to release microspore mother cells (MMC). They were then stained with 4′,6-diamidino-2-phenylindole (1 µg/ml DAPI in a buffer containing 50% glycerol and 10 mM citrate, pH 4.5). Paraffin embedding and sectioning were performed using a previous protocol described by Feng et al. [18]. Briefly, the spikelets were fixed overnight in 2.5% glutaraldehyde (pH 6.8) at 4°C and washed twice using 0.1 M phosphate buffer (pH 6.8). They were then dehydrated in an ethanol series and embedded in paraffin (Segma) for polymerization at 45°C for 4 hours. Sections were made using a rotary microtome (Leica, RM2235).
Experimental Design and Statistical Analysis
Thirty F1s and their parents were sown on April 4 and transplanted on May 20, 2006 in the Sichuan Agricultural University paddy (Chengdu, Sichuan, China) to evaluate cytoplasmic effects. A randomized complete block design with three replications was used. For each replication, three rows with 12 plants in each row were planted in plots 2.12 m×0.8 m in size. Rows were 26.6 cm apart and plants within rows were 17.7 cm apart. Ten randomly selected plants from each plot were measured for plant height (cm), effective panicle number, 1,000-grain weight (g), grain number per panicle, seed set rate (%), and weight per panicle (g). Mean values were used for analysis of variance (ANOVA). Most of the plants from each plot were bulk harvested for grain yield, but one plant from each end of each row was omitted to exclude any border effect. This experiment was repeated in the summer of 2008, with the same design. A fixed model with type III sum of squares in SPSS software (Version 21.0. Armonk, NY, U.S.: IBM Corp) was adopted and used to perform an ANOVA. Least significant difference (LSD) was estimated for mean comparison of general combining ability (GCA) effects. The A1–A6 GCA was calculated by the difference between a mean over all combinations for a line A such as A1 to be a parent with all restores (R1–R5) and the overall mean for a trait. The effects of h2s cytoplasm on plant height and yield-related traits were estimated as follows: [h2s (A1)/R (R1–R5)] F1– [isonuclear alloplasmic line (A2–A6)/R (R1–R5)] F1.
Molecular Mapping
The h2s gene was mapped using a procedure described previously by Chen et al. [19]. Two F2 populations were generated by crossing h2s as a female with Zhenshan97B and Nipponbare, respectively. We used 342 SSR markers to examine polymorphism between h2s and Zhenshan97B. Preliminary mapping was based on 1532 male sterile F2 individuals from the cross between h2s and Zhenshan97B. For fine mapping, 35 SSRs and 74 indel markers were used to examine polymorphism for the target region between h2s and Nipponbare, and 2400 male sterile F2 individuals produced from this cross were analyzed. Among the 74 indel markers, the closest marker to the mutation locus was W11 (F: TTGGTCCCACAAATAAGTCATG; R: TTGGAGCAACTGAAGCAAGGAA). Genetic distance was estimated using Mapmaker 3.0 software [20]. The expression patterns of candidate genes were analyzed using Rice eFP Browser (http://bar.utoronto.ca/efprice/cgi-bin/efpWeb.cgi) and the rice anther expression database [21].
Expression Analysis for Candidate Gene
Total RNA was isolated using a Qiagen RNA plant mini kit with on-column DNAse digestion (Qiagen). Two micrograms of RNA was used for reverse transcription using M-MLVRT (Promega) with oligo (dT18) primer, and 1 µL RT product diluted with 20 µL ddH2O was used as a template for PCR. The RNA used for RT-PCR was from wild type and mutant anthers at the post-meiosis stage, and the primer pair for Loc_Os06g40550 was W70 (F: CACCACCTACAGTCCCTGCCTCAAA; R: ATGCCGCCCCGCCTATCCTTCCTCA) and OsActin1 (F: ACGGCGATAACAGCT CCTCTT; R: CCTCTT CCAGCCTTCCTTCAT).
