Wirth B, el-Agwany A, Baasner A, Burghes A, Koch A, Dadze A, Piechaczeck-Wappenschmidt B, Rudnik-Schöneborn S, Zerres K, Schönling J
Institute of Human Genetics, Bonn, Germany.
Eur J Hum Genet. 1995;3(1):56-60. doi: 10.1159/000472274.
The gene for autosomal recessive proximal spinal muscular atrophy (SMA) has recently been mapped between D5S629 and D5S557. We report here a new single-locus microsatellite A31 (D5S823) and two multicopy microsatellites 97T-CA and 95/23-CA. The marker A31 maps to the region of overlap between YACs y116, y55 and y122, distal to D5S629; 97T-CA originates from a cosmid corresponding to the STS 97T, localized distally to A31, while 95/23-CA derives from a cosmid corresponding to the STS 97U, localized proximally to D5S557. We tested all our key recombinant families with these markers. In one type I/II SMA family, a recombinant was found that placed the SMA locus distal to D5S823. Homozygosity mapping in a consanguineous type I SMA family indicates that the SMA gene lies proximal to 95/23-CA. Thus, the two new markers, A31 and 95/23-CA further refine the SMA gene to an approximately 750-kb interval.
常染色体隐性遗传性近端脊髓性肌萎缩症(SMA)的基因最近被定位于D5S629和D5S557之间。我们在此报告一个新的单基因座微卫星A31(D5S823)以及两个多拷贝微卫星97T-CA和95/23-CA。标记A31定位于YACs y116、y55和y122之间的重叠区域,在D5S629的远端;97T-CA源自一个与STS 97T对应的黏粒,定位于A31的远端,而95/23-CA源自一个与STS 97U对应的黏粒,定位于D5S557的近端。我们用这些标记对所有关键的重组家系进行了检测。在一个I/II型SMA家系中,发现了一个重组个体,该个体将SMA基因座定位于D5S823的远端。在一个近亲婚配的I型SMA家系中进行纯合性定位表明,SMA基因位于95/23-CA的近端。因此,这两个新标记A31和95/23-CA将SMA基因进一步定位到了一个约750 kb的区间内。