Abstract

Association analysis between constructed single nucleotide polymorphism linkage disequilibrium blocks (SNPLDBs) and general combining ability (GCA) effects is a novel approach to uncover the genetic basis of GCA within the sequence genomes of parents of hybrid rice. Here, we calculated the GCA effect values of 33 parents of hybrid rice and sequenced them to identify genome-wide single nucleotide polymorphisms (SNPs). In total, 64.6 % of the uniquely mapped paired-end short reads revealed a final total of 291 959 SNPs between the 33 parental genomes and the Nipponbare reference genome. The identified SNPs were non-randomly distributed among all chromosomes of rice, whereas one-fourth of the SNPs were situated in the exonic regions with 16 % being non-synonymous. Further, the identified SNPs were merged and optimized for construction of 2612 SNPLDB markers, using linkage disequilibrium information. The single-factor analysis of variance-based association method between the constructed SNPLDB markers and GCA effects values detected 99 significant SNPLDBs for GCA of 11 yield-related traits. The associated SNPLDB markers explained 26.4 % of phenotypic variations with traits, on average. We mined 50 favourable GCA alleles at the associated SNPLDBs regions, distributed across the 33 parental genomes. The parental genomes possessed a small number of favourable GCA alleles for studied traits, with the exception of days to heading and plant height. Our results suggest that the identified GCA alleles could be used to improve the GCA performance of parents of hybrid rice through optimal crossing design. Moreover, favourable GCA alleles should be incorporated in the parental genomes through marker-assisted selection experiments, and the parental lines carrying more alleles could be utilized in breeding as superior parents for developing rice hybrids of desirable characteristics.

Highlights

  • 256A ( WA type) Zhenpin A ( WA type) 257A ( WA type) II-32A ( ID type) Zhenshan 97 A ( WA type) Yuetai A ( ID type) You 1A( WA type) Zhong 9A ( WA type) 863A ( BT type) 9201A ( BT type) Xu 2A ( BT type Nanjing 46A ( BT type) 731A ( BT type) Liuqianxin A ( BT type) 6427A ( BT type) Zhendao 88A ( BT type) Qingkong A ( BT type) Yueguang A ( BT type) Wuqiang A ( BT type) Wuyujing 3A ( BT type) Liuyan 189A ( BT type) Minghui 63 Zhenhui 084 Yanhui 559 Huizi 04 Hui 9368 Kanghui[98] C418 Ninghui8hao Yunhui 4 hao Zhehui 315 Yanhui R50 Xiushui 04R

  • that none of the superior alleles of GCA are situated within the sequenced genome of parents

  • PH are positive in sense of favoring shorter plant height

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Summary

Supporting Information

256A ( WA type) Zhenpin A ( WA type) 257A ( WA type) II-32A ( ID type) Zhenshan 97 A ( WA type) Yuetai A ( ID type) You 1A( WA type) Zhong 9A ( WA type) 863A ( BT type) 9201A ( BT type) Xu 2A ( BT type Nanjing 46A ( BT type) 731A ( BT type) Liuqianxin A ( BT type) 6427A ( BT type) Zhendao 88A ( BT type) Qingkong A ( BT type) Yueguang A ( BT type) Wuqiang A ( BT type) Wuyujing 3A ( BT type) Liuyan 189A ( BT type) Minghui 63 Zhenhui 084 Yanhui 559 Huizi 04 Hui 9368 Kanghui[98] C418 Ninghui8hao Yunhui 4 hao Zhehui 315 Yanhui R50 Xiushui 04R

Developed year Subspecies indica indica indica indica japonica japonica japonica
Chr Allele No
Indica Combinations
NPPP NSPP NFGPP PL SW ST SL TG GYPP
Yueguang A
SW ST SL TGW GYPP
Nucleotide Biological process Molecular process Ref length
DNA binding transcription factor
NPPP response to abiotic
CAAX amino terminal protease family protein metabolic
Leucine Rich Repeat domain containing

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