- Original article
- Open Access
Analysis of QTL for Grain Size in a Rice Chromosome Segment Substitution Line Z1392 with Long Grains and Fine Mapping of qGL-6
Rice volume 13, Article number: 40 (2020)
Grain size affects not only rice yield but is also an important element in quality of appearance. However, the mechanism for inheritance of grain size is unclear.
A rice chromosome segment substitution line Z1392, which harbors three substitution segments and produces grains of increased length, was identified. The three chromosome segments were located on chromosomes 1, 5, and 6, and the average length of the substitution segment was 3.17 Mb. Cytological analysis indicates that the predominant cause of increased grain length in Z1392 could be cell expansion in the glumes. Seven quantitative trait loci (QTLs) for grain size related traits were identified using the secondary F2 population produced by Nipponbare/Z1392. The inheritance of grain length in Z1392 was mainly controlled by two major QTLs, qGL-5 and qGL-6. qGL-6 was localized on a 1.26 Mb region on chromosome 6, and OsARF19 may be its candidate gene. Based on QTL mapping, three single-segment substitution lines (S1, S2, and S3) and two double-segment substitution lines (D1 and D2) were selected, and the mapping accuracy for qGL-5 and qGL-6 was further verified using three single-segment substitution lines. Analysis of QTL additive and epistatic effects revealed that the additive effect of alleles qGL-5 and qGL-6 from ‘Xihui 18’ was estimated to increase grain length of Z1392 by 0.22 and 0.15 mm, respectively. In addition, a positive epistatic interaction between qGL-5 and qGL-6 was detected, which indicates that the pyramiding of qGL-5 and qGL-6 for grain length produces a novel genotype with longer grains.
Inheritance of grain length in the triple-segment substitution line Z1392 is mainly controlled by two major QTLs, qGL-5 and qGL-6. qGL-6 was found to be located in a 1.26 Mb region on chromosome 6, and OsARF19 may be its candidate gene. A positive epistatic interaction between qGL-5 and qGL-6 results in longer grains. The present results can be used to facilitate cloning of the qGL-5 and qGL-6 genes and contribute to improvement of grain yield in rice.
Rice (Oryza sativa L.) is an important cereal crop throughout Asia. On the basis of the length: width ratio, rice grains are divided into three size classes, namely long, medium, and short grain, for which the ratios range from greater than 3.0, 2.1–2.9, and less than 2, respectively (Bai et al. 2010). Improvements in grain size are directly associated with yield, therefore grain size and yield-related traits are an important focus in research on rice. Chromosome segment substitution lines (CSSLs) are invaluable material in quantitative trait locus (QTL) research for the separation and localization of specific traits (Kubo and Yoshimura 2002). Quantitative traits, such as grain size, plant height, heading stage, and grain filling, are controlled by multiple genes. The construction of CSSLs has formed a strong foundation on which to base further research on quantitative traits.
