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酿酒酵母核基因对线粒体基因表达的翻译调控

Translational regulation of mitochondrial gene expression by nuclear genes of Saccharomyces cerevisiae.

作者信息

Fox T D, Costanzo M C, Strick C A, Marykwas D L, Seaver E C, Rosenthal J K

机构信息

Section of Genetics and Development, Cornell University, Ithaca, New York 14853.

出版信息

Philos Trans R Soc Lond B Biol Sci. 1988 May 31;319(1193):97-105. doi: 10.1098/rstb.1988.0034.

Abstract

We describe several yeast nuclear mutations that specifically block expression of the mitochondrial genes encoding cytochrome c oxidase subunits II (COXII) and III (COXIII). These recessive mutations define positive regulators of mitochondrial gene expression that act at the level of translation. Mutations in the nuclear gene PET111 completely block accumulation of COXII, but the COXII mRNA is present in mutant cells at a level approximately one-third of that of the wild type. Mitochondrial suppressors of pet111 mutations correspond to deletions in mtDNA that result in fusions between the coxII structural gene and other mitochondrial genes. The chimeric mRNAs encoded by these fusions are translated in pet111 mutants; this translation leads to accumulation of functional COXII. The PET111 protein probably acts directly on coxII translation, because it is located in mitochondria. Translation of the mitochondrially coded mRNA for COXIII requires the action of at least three nuclear genes, PET494, PET54 and a newly discovered gene, provisionally termed PET55. Both the PET494 and PET54 proteins are located in mitochondria and therefore probably act directly on the mitochondrial translation system. Mutations in all three genes are suppressed in strains that contain chimeric coxIII mRNAs with the 5'-untranslated leaders of other mitochondrial transcripts fused to the coxIII coding sequence. The products of all three nuclear genes may form a complex and carry out a single function.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

我们描述了几种酵母核突变,这些突变特异性地阻断了编码细胞色素c氧化酶亚基II(COXII)和亚基III(COXIII)的线粒体基因的表达。这些隐性突变定义了线粒体基因表达的正向调节因子,其作用于翻译水平。核基因PET111中的突变完全阻断了COXII的积累,但COXII mRNA在突变细胞中的水平约为野生型的三分之一。pet111突变的线粒体抑制子对应于线粒体DNA中的缺失,这些缺失导致coxII结构基因与其他线粒体基因之间发生融合。这些融合编码的嵌合mRNA在pet111突变体中被翻译;这种翻译导致功能性COXII的积累。PET111蛋白可能直接作用于coxII的翻译,因为它位于线粒体中。COXIII的线粒体编码mRNA的翻译需要至少三个核基因PET494、PET54和一个新发现的基因(暂称为PET55)的作用。PET494和PET54蛋白都位于线粒体中,因此可能直接作用于线粒体翻译系统。在含有嵌合coxIII mRNA的菌株中,所有这三个基因中的突变都被抑制,这些嵌合mRNA的5'非翻译前导序列与其他线粒体转录本的5'非翻译前导序列融合到coxIII编码序列上。所有这三个核基因的产物可能形成一个复合物并执行单一功能。(摘要截短于250字)

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