- Research article
- Open Access
Association analysis between constructed SNPLDBs and GCA effects of 9 quality-related traits in parents of hybrid rice (Oryza sativa L.)
BMC Genomics volume 21, Article number: 31 (2020)
The general combining ability (GCA) of parents in hybrid rice affects not only heterotic level of grain yield and other important agronomic traits, but also performance of grain quality traits of F2 bulk population which is the commodity consumed by humans. In order to make GCA improvement for quality traits in parents of hybrid rice by molecular marker assisted selection feasible, genome-wide GCA loci for quality traits in parents were detected through association analysis between the effects of GCA and constructed single nucleotide polymorphism linkage disequilibrium blocks (SNPLDBs), by using unhusked rice grains harvested from F1 plants of 48 crosses of Indica rice and 78 crosses of Japonica rice. GCA-SNPLDBs association analysis.
Among the 8 CMS and 6 restorer lines of indica rice subspecies, CMS lines Zhenpin A, Zhenshan97 A, and 257A, and restorers Kanghui98, Minghui63 and Yanhui559 were recognized as good general combiners based on their GCA effect values for the 9 quality traits (brown rice rate, milled rice rate, head rice rate, percentage of chalky grains, chalky area size, chalkiness degree, gelatinization temperature, gel consistency and amylose content). Among the 13 CMS and 6 restorer lines of japonica rice subspecies, CMS 863A, 6427A and Xu 2A, and restorers C418, Ninghui8hao and Yunhui4hao showed elite GCA effect values for the 9 traits. GCA-SNPLDB association analysis revealed 39 significant SNPLDB loci associated with the GCA of the 9 quality-related traits, and the numbers of SNPLDB loci located on chromosome 1, 2, 3, 4, 5, 8, 9, 11 and 12 were 1, 4, 3, 9, 6, 5, 5, 4 and 2, respectively. Number of superior GCA alleles for the 9 traits among the 33 parents ranged from 1 to 26.
Thirty-nine significant SNPLDBs loci were identified associated with the GCA of 9 quality-related traits, and the superior SNPLDB alleles could be used to improve the GCA of parents for the traits in the future by molecular marker assisted selection. The genetic basis of trait GCA in parents is different from that of trait itself.
Rice (Oryza sativa L.) is a crucial staple crop for more than half of the world population. Recently, due to the increase in their living standards, people started to demand high-quality rice, including high eating and cooking quality, with various preferences in different geographic regions. Breeding researcher more centered on enhancing the quality of rice to cope with the demanded quality standards of direct consumers, and the other various commercial uses. Grain quality in rice is determined through many factors, e.g., nutritional value, grain appearance, cooking and eating quality. Among 117 rice-growing countries, hybrid rice breeding technologies have been adopted by 27 countries. Grain quality of hybrid rice has its speciality since the commodity consumed by people is a F2 bulk population.
From a commercial perspective, the key to gain high grain quality from hybrid rice depends on the choice of parental material. The prime initiative of rice breeders for developing superior hybrid rice cultivar is to choose suitable mating parents . These parental characteristics are heritable and were able to appear in the F1 generation. The combining ability is the basic breeding tool for identification of prospective parents of hybrid cultivars for both yield and quality traits. Generally, combining ability is an estimation and prediction of parental values relayed on their developed offspring performances . Typically, evaluation of inbred parents and crosses for GCA following the traditional plant breeding methods are laborious, tedious and time-consuming . In addition, as the number of parents involved in combining ability manipulation increased, their hybrids affected the feasibility of the experiment . Many studies based on association analysis between combining ability and markers also revealed genomic loci significantly found associated with the combining ability of parental traits [13, 16, 18, 19, 22, 27, 37]. Several SSR marker loci associated with the CA of quality traits have been published. However, these studies were confined to SSR markers. Thus far, no SNP-based analyses were reported to discover SNPLDB locus/loci associated with the GCA of parental quality traits in rice.
In this study, to increase the power of association analysis for discovery of GCA loci of quality-related traits, we suggest a grouping of identified SNPs into haplotype blocks (SNPLDBs). The principle of blocking was determined based totally on tightly linked genetic loci. SNPs are usually located close to each other and trend to move together. In general, genetic loci located more adjutants to others on a chromosome had strong LD compared to those present distantly. The construction of SNPLDBs and treating them as an independent unit (marker), we are minimizing the number of assumptions being tested and thus relaxing the strict criteria for gaining maximum significance of association analysis. Merging SNPs together in a proper way extends the dimension of association analysis. Furthermore, if there are multiple independent SNPs, by considering their joint effect, we will have the power to detect this joint effect on the trait. Recently, the LD blocks-based SNPLDB marker have been proposed for association analysis and showed practical utility value in the experiments of plant breeding [25, 40].
Here, we treated the constructed SNPLDB as a marker and examined in the associations with the values of GCA for 33 parents of hybrid rice for 9 quality-related traits, using the single factor ANOVA method of marker-trait association. The sequence data were obtained by performing genotyping by sequencing of parental genomes, whereas, the GCA effects were estimated by evaluation of developed hybrids.
The objectives of our study were: (1) to evaluate parents of hybrid rice for GCA effect of quality traits; (2) to associate SNPLDB with the parents GCA to determine genome-wide GCA loci and superior SNPLDB alleles related to grain quality traits; (3) to predict combinations that can improve GCA effect values of parents for the quality traits through pyramiding or substituting SNPLDB alleles.