Rice grain size is controlled by a combination of grain length, grain width, and grain thickness. Previous studies have shown that the development of grain size is dependent on multiple pathways. The mitogen-activated protein kinases (MAPK) pathway contains three cascade reactions, which play an important role in regulation of grain size (Li and Li 2016). SMG1 encod es Mitogen Activated Protein Kinase Kinase 4 (OsMKK4), which is involved in the MAPK signaling pathway. The smg1 mutant produces small and light grains due to a decreased cell number (Duan et al. 2014). OsMAPK6 may be a downstream effector of OsMAKK4. Mutation of OsMAPK6 also causes small-grain and dwarf phenotypes as a result of limited cell proliferation (Liu et al. 2015b). GRAIN SIZE AND NUMBER 1 (GSN1) is a negative regulator of the SMALL GRAIN 2 (OsMKKK10)–SMALL GRAIN 1 (OsMKK4)–OsMPK6 cascade reaction, and regulates cell differentiation and proliferation through the GSN1–MAPK pathway, thus regulating the number and length of grains (Guo et al. 2018). Guanine nucleotide-binding proteins (G proteins) consist of three subunits (α, β, and γ), and G protein-coupled receptors are also involved in the transduction of signaling pathways in rice (Liu et al. 2018). qLGY3 encodes a variable splicing protein, OsMADS1lgy3, which is a crucial effector downstream of the G protein βγ dimer (Liu et al. 2018). The Gγ subunit LONG KERNEL 3 (GS3) interacts with DENSE AND ERECT PANICLE 1 (DEP1) and MADS-domain transcription factors, and participates in the G-protein regulation pathway as a cofactor in the regulation of grain size. Concurrent expression of an allele of the grain size gene OsMADS1lgy3, GS3, and panicle DEP1 may result in traits that enhance yield and quality (Liu et al. 2018). Several recent studies have demonstrated that the ubiquitin–proteasome pathway may also regulate the development of grain size in rice. GRAIN WEIGHT 2 (GW2) encodes a RING-type protein with E3 ubiquitin ligase activity, which regulates proteolysis by targeting substrate binding to the proteasome, thereby negatively regulating cell proliferation and playing a role in the degradation of the ubiquitin–proteasome pathway. Loss of GW2 increases cell number, which results in broader glumes and an accelerated rate of grain filling, thus increasing grain width, weight, and yield (Song et al. 2007). Epigenetic modification also regulates the development of grain size. RELATED TO ABSCISIC ACID INSENSITIVE 3 (ABI3)/VIVIPAROUS 1 (VP1) 6 (RAV6) encodes a B3 DNA-binding protein, which affects the brassinosteroid (BR) pathway by controlling the degree of promoter methylation, thereby regulating the leaf angle and grain size (Zhang et al. 2015b). GW6a encodes a novel GANT-like protein with histone acetyltransferase activity, which regulates rice grain size and yield by regulating the overall acetylation level of histone H4 (Song et al. 2015). In addition, many phytohormone-regulated pathways in rice control the proliferation and longitudinal growth of cells. Multiple genes are involved in the BR signaling pathway, for example, DWARF EBISU (D2/SMG11) encodes cytochrome P450, which regulates grain size by controlling cell elongation (Fang et al. 2016). Several genes are involved in auxin regulation, such as BIG GRAIN 1 (BG1), which encodes a novel membrane-localized protein. Overexpression of BG1 leads to a significant increase in grain size, with clearly perturbed gravitropism in severe cases, by changing the auxin basipetal transport and altered auxin distribution; this suggests that BG1 plays a role in the auxin regulatory pathway (Liu et al. 2015a). Genes involved in the cytokinin regulatory pathway, such as REGULATOR OF AWN ELONGATION 2 (GAD1), which encodes an epidermal pattern factor, regulate the content of endogenous cytokinins by interacting with GRAIN NUMBER 1A (OsCKX2) and DROUGHT AND SALT TOLERANCE (DST) to regulate grain size (Jin et al. 2016). In general, many of the modes that regulate rice grain size remain unexplained and require further study, owing to the complex regulatory modes within and among the pathways.
In this study, a novel rice CSSL with long grains Z1392 and carrying three substitution segments was derived from a cross between ‘Nipponbare’ as the recipient parent and the indica restorer line ‘Xihui 18’ as the donor parent. We performed QTL mapping of grain size traits using a secondary F2 population derived from the cross between ‘Nipponbare’ and Z1392. qGL-6 was localized on a 1.26 Mb region on chromosome 6, and OsARF19 may be its candidate gene. On the basis of the QTL mapping results, we selected single-segment (SSSL), double-segment (DSSL), and triple-segment substitution lines (TSSL) for each QTL in the F3 generation using marker-assisted selection (MAS). We also carried out analysis of the additive and epistatic effects of QTLs on grain length. The results in the present study will be helpful in cloning of QTLs for grain length and their breeding application in the future.
