Construction of a high-density linkage map and mapping quantitative trait loci for somatic embryogenesis using leaf petioles as explants in upland cotton (Gossypium hirsutum L.)

被引:7
作者
Xu, Zhenzhen [1 ,2 ]
Zhang, Chaojun [1 ]
Ge, Xiaoyang [1 ]
Wang, Ni [1 ]
Zhou, Kehai [1 ]
Yang, Xiaojie [1 ]
Wu, Zhixia [1 ]
Zhang, Xueyan [1 ]
Liu, Chuanliang [1 ]
Yang, Zuoren [1 ]
Li, Changfeng [1 ]
Liu, Kun [1 ]
Yang, Zhaoen [1 ]
Qian, Yuyuan [1 ]
Li, Fuguang [1 ]
机构
[1] Chinese Acad Agr Sci, Inst Cotton Res, State Key Lab Cotton Biol, Anyang 455000, Peoples R China
[2] Jiangsu Acad Agr Sci, Inst Ind Crops, Nanjing 210014, Peoples R China
关键词
Quantitative trait loci; Somatic embryogenesis; Genetic map; Simple sequence repeat; Cotton; SIMPLE SEQUENCE REPEAT; PLANT-REGENERATION; FIBER QUALITY; BARBADENSE L; EST-SSRS; MARKERS; GENOME; TRANSFORMATION; CALLUS; GENE;
D O I
10.1007/s00299-015-1776-y
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
The first high-density linkage map was constructed to identify quantitative trait loci (QTLs) for somatic embryogenesis (SE) in cotton ( Gossypium hirsutum L.) using leaf petioles as explants. Cotton transformation is highly limited by only a few regenerable genotypes and the lack of understanding of the genetic and molecular basis of somatic embryogenesis (SE) in cotton (Gossypium hirsutum L.). To construct a more saturated linkage map and further identify quantitative trait loci (QTLs) for SE using leaf petioles as explants, a high embryogenesis frequency line (W10) from the commercial Chinese cotton cultivar CRI24 was crossed with TM-1, a genetic standard upland cotton with no embryogenesis frequency. The genetic map spanned 2300.41 cM in genetic distance and contained 411 polymorphic simple sequence repeat (SSR) loci. Of the 411 mapped loci, 25 were developed from unigenes identified for SE in our previous study. Six QTLs for SE were detected by composite interval mapping method, each explaining 6.88-37.07 % of the phenotypic variance. Single marker analysis was also performed to verify the reliability of QTLs detection, and the SSR markers NAU3325 and DPL0209 were detected by the two methods. Further studies on the relatively stable and anchoring QTLs/markers for SE in an advanced population of W10 x TM-1 and other cross combinations with different SE abilities may shed light on the genetic and molecular mechanism of SE in cotton.
引用
收藏
页码:1177 / 1187
页数:11
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