Performance of 9 quality traits of F2 bulks in two sets of NCII combinations
The mean performances of 9 quality-related traits in 48 hybrids obtained from 8 indica rice CMS lines crossed with 6 indica restorers are presented in Additional file 1: Table S1. Among the 48 Indica developed crosses, the highest brown rice rate (86.3%), gelatinization temperature (6.2ASS) and amylose content (23.9%) in addition to the least chalkiness degree (1.6%) were observed in Zhenshan97A × Kanghui98. The cross between CMS Yuetai A and restorer Yanhui559 recorded the highest milled rice rate (76.2%) and head rice rate (69.5%), while, The least percentage of chalky grains (36.0%), chalky area size (16.7%) and gel consistency (37.5 mm) was detected in 256A × Zhenhui084.
The mean performances of 9 quality-related traits in 78 hybrids obtained from 13 japonica rice CMS crossed with 6 japonica restorers are presented in Additional file 2: Table S2. Among the 78 japonica developed crosses, the mean performance of Wuyujing3A × Ninghui8hao showed the highest brown rice rate (83.8%), milled rice rate (73.7%), head rice rate (67.1%) and gel consistency (62.0 mm) in addition to the least chalkiness degree (1.6%). The cross between CMS 731A and restorer Yanhui R50 recorded the least percentage of chalky grains (30.5%), chalky area size (11.5%) and gelatinization temperature (1.1ASS), whereas, the least amylose content (9.6%) was detected in Liuyan 189A × Yanhui R50.
Estimations of GCA effects of indica rice CMS and restorer lines
In our study, the effect values of GCA for CMS and restorer lines in indica rice varied significantly for 9 quality-related traits. The 14 parents (8 CMS lines + 6 restorer lines) of indica rice set showed both positive and negative GCA effect values. For example, the GCA of II-32A showed a negative effect for chalky area size, percentage of chalky grains, chalkiness degree and amylose content, but positive effect on head rice rate, milled rice rate, brown rice rate, gel consistency and gelatinization temperature. Among the 8 indica CMS lines, the GCA effects of CMS Zhenpin A showed maximum positive values for all traits (Table 1). Also, the CMS Zhenshan97A was observed to be good general combiner for chalky area size, percentage of chalky grains, chalkiness degree and gel consistency.
Among the 6 indica restorer lines, Minghui63 had maximum GCA effect values for head rice rate, chalky area size, percentage of chalky grains, chalkiness degree and amylose content; Kanghui98 showed maximum positive GCA values for milled rice rate, brown rice rate and gel consistency; Yanhui559 showed maximum positive GCA value for gelatinization temperature (Table 1). In terms of elite parental lines, the CMS Zhenpin A, Zhenshan97A and restorer Minghui63, Kanghui98 and Yanhui559 had the most favorable GCA effects for the studied traits.
Based on the five level evaluation criteria and comprehensive scoring standards for nine grain quality traits in indica rice shown in Additional file 3: Table S3. the comprehensive evaluation scores of 48 F2s ranged from 43 to 75 (Full score of nine traits is 90) (Fig. 1). The combination crossed by Yuetai A and Yanhui559 recorded the highest score among the 48 F2s (Fig. 1). The grain quality performance of F2 derived from the combination of Yuetai A × Yanhui559 were showed in Fig. 2. According to China’s Ministry of Agriculture’s Edible Rice Quality Industry Standard (NY/T 593-2002) , the quality traits of grain could be divided into five levels and the first level is the best. The HRR, MRR, BRR and CD of F2 grains crossed by Yuetai A and Yanhui559 belonged to level 1. The GT and AC belonged to level 2. And the remaining traits, i.e. CAS, PCG and GC belonged to level 3, 3 and 4, respectively (Fig. 2). The comprehensive evaluation scores of the combinations considering Yuetai A, Zhenpin A, Zhenshan97A, Yanhui559, Hui9368 and Kanghui98 as parents were generally higher, which was basically consistent with the results of general combining ability analysis (Fig. 1 and Table 1).
Estimations of GCA effects of japonica CMS and restorer lines
The parents of japonica hybrid rice showed both positive and negative GCA effects values for 9 quality-related traits. Among the 13 japonica CMS lines, CMS 863 A was observed to be the best general combiner for all the studied traits except GT (Table 2). Maximum GCA value of gelatinization temperature was showed by 6427 A.
Among the 6 japonica rice restorer lines, C418 recorded the maximum GCA effects for most of traits; Ninghui8hao, Yunhui4hao also showed good general combiners for all the studied traits (Table 2). In terms of GCA performances of all quality-related traits, CMS 863 A, 6427 A and restorers C418, Ninghui8hao and Yunhui4hao had a favorable GCA effects for developing japonica hybrids of superior performances.