Identification of Substitution Segments in Z1392
Three substitution segments of Z1392 originating in Xihui 18 were located on chromosomes 1, 5, and 6. The substitution segment on chromosome 1 was the the short arm--RM3426--RM1167 and its estimated length was 2.1 Mb. The substitution segment on chromosome 5 was RM3345--nSSR505–RM18119-RM289--RM6082 and it had an estimated length of 3.9 Mb. The substitution segment on chromosome 6 was RM5371--RM7412–RM494--long arm and its estimated length was 3.5 Mb. The total substitution length was 9.5 Mb and the mean length was 3.17 Mb (Fig. 1).
Grain Size Related Traits Analysis of Z1392
Z1392 has similar plant type with the recipient Nipponbare (Fig. 2 A, B). However, Compared with Nipponbare, Z1392 showed a grain length that was increased by 18.43%, a grain width decreased by 13.49% and a ratio of length to width increased by 36.41% (p < 0.01 for each trait) (Fig. 2 C-I). There was no difference for 1000-grain weight between Z1392 and Nipponbare (Fig. 2j).
Cytological Analysis of Glumes in Z1392 and Nipponbare
To examine the factors responsible for the increase in grain length of the substitution line Z1392, scanning electron microscopy was used to observe the cell morphology of glumes in Nipponbare and Z1392 at the heading stage. We measured cell size in the inner epidermis of the glumes of mature grains. The glume cell length in Z1932 was 25.93 μm longer than that of Nipponbare, whereas the cell width was narrower by 4.42 μm on average (Fig. 3a, b, d, e, g, h). No significant difference in total cell number in the outer epidermis of the glume along the longitudinal axis was observed between Nipponbare and Z1392 (Fig. 3c, f, i). These findings suggest that the increase in grain length of Z1392 might have resulted predominantly from cell expansion, and not from an increase in cell number.
Genetic Analysis of Grain Size Related Traits of Z1392
The grain size in Nipponbare displayed a short and broad phenotype, whereas the grain was long and narrow in Xihui 18 and Z1392. The grain size in F1 individuals derived from the cross between Nipponbare and Z1392 was long and narrow, which indicates that the long grain trait exhibited dominance over the short grain phenotype. In the F2 population of 216 individuals, the traits related to grain size, including grain length, grain width, ratio of length to width and 1000-grain weight showed basically a normal distribution, which indicates that these traits in Z1392 were still controlled by multiple genes (Fig. 4).
QTL Mapping for Grain Size Related Traits in the Secondary F2 Population of Nipponbare /Z1392
Seven quantitative trait loci for grain size related traits were identified in the secondary F2 population obtained from the cross between Nipponbare and Z1392. The inheritance of grain length in Z1392 was controlled by two major QTLs, qGL-5 and qGL-6. The additive effect of alleles of qGL-5 and qGL-6 inherited from Xihui 18 was estimated to increase the grain length by 0.22 mm and 0.15 mm in Z1392, implying contribution rates of 32.25% and 15.07%, respectively. The grain width of Z1392 was controlled by the negative effect of qGW-5, which could reduce grain width in Z1392 by 0.09 mm per grain, and its contribution rate was 73.38%. Similarly, the ratio of length to width of Z1392 was controlled by two QTLs, qRLW-5 and qRLW-6, and the contribution rates were 19.01% and 13.52%, respectively. Two QTLs (qKWT-5 and qKWT-6) showed negative and positive effects on 1000-grain weight, and the contribution rates were 20.12% and 21.81%, respectively (Table 1).
Fine Mapping of Putative qGL-6 and Sequence Analysis of Candidate Genes
On the basis of QTL mapping, 241 recessive individuals with short grains excluding those with bands of Nipponbare in the qGL-5 locus of the F2 population were used for fine mapping of qGL-6. The grain length was 7.40 mm in the 241 recombinant types, which shows no real difference from that (7.0 mm) seen in Nipponbare (Fig. 5b). This enabled qGL-6 to be fine-mapped between RM439 and RM103 on chromosome 6, with a physical distance of 1.26 Mb (Fig. 5a). Through gene prediction and sequencing, the auxin response factor OsARF19 was identified as a candidate gene of qGL-6, and this highlighted a number of differences in the DNA sequence of OsARF19 between Nipponbare and Z1392. Firstly, there are 6 CAGs in the CAG repeat region after the 1803rd bases in Nipponbare, but only 5 CAGs in Z1392, and the CAG encodes glutamine. Thus, a glutamine of the OsARF19 protein in Z1392 is reduced compared to Nipponbare. Secondly, a base in the 1830th and 1833rd bases in Nipponbare was changed to G base in Z1392. Thus the CAA in Nipponbare was changed to the CAG in Z1392, but both of these encoded glutamine, and did not cause amino acid changes (Fig. 5c).