Results
Identification and Characterization of h2s
The h2s mutant showed shorter spikelets with smaller anthers than the wild type (Figure 1B, C, D) but exhibited normal pistil and vegetative development with only slightly shorter plant height (Figure 1A). The h2s mutant failed to produce mature pollen (Figure 1E and F). To characterize defects during anther development in the h2s mutant, we performed 4′, 6-diamidino-2-phenylindole staining. No abnormal activity was observed in h2s during meiosis (Figures 2A–P). However, the cytoplasm of the young h2s microspores collapsed after they were released from tetrads (Figure 2Q and R). At the vacuolated pollen stage, the microspores were completely collapsed and only nuclei were left with some residual cytoplasm in the locule (Figure 2S and T). These observations suggest that the developmental defect in the h2s mutant occurred after the release of young microspores from tetrads.
Comparison between WT (left) and h2s (right) for heading plant (A), headed panicle (B, C), flower (D) and pollen of WT (E) and anther of h2s (F).
(A–I) and (K–S) for WT, (B–J) and (L–T) for h2s; (A) and (B) Pachytene, (C) and (D) diakinesis, (E) and (F) metaphase I, (G) and (H) anaphase I, (I) and (J) telophase I, (K) and (L) prophase II, (M) and (N) metaphase II, (O) and (P) tetrad, (Q) and (R) young microspore stage, and (S) and (T) vacuolated pollen stage. No difference in the process of meiosis was observed between WT and h2s. Bars = 10 µm.
To obtain more information regarding the morphological defects of h2s anthers, we examined thin sections of wild-type and h2s anthers. At the meiosis stage, as with 4′, 6-diamidino-2-phenylindole staining, no obvious difference between the wild type and the h2s mutant was observed (Figure 3A and E). At the post-meiotic stage, MMC went through meiosis and formed tetrads in the wild type (Figure 3B). In this way, young microspores in tetrads were released in the anther locule at the young microspore stage (Figure 3C). At the vacuolated pollen stage, the microspore nucleus was pressed near the cytoplasmic membrane by the vacuole and underwent mitosis twice to form mature pollen grains. The tapetum became condensed and degraded (Figure 3D). In contrast, at the post-meiotic stage, the h2s mutant showed young microspores but there was no clear boundary around them (Figure 3F). At the young microspore stage, as with 4′, 6-diamidino-2-phenylindole staining, the young h2s microspores appeared degraded. The microspores in h2s seemed to lack exine, so the microspore degradation might be due to the absence of exine. At the vacuolated pollen stage, the microspores in h2s were completely degraded and formed empty anther locules.
(A–D) for WT, (E–G) for h2s. (A) and (E) Meiosis, (B) and (F) post-meiotic stage, (C) and (G) young microspore stage. The young microspores in h2s exhibited defects at the post-meiotic stage (D) and vacuolated pollen stage (H). However, no microspore was observed at the vacuolated pollen stage. E: epidermis; En: endothecium; T: tapetum; Ms: microsporocyte; Msp: microspore; Tds: tetrad; bars = 15 µm.
Genetic Analysis of the h2s Mutant
All F1 plants from the cross between h2s and 9311 produced normal mature pollen and seed sets. Among 120 F2 plants, 87 had normal pollen and 33 had no pollen, (χ2[3∶1] = 0.259; P>0.5), indicating a single recessive mutation in the spontaneous h2s mutant. h2s also showed stable MS in both Sichuan (E103°82′, N30°97′) and Hainan (E110°05′, N18°28′), suggesting that h2s was not a PTMS.
Cytoplasmic Effects of h2s on Plant Height and Yield-related Traits
No differences in genetic background among the six isonuclear alloplasmic lines (A1–A6) were detected (Figure S1), indicating that the nuclei of Zhenshan97A, D702A, G46A, K18A, and XieqingzaoA were successfully substituted by the h2s nucleus. This allowed reliable comparison of the cytoplasmic effects among A1–A6.
