Jia J, Yang Z, Li G, Liu Ch, Lei M, Zhang T, Zhou J, Ren Z
School of Life Science and Technology, University of Electronic Science and Technology of China, Chengdu, Sichuan, China.
J Appl Genet. 2009;50(1):25-8. doi: 10.1007/BF03195648.
A repetitive sequence of 411 bp, named pSaO5411, was identified in the Secale africanum genome (Ra) by random amplified polymorphic DNA (RAPD) analysis of wheat and wheat-S. africanum amphiploids. GenBank BLAST search revealed that the sequence of pSaO5411 was highly homologous to a part of a Ty1-copia retrotransposon. Fluorescence in situ hybridization (FISH) analyses indicated that pSaO5411 was significantly hybridized to S. africanum chromosomes of a wheat-S. africanum amphiploid, and it was dispersed along the Secale chromosome arms except the terminal regions. Basing on the sequence of pSaO5411, a pair of sequence-characterized amplified region (SCAR) primers were designed, and the resultant SCAR marker was able to target both cultivated rye and the wild Secale species, which also enabled to identify effectively the S. africanum chromatin introduced into the wheat genome.
通过对小麦和小麦-非洲黑麦双体异附加系进行随机扩增多态性DNA(RAPD)分析,在非洲黑麦基因组(Ra)中鉴定出一段411 bp的重复序列,命名为pSaO5411。GenBank BLAST搜索显示,pSaO5411的序列与Ty1-copia逆转座子的一部分高度同源。荧光原位杂交(FISH)分析表明,pSaO5411与小麦-非洲黑麦双体异附加系的非洲黑麦染色体有明显杂交,并且除末端区域外,它沿着黑麦染色体臂分散分布。基于pSaO5411的序列,设计了一对序列特异性扩增区域(SCAR)引物,所得的SCAR标记能够靶向栽培黑麦和野生黑麦物种,这也能够有效地鉴定导入小麦基因组中的非洲黑麦染色质。