首页> 外文期刊>The Journal of Clinical Investigation: The Official Journal of the American Society for Clinical Investigation >Molecular and biochemical basis of intermediate maple syrup urine disease. Occurrence of homozygous G245R and F364C mutations at the E1 alpha locus of Hispanic-Mexican patients.
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Molecular and biochemical basis of intermediate maple syrup urine disease. Occurrence of homozygous G245R and F364C mutations at the E1 alpha locus of Hispanic-Mexican patients.

机译:中间枫糖浆尿病的分子和生化基础。西班牙裔-墨西哥患者的 E1 α 位点出现纯合 G245R 和 F364C 突变。

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摘要

Maple syrup urine disease (MSUD) is caused by a deficiency of the mitochondrial branched-chain alpha-keta acid dehydrogenase (BCKAD) complex. The multienzyme complex comprises five enzyme components, including the E1 decarboxylase with a heterotetrameric (alpha 2 beta 2) structure. Four unrelated Hispanic-Mexican MSUD patients with the intermediate clinical phenotype were diagnosed 7 to 22 mo after birth during evaluation for developmental delay. Three of the four patients were found homozygous for G to A transition at base 895 (exon 7) of the E1 alpha locus, which changes Gly-245 to Arg (G245R) in that subunit. The remaining patient was homozygous for T to G transversion at base 1,253 in the E1 alpha gene, which converts Phe-364 to Cys (F364C) in the gene product. Transfection studies in E1 alpha-deficient lymphoblasts indicate that both G245R and F364C mutant E1 alpha subunits were unable to significantly reconstitute BCKAD activity. Western blotting showed that both mutant E1 alpha subunits in transfected cells failed to efficiently rescue the normal E1 beta through assembly. The putative assembly defect was confirmed by pulse-chase labeling of E1 subunits in a chaperone-augmented bacterial overexpression system. The kinetics of initial assembly of the G245R E1 alpha subunit with the normal E1 beta was shown to be slower than the normal E1 alpha. No detectable assembly of the F364C E1 alpha with normal E1 beta was observed during the 2 h chase. Small amounts of recombinant mutant E1 proteins were produced after 15 h induction with isopropyl thiogalactoside and exhibited very low or no E1 activity. Our study establishes that G245R and F364C mutations in the E1 alpha subunit disrupt both the E1 heterotetrameric assembly and function of the BCKAD complex. Moreover, the results suggest that the G245R mutant E1 alpha allele may be important in the Hispanic-Mexican population.
机译:枫糖浆尿病 (MSUD) 是由线粒体支链 α-酮酸脱氢酶 (BCKAD) 复合物缺乏引起的。多酶复合物由五种酶组成,包括具有异四聚体(α 2 β 2)结构的 E1 脱羧酶。在评估发育迟缓期间,在出生后 7 至 22 个月诊断出具有中间临床表型的无关西班牙裔-墨西哥 MSUD 患者。四名患者中有三名被发现在 E1 α 位点的碱基 895(外显子 7)处发生 G 到 A 转变的纯合子,该基因座将该亚基中的 Gly-245 变为 Arg (G245R)。其余患者在 E1 α 基因的碱基 1,253 处为 T 到 G 转位纯合子,该基因将 Phe-364 转化为基因产物中的 Cys (F364C)。对 E1 α 缺陷淋巴母细胞的转染研究表明,G245R 和 F364C 突变体 E1 α 亚基均无法显着重建 BCKAD 活性。Western blotting 显示转染细胞中的两个突变 E1 α 亚基都未能通过组装有效地挽救正常的 E1 β。通过伴侣增强细菌过表达系统中 E1 亚基的脉冲追逐标记证实了推定的组装缺陷。G245R E1 α 亚基与正常 E1 β 的初始组装动力学比正常 E1 α 慢。在 2 小时追逐期间,未观察到 F364C E1 α 与正常 E1 β 的可检测组装。用异丙基硫代半乳糖苷诱导 15 小时后产生少量重组突变 E1 蛋白,并且表现出非常低或没有 E1 活性。我们的研究表明,E1 α 亚基中的 G245R 和 F364C 突变破坏了 E1 异源四聚体组装和 BCKAD 复合物的功能。此外,结果表明,G245R突变体E1α等位基因在西班牙裔-墨西哥人群中可能很重要。

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