Analysis of Additive and Epistatic Effects of QTLs on Grain Length
On the basis of the QTL mapping results, eight individuals were selected from the F2 population by MAS, and F3 lines were obtained from each individual. Ten individuals for each F3 line were sampled for further molecular marker selection using heterozygous markers in the selected plant lines. Ultimately, three SSSLs (S1, S2, and S3) and two DSSLs (D1 and D2) were selected. S1 carried the substitution fragment of chromosome 1 and lacked the QTLs for grain length and grain width. S2 carried the substitution fragment of chromosome 5, which included the grain length QTL qGL-5, for which the additive effect was estimated to be an increased grain length of S2 by 0.3 mm. S3 carried the chromosome 6 substitution fragment containing the grain length QTL qGL-6, for which the additive effect was estimated to be an increased grain length of S3 by 0.13 mm (Fig. 6). These QTLs were repeatedly detected in different years (qGL-5: a2017 = 0.22, P = 0.0012; a2018 = 0.22, P = 0.0012; qGL-6: a2017 = 0.15, P = 0.028; a2018 = 0.22, P = 0.0012), which indicates that the QTLs were mapped accurately, and differences in the additive effect of the QTLs were detected in comparison with the previous season, which suggests that different environments have interactive effects on grain length.
The DSSL D1 carried the substitution fragments of chromosomes 1 and 6. The substitution fragment of chromosome 1 lacked a grain length QTL, whereas the substitution fragment of chromosome 6 contained qGL-6. The additive effect of qGL-6 was 0.13 mm, and an epistatic effect between the two substitution segments of 0.41 mm was observed. The DSSL D2 carried substitution fragments of chromosomes 5 and 6. The substitution fragment of chromosome 5 contained qGL-5, for which the additive effect was 0.3 mm, the substitution fragment of chromosome 6 contained qGL-6, which showed an additive effect of 0.13 mm, and an epistatic effect between the two substitution fragments of 0.31 mm was observed. The TSSL T3 (Z1392) carried the three substitution fragments. As indicated in the preceding discussion, the substitution fragment of chromosome 1 lacked grain length QTL, whereas those of chromosomes 5 and 6 contained qGL-5 and qGL-6, respectively. An epistatic effect among the three substitution fragments of 0.26 mm was observed. Therefore, the theoretical genetic effects on grain length of D1, D2, and T3 were 0.44 mm, 0.74 mm, and 0.69 mm, respectively. Given that the grain length of the recipient parent Nipponbare was 7.2 mm, the grain length of D1, D2, and T3 was predicted to be 8.15 mm, 8.29 mm, and 8.24 mm, respectively. However, the actual average grain length of D1, D2, and T3 was 8.45 mm, 8.67 mm, and 8.58 mm, which may be the result of errors or environmental effects between individuals (Fig. 6). Taken together, the combination of qGL-5 and qGL-6 resulted in the development of a longer grain.
