Velasco E, Valero C, García E, de la Puente A, Cruces J, San Millán J L, del Castillo I, Coloma A, Moreno F, Hernández-Chico C
Unidad de Genética Molecular, Hospital Ramón y Cajal, Madrid, Spain.
Eur J Hum Genet. 1995;3(2):96-101. doi: 10.1159/000472282.
A locus responsible for autosomal recessive spinal muscular atrophy (SMA) on chromosome 5q11.2-q13.3 has been mapped to a critical interval delimited by markers D5S435 and D5S557. By a modification of the Vectorette-(GT)n method, we have isolated three polymorphic CA repeats from two YACs of the SMA region. Two of them (D5S1417 and D5S1416) map within the SMA critical region, and the other (D5S1415) is centromeric to D5S435. Linkage analysis in Spanish SMA families with eleven markers showed that in our families the disease is linked to this region and confirmed that the novel markers are tightly linked to the SMA locus. The most likely order of markers was 5cen-(D5S63/D5S1356)-(D5S125/D5S465)- (D5S435/D5S1417/D5S1416/D5S557)-D5S610- D5S112-D5S127-5qter, with odds against alternative orders > 1,000:1. Genetic distances are in agreement with those previously published. However, the recombination fraction between D5S610 and D5S112 is remarkably greater than expected from the physical distance, suggesting a hot spot for recombination in this region. Our results from haplotype and multipoint analyses show that the SMA locus must lie between D5S465 and D5S112, and lend further support to the current location of the SMA locus.
5号染色体q11.2 - q13.3上一个导致常染色体隐性脊髓性肌萎缩症(SMA)的基因座已被定位到由标记D5S435和D5S557界定的关键区间。通过改良的Vectorette - (GT)n方法,我们从SMA区域的两个酵母人工染色体(YAC)中分离出三个多态性CA重复序列。其中两个(D5S1417和D5S1416)定位于SMA关键区域内,另一个(D5S1415)位于D5S435的着丝粒侧。对西班牙SMA家系进行的11个标记的连锁分析表明,在我们的家系中该疾病与该区域连锁,并证实这些新标记与SMA基因座紧密连锁。标记最可能的顺序是5cen - (D5S63/D5S1356) - (D5S125/D5S465) - (D5S435/D5S1417/D5S1416/D5S557) - D5S610 - D5S112 - D5S127 - 5qter,与其他顺序相比的优势比大于1000:1。遗传距离与先前发表的结果一致。然而,D5S610和D5S112之间的重组率明显高于根据物理距离预期的值,表明该区域存在重组热点。我们单倍型和多点分析的结果表明,SMA基因座必定位于D5S465和D5S112之间,并进一步支持了SMA基因座的当前定位。