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编码酵母寡霉素敏感性赋予蛋白的基因。

The gene coding for the yeast oligomycin sensitivity-conferring protein.

作者信息

Uh M, Jones D, Mueller D M

机构信息

Department of Biological Chemistry and Structure, Chicago Medical School, University of Health Sciences, Illinois 60064.

出版信息

J Biol Chem. 1990 Nov 5;265(31):19047-52.

PMID:2146269
Abstract

The gene coding for the yeast Saccharomyces cerevisiae mitochondrial oligomycin sensitivity-conferring protein (OSCP) has been sequenced, and the gene products have been characterized. The OSCP is subunit 5 of the mitochondrial ATP synthase, a multimeric protein complex. As such, the gene coding for the yeast OSCP is referred to here as the ATP5 gene. From the predicted primary sequence, the calculated molecular weight of the immature yeast OSCP is 22,813 and the amino acid sequence is 35% identical and 65% homologous to bovine OSCP. A null mutant has been constructed. This mutant strain is unable to grow on glycerol medium, has no detectable oligomycin-sensitive ATPase activity, and has no detectable immune reactive proteins with the corresponding molecular weight of the OSCP (using antibodies