Melki J, Lefebvre S, Burglen L, Burlet P, Clermont O, Millasseau P, Reboullet S, Bénichou B, Zeviani M, Le Paslier D
Unité de Recherches sur les Handicaps Génétiques de l'Enfant, INSERM U-393, Hôpital des Enfants-Malades, Paris, France.
Science. 1994 Jun 3;264(5164):1474-7. doi: 10.1126/science.7910982.
Spinal muscular atrophies (SMAs) represent the second most common fatal autosomal recessive disorder after cystic fibrosis. Childhood spinal muscular atrophies are divided into severe (type I) and mild forms (types II and III). By a combination of genetic and physical mapping, a yeast artificial chromosome contig of the 5q13 region spanning the disease locus was constructed that showed the presence of low copy repeats in this region. Allele segregation was analyzed at the closest genetic loci detected by markers C212 and C272 in 201 SMA families. Inherited and de novo deletions were observed in nine unrelated SMA patients. Moreover, deletions were strongly suggested in at least 18 percent of SMA type I patients by the observation of marked heterozygosity deficiency for the loci studied. These results indicate that deletion events are statistically associated with the severe form of spinal muscular atrophy.
脊髓性肌萎缩症(SMA)是仅次于囊性纤维化的第二常见致命常染色体隐性疾病。儿童脊髓性肌萎缩症分为严重型(I型)和轻型(II型和III型)。通过基因和物理图谱相结合的方法,构建了跨越疾病位点的5q13区域的酵母人工染色体重叠群,该重叠群显示该区域存在低拷贝重复序列。在201个SMA家族中,对标记C212和C272检测到的最接近的基因座进行了等位基因分离分析。在9名无亲缘关系的SMA患者中观察到遗传和新生缺失。此外,通过观察所研究基因座的明显杂合性缺陷,强烈提示至少18%的I型SMA患者存在缺失。这些结果表明,缺失事件在统计学上与严重型脊髓性肌萎缩症相关。