首页> 美国卫生研究院文献>The Journal of 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。在西班牙裔墨西哥患者的E1 alpha位点发生纯合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)复合体缺乏引起的。所述多酶复合物包含五个酶成分,包括具有异四聚体(α2β2)结构的E 1脱羧酶。在评估发育迟缓期间,出生后7至22 mo确诊了4名具有中间临床表型的无关的西班牙裔-墨西哥MSUD患者。在四名患者中的三名被发现在E1α基因座的895碱基(外显子7)处由G到A的纯合子转变,使该亚基中的Gly-245变成Arg(G245R)。其余患者在E1 alpha基因的1,253位碱基处发生了T到G的纯合,这将基因产物中的Phe-364转换为Cys(F364C)。 E1 alpha缺陷淋巴母细胞的转染研究表明,G245R和F364C突变E1 alpha亚基均不能显着重构BCKAD活性。蛋白质印迹显示转染细胞中的两个突变E1α亚基均无法通过组装有效地拯救正常的E1β。通过在伴侣伴侣增强的细菌过表达系统中对E1亚基进行脉冲追踪标记,证实了推定的装配缺陷。 G245R E1 alpha亚基与正常E1 beta的初始组装动力学被证明比正常E1 alpha慢。在追赶2小时的过程中,未观察到F364C E1 alpha与正常E1 beta的组装。用异丙基硫代半乳糖苷诱导15小时后,产生了少量的重组突变E1蛋白,并表现出非常低的E1活性或没有E1活性。我们的研究表明,E1α亚基中的G245R和F364C突变会破坏E1异四聚体装配和BCKAD复合物的功能。此外,结果表明,G245R突变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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