Based on the five level evaluation criteria and comprehensive scoring standards for the nine grain quality traits shown in Additional file 4: Table S4. the comprehensive evaluation scores of 78 F2s ranged from 33 to 48 (Full score of nine traits is 90) (Fig. 3). The highest score was observed in the combination crossed by Wuyujing3A and Ninghui8hao (Fig. 3). Figure 4 showed the values of 7 grain quality traits of the aforementioned cross. According to the NY/T 593-2002 mentioned above, the CD and BRR of F2 grains in the combination crossed by Wuyujing3A and Ninghui8hao belonged to level 2; the HRR, MRR, GT and GC belonged to level 3; and the remaining traits, i.e. PCG, CAS and AC belonged to level 4, 5 and 5, respectively (Fig. 4). The comprehensive evaluation scores of the combinations considering Wuyujing3A, 92101A, Ninghui8hao and Yanhui R50 as parents were generally higher, which was basically consistent with the results of general combining ability analysis (Fig. 3 and Table 2).
Association analysis between constructed SNPLDBs and GCA effects
The association analysis between the effect values of GCA and constructed SNPLDBs revealed a total of 39 significant SNPLDBs for GCA of 9 quality-related traits. The identified SNPLDBs were distributed on nine of the 12 chromosomes of rice. The number of associated SNPLBDs for each trait varied and, on average over the 39 SNPLDBs, 41.6% of phenotypic variation was explained by each SNPLDB. The detail information of the 39 associated SNPLDBs is presented in Fig. 5 and Table 3.
Brown rice rate
Two SNPLDBs situated on 2 different chromosomes (Chr4, Chr5) showed significant associations with the GCA of brown rice rate. The associated GCA-SNPLDBs of brown rice rate explained phenotypic variance in the range of 49.1% (S5_12092551) to 54.9% (4_BLOCK_17882078_17907416) (Table 3). The SNPLDB detected on chromosome 4 showed a positive effect with GCA of the trait. The elite SNP genotype (A/C at 17907065 bp position) of gene Os04g0368800/LOC_Os04g30010 situated on chromosome 4 increased BRR by 10.28% (Table 4).
Milled rice rate
Two SNPLDBs situated on 2 different chromosomes (Chr4, Chr5) showed significant relationships with the GCA of milled rice rate. The phenotypic variation caused by these SNPLDBs ranged from 49.4% (S5_12092551) to 53.6% (4_BLOCK_17882078_17907416) (Table 3). The SNPLDB detected on chromosome 4 showed a positive effect on GCA of MRR. The elite SNP genotype (A/C at 17907065 bp position) of gene Os04g0368800/LOC_Os04g30010 situated on chromosome 4 increased MRR by 10.62% (Table 4).
Head rice rate
Three SNPLDBs distributed over chromosome 4, 5, and 8 revealed significant associations with the GCA of head rice rate. The phenotypic variations caused by these associated SNPLDBs were 52.0% (4_BLOCK_17882078_17907416), 49.9% (S5_12092551) and 35.5% (8_BLOCK_26862470_27057202), respectively (Table 3). The SNPLDB (4_BLOCK_17882078_17907416) detected on chromosome 4 favored larger phenotypic variation and both SNPLDBs on chromosomes 4 and 8 showed a positive effect on the GCA of HRR. The elite SNP genotypes (AC/CT at the position of 17,907,065 bp and 26,969,210 bp) of genes Os04g0368800 and Os08g0539400 located on chromosomes 4 and 8 increased HRR by 12.85 and 17.35%, respectively (Table 4).
Percentage of chalky grains
One SNPLDB situated on chromosome 4 showed associations with the GCA of the percentage of chalky grains. The phenotypic variance explained by the SNPLDB (4_BLOCK_17882078_17907416) was 51.1% (Table 3). The SNP genotype (A/C at 17907065 bp position) of gene Os04g0368800 situated on chromosome 4 decreased PCG by 10.63% (Table 4).
Chalky area size
Twelve SNPLDBs situated on 9 various chromosomes (Chr1, Chr2, Chr3, Chr4, Chr5, Chr8, Chr9, Chr11 and Chr12) were associated with the GCA of chalky area size. The percentages of phenotypic variation explained by these SNPLDBs were ranged from 19.6% (2_BLOCK_23246549_23402926) to 60.9% (11_BLOCK_16710912_16770852) (Table 3). Among the eight genes associated with the combining ability of CAS, the SNP genotype of gene Os08g0539400 (C/T at 26969210 bp position) situated on chromosome 8 recorded the largest decrement 22.68% (Table 4).
One SNPLDB situated on chromosome 4 showed associations with the GCA of chalkiness degree. The phenotypic variance caused by the SNPLDB was 52.2% (4_BLOCK_17882078_17907416) (Table 3). The elite SNP genotype (A/C at 17907065 bp position) of gene Os04g0368800 situated on chromosome 4 made CD of heterozygous group decreased from 1.96 to 1.76% (Table 4).
One SNPLDB situated on chromosome 4 showed associations with the GCA of gelatinization temperature. The phenotypic variance caused by the SNPLDB (4_BLOCK_17882078_17907416) was 50.3% (Table 3). The SNP genotype (A/C at 17907065 bp position) of gene Os04g0368800 situated on chromosome 4 in the heterozygous group has a 43.57% larger GT than that in homozygous group (Table 4).
Two SNPLDBs situated on 2 different chromosomes (Chr4, Chr5) revealed significant relationships with the GCA of gel consistency. The percentage of phenotypic variation explained by these SNPLDBs ranged from 41.3% (S5_12092551) to 50.3% (4_BLOCK_17882078_17907416) (Table 3) The elite SNP genotype (A/C at 17907065 bp position) of gene Os04g0368800 situated on chromosome 4 increased GC by 8.9% (Table 4).