The combined ANOVA for the data collected in two years (Figures S2, S3, S4, S5, S6, S7, and S8) showed that the cytoplasm (P1) had significant effects on all investigated traits except effective panicle number (Table 1). The year effect was significant on all traits except the 1000-grain number and grain number per panicle. The interaction between year and cytoplasm showed a significant effect on effective panicle number, grain number per panicle, and yield. The cytoplasmic effects of h2s on plant height and yield-related traits were estimated by comparing two hybrids with the same male parent. Out of 25 paired comparisons, all but two showed that h2s cytoplasm had a positive effect on yield. These positive effects were significant in 12 (48%) and 10 (40%) paired comparisons in 2006 and 2008, respectively (Table 2). Similarly, all but two paired comparisons showed that h2s cytoplasm had positive effects on the seed set rate. Thirteen (52%) and fourteen (56%) of such comparisons were found to be significant in 2006 and 2008, respectively. Six (24%) and seven (28%) paired comparisons showed significant positive cytoplasmic effect on weight per panicle in 2006 and 2008, respectively. For plant height, effective panicle number, and 1000-grain weight, there were fewer comparisons with significant positive cytoplasmic effects, even though the high proportion of paired comparisons showed positive cytoplasmic effects (Table S2). In contrast, 4 and 9 paired comparisons showed significant negative cytoplasmic effects on grain number per panicle in 2006 and 2008, respectively (Table S2). In conclusion, the cytoplasm of h2s showed a significant and positive effect on yield, seed set rate, weight per panicle, and a significant and negative effect on the grain number per panicle, but plant height, 1000-grain weight, and grain number per panicle were less affected.
Cytoplasmic Effects of h2s on General Combining Ability (GCA)
Studies on GCA have provided information on the potential of specific rice lines as parents in breeding programs. Compared with isonuclear alloplasmic parents A2, A3, A4, A5, and A6, h2s showed significant positive cytoplasmic effects on GCA with respect to yield-related traits (seed set rate, weight per panicle, and yield) (Table 3) and plant height (Table S3) in both years. However, no cytoplasmic effect on GCA with respect to effective panicle number or grain number per panicle was observed for h2s in either year (Table S3). The significant and positive cytoplasmic effect on GCA, especially with respect to yield, suggests that the h2s mutant is a good parent for rice breeding.
Molecular Mapping of the h2s Mutation
Although cytoplasmic analysis of agronomic traits and GCA indicated that h2s had considerable potential for the improvement of rice yield, the male sterility of h2s severely restricts its utility in the production of hybrid seeds. This is because h2s is a non-photoperiod/thermo-sensitive genic male sterile mutant. However, one previously described approach provides a possibility to maintain the MS of recessive GMS, so that h2s could be used to produce hybrid seed in breeding practices [7]. This approach requires cloning the gene responsible for MS. For this reason, we tried to clone the H2S gene using a mapping-based approach.
A F2 population was generated from a cross between h2s and Zhensan97B to map the h2s gene. A bulk segregant analysis was conducted using 52 polymorphic SSR markers between h2s and Zhensan97B with two DNA bulks, each with ten sterile F2 plants and ten fertile F2 plants. Of the 52 SSRs, only RM3 on chromosome 6 was polymorphic between the two DNA bulks, indicating that the putative h2s gene was located on chromosome 6. We then examined 23 SSRs flanking RM3 for polymorphisms between h2s and Zhensan97B, and the polymorphic SSRs were used to analyze 612 male sterile F2 individuals. Both RM454 (located at 27832 kb) and RM528 (located at 26544 kb) were found to be linked with the h2s locus, with 7.47 and 9.19 cM genetic distance, respectively (Figure 4A). Because no other SSRs were found to be polymorphic between h2s and Zhensan97B for the region between RM454 and RM528, 35 SSRs and 74 indel markers were examined for polymorphism between h2s and Nipponbare. The identified polymorphic markers were used to analyze 2400 male sterile F2 individuals in the cross between h2s and Nipponbare. The h2s locus was mapped to a 152 kb region between indel W11 (located at 24044 kb) and RM20366 (located at 24196 kb) with 0.2 and 0.3 cM genetic distance, respectively (Figure 4B). A total of 22 genes were predicted in this mapped region [22] (Table 4), and none of them have been previously reported for the h2s phenotype. This result suggests that H2S is a novel gene controlling post-meiotic anther and pollen development.
