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线粒体NADH-泛醌还原酶:牛和人24 kDa亚基导入前体的互补DNA序列

Mitochondrial NADH-ubiquinone reductase: complementary DNA sequences of import precursors of the bovine and human 24-kDa subunit.

作者信息

Pilkington S J, Walker J E

机构信息

Medical Research Council, Laboratory of Molecular Biology, Cambridge, U.K.

出版信息

Biochemistry. 1989 Apr 18;28(8):3257-64. doi: 10.1021/bi00434a021.

DOI:10.1021/bi00434a021
PMID:2500970
Abstract

The 24-kDa subunit of mitochondrial NADH-ubiquinone reductase (complex I) is an iron-sulfur protein that is present in the flavoprotein or NADH dehydrogenase II subcomplex. It is a nuclear gene product and is imported into the organelle. A group of human patients with mitochondrial myopathy have been shown to have reduced levels of subunits of complex I in skeletal muscle mitochondria, and in one patient the 24-kDa subunit appears to be absent (Schapira et al., 1988). To investigate the genetic basis of this type of myopathy, cDNA clones have been isolated from a bovine library derived from heart and liver mRNA by hybridization with two mixtures of 48 synthetic oligonucleotides 17 bases in length that were designed on the basis of known protein sequences. The recombinant DNA sequence has been determined, and it encodes a precursor of the mature 24-kDa protein. The N terminus of the mature protein is preceded by a presequence of 32 amino acids that has properties that are characteristic of mitochondrial import sequences. The sequence of the mature protein deduced from the cDNA contains a segment of nine amino acids that was not determined in an earlier partial protein sequence analysis. The bovine clone has been employed as a hybridization probe to identify cDNA clones of the human homologue of the 24-kDa protein. Its DNA sequence has also been determined, and it codes for a protein that is closely related to the bovine protein.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

线粒体NADH-泛醌还原酶(复合体I)的24 kDa亚基是一种铁硫蛋白,存在于黄素蛋白或NADH脱氢酶II亚复合体中。它是一种核基因产物,可被导入细胞器。已证明一组线粒体肌病患者骨骼肌线粒体中复合体I亚基水平降低,且有一名患者似乎不存在24 kDa亚基(沙皮拉等人,1988年)。为了研究这类肌病的遗传基础,通过与基于已知蛋白质序列设计的两种由48个17个碱基长的合成寡核苷酸混合物杂交,从源自心脏和肝脏mRNA的牛文库中分离出了cDNA克隆。已确定了重组DNA序列,它编码成熟24 kDa蛋白的前体。成熟蛋白的N端之前有一段32个氨基酸的前序列,具有线粒体导入序列的特征。从cDNA推导的成熟蛋白序列包含一段九个氨基酸的片段,该片段在早期的部分蛋白质序列分析中未确定。牛克隆已被用作杂交探针来鉴定24 kDa蛋白人类同源物的cDNA克隆。其DNA序列也已确定,它编码一种与牛蛋白密切相关的蛋白质。(摘要截短于250字)

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