Fifteen SNPLDBs situated on 8 various chromosomes (Chr2, Chr3, Chr4, Chr5, Chr8, Chr9, Chr11 and Chr12) were found associated with the GCA of amylose content. Three significant SNPLDBs were observed on chromosome 9 and 11, respectively. The percentage of phenotypic variations explained by these SNPLDBs ranged from 19.8% (9_BLOCK_20278565_20464993) to 63.5% (11_BLOCK_16710912_16770852) (Table 3). A total of eight SNPLDBs, 11 elite SNPs genotype were detected decreasing GCA of AC. The highest decrease percentage between the heterozygous group and the homozygous group is the elite SNP genotype (C/T at 26969210 bp position) ofOs08g0539400 situated on chromosome 8, and the decreased value was 26.65% (Table 4).
Distribution of superior alleles among the 33 parents
In this study, the alleles which caused positive effects on GCA of quality traits of parents of hybrid rice were considered as the superior alleles. For BRR, MRR, HRR and GC traits, the higher GCA effect value was considered as positive effects, and for PCG, CAS, CD, GT and AC traits, the lower GCA effect value was considered positive effects. The number of superior alleles for BRR, MRR, HRR, PCG, CAS, CD, GT, GC and AC detected across 33 parents were 4, 4, 16, 2, 66, 2, 2, 4 and 90, respectively (Table 5).
Among the 8 Indica CMS lines, CMS Zhenpin A showed 12 positive GCA alleles, including one for HRR, 4 for CAS and 7 for AC.. CMS Yuetai A demonstrated 11 positive GCA alleles, including one for HRR, 4 for CAS and 6 for AC (Table 5). Meanwhile, among the 6 Indica restorer lines, restorer Minghui 63 had 15 positive GCA alleles, including one for HRR, 6 for CAS and 8 for AC. Restorer Zhenhui 084 contained 16 positive GCA alleles, including one for BRR, 1 for MRR, 1 for HRR, 5 for CAS, 1 for GC and 7 for AC.. Restorer Kanghui98 contained 2 positive GCA alleles for CAS and 5 positive GCA alleles for AC.
Among the 13 Japonica CMS lines, CMS Zhendao 88A had a maximum number of positive GCA alleles for all traits. The CMS 9201A, Liuqianxin A and Wuqiang A each had 2 positive GCA alleles for CAS and AC, respectively (Table 5). Among the 6 Japonica restorer lines, restorer Yanhui R50 had 26 GCA alleles in genomes for all the 9 quality. The restorer Ninghui8hao showed the presence of 4 and 7 positive GCA alleles for CAS and AC, respectively. The restorer Zhehui315 carried 1, 2 and 4 positive GCA alleles for HRR, CAS and AC, respectively. The restorer C418 contained 1,1 and 3 positive GCA alleles for HRR, CAS and AC, respectively.
Elite parental lines for developing of superior hybrid cultivars
Based on the presence of detected superior GCA-SNPLDB alleles that could be combined (pyramided) into a maintainer (CMS has no fertile pollens) or restorer lines, the elite parental combinations of improved GCA of quality-related traits were suggested. The superior alleles carried by the CMS and restorer lines are presented in (Table 5). The parental lines carrying a maximum number of superior GCA-SNPLDB alleles could be the elite parental lines of superior GCA performances, which had the potential of developing hybrids of promising performances. Alleles detected in CMS and restorer lines will improve the GCA of traits which will alternatively cause positive effect on rice quality trait values of F2 bulk population.
Among the Indica CMS and restorer lines, the crossing combinations between CMS Zhenpin A and restorers Minghui 63 and Kanghui98 are the elite Indica parental lines for developing of superior hybrids of head rice rate, chalky area size and amylose content. Subsequently, among the Japonica parents of hybrid rice, CMS 863A, Liuqianxin A, Wuqiang A and Zhendao 88A with restorers C418, Yanhui R50 and Ninghui8hao were found to be elite parental combinations containing a maximum number of superior GCA alleles for most of the quality-related traits.
In this study, we prepared two sets of F1 crosses using NCII genetic design to evaluate GCA effect values of 9 quality-related traits in parents in rice. One set was consisted of 48 F1 crosses made by 8 CMS and 6 restorer lines within indica rice subspecies, and the other set contained 78 F1 crosses made by 13 CMS and 6 restorer lines within japonica rice subspecies. Significant variations of the GCA effect values of the 9 traits were observed in 33 parents. Among the parental lines in Indica subspecies, CMS Zhenpin A, Zhenshan97 A, and 257A and restorers Kanghui98, Minghui63 and Yanhui559 were recognized as good general combiners due to their maximum positive GCA effect values for most of the traits. Among the parental lines in Japonica subspecies, CMS 863A, 6427A and Xu 2A and restorers C418, Ninghui8hao and Yunhui4hao recorded maximum positive GCA effect values for traits.
