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首页> 外文期刊>Molecular and Cellular Biology >MIP1, a new yeast gene homologous to the rat mitochondrial intermediate peptidase gene, is required for oxidative metabolism in Saccharomyces cerevisiae.
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MIP1, a new yeast gene homologous to the rat mitochondrial intermediate peptidase gene, is required for oxidative metabolism in Saccharomyces cerevisiae.

机译:MIP1是与大鼠线粒体中间肽酶基因同源的新酵母基因,是酿酒酵母中氧化代谢所必需的。

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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.
机译:线粒体中间肽酶(MIP)切割氨基末端八肽(F / L / IXXS / T / GXXXX)是导入到基质和内膜的许多线粒体前体蛋白的典型特征。我们先前描述了大鼠肝MIP(RMIP)的分子特征,并指出了从酵母染色体III的基因YCL57w预测的序列中的推定同源物。现在,已经通过使用RMIP cDNA探针筛选啤酒酵母基因组文库来分离出一种新的酵母基因MIP1。 MIP1预测一种772个氨基酸的蛋白质(YMIP),与RMIP相似,相似度为54%,相同性为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,其中包含一个锌结合基序HEXXH,而预测的YCL57w蛋白则包含具有较低同源性的可比序列。在染色体破坏的ycl57w突变体中未观察到明显的生化表型。相反,mip1突变体无法在不可发酵的底物上生长,而mip1 ycl57w的双重破坏并不会导致更严重的表型。 mip1突变体显示呼吸链复合物III和IV的缺陷,是由于未能对细胞色素氧化酶亚基IV(CoxIV)和铁硫蛋白(Fe- S)的bc1复合物成熟的蛋白质。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线粒体级分无法进行人鸟氨酸转氨甲酰酶中间体(iOTC)的成熟,特别是被RMIP裂解。 CEN质粒编码的YMIP蛋白可恢复正常的MIP活性以及呼吸功能。因此,YMIP是RMIP的功能同源物,代表了酵母线粒体导入机制的新组成部分。

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