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大鼠NADH:泛醌氧化还原酶13.2 kDa亚基的基因组序列、结构组织及进化保守性

Genomic sequence, structural organization and evolutionary conservation of the 13.2-kDa subunit of rat NADH:ubiquinone oxidoreductase.

作者信息

Watson J D, Beckett-Jones B, Roy R N, Green N C, Flynn T G

机构信息

Department of Biochemistry, Queen's University, Kingston, Ontario, Canada.

出版信息

Gene. 1995 Jun 9;158(2):275-80. doi: 10.1016/0378-1119(95)00029-6.

Abstract

The 13.2-kDa subunit of NADH:ubiquinone oxidoreductase has been shown to be an integral part of the bovine iron-sulfur (IP) part of the protein. This subunit has been shown to interact with at least two other protein subunits of the IP fragment. The amino acid (aa) sequence of this subunit, determined from an acid extract of rat heart was used to generate an oligodeoxyribonucleotide probe which allowed isolation of a cDNA coding for the rat homologue of 13.2-kDa IP. The cDNA was used as a probe of a rat genomic DNA library and two clones were isolated, one of which contained the entire coding region for 13.2-kDa IP. Southern analysis indicates that the IP13 sequence exists as a single copy gene. The sequence of the genomic clone contains one intron and promoter elements including a TATAAA region. The 5' flank region has several potential regulatory sites, most notably regions similar to the nuclear respiratory factor 1 (NRF-1) motif, found in other genes which code for mitochondrial proteins [Evans and Scarpulla, Genes Dev. 4 (1990) 1023-1034]. The core domain of the deduced rat aa sequence has a high degree of identity with the mouse and cow homologues of this protein. The high degree of conservation of this protein indicates that the protein is essential for the function of complex I.

摘要

NADH

泛醌氧化还原酶的13.2 kDa亚基已被证明是该蛋白质牛铁硫(IP)部分的一个组成部分。该亚基已被证明与IP片段的至少两个其他蛋白质亚基相互作用。从大鼠心脏的酸提取物中确定的该亚基的氨基酸(aa)序列被用于生成一个寡脱氧核糖核苷酸探针,该探针可用于分离编码13.2 kDa IP大鼠同源物的cDNA。该cDNA被用作大鼠基因组DNA文库的探针,并分离出两个克隆,其中一个包含13.2 kDa IP的完整编码区。Southern分析表明,IP13序列以单拷贝基因形式存在。基因组克隆的序列包含一个内含子和启动子元件,包括一个TATAAA区域。5'侧翼区域有几个潜在的调控位点,最显著的是与核呼吸因子1(NRF-1)基序相似的区域,在其他编码线粒体蛋白的基因中也有发现[Evans和Scarpulla,《基因与发育》4(1990)1023 - 1034]。推导的大鼠aa序列的核心结构域与该蛋白质的小鼠和牛同源物具有高度的同一性。这种蛋白质的高度保守性表明该蛋白质对于复合体I的功能至关重要。

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