By association analysis between the effects of GCA and SNPLDBs, we detected 39 significant SNPLDB loci associated with the GCA of the 9 traits, and the SNPLDB loci were located on chromosome 1 (1), 2 (4), 3 (3), 4 (9), 5 (6), 8 (5), 9 (5), 11 (4) and 12 (2). By searching the website www.ricedata.cn/gene/index.htm, we found that on chromosome 2, our associate region 23,246,549 − 23,402,926 responsible for GCA of AC/CAS was near to the cloned rice quality-related gene du3 (OsCBP20, Os02g0612300, 24,100,174 − 24,103,481), away from 697,248 bp (24,100,174 − 23,402,926) each other. Also, on chromosome 9, the associate region (S9_21,092,077) responsible for GCA of CAS/AC was 343,568 bp apart from the cloned rice quality-related gene OsVPS22 (Os09g0529700, 20,744,838 − 20,748,509). We did not find SNPLDB loci harboring the cloned Wx and ALK genes on chromosome 6 associated with GCA of the these traits. Togather, we inferred that the genetic basis of trait GCA in the parents is different from that of trait itself in rice. And we explained the results as that trait GCA in the parents is mainly related with polygenes rather than with major gene controlling the trait itself.
From the perspective of enhancing the hybrid rice quality, F2 bulk seed analysis is effective and unavoidable choice in our study, and it is feasible to associated SNPLDB with combining ability for grain quality traits in hybrid rice parents through combining the SNP genotypes of parents and the quality phenotypes of F2 directly. All the elite SNPLDBs detected in our research are useful for enhancement grain quality traits in hybrid rice.
Significance of GCA evaluation by markers
Traditional methods, such as Grifing’s mehods, NC methods, can be used to estimate the GCA effects of parental lines. However, if we want to improve GCA of parents, we need to breed new parents by many years and evaluate them again. It is a time-consuming and laborious work in field trials. The ongoing progress in genomics has provided a wide range of molecular markers for crop improvement. Since there are enormous types of molecular markers are available for tagging the genomic regions of important phenotypes in parental genomes of hybrid rice, the information of GCA may become predictable based on dissection of parental lines using markers. By genotyping GCA of parents with the use of molecular markers, we can not only detect the GCA loci in parental genomes but can also improve the GCA of a parent by pyramiding the favorable GCA alleles exiting in various parents into a single parent (maintainer (CMS) or restorer) and/or removing of unfavorable GCA alleles by marker-assisted selection. Previously, based on the identified favorable and unfavorable SSR alleles, the combining ability of an elite rice restorer line (Minhui63) was enhanced by the incorporation of favorable combining ability alleles and elimination of unfavorable CA alleles .
Advantage of SNPLDBs for association analysis
SNPs always show more biological significance when SNP clusters are tightly organized into haplotype blocks in the examined genomic region . Association analysis with SNPLDBs increases the power of association [6, 30]. In fact, compared with individual SNPs, constructed SNPLDB has a higher meaning, enhancing the accuracy and robustness of association analysis [8, 11]. Association analysis using SNPLDB can significantly improve the efficiency of detecting QTLs [23, 24, 38]. In addition, association analysis using SNPLDB can provide new biological insights for genomic regions that determine trait control, which is not available with a single SNP method . Efforts to construct SNPLDB from large genomic sequence data are being successful in various crops, such as Chinese soybean , rice , and corn , and wheat .
Association analysis by single-factor test
To date, many studies were conducted to dissect the genomic regions (or QTLs) underlying important phenotypes of rice using marker-trait association strategy. Different methods were used for different populations. GWAS method is suitable for natural population. Interval mapping method is suitable for bi-parent-derived segregation populations. For our NCII-derived population, the single-factor test method was used for testing associations between marker and phenotype . This association method provides maximum resolution that enables the identification of significant candidate loci. Using this single-factor association analysis, we found 39 significant SNPLDBs associated with the GCA of 9 quality-related traits. The SNPLDBs distributed on chromosome 1, 2, 3, 4, 5, 8, 9, 11 and 12 (Table 3). According to the distribution of the superior SNPLDB alleles (Table 5), GCA of the quality traits in parents could be improved by pyramiding or substituting process though molecular marker assisted selection. For example, GCA of the 9 traits in japonica restorer Xiushui 04R could be enhanced by crossing it with another japonica restorer Yanhui R50 (Table 5).
We identified 39 significant SNPLDBs associated with the GCA of 9 quality-related traits among the parents used and the SNPLDB information could be used to improve the GCA of parents for the quality traits in the future. The genetic basis of trait GCA in parents is different from that of trait itself.
In our study, two sets of F1 hybrids were prepared using the North Carolina mating design II . One set contained 48 F1 hybrids made by 8 CMS and 6 restorer lines in Indica rice subspecies, and the other set consisted of 78 F1 hybrids made by 13 CMS and 6 restorer lines in Japonica rice subspecies. These parental lines are widely utilized for the commercial production in three-line hybrid rice in China. Dry seeds of the 33 parents were sown in the first week of May 2014 on the seedling nursery in paddy field at the Jiangpu Experimental station (32°07′N, 118°64′E), Nanjing Agricultural University, Nanjing, China. Thirty days after sowing, the seedlings were transplanted by hand into the paddy field with each plot containing 5 rows with 8 plants per row at a space of 20 cm × 20 cm. At heading stage, the spikelets of CMS plants were cut one third using scissors by hand before floret flowering, pollinated with restorer pollen and covered with Kraft paper bag (Fig. 6a). Twenty five days after pollination, the F1 seeds were harvested (Fig. 6b), dried by air, threshed by hand and stored in room temperature. The F1 hybrids’ seeds and their parents (restorer lines, and maintainer lines instead of CMS lines) were nursed in the first week of May 2015. Thirty days later, the seedlings were transplanted into the paddy field with one seedling per hill using a randomized complete block design and three replications. Each plot contained 5 rows with 8 plants per row at a space of 20 cm × 20 cm,. Field management practices were implemented according to the local standards. After the lowest grain on main stem panicle in all plants within a plot became yellow, all the panicles of randomly-selected 6 plants within the plot were harvested by hand, put them into a Nylon mesh bag, dried them under the sun, and threshed by hand. The dried grains were stored three months at room temperature for stabling the physicochemical traits of rice qualities.
