Kobayashi H, Baumbach L, Matise T C, Schiavi A, Greenberg F, Hoffman E P
Department of Molecular Genetics and Biochemistry, University of Pittsburgh School of Medicine, PA 15261, USA.
Hum Mol Genet. 1995 Jul;4(7):1213-6. doi: 10.1093/hmg/4.7.1213.
X-linked arthrogryposis Type I (X-linked infantile spinal muscular atrophy) is a rare disorder showing hypotonia, areflexia, and multiple congenital contractures (arthrogryposis) associated with loss of anterior horn cells and death in infancy. We have studied an X-linked arthrogryposis family using highly polymorphic microsatellite markers throughout the X chromosome. Meiotic breakpoint analysis (concordance analysis) based on shared regions of the founder X chromosome was successful in localizing the X-linked arthrogryposis gene to Xp11.3-q11.2. In this region, the highest two-point lod score was found with DXS991 (Zmax = 2.63, theta = 0.00). In multipoint linkage analysis covering the entire X chromosome, only the region defined by MAOB and DXS991 showed positive lod scores and all other regions showed negative lod scores. These data establish the first gene mapping assignment of an X-linked lethal form of human lower motor neuron disease.
I型X连锁先天性多发性关节挛缩症(X连锁婴儿型脊髓性肌萎缩症)是一种罕见的疾病,表现为肌张力减退、反射消失以及与前角细胞丧失相关的多发性先天性挛缩(关节挛缩症),并在婴儿期死亡。我们使用整个X染色体上的高度多态性微卫星标记对一个X连锁先天性多发性关节挛缩症家族进行了研究。基于奠基者X染色体的共享区域进行的减数分裂断点分析(一致性分析)成功地将X连锁先天性多发性关节挛缩症基因定位到Xp11.3-q11.2。在该区域,与DXS991的两点连锁值最高(Zmax = 2.63,θ = 0.00)。在覆盖整个X染色体的多点连锁分析中,只有由MAOB和DXS991定义的区域显示出正连锁值,而所有其他区域显示出负连锁值。这些数据确立了人类下运动神经元疾病的X连锁致死形式的首次基因定位。