Development of an allele-specific marker for Glu-B3 alleles in common wheat and establishment of a multiplex PCR assay

被引:3
作者
Sui, Xinxia [1 ,2 ]
Wang, Linhai [1 ]
Xia, Xianchun [1 ]
Wang, Zhenlin [3 ]
He, Zhonghu [1 ,4 ]
机构
[1] Chinese Acad Agr Sci, Inst Crop Sci, Natl Wheat Improvement Ctr, Natl Key Facil Crop Gene Resources & Genet Improv, Beijing 100081, Peoples R China
[2] Shandong Acad Agr Sci, Crop Res Inst, Jinan 250100, Peoples R China
[3] Shandong Agr Univ, Coll Life Sci, Tai An 271018, Shandong, Peoples R China
[4] Chinese Acad Agr Sci, China Off, Int Maize & Wheat Improvement Ctr CIMMYT, Beijing 100081, Peoples R China
基金
中国国家自然科学基金;
关键词
Functional marker; LMW-GS; multiplex PCR; Triticum aestivum L; LOW-MOLECULAR-WEIGHT; TRITICUM-AESTIVUM L; GLUTENIN SUBUNIT GENES; CHINESE BREAD WHEATS; DOUGH PROPERTIES; STS MARKERS; QUALITY; LMW; PROTEINS; LOCI;
D O I
10.1071/CP10241
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Low-molecular-weight glutenin subunits (LMW-GS) have significant effects on the processing quality of enduse products of common wheat. It is more efficient to discriminate LMW-GSalleles with PCR-based molecular markers than with SDS-PAGE. In the present study, we developed an allele-specific PCR marker, designated Glu-B3abefg, which can be used to discriminate protein alleles Glu-B3a, b,e,f, and g simultaneously. Based on ten previously developed allele-specific STS markers, three multiplex PCRs, viz. Glu-B3c + Glu-B3d, Glu-B3b + Glu-B3g, and Glu-B3h + Glu-B3i, were established. Six Glu-B3 alleles (b, c, d, g, h, and i) could be discriminated using the three multiplex PCRs. Results of tests on 158 wheat varieties and lines using Glu-B3abefg and the three multiplex PCRs were consistent with those using the ten STS markers separately. The new allele-specific marker and three multiplex PCRs represent an efficient way to undertake marker-assisted selection of Glu-B3 alleles.
引用
收藏
页码:978 / 987
页数:10
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