Brown rice rate is calculated using the following formula:
Where, brown rice or husked rice was obtained by removing the husk of raw rice (Fig. 7a, b) by a brown rice machine (JE0826, Zhejiang Taizhou grain Instrument Factory).
Milled rice rate is calculated by using the formula:
Where, milled rice was obtained by removing all or part of the bran and embryo from the husked rice grains using the Laboratory Huller (JMNJG3, Zhejiang Taizhou grain Instrument Factory).
Head rice rate is calculated by using the formula:
Head rice indicates to milled rice grains whose length is greater than or equal to three quarters of the average length of the intact grain (Fig. 7c).
Percentage of chalky grains, chalky area size and chalkiness degree
Grain chalkiness was assessed by a visual rating of the chalky percentage of the grain (Fig. 7d,e) based totally on the standard Evaluation System (SES). Selection, segregation and weighing the chalky grains was performed. The test method of PCG, CAS and CD were in accordance to the method of Han et al.  and Hong . The following formula was used to calculate the percentage of chalky grains:
The GT was indirectly estimated as the alkali spreading score (ASS) according to Little et al.  with slightly modified. Briefly, 6 grains of intact milled white rice of each accession were put in a petri dish of 60 mm in diameter and add 10 ml of 1.7% KOH water solution. The samples were separated from each other by using the forceps and incubated at 30 ± 0.5 °C for 23 h to allow spreading of the grains. The spreading score of the grains was recorded through visual assessment according to the description of Jennings et al. . ASS values were recorded as grade 1 to grade 7, according to the appearance of the endosperm and the degree of dispersion. Endosperm that was unaffected were recorded 1, and that were disappeared completely (Fig. 7f) were recorded 7, ASS is inversely proportional to GT. There are three classes of gelatinization temperature: the ASS from 1 to 3 grades is high GT (> 75 °C), from 4 to 5 grades is intermediate GT (70–74 °C), and from 6 to 7 grades is low GT (< 70 °C).
The GC was determined following the method of Cagampang et al. . Briefly, 100 mg of rice flour about 12% of the moisture content was weighed in a test tube, to which 0.2 ml of 95% ethanol containing thymol blue was added and gently shaken to forestall cluttering of the powder during gelatinization. Two milliliters of 0.2 mol/L KOH was added and thoroughly shaken. The tubes were covered with the glass marbles and boiled in a water bath to reflux for 8 min. After cooling down at room temperature for 5~10 min, the tubes were placed on ice for 20 min, and then placed horizontally on the surface of the table for 1 h. The length of the gel (mm), that is, the distance from the bottom of the tube to the front of the gel migration, is a measurement of GC (Fig. 7g). The longer the gel is, the softer the GC is.
The AC of head rice grains was measured by using the automatic microplate spectrophotometer followed the method described by Zhu et al. . Briefly, each 50 mg of test sample flour was taken in a test tube with scale, added 0.5 ml of 95% ethanol and 1.5 ml of 3 mol/L NaOH, respectively. The tube was placed overnight (12-16 h) in 30 °C thermostat after fully skimmed then shaken lightly with distilled water to 40 ml. 10 μl mixture was added on the ELISA plate with 96 holes (Fig. 7h), remaining reaction solution consisted of 2 μl of 1 mol/L acetic acid and 3 μl of 2% I2-KI, finally adding distilled water 185 μl, so that each hole volume to 200 μl. The remaining step is setting the wavelength of 620 nm, the microplate spectrophotometer automatically recorded the optical density (OD) value, which was showed in the computer monitor. The content of amylose was calculated by a standard curve.
Calculation of effect values of GCA
According to the statistical model , the obtained phenotypic data of the hybrids have been subjected to analysis of variance (ANOVA) by using excel software (2007). The following equations were used to analyze the effect values of GCA in 9 quality-related traits for the 33 parents .
where, μ =mean,
gi= general combining ability effect of ith genotype,
εik = error term associated with ith genotype and kth replication.
Significance of genotype differences was tested using the method of least significant difference (LSD) at α = 0.01 probability level.
Construction of SNPLDBs
The SNP data of this study were obtained from Zaid et al. , and are available at NCBI under accession number SRR7250921. The missing genotypes in the sequence data were precisely predict through the fastPHASE software . Then, The linkage disequilibrium (LD) blocks were defined by Haploview software . The confidence intervals block partitioning approach was used with default settings, except that 200 kb and 0.01 were the maximum distance and minimum major allele frequency (MAF), respectively . To construct SNPLDB, the SNPs inside the block have been grouped into a single marker with haplotype as its alleles. Each constructed SNPDB was tested in association analysis after treating it as a marker. The markers of constructed SNPLDB were characterized in detail by using Power Marker software (v3.25) through calculating their MAF, genetic diversity and polymorphism information content (PIC) .
