Billaut-Laden Ingrid, Rat Emmanuel, Allorge Delphine, Crunelle-Thibaut Aurélie, Cauffiez Christelle, Chevalier Dany, Lo-Guidice Jean-Marc, Broly Franck
Equipe d'accueil EA2679, Faculté de Médecine, Pôle Recherche, 1 place de Verdun, 59045 Lille Cedex, France.
Toxicol Lett. 2006 Aug 20;165(2):101-11. doi: 10.1016/j.toxlet.2006.02.002. Epub 2006 Mar 20.
Mercaptopyruvate sulfurtransferase (MPST) plays a central role in both cysteine degradation and cyanide detoxification. Moreover, deficiency in MPST activity has been suggested to be responsible for a rare inheritable disorder known as mercaptolactate-cysteine disulfiduria (MCDU). To date, no mutation of the human MPST gene has been reported. We developed a screening strategy to search for mutations in the MPST gene of 50 unrelated French individuals. Two intronic polymorphisms (IVS1-110C>G and IVS2+39C>T) and a nonsense mutation (Tyr(85)Stop) were identified and their functional consequences were assessed in vivo by measurement of erythrocyte MPST activity and/or in vitro using heterologous expression or transient transfection assay. The nonsense mutation likely leads to the synthesis of a severely truncated protein without enzymatic activity, as supported by our in vitro data. This work constitutes the first report of the existence of a functional genetic polymorphism affecting MPST and should be of great help to investigate certain disorders such as MCDU.
巯基丙酮酸硫转移酶(MPST)在半胱氨酸降解和氰化物解毒过程中都起着核心作用。此外,有人提出MPST活性缺乏是导致一种罕见的遗传性疾病——巯基乳酸 - 半胱氨酸二硫尿症(MCDU)的原因。迄今为止,尚未报道过人类MPST基因的突变情况。我们开发了一种筛选策略,用于在50名无亲缘关系的法国个体的MPST基因中寻找突变。我们鉴定出了两个内含子多态性(IVS1 - 110C>G和IVS2 + 39C>T)以及一个无义突变(Tyr(85)Stop),并通过测量红细胞MPST活性在体内和/或使用异源表达或瞬时转染试验在体外评估了它们的功能后果。我们的体外数据表明,该无义突变可能导致合成一种严重截短且无酶活性的蛋白质。这项工作首次报道了存在影响MPST的功能性基因多态性,对于研究诸如MCDU等某些疾病应该会有很大帮助。