In this study, the rice CSSL Z1392 was identified, having been derived from a cross between Nipponbare as the recipient parent and the indica restorer line Xihui 18 as the donor parent. Z1392 carried three substitution segments and exhibited a long-grain phenotype. The major QTLs carried by Z1392, qGL-5 and qGL-6, contributed to grain length, which affords the opportunity for future research on the molecular mechanisms underlying the development and regulation of grain length. In addition, we analyzed two SSSLs that carried qGL-5 or qGL-6, which positively affected grain length, and one DSSL that carried qGL-5 and qGL-6. Interaction of qGL-5 and qGL-6 resulted in positive epistatic effects in the DSSL, with longer grain length compared with the single long-grain SSSL. Thus, combination of major QTLs that positively affect grain length resulted in a further increase in grain length. However, a previous study showed that combination of two QTLs, qGL3 and qGL4-b, which each have positive effects on grain length, resulted in negative epistatic effects in the DSSL and thus did not result in a longer grain (Zhao et al. 2011). Nevertheless, these results are not contradictory, but rather verify the finding that QTLs with different effects on grain length will produce different interactive effects when combined, and only when the epistatic effect is in the same direction as the additive effect of the target gene can any significant improvement in grain length be achieved. To achieve the desired effect of the target gene, it is first necessary to predict whether two genes interact with each other, and the effect of that interaction. Therefore, given that Z1392 harbors qGL-5 and qGL-6, this line is an important resource for molecular breeding of rice.
Senven QTLs for grain size related traits were identified in Z1392. Compared with the reported QTLs, the grain size QTLs qGW-5 and qKWT-5 are located in the same chromosomal region as GW5, which participates in the ubiquitin–proteasome pathway to regulate cell division during seed development (Weng et al. 2008). The grain length QTL qGL-6 was fine-mapped on chromosome 6, with a physical distance of 1.26 Mb, and 3-bp Indel (CAG) occurred in the coding region of OsARF19, which encodes an auxin response factor. The null mutant osarf19 (isolated from a T-DNA) and RNAi lines of OsARF19 displayed enlarged organs and plant architecture caused by cell elongation (Zhang et al. 2015a, 2015b). Similarly, mutation of qGL-6 showing increased grain length and plant height in Z1392 might also result predominantly from cell expansion. We therefore suppose that OsARF19 is the candidate for qGL-6. The localization interval for the grain length QTL qGL-5 may contain five genes associated with the development of grain size, and which encode a Serine/Threonine protein phosphatase, a rapid alkalization factor (RALF) family protein precursor, a GSK3/SHAGGY-Like kinase, a protein kinase, and an expressed protein containing a PPR repeat sequence. Although these genes that control different traits are located in the same chromosomal interval as the QTLs identified in the present study, further sequencing and functional complementation are still needed to determine whether the genes are alleles of the identified QTLs. Therefore, the present results lay the foundations for additional fine localization of the QTLs, cloning of the candidate genes, and functional research on grain size.
The rice TSSL line Z1392 was identified, which exhibited increased grain length. The chromosomal substitution fragments were located on chromosomes 1, 5, and 6, and the average substitution length was 3.17 Mb. The increased grain length in Z1392 might be caused predominantly by cell expansion in the glumes. Inheritance of the long-grain phenotype in Z1392 is mainly controlled by two major QTLs, qGL-5 and qGL-6. qGL-6 was localized to a 1.26 Mb region on chromosome 6, and OsARF19 may be its candidate gene. On the basis of QTL mapping, three SSSLs and two DSSLs were selected. Epistatic effect analysis revealed a positive epistatic interaction between qGL-5 and qGL-6, which indicates that pyramiding of qGL-5 and qGL-6 enhances the long-grain phenotype.
Materials and Methods
The rice CSSL Z1392 was developed using the rice cultivars ‘Nipponbare’ as the recipient parent and excellent indica restore line ‘Xihui 18’ as the donor parent. After continuous backcrossing and selfing, in combination with phenotype-based selection and simple sequence repeat (SSR) marker selection, a genetically stable CSSL with three substitution segments was identified and designated Z1392.
The plant material used for QTL mapping was a secondary F2 population derived from a cross between Nipponbare and Z1392.
On the basis of QTL mapping results obtained in 2017, eight individual plants were selected by MAS and planted in 2018. Ten individual plants were selected from each line to allow further selection of molecular markers for hybrid markers, and homozygous single-fragment substitution lines and double-fragment substitution lines were then selected.
