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粗糙脉孢菌中复合物I外周臂21.3 kDa亚基编码基因的破坏。

Disruption of the gene coding for the 21.3-kDa subunit of the peripheral arm of complex I from Neurospora crassa.

作者信息

Alves P C, Videira A

机构信息

Instituto de Ciências Biomédicas de Abel Salazar, Universidade do Porto, Portugal.

出版信息

J Biol Chem. 1994 Mar 11;269(10):7777-84.

PMID:8126004
Abstract

A 21.3-kDa subunit of the peripheral arm of complex I from Neurospora is encoded by a single chromosomal gene, nuo-21.3b. It is located on linkage group V of the fungal genome, linked to inl. We have isolated and characterized a genomic clone containing this nuclear gene. A DNA fragment containing a portion of the coding region of the gene and upstream flanking sequences was introduced by transformation into a wild-type strain of Neurospora crassa. A single copy transformant was selected and crossed with another strain, leading to inactivation of nuo-21.3b through repeat-induced point mutations. We have analyzed random progeny from this cross and isolated two mutant strains lacking the 21.3-kDa subunit of complex I. One of them was further characterized. Our results suggest that most, if not all, other subunits of complex I are present in the mitochondria of the mutant and assembled in a structure similar to complex I, representing delta 25% of the amounts of enzyme found in the wild type. Nevertheless, a major intermediate, containing proteins of the peripheral arm of complex I, accumulates in the mutant mitochondria. This indicates that the absence of the 21.3-kDa polypeptide results in a disturbed assembly of the enzyme complex, suggesting a role for this polypeptide. We observed similar rates of rotenone-sensitive NADH:ubiquinone oxido-reductase activity in mitochondrial membranes from the mutant and wild-type strains and discuss the possibility that this electron transfer is independent of the more hydrophobic part of complex I. Transformation of the mutant with the intact gene and flanking sequences restored the wild-type phenotype.

摘要

粗糙脉孢菌复合体I外周臂的一个21.3 kDa亚基由单个染色体基因nuo - 21.3b编码。它位于真菌基因组的V连锁群上,与inl连锁。我们分离并鉴定了一个包含该核基因的基因组克隆。通过转化将一个含有该基因部分编码区和上游侧翼序列的DNA片段导入粗糙脉孢菌的野生型菌株。挑选出一个单拷贝转化体并与另一个菌株杂交,通过重复诱导点突变使nuo - 21.3b失活。我们分析了该杂交的随机后代,分离出两个缺乏复合体I 21.3 kDa亚基的突变菌株。对其中一个进行了进一步鉴定。我们的结果表明,复合体I的大多数(如果不是全部)其他亚基存在于突变体的线粒体中,并组装成类似于复合体I的结构,其含量约为野生型中该酶含量的25%。然而,一种主要的中间体,包含复合体I外周臂的蛋白质,在突变体线粒体中积累。这表明21.3 kDa多肽的缺失导致酶复合体组装受到干扰,提示该多肽具有一定作用。我们在突变体和野生型菌株的线粒体膜中观察到对鱼藤酮敏感的NADH:泛醌氧化还原酶活性的相似速率,并讨论了这种电子传递可能独立于复合体I更疏水部分的可能性。用完整基因和侧翼序列对突变体进行转化恢复了野生型表型。

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