Uchida K, Koopman P, Mita A, Wakana S, Wright E, Kikkawa Y, Yonekawa H, Moriwaki K, Shiroishi T
Mammalian Genetics Laboratory, National Institute of Genetics, Yata 1111, Mishima, Shizuoka-ken 411, Japan.
Mamm Genome. 1996 Jul;7(7):481-5. doi: 10.1007/s003359900147.
The Sry-related gene Sox9 has been proposed as the gene responsible for the mouse skeletal mutant Tail-short (Ts), on the basis of its expression in skeletogenic mesenchymal condensations in the mouse embryo and its chromosomal location in the region of Ts on distal Chromosome (Chr) 11. We present here detailed mapping of Ts locus relative to the Sox9, using an intersubspecific cross. Among 521 backcross progeny, 16 recombinants were detected between Sox9 and Ts, suggesting a separation of 3.5 +/- 0.01 cM, and excluding Sox9 as a candidate for Ts. A further nine recombinants were detected between Ts and the polycomb-like gene M33, suggesting that these loci are separated by 1.8 +/- 0.011 cM. Six microsatellite markers were co-localized to the Ts locus, providing reagents for positional cloning of Ts.
基于与性别决定相关的基因Sox9在小鼠胚胎骨骼发生间充质凝聚中的表达及其在远端11号染色体(Chr)上Ts区域的染色体定位,有人提出该基因是导致小鼠骨骼突变体短尾(Ts)的基因。我们在此使用种间杂交展示了Ts基因座相对于Sox9的详细定位。在521个回交后代中,在Sox9和Ts之间检测到16个重组体,表明二者相距3.5±0.01厘摩,从而排除了Sox9作为Ts候选基因的可能性。在Ts和多梳样基因M33之间又检测到9个重组体,表明这些基因座相距1.8±0.011厘摩。六个微卫星标记与Ts基因座共定位,为Ts的位置克隆提供了试剂。