Laporte J, Guiraud-Chaumeil C, Vincent M C, Mandel J L, Tanner S M, Liechti-Gallati S, Wallgren-Pettersson C, Dahl N, Kress W, Bolhuis P A, Fardeau M, Samson F, Bertini E
IGBMC, CNRS/INSERM/ULP, Illkirch, France.
Hum Mol Genet. 1997 Sep;6(9):1505-11. doi: 10.1093/hmg/6.9.1505.
X-linked recessive myotubular myopathy (XLMTM) is characterized by severe hypotonia and generalized muscle weakness, with impaired maturation of muscle fibres. The gene responsible, MTM1, was identified recently by positional cloning, and encodes a protein (myotubularin) with a tyrosine phosphatase domain (PTP). Myotubularin is highly conserved through evolution and defines a new family of putative tyrosine phosphatases in man. We report the identification of MTM1 mutations in 55 of 85 independent patients screened by single-strand conformation polymorphism for all the coding sequence. Large deletions were observed in only three patients. Five point mutations were found in multiple unrelated patients, accounting for 27% of the observed mutations. The possibility of detecting mutations and determining carrier status in a disease with a high proportion of sporadic cases is of importance for genetic counselling. More than half of XLMTM mutations are expected to inactivate the putative enzymatic activity of myotubularin, either by truncation or by missense mutations affecting the predicted PTP domain. Additional mutations are missenses clustered in two regions of the protein. Most of these affect amino acids conserved in the homologous yeast and Caenorhabditis elegans proteins, thus indicating the presence of other functional domains.
X连锁隐性肌管性肌病(XLMTM)的特征为严重的肌张力减退和全身肌肉无力,伴有肌纤维成熟障碍。致病基因MTM1最近通过定位克隆得以确定,它编码一种带有酪氨酸磷酸酶结构域(PTP)的蛋白质(肌管素)。肌管素在进化过程中高度保守,在人类中定义了一个新的假定酪氨酸磷酸酶家族。我们报告了在85例独立患者中,通过单链构象多态性对所有编码序列进行筛查,发现了55例MTM1突变。仅在3例患者中观察到大片段缺失。在多个不相关患者中发现了5个点突变,占所观察到突变的27%。对于遗传咨询而言,在散发病例比例较高的疾病中检测突变并确定携带者状态具有重要意义。预计超过一半的XLMTM突变会通过截短或影响预测的PTP结构域的错义突变使肌管素的假定酶活性失活。其他突变是聚集在该蛋白质两个区域的错义突变。其中大多数影响在同源酵母和秀丽隐杆线虫蛋白质中保守的氨基酸,从而表明存在其他功能结构域。