(A) Preliminary mapping results using a population of h2s/Zhensan97B and (B) fine mapping results using a population of h2s/Nipponbare. Genetic distance between a marker and the h2s gene is given on the left in centimorgans (cM).D.
Analysis of Candidate Genes
Analysis of expression patterns for the 22 candidate genes showed that ten are expressed in the inflorescence [23] (Table 4). Among the ten candidates, Loc_Os06g40490 encodes a glycosyl hydrolase that is likely to be involved in carbohydrate metabolic processes [24]. Loc_Os06g40550 encodes a protein with an ATP binding cassette (ABC) transporter domain. Its homolog in Arabidopsis, ABCG26/WBC27, has been reported to be involved in pollen exine formation, and the abcg26/wbc27 mutant exhibits impaired pollen wall formation that causes MS in Arabidopsis [25], [26], [27]. The homolog of SNF7 (sucrose non-fermenting 7) protein encoded by Loc_Os06g40620 in Arabidopsis is a subunit of the ESCRT III complex. It may be involved in vesicle-mediated transport [28]. Loc_Os06g40630 encodes a protein containing a SFT2 domain, its homolog in yeast is involved in trafficking to the Golgi complex [29]. Loc_Os06g40650 encodes copine-1, whose homolog in Arabidopsis (ring domain ligase 2) negatively regulates drought stress response [30]. Two genes (LOC_Os06g40540 and LOC_Os06g40660) are predicted to be retro-transposons, and the genetic functions of three other genes (LOC_Os06g40500, LOC_Os06g40580, and LOC_Os06g40609) are unknown at present. Among the ten candidate genes, Loc_Os06g40550 is the only one to be expressed in anthers around the tetrad stage [21]. Considering that a mutant of the Loc_Os06g40550 homolog in Arabidopsis, abcg26/wbc27, also exhibits MS, and the spatial and temporal expression of Loc_Os06g40550 was consistent with h2s phenotype, we chose Loc_Os06g40550 as a top candidate gene for further study.
A twelve-nucleotide (GCCACCCTCCTC) deletion in the predicted sixth exon of Loc_Os06g40550 was detected in the h2s genomic DNA and RNA by sequencing and RT-PCR analysis (Figure5A and B). However, the deletion did not change the reading frame. These results suggest that the deletion in Loc_Os06g40550 may be responsible for the h2s phenotype, but a complementary experiment is needed.
(A) Schematic structure of gene Loc_Os06g40550, 12 bp deletion was detected at the predicted sixth exon. White and grey boxes for UTR regions and exons, respectively. The gray lines for introns, and the black dash box for ABC transporter domain region. (B) RT-PCR examination of 12 deletion in Loc_Os06g40550 RNA. The deletion was detected in the RNA of heterozygous and homozygous plants.
Discussion
In CMS, cytoplasmic effects on most of the agronomic traits are either negative or not actively favorable to the achievement of high grain yield. Our study showed that the cytoplasmic effects of h2s on yield and GCA of yield were positive and significant in both years, suggesting that h2s may be more useful in improving rice yield than CMS. GMS does not have male sterile cytoplasm which is responsible for negative cytoplasmic effect on agronomic traits in the CMS [1], [5], [31]. For this reason, the cytoplasmic effects are probably positive in the GMS as h2s. The positive-cytoplasmic effects on yield in the GMS should be seriously considered in rice breeding.
