QTL Scanning for Rice Yield Using a Whole Genome SNP Array

被引:21
作者
Tan, Cong [1 ]
Han, Zhongmin [1 ]
Yu, Huihui [2 ]
Zhan, Wei [1 ]
Xie, Weibo [1 ]
Chen, Xun [1 ]
Zhao, Hu [1 ]
Zhou, Fasong [2 ]
Xing, Yongzhong [1 ]
机构
[1] Huazhong Agr Univ, Natl Ctr Plant Gene Res, Natl Key Lab Crop Genet Improvement, Wuhan 430070, Peoples R China
[2] China Natl Seed Grp Co Ltd, Life Sci & Technol Ctr, Wuhan 430075, Peoples R China
关键词
RILs; RICE6K SNP array; Bin map; Segregation distortion; QTL; QUANTITATIVE TRAIT LOCI; SINGLE-NUCLEOTIDE POLYMORPHISMS; ORYZA-RUFIPOGON; DEVELOPMENTAL BEHAVIOR; NATURAL VARIATION; TILLER NUMBER; GENETIC-BASIS; MALE MEIOSIS; LINKAGE MAP; GRAIN-SIZE;
D O I
10.1016/j.jgg.2013.06.009
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
High-throughput SNP genotyping is widely used for plant genetic studies. Recently, a RICE6K SNP array has been developed based on the Illumina Bead Array platform and Infinium SNP assay technology for genome-wide evaluation of allelic variations and breeding applications. In this study, the RICE6K SNP array was used to genotype a recombinant inbred line (RIL) population derived from the cross between the indica variety, Zhenshan 97, and the japonica variety, Xizang 2. A total of 3324 SNP markers of high quality were identified and were grouped into 1495 recombination bins in the RIL population. A high-density linkage map, consisting of the 1495 bins, was developed, covering 1591.2 cM and with average length of 1.1 cM per bin. Segregation distortions were observed in 24 regions of the 11 chromosomes in the RILs. One half of the distorted regions contained fertility genes that had been previously reported. A total of 23 QTLs were identified for yield. Seven QTLs were firstly detected in this study. The positive alleles from about half of the identified QTLs came from Zhenshan 97 and they had lower phenotypic values than Xizang 2. This indicated that favorable alleles for breeding were dispersed in both parents and pyramiding favorable alleles could develop elite lines. The size of the mapping population for QTL analysis using high throughput SNP genotyping platform is also discussed.
引用
收藏
页码:629 / 638
页数:10
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