Schwarz Gerhard, Sift Andreas, Wenzel Gerhard, Mohler Volker
EpiGene GmbH, Biotechnology in Plant Protection, Hohenbachernstrasse 19-21, 85354 Freising, Germany.
J Agric Food Chem. 2003 Jul 16;51(15):4263-7. doi: 10.1021/jf0261304.
The promoter regions of HMW glutenin x-type genes at the Glu-D1 locus were surveyed for SNPs within a subpopulation of German bread wheat cultivars. On the basis of the promoter sequences of HMW glutenin subunit genes Glu-A1-x1, Glu-A1-x2, Glu-B1-x1, Glu-B1-x7, Glu-D1-x2, and Glu-D1-x5, an amplification refractory mutation system assay was designed to selectively amplify Dx-specific PCR fragments. Comparative sequence analysis among seven Glu-D1-x2 and seven Glu-D1-x5 wheat cultivars only confirmed a G-A transition in the promoter sequence to be a true polymorphism. SNP scoring by DHPLC of 95 German bread wheat cultivars, with the exception of cv. Anemos, showed that the transition completely agreed with the presence of HMW glutenin subunits 1Dx5 + 1Dy10 in SDS-PAGE. Therefore, the developed DHPLC assay is suitable for high-throughput genotyping to assist the selection of HMW glutenin genes in wheat quality breeding programs.
在德国面包小麦品种的一个亚群中,对位于Glu-D1位点的高分子量谷蛋白x型基因的启动子区域进行了单核苷酸多态性(SNP)检测。基于高分子量谷蛋白亚基基因Glu-A1-x1、Glu-A1-x2、Glu-B1-x1、Glu-B1-x7、Glu-D1-x2和Glu-D1-x5的启动子序列,设计了一种扩增阻滞突变系统分析法,以选择性扩增Dx特异性PCR片段。对7个Glu-D1-x2小麦品种和7个Glu-D1-x5小麦品种进行的比较序列分析仅证实启动子序列中的G-A转换是一个真正的多态性。通过变性高效液相色谱(DHPLC)对95个德国面包小麦品种(除品种Anemos外)进行SNP评分,结果表明该转换与十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)中高分子量谷蛋白亚基1Dx5 + 1Dy10的存在完全一致。因此,所开发的DHPLC分析法适用于高通量基因分型,以协助小麦品质育种计划中高分子量谷蛋白基因的选择。