Liu Fu-Xia, Cao Mo-Ju, Rong Ting-Zhao, Pan Guang-Tang
Maize Research Institute of Sichuan Agricultural University, Ya' an 625014, China.
Yi Chuan Xue Bao. 2005 Jul;32(7):753-7.
Two F2 populations with different kinds of spike derived from maize male sterility materials RP(3)195 (A) x S37 (inbred line) ,which had been sib-bred for many generations,were used for sterility analysis and gene location. There were 138 and 247 plants in the two F2 populations respectively. Among the 326 pairs of microsatellite primers selected,56 were found polymorphic. Linkage analysis of F2 populations with the 56 pairs of primers showed that microsatellite markers bnlg197 and umc1012 were linked with the male sterility gene. The genetic distance between marker bnlgl97 and the male sterility gene in the two different F2 populations were 7 cM and 14.5 cM respectively. The genetic distance between marker umc1012 and the male sterility gene in the 138 plants was 28.5 cM. Thus the male sterility gene was located on chromosome 3L.
以玉米雄性不育材料RP(3)195(A)×S37(自交系)衍生的两种不同穗型的F2群体为材料,这两个群体已经连续多代兄妹交,用于不育性分析和基因定位。两个F2群体分别有138株和247株。在所选的326对微卫星引物中,发现56对具有多态性。用这56对引物对F2群体进行连锁分析,结果表明微卫星标记bnlg197和umc1012与雄性不育基因连锁。在两个不同的F2群体中,标记bnlgl97与雄性不育基因之间的遗传距离分别为7 cM和14.5 cM。在138株植株中,标记umc1012与雄性不育基因之间的遗传距离为28.5 cM。因此,雄性不育基因位于第3L染色体上。