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Converting restriction fragment length polymorphism to single‐strand conformation polymorphism markers and its application in the fine mapping of a trichome gene in cotton
Author(s) -
He Shae,
Zheng Yunna,
Chen Aiqun,
Ding Mingquan,
Lin Lifeng,
Cao Yuefen,
Zhou Wei,
Rong Junkang
Publication year - 2013
Publication title -
plant breeding
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.583
H-Index - 71
eISSN - 1439-0523
pISSN - 0179-9541
DOI - 10.1111/pbr.12030
Subject(s) - single strand conformation polymorphism , biology , genetics , restriction fragment length polymorphism , genetic marker , gene mapping , cleaved amplified polymorphic sequence , genome , molecular marker , gene , polymerase chain reaction , chromosome
A well‐characterized and systematically organized collection of genetic markers is crucial in the study of any crop species. It is the basis of map‐based gene cloning and crop improvements through marker‐assisted selections. Single‐strand conformation polymorphism ( SSCP ) has been a robust way of discovering new polymorphisms in marker development without the requirement of sequencing. Here, we report the first approach of applying SSCP marker discovery methods in the genetic map construction and gene mapping of cotton species. A total of 80 restriction fragment length polymorphism ( RFLP ) markers were selected from a region on published cotton genetic maps around the T 1 gene related to cotton trichome. Among the 80 RFLP s, 28 showed polymorphisms through SSCP , showing a polymorphic rate of approximately 35%, which is much higher than that of simple sequence repeat ( SSR ) markers in the same region (7.8%). By integrating these newly generated SSCP markers, a detailed genetic map was reconstructed around this region using an F 2 population derived from a cross between G ossypium arboreum and G . herboceum . The reconstructed region comprises 22 SSCP markers, eight SSR markers and the T 1 gene, spanning 21.6 cM. The marker order of the new map agrees well with published reference RFLP maps. The above results suggest that SSCP method can be applied very efficiently and reliably to the marker development of cotton genomes. It will prove to be even more valuable and robust after the public release of cotton whole‐genome sequences.