In order to identify significantly associated SNPLDBs with the effect values of GCA for the parents of hybrid rice, the single-factor analysis of variance (ANOVA) was used to test the association between the effect values of GCA for 9 quality-related traits and the constructed SNPLBDs . The linear model is
Where yij is the ith allele jth observation at the SNPLDB under testing.
μ is the mean of population,
ai is the ith allele effect and
εij is error of random.
SAS PROC GLM (Release 9.1.3; SAS Institute, Cary, NC) was used to perform all the computation processes. The significant SNPLDBs on the chromosomal region had been selected at the least P value (α = 0.001 probability level) for all traits except chalky area size and amylose content which were selected at P value (α = 0.01 probability level). The coefficient of determination (R2) was estimated to determine the percentage of phenotypic variation explained by each associated SNPLDB marker.
Availability of data and materials
All data generated or analyzed during this study are included in this published article and supplementary information files. All the SNP data of this study obtained from previous studies on rice CMS in our State Key Laboratory of Crop Genetics and Germplasm Enhancement, Nanjing Agricultural University, and are available at NCBI under accession number SRR7250921.
Brown rice rate
Chalky area size
Cytoplasmic male sterile
General combining ability
Head rice rate
Milled rice rate
Percentage of chalky grains
Single nucleotide polymorphism
Simple sequence repeats
Abdel-Shafy H, Bortfeldt RH, Tetens J, Brockmann GA. Single nucleotide polymorphism and haplotype effects associated with somatic cell score in German Holstein cattle. Genet Sel Evol. 2014;46(1):35.
Barrett JC, Fry B, Maller J, Daly MJ. Haploview: analysis and visualization of LD and haplotype maps. Bioinformatics. 2005;21(2):263–5.
Bertan I, Carvalho F, Oliveira AD. Parental selection strategies in plant breeding programs. J Crop Sci Biotechnol. 2007;10:211–22.
Cagampang GB, Perez CM, Juliano BO. A gel consistency test for eating quality of rice. J Sci Food Agric. 1973;24(12):1589–94.
Cao L, Zhan X. Chinese experiences in breeding three-line, two-line and super hybrid Rice. Rijeka: INTECH; 2014.
Ferdosi MH, Henshall J, Tier B. Study of the optimum haplotype length to build genomic relationship matrices. Genet Sel Evol. 2016;48(1):75.
Gabriel SB, Schaffner SF, Nguyen H, Moore JM, Roy J, Blumenstiel B, et al. The structure of haplotype blocks in the human genome. Science. 2002;296(5576):2225.
Grapes L, Dekkers JCM, Rothschild MF, Fernando RL. Comparing linkage disequilibrium-based methods for fine mapping quantitative trait loci. Genetics. 2004;166(3):1561.
Haile JK, Hammer K, Badebo A, Singh RP, Röder MS. Haplotype analysis of molecular markers linked to stem rust resistance genes in Ethiopian improved durum wheat varieties and tetraploid wheat landraces. Genet Resour Crop Evol. 2013;60(3):853–64.
Han L, XW. Description and specification of rice germplasm resources. Beijing: China Agriculture Press; 2006.
Hayes BJ, Chamberlain AJ, McPartlan H, Macleod I, Sethuraman L, Goddard ME. Accuracy of marker-assisted selection with single markers and marker haplotypes in cattle. Genet Res. 2007;89(4):215–20.
Hong DL. Experimental technique of crop breeding. Beijing: Science Press; 2010.
Huang J, Qi H, Feng X, Huang Y, Zhu L, Yue B. General combining ability of most yield-related traits had a genetic basis different from their corresponding traits per se in a set of maize introgression lines. Genetica. 2013;141(10):453–61.
Jennings PR, Coffman WR, HEK. Grain Quality. In: Rice improvement. Philippines: Intl Rice Res Inst Los Banos; 1979. p. 101–20.
Lestari P, Lee G, Ham T-H, Reflinur WM-O, Piao R, et al. Single nucleotide polymorphisms and haplotype diversity in Rice sucrose synthase 3. J Hered. 2011;102(6):735–46.
Liang K, Huang D-C, Zhao K-M, Nguyen P-T, Xie H, Ma W-X, et al. Marker genotypes for parents of japonica hybrid Rice with high combining ability of yield traits. Acta Agron Sin. 2010;36(8):1270–9.
Little RR, Hilder GB, Dawson EH. Differential effect of dilute alkali on 25 varieties of milled white rice. Cereal Chem. 1958;35(2):111–26.
Liu C, Song G, Zhou Y, Qu X, Guo Z, Liu Z, et al. OsPRR37 and Ghd7 are the major genes for general combining ability of DTH, PH and SPP in rice. Sci Rep. 2015a;5:12803.
Liu EB, Liu Y, Liu XL, Liu QM, Zhao KM, Edzesi WM, et al. Detecting marker genotypes with elite combining ability for yield traits in parents of hybrid japonica rice. Chinese J Rice Sci. 2013;27:473–81.
Liu K, Muse SV. PowerMarker: an integrated analysis environment for genetic marker analysis. Bioinformatics. 2005;21(9):2128–9.
Liu X-C, Chen S-G, Chen J-S, Ishiki K, Wang W-X, Yu L-Q. Improvement of combining ability for restorer lines with the identified SSR markers in hybrid Rice breeding. Breed Sci. 2004;54(4):341–6.
