Long Hai, Wei Yu-Ming, Yan Ze-Hong, Baum Bernard, Nevo Eviatar, Zheng You-Liang
Triticeae Research Institute, Sichuan Agricultural University, Dujiangyan, Sichuan 611830, China.
Theor Appl Genet. 2005 Nov;111(7):1251-9. doi: 10.1007/s00122-005-0024-1. Epub 2005 Nov 15.
On the basis of sequence analysis, 69 known low-molecular-weight glutenin subunit (LMW-GS) genes were experimentally classified into nine groups by the deduced amino acid sequence of the highly conserved N-terminal domain. To clarify the chromosomal locations of these groups, 11 specific primer sets were designed to carry out polymerase chain reactions (PCR) with the genomic DNA of group 1 ditelosomic lines of Chinese Spring, among which nine primer sets proved to be LMW-GS group-specific. Each group of LMW-GS genes was specifically assigned on a single chromosome arm and hence to a specific locus. Therefore, these results provided the possibility to predict the chromosome location of a new LMW-GS gene based on its deduced N-terminal sequence. The validity of the classification was confirmed by the amplifications in 27 diploid wheat and Aegilops accessions. The length polymorphisms of LMW-GS genes of groups 1 and 2, and groups 3 and 4.1 were detected in diploid A-genome and S-genome accessions, respectively. The diploid wheat and Aegilops species could be used as valuable resources of novel allele variations of LMW-GS gene in the improvement of wheat quality. The nine LMW-GS group-specific primer sets could be utilized to select specific allele variations of LMW-GS genes in the marker-assisted breeding.
基于序列分析,通过推导高度保守的N端结构域的氨基酸序列,将69个已知的低分子量麦谷蛋白亚基(LMW-GS)基因实验性地分为9组。为了明确这些组在染色体上的位置,设计了11对特异性引物,以中国春1组双端体品系的基因组DNA进行聚合酶链反应(PCR),其中9对引物被证明是LMW-GS组特异性的。每组LMW-GS基因都被特异性地定位在一条染色体臂上,从而定位到一个特定的位点。因此,这些结果为根据新的LMW-GS基因推导的N端序列预测其染色体位置提供了可能性。通过在27个二倍体小麦和节节麦材料中的扩增,证实了分类的有效性。在二倍体A基因组和S基因组材料中分别检测到了1组和2组以及3组和4.1组LMW-GS基因的长度多态性。二倍体小麦和节节麦物种可作为LMW-GS基因新等位变异的宝贵资源用于小麦品质改良。这9对LMW-GS组特异性引物可用于在分子标记辅助育种中选择LMW-GS基因的特异性等位变异。