Suppr超能文献

MIP1是一种与大鼠线粒体中间肽酶基因同源的新酵母基因,是酿酒酵母氧化代谢所必需的。

MIP1, a new yeast gene homologous to the rat mitochondrial intermediate peptidase gene, is required for oxidative metabolism in Saccharomyces cerevisiae.

作者信息

Isaya G, Miklos D, Rollins R A

机构信息

Department of Genetics, Yale University School of Medicine, New Haven, Connecticut 06520-8005.

出版信息

Mol Cell Biol. 1994 Aug;14(8):5603-16. doi: 10.1128/mcb.14.8.5603-5616.1994.

Abstract

Cleavage of amino-terminal octapeptides, F/L/IXXS/T/GXXXX, by mitochondrial intermediate peptidase (MIP) is typical of many mitochondrial precursor proteins imported to the matrix and the inner membrane. We previously described the molecular characterization of rat liver MIP (RMIP) and indicated a putative homolog in the sequence predicted from gene YCL57w of yeast chromosome III. A new yeast gene, MIP1, has now been isolated by screening a Saccharomyces cerevisiae genomic library with an RMIP cDNA probe. MIP1 predicts a protein of 772 amino acids (YMIP), which is 54% similar and 31% identical to RMIP and includes a putative 37-residue mitochondrial leader peptide. RMIP and YMIP contain the sequence LFHEMGHAM HSMLGRT, which includes a zinc-binding motif, HEXXH, while the predicted YCL57w protein contains a comparable sequence with a lower degree of homology. No obvious biochemical phenotype was observed in a chromosomally disrupted ycl57w mutant. In contrast, a mip1 mutant was unable to grow on nonfermentable substrates, while a mip1 ycl57w double disruption did not result in a more severe phenotype. The mip1 mutant exhibited defects of complexes III and IV of the respiratory chain, caused by failure to carry out the second MIP-catalyzed cleavage of the nuclear-encoded precursors for cytochrome oxidase subunit IV (CoxIV) and the iron-sulfur protein (Fe-S) of the bc1 complex to mature proteins. In vivo, intermediate-size CoxIV was accumulated in the mitochondrial matrix, while intermediate-size Fe-S was targeted to the inner membrane. Moreover, mip1 mitochondrial fractions failed to carry out maturation of the human ornithine transcarbamylase intermediate (iOTC), specifically cleaved by RMIP. A CEN plasmid-encoded YMIP protein restored normal MIP activity along with respiratory competence. Thus, YMIP is a functional homolog of RMIP and represents a new component of the yeast mitochondrial import machinery.

摘要

线粒体中间肽酶(MIP)对氨基末端八肽F/L/IXXS/T/GXXXX的切割是许多导入线粒体基质和内膜的线粒体前体蛋白的典型特征。我们之前描述了大鼠肝脏MIP(RMIP)的分子特征,并指出酵母III号染色体基因YCL57w预测序列中有一个假定的同源物。现在,通过用RMIP cDNA探针筛选酿酒酵母基因组文库,分离出了一个新的酵母基因MIP1。MIP1预测的蛋白质由772个氨基酸组成(YMIP),与RMIP的相似度为54%,一致性为31%,并包含一个假定的37个残基的线粒体前导肽。RMIP和YMIP包含序列LFHEMGHAM HSMLGRT,其中包括一个锌结合基序HEXXH,而预测的YCL57w蛋白包含一个同源性较低的类似序列。在染色体破坏的ycl57w突变体中未观察到明显的生化表型。相比之下,mip1突变体无法在非发酵底物上生长,而mip1 ycl57w双破坏并未导致更严重的表型。mip1突变体表现出呼吸链复合物III和IV的缺陷,这是由于未能对细胞色素氧化酶亚基IV(CoxIV)和bc1复合物的铁硫蛋白(Fe-S)的核编码前体进行第二次MIP催化切割,使其成熟为蛋白质。在体内,中等大小的CoxIV积累在线粒体基质中,而中等大小的Fe-S靶向内膜。此外,mip1线粒体组分无法使人类鸟氨酸转氨甲酰酶中间体(iOTC)成熟,iOTC可被RMIP特异性切割。一个CEN质粒编码的YMIP蛋白恢复了正常的MIP活性以及呼吸能力。因此,YMIP是RMIP的功能同源物,代表酵母线粒体导入机制的一个新组分。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a37a/359079/1a6ff92c2130/molcellb00008-0600-a.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验