Although the GMS mutant h2s shows promise for rice breeding, the challenge of maintaining the MS of h2s for the production of hybrid seeds limits its practical application. In order to utilize the positive-cytoplasmic effects of h2s and resolve the challenge, we could generate a PTMS line with both h2s cytoplasm and PTMS nuclei using nuclear substitutions. However, the fact that the fertility of PTMS line with h2s cytoplasm is easily affected by environment also restricts the wide application of positive cytoplasmic effects of h2s. The approach described by Marc et al. [7] has been proposed to maintain the male sterile condition of recessive genic MS and provide an alternative way of utilizing the positive-cytoplasmic effects of h2s in rice breeding. This approach requires cloning the gene responsible for the h2s phenotype. Our mapping results showed that no gene in the fine-mapping region has been reported to be responsible for h2s phenotype, suggesting that h2s is a novel gene essential to male reproductive development. Sequencing and bioinformatics analysis of the candidate genes suggested that Loc_Os06g40550, encoding a protein with ABC transporter domain, was the best candidate. This lays a strong basis for cloning the H2S gene and for using the h2s mutant in rice breeding. Because the h2s mutant showed defective rice anther and pollen wall development, our work may also be helpful for understanding the molecular mechanisms underlying the development of these structures.
Supporting Information
Figure S1.
Two representative results of checking A1–A6 background using ISSR primers and SSRs.
https://doi.org/10.1371/journal.pone.0061719.s001
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Figure S2.
Seed set rate and CV (coefficient of variation) of 30 combinations of 6 isonuclear alloplasmic lines (A1–A6) with 5 restorers (R1–R5) during both years.
https://doi.org/10.1371/journal.pone.0061719.s002
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Figure S3.
Mean grain number per panicle and CV (coefficient of variation) of 30 combinations of 6 isonuclear alloplasmic lines (A1–A6) with 5 restorers (R1–R5) during both years.
https://doi.org/10.1371/journal.pone.0061719.s003
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Figure S4.
Mean 1000-grain weight and CV (coefficient of variation) of 30 combinations of 6 isonuclear alloplasmic lines (A1–A6) with 5 restorers (R1–R5) during both years.
https://doi.org/10.1371/journal.pone.0061719.s004
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Figure S5.
Mean effective panicle number and CV (coefficient of variation) of 30 combinations of 6 isonuclear alloplasmic lines (A1–A6) with 5 restorers (R1–R5) during both years.
https://doi.org/10.1371/journal.pone.0061719.s005
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Figure S6.
Mean plant height and CV (coefficient of variation) of 30 combinations of 6 isonuclear alloplasmic lines (A1–A6) with 5 restorers (R1–R5) during both years.
https://doi.org/10.1371/journal.pone.0061719.s006
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Figure S7.
Mean yield and CV (coefficient of variation) of 30 combinations of 6 isonuclear alloplasmic lines (A1–A6) with 5 restorers (R1–R5) during both years.
https://doi.org/10.1371/journal.pone.0061719.s007
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Figure S8.
Mean weight per panicle and CV (coefficient of variation) of 30 combinations of 6 isonuclear alloplasmic lines (A1–A6) with 5 restorers (R1–R5) during both years.
https://doi.org/10.1371/journal.pone.0061719.s008
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Table S1.
Isonuclear alloplasmic lines used in cytoplasm effects analysis.
https://doi.org/10.1371/journal.pone.0061719.s009
(DOCX)
Table S2.
h2s cytoplasmic effects on seed set rate, weight/panicle and yield in comparison with Zhenshan97A (A2), D702A (A3), G46A (A4), K18A (A5) and XieqingzaoA (A6).
https://doi.org/10.1371/journal.pone.0061719.s010
(DOCX)
Table S3.
GCA effects on seed set rate, weight per panicle and yield among cytoplasms of h2s (A1), Zhenshan97A (A2), D702A (A3), G46A (A4), K18A (A5) and XieqingzaoA (A6).
https://doi.org/10.1371/journal.pone.0061719.s011
(DOCX)
Acknowledgments
We gratefully acknowledge Yuanqi Wu at Sichuan Agricultural University (SAU) for statistical analysis and Yuanyuan Li at SAU for sectioning tissue samples, Wenming Wang at SAU, Sheila McCormick at UC-Berkeley, and Shuizhang Fei at Iowa State University for editing and comments on the manuscript.
Author Contributions
Conceived and designed the experiments: SL YW BM. Performed the experiments: PQ YW YL. Analyzed the data: PQ YW SL. Contributed reagents/materials/analysis tools: YW BM SL. Wrote the paper: PQ YW SL.
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