Laporte J, Guiraud-Chaumeil C, Tanner S M, Blondeau F, Hu L J, Vicaire S, Liechti-Gallati S, Mandel J L
Institut de Génétique et de Biologie Moléculaire et Cellulaire, CNRS, Illkirch, France.
Eur J Hum Genet. 1998 Jul-Aug;6(4):325-30. doi: 10.1038/sj.ejhg.5200189.
X-linked recessive myotubular myopathy (XLMTM) is a very severe congenital muscular disease characterised by an impaired maturation of muscle fibres, and caused by defects in the MTM1 gene. This gene defines a new family of putative tyrosine phosphatases conserved through evolution. We have determined intronic flanking sequences for all the 15 exons to facilitate the detection of mutations in patients and genetic counselling. We characterised a new polymorphic marker in the immediate vicinity of the gene, which might prove useful for linkage analysis. Sequencing of the TATA-less predicted promoter provides the basis for transcriptional regulatory studies.
X连锁隐性肌管性肌病(XLMTM)是一种非常严重的先天性肌肉疾病,其特征为肌纤维成熟受损,由MTM1基因突变所致。该基因定义了一个在进化过程中保守的假定酪氨酸磷酸酶新家族。我们已确定了所有15个外显子的内含子侧翼序列,以利于检测患者的突变及进行遗传咨询。我们对该基因紧邻区域的一个新的多态性标记进行了特征分析,这可能对连锁分析有用。对无TATA框的预测启动子进行测序为转录调控研究提供了基础。