Material Planting Method
In June 2016, the F1 was generated at the experimental station of Southwest University in Chongqing, China, by crossing Nipponbare with Z1392. In August, hybrid seeds were planted in LingShui, Hainan Province. All 30 F1 seeds and seeds of the parents were planted at the experimental station of Southwest University in Chongqing on March 10, 2017. In March 2018, on the basis of QTL mapping results in 2017, 30 seeds of eight individual plants were used for breeding of secondary substitution fragment lines, and the parents were planted in the same experimental field. On April 15, 2018, all plants were transplanted to the same experimental field. The spacing between hills was 16.67 cm and the spacing between rows was 26.67 cm. Conventional field management practices were applied.
Identification of Substitution Segments in Z1392
A set of 263 markers polymorphic between Nipponbare and Xihui 18 were selected from 429 markers that covered the entire rice genome. The long-grain substitution line Z1392, harboring three substitution segments, was selected from the BC3F4 generation by selection of molecular marker and phenotype. The identification of substitution segments was performed as described previously (Zhao et al. 2016), and the estimated length of the substitution segments was calculated following an established method (Paterson et al. 1991). The distance of the substitution markers from the donor plus half of the distance between the boundary markers from Nipponbare and the substitution markers was taken to be the estimated substitution length. Mapchart 2.2 was used to draw a chromosome substitution fragment map.
Grain Size Related Traits Assessment
At maturity, 10 plants on the third to seventh hills of the central two rows of the Nipponbare and Z1392 plots, and 10 plants of selected SSSLs and DSSLs, and 216 individuals were harvested for QTL mapping. For each plant, grain length, grain width, ratio of length to width, and 1000-grain weight, were measured. A Student’s t-test was conducted for each trait to assess the significance of differences between Nipponbare and Z1392, and descriptive statistics such as skewness and kurtosis were obtained for the F2 population using the statistical functions in Microsoft Excel 2010.
Scanning Electron Microscopy
At the completion of the booting stage and before the heading period, the phenotypic characteristics of the inner and outer epidermal cells of the glume in Nipponbare and Z1392 were investigated using a Hitachi SU3500 scanning electron microscope (Hitachi, Tokyo, Japan) with a frozen stage (− 40 °C) under a low-vacuum environment.
Total genomic DNA of Nipponbare, Xihui 18, Z1392, and the 216 plants from the F2 population was extracted using the cetyltrimethylammonium bromide method (Mccouch et al. 1988). PCR amplification, non-denaturing polyacrylamide gel electrophoresis, and rapid silver staining were performed as described previously (Zhao et al. 2016). Nipponbare bands were scored as “− 1”, Z1392 bands were scored as “1”, heterozygous bands were scored as “0”, and the absence of marker bands was scored as “.”. The marker assignments of all six SSR markers on the substitution segments of Z1392, together with the phenotypic values of each individual in the F2 population, were used for QTL mapping. QTL mapping was performed using the restricted maximum likelihood method by mixed linear models (MLM) implemented in the HPMIXED procedure of SAS (SAS Institute Inc., Cary, NC, USA), with significance determined at α = 0.05 (Hu and Xu 2009; Cui et al. 2017; Spilke et al. 2005).
Development of SSSLs and DSSLs, and Additive and Epistatic Effect Analysis
On the basis of the QTL mapping results obtained in 2017, eight plants were selected using a MAS method and were planted in 2018. Ten plants from each line were selected for further molecular marker assisted selection. Ultimately, homozygous SSSLs and DSSLs were selected. At the maturity stage, 10 plants from each SSSL, DSSL, and TSSL (Z1392) were sampled and the grain length and grain width of each plant were measured, with three replicate measurements per plant recorded. Additive and epistasis effects of unlinked QTLs for grain length and grain width were calculated following the descriptions of Eshed and Zamir (Eshed and Zamir 1996). The additive effect was taken as half the difference between each SSSL and the recipient Nipponbare at P < 0.01 according to the student t-test. QTL interaction in each DSSL was determined by comparing the difference between the effect of DSSL and its corresponding SSSL pairs (SSSLa and SSSLb) at P < 0.01. QTL interaction in TSSL was determined by comparing the difference between the effect of (TSSL+ Nipponbare +Nipponbare) and its corresponding SSSL pairs (SSSLa+ SSSLb + SSSLc) at P < 0.01 by student t-test. The epistatic effect in DSSL was estimated using phenotypic values according to the value of half [DSPL + Nipponbare) - (SSSLa + SSSLb)]. The epistatic effect in TSSL was estimated using phenotypic values according to the value of half [(TSSL + Nipponbare+ Nipponbare) - (SSSLa + SSSLb+ SSSLc)]. Then, a t-test was used to validate QTLs for all traits between each SSSL and Nipponbare. The additive effect of a QTL is half the difference between each SSSL and Nipponbare, and the threshold probability value for a QTL is less than 0.05 (Eshed and Zamir 1996).
