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酿酒酵母ATP合酶亚基6和8线粒体合成的核基因调控

Regulation by nuclear genes of the mitochondrial synthesis of subunits 6 and 8 of the ATP synthase of Saccharomyces cerevisiae.

作者信息

Pelissier P P, Camougrand N M, Manon S T, Velours G M, Guerin M G

机构信息

Institut de Biochimie Cellulaire et Neurochimie, Université de Bordeaux II, France.

出版信息

J Biol Chem. 1992 Feb 5;267(4):2467-73.

PMID:1531141
Abstract

The nuclear mutant AB1-4A/8/100, a respiratory-competent strain altered in the regulation of ATP synthesis, has been shown to be modified in the relative stoichiometry of the mtDNA-encoded proteolipids of the F0 sector of ATP synthase: the ratios mutant/wild type of the proteolipids were equal to 0.4/0.7/1 for Su8/Su6/Su9, respectively. This defect results from the simultaneous presence of two nuclear genes which promote a cryosensitive phenotype on a nonfermentable carbon source. Measurements of mitochondrial protein synthesis carried out "in vivo" and "in organello" evidenced a specific defect in the synthesis of subunits 6 and 8. Measurements of the steady state levels of mitochondrial mRNA showed that the defect in subunits 6 and 8 was correlated with a modification of the expression of a cotranscript ATP8-ATP6. This cotranscript is matured at a unique site to give two cotranscripts of 4600 and 5200 bases in length. In mutant mitochondria, the ratio between both cotranscripts, 5200/4600, was lowered. In parallel, expression of the whole mitochondrial transcription unit supporting the genes COXI, ATP8, ATP6, and RF3 was enhanced. However, despite this over expression, the amount of the long cotranscript ATP8-ATP6 remained lower than in wild type mitochondria.

摘要

核突变体AB1-4A/8/100是一种呼吸功能正常的菌株,其ATP合成调节发生改变,已证明其ATP合酶F0区段的线粒体DNA编码的蛋白脂质的相对化学计量发生了改变:对于Su8/Su6/Su9,蛋白脂质的突变体/野生型比率分别等于0.4/0.7/1。这种缺陷是由两个核基因同时存在导致的,这两个基因在不可发酵碳源上促进冷敏感表型。“体内”和“细胞器内”进行的线粒体蛋白质合成测量证明了亚基6和8合成存在特定缺陷。线粒体mRNA稳态水平的测量表明,亚基6和8的缺陷与共转录本ATP8-ATP6表达的改变相关。该共转录本在一个独特位点成熟,产生两个长度分别为4600和5200个碱基的共转录本。在突变体线粒体中,两种共转录本之间的比率5200/4600降低。同时,支持基因COXI、ATP8、ATP6和RF3的整个线粒体转录单元的表达增强。然而,尽管有这种过表达,长共转录本ATP8-ATP6的量仍低于野生型线粒体。

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