Echt C S, Erdahl L A, McCoy T J
Department of Plant and Soil Science, Montana State University, Bozeman, MT 59717.
Genome. 1992 Feb;35(1):84-7. doi: 10.1139/g92-014.
Polymerase chain reaction was used, with single 10-mer primers of arbitrary sequence, to amplify random regions of genomic DNA from a diploid cultivated alfalfa backcross population. Segregation of the random amplified polymorphic DNA (RAPD) fragments was analysed to determine if RAPD markers are suitable for use as genetic markers. Of the 19 primers tested, 13 amplified a total of 37 polymorphic fragments, of which 28 (76%) segregated as dominant Mendelian traits. RAPD markers appear useful for the rapid development of genetic information in species like alfalfa where little information currently exists or is difficult to obtain.
利用聚合酶链反应,使用任意序列的单链10聚体引物,从二倍体栽培苜蓿回交群体中扩增基因组DNA的随机区域。分析随机扩增多态性DNA(RAPD)片段的分离情况,以确定RAPD标记是否适合用作遗传标记。在测试的19种引物中,13种引物共扩增出37个多态性片段,其中28个(76%)表现为显性孟德尔性状分离。RAPD标记对于像苜蓿这样目前几乎没有信息或难以获得信息的物种中快速开发遗传信息似乎很有用。