Liu Y, Liu EB, Zeng SY, Pu W, Liu QM, Liang LJ, et al. Identification of molecular marker fragments associated with combining ability for quality traits in parents of hybrid japonica rice (Oryza sativa L.). Chinese J Rice Sci. 2015b;29:373–81.
Lorenz AJ, Hamblin MT, Jannink J-L. Performance of single nucleotide polymorphisms versus haplotypes for genome-wide association analysis in barley. PLoS One. 2010;5(11):e14079.
Lu Y, Zhang S, Shah T, Xie C, Hao Z, Li X, et al. Joint linkage–linkage disequilibrium mapping is a powerful approach to detecting quantitative trait loci underlying drought tolerance in maize. Proc Natl Acad Sci. 2010;107(45):19585.
Meng S, He J, Zhao T, Xing G, Li Y, Yang S, et al. Detecting the QTL-allele system of seed isoflavone content in Chinese soybean landrace population for optimal cross design and gene system exploration. Theor Appl Genet. 2016;129:1557–76.
Montana G. Statistical methods in genetics. Brief Bioinform. 2006;7(3):297–308.
Qi H, Huang J, Zheng Q, Huang Y, Shao R, Zhu L, et al. Identification of combining ability loci for five yield-related traits in maize using a set of testcrosses with introgression lines. Theor Appl Genet. 2013;126(2):369–77.
Rafalski A. Applications of single nucleotide polymorphisms in crop genetics. Curr Opin Plant Biol. 2002;5(2):94–100.
Rice Editorial Office of China. Industry standard of Ministry of Agriculture of China -- Cooking rice variety quality (NY/T 593-2002). China Rice. 2003;(1):41-42.
Saad MN, Mabrouk MS, Eldeib AM, Shaker OG. Identification of rheumatoid arthritis biomarkers based on single nucleotide polymorphisms and haplotype blocks: a systematic review and meta-analysis. J Adv Res. 2016;7(1):1–16.
Shukla SK, Pandey MP. Combining ability and heterosis over environments for yield and yield components in two-line hybrids involving thermosensitive genic male sterile lines in rice (Oryza sativa L.). Plant Breed. 2008;127(1):28–32.
Singh RK, Chaudhary BD. Biometrical methods in quantitative genetics analysis. New Delhi: Kalyani Publishers; 1977.
Smith JSC, Hussain T, Jones ES, Graham G, Podlich D, Wall S, et al. Use of doubled haploids in maize breeding: implications for intellectual property protection and genetic diversity in hybrid crops. Mol Breed. 2008;22(1):51–9.
Sprague GF, Tatum LA. General vs. specific combining ability in single crosses of Corn1. Agron J. 1942;34(10):923–32.
Stephens M, Scheet P. Accounting for decay of linkage disequilibrium in haplotype inference and missing-data imputation. Am J Hum Genet. 2005;76(3):449–62.
Van Inghelandt D, Melchinger AE, Martinant J-P, Stich B. Genome-wide association mapping of flowering time and northern corn leaf blight (Setosphaeria turcica) resistance in a vast commercial maize germplasm set. BMC Plant Biol. 2012;12(1):56.
Xie H, Dang X-J, Liu E-B, Zeng S-Y, Hong D-L. Identifying SSR Marker Locus Genotypes with Elite Combining Ability for Yield Traits in Backbone Parents ofJaponicaHybrid Rice (Oryza satival.) in Jianghuai Area. Acta Agronomica Sinica. 2016;42(3):330.
Yan J, Warburton M, Crouch J. Association mapping for enhancing maize (Zea mays L.) genetic improvement. Crop Sci. 2011;51(2):433–49.
Zaid IU, Tang W, Liu E, Khan SU, Wang H, Mawuli EW, et al. Genome-Wide Single-Nucleotide Polymorphisms in CMS and Restorer Lines Discovered by Genotyping Using Sequencing and Association with Marker-Combining Ability for 12 Yield-Related Traits in Oryza sativa L. subsp. Japonica. Front Plant Sci. 2017;8:143.
Zhang Y, He J, Wang Y, Xing G, Zhao J, Li Y, et al. Establishment of a 100-seed weight quantitative trait locus–allele matrix of the germplasm population for optimal recombination design in soybean breeding programmes. J Exp Bot. 2015;66(20):6311–25.
Zhu L, Liu Q, Sang Y, Gu M, Shi YC. Underlying reasons for waxy rice flours having different pasting properties. Food Chem. 2010;120(1):94–100.
The first author is grateful to Mr. Hossam-eldin Seddik for language help.
Funding support was provided by a grant from National Natural Science Foundation of China (31671658, to Delin Hong) which was used for collection of 9 quality traits, analysis of the data and manuscript processing charge.
Ethics approval and consent to participate
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
Eltahawy, M.S., Ali, N., Zaid, I.U. et al. Association analysis between constructed SNPLDBs and GCA effects of 9 quality-related traits in parents of hybrid rice (Oryza sativa L.). BMC Genomics 21, 31 (2020) doi:10.1186/s12864-019-6428-0
- Hybrid rice
- Combining ability of parents
- Single nucleotide polymorphism linkage disequilibrium blocks
- Association analysis
- Quality traits