Availability of Data and Materials
The datasets supporting the conclusions of this article are included within the article.
Quantitative trait loci
Chromosome segment substitution lines
Triple-segment substitution lines
Simple sequence repeat
Scanning electron microscopy
Bai XF, Luo LJ, Yan WH, Kovi MR, Zhan W, Xing YZ (2010) Genetic dissection of rice grain shape using a recombinant inbred line population derived from two contrasting parents and fine mapping a pleiotropic quantitative trait locus qGL7. BMC Genet 11:16
Cui TT, He KH, Chang LG, Zhang XH, Xue JQ, Liu JC (2017) QTL mapping for leaf area in maize (Zea mays L.) under multi-environments. J Integr Agric 16(4):800–808
Duan PG, Rao YC, Zeng DL, Yang YL, Xu R, Zhang BL, Dong GJ, Qian Q, Li YH (2014) SMALL GRAIN 1, which encodes a mitogen-activated protein kinase kinase 4, influences grain size in rice. Plant J 77(4):547–557
Eshed Y, Zamir D (1996) Less-than-additive epistatic interactions of quantitative trait loci in tomato. Genetics 143(4):1807–1817
Fang N, Xu R, Huang LJ, Zhang BL, Duan PG, Li N, Luo YH, Li YH (2016) SMALL GRAIN 11 controls grain size, Grain Number and Grain Yield in Rice. Rice 9:64
Guo T, Chen K, Dong NQ, Shi CL, Ye WW, Gao JP, Shan JX, Lin HX (2018) GRAIN SIZE AND NUMBER1 negatively regulates the OsMKKK10-OsMKK4-OsMPK6 Cascade to coordinate the trade-off between grain NUMBER per panicle and grain size in Rice. Plant Cell 30(4):871–888
Hu Z, Xu S (2009) PROC QTL-A SAS procedure for mapping quantitative trait loci. Int J Plant Genomics 2009:141234
Jin J, Hua L, Zhu ZF, Tan LB, Zhao XH, Zhang WF, Liu FX, Fu YC, Cai HW, Sun XY, Gu P, Xie DX, Sun CQ (2016) GAD1 encodes a secreted peptide that regulates grain number, grain length, and awn development in Rice domestication. Plant Cell 28(10):2453–2463
Kubo T, Yoshimura A (2002) Genetic basis of hybrid breakdown in a japonica/Indica cross of rice, Oryza sativa L. Theor Appl Genet 105(6–7):906–911
Li N, Li YH (2016) Signaling pathways of seed size control in plants. Curr Opin Plant Biol 33:23–32
Liu LC, Tong HN, Xiao YH, Che RH, Xu F, Hu B, Liang CZ, Chu JF, Li JY, Chu CC (2015a) Activation of big Grain1 significantly improves grain size by regulating auxin transport in rice (vol 112, pg 11102, 2015). Proc Natl Acad Sci U S A 112(39):E5446–E5446
Liu Q, Han RX, Wu K, Zhang JQ, Ye YF, Wang SS, Chen JF, Pan YJ, Li Q, Xu XP, Zhou JW, Tao DY, Wu YJ, Fu XD (2018) G-protein beta gamma subunits determine grain size through interaction with MADS-domain transcription factors in rice. Nat Commun 9(1):852
Liu SY, Hua L, Dong SJ, Chen HQ, Zhu XD, Jiang JE, Zhang F, Li YH, Fang XH, Chen F (2015b) OsMAPK6, a mitogen-activated protein kinase, influences rice grain size and biomass production. Plant J 84(4):672–681
Mccouch SR, Kochert G, Yu ZH, Wang ZY, Khush GS, Coffman WR, Tanksley SD (1988) Molecular mapping of Rice chromosomes. Theor Appl Genet 76(6):815–829
Paterson AH, Damon S, Hewitt JD, Zamir D, Rabinowitch HD, Lincoln SE, Lander ES, Tanksley SD (1991) Mendelian factors underlying quantitative traits in tomato - comparison across species, generations, and environments. Genetics 127(1):181–197
Song XJ, Huang W, Shi M, Zhu MZ, Lin HX (2007) A QTL for rice grain width and weight encodes a previously unknown RING-type E3 ubiquitin ligase. Nat Genet 39(5):623–630
Song XJ, Kuroha T, Ayano M, Furuta T, Nagai K, Komeda N, Segami S, Miura K, Ogawa D, Kamura T, Suzuki T, Higashiyama T, Yamasaki M, Mori H, Inukai Y, Wu JZ, Kitano H, Sakakibara H, Jacobsen SE, Ashikari M (2015) Rare allele of a previously unidentified histone H4 acetyltransferase enhances grain weight, yield, and plant biomass in rice. Proc Natl Acad Sci U S A 112(1):76–81
Spilke J, Piepho HP, Hu X (2005) Analysis of unbalanced data by mixed linear models using the MIXED procedure of the SAS system. J Agron Crop Sci 191(1):47–54
Weng JF, Gu SH, Wan XY, Gao H, Guo T, Su N, Lei CL, Zhang X, Cheng ZJ, Guo XP, Wang JL, Jiang L, Zhai HQ, Wan JM (2008) Isolation and initial characterization of GW5, a major QTL associated with rice grain width and weight. Cell Res 18(12):1199–1209
Zhang S, Wu T, Liu S et al (2015b) Disruption of OsARF19 is Critical for Floral Organ Development and Plant Architecture in Rice (Oryza sativa L.). Plant Mol Biol Report 34(4):748–760
Zhang XQ, Sun J, Cao XF, Song XW (2015a) Epigenetic mutation of RAV6 affects leaf angle and seed size in Rice. Plant Physiol 169(3):2118–2128
Zhao FM, Tan Y, Zheng LY, Zhou K, He GH, Ling YH, Zhang LH, Xu SZ (2016) Identification of Rice chromosome segment substitution line Z322-1-10 and mapping QTLs for agronomic traits from the F-3 population. Cereal Res Commun 44(3):370–380
Zhao FM, Zhang GQ, Zeng RZ, Yang ZL, Ling YH, Sang XC, He GH (2011) Analysis of Epistatic and additive effects of QTLs for grain shape using single segment substitution lines in Rice (Oryza sativa L.). Acta Agron Sin 37(3):469–476
We thank Professor Shizhong Xu at University of California, Riverside, USA for writing the stem program for the QTL mapping.
The study was supported by the National Key Research Plan Project (2017YFD0101107), the National Natural Science Foundation of China (grant no. 31900612), and the Chongqing Technical Innovation and Application Development Project (cstc2019jscx-msxmX0392).
Ethics Approval and Consent to Participate
This study complied with the ethical standards of China, where this research work was carried out.
Consent for Publication
All authors are consent for publication.
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Zhang, T., Wang, S., Sun, S. et al. Analysis of QTL for Grain Size in a Rice Chromosome Segment Substitution Line Z1392 with Long Grains and Fine Mapping of qGL-6. Rice 13, 40 (2020). https://doi.org/10.1186/s12284-020-00399-z
- Chromosome segment substitution line
- Grain length
- QTL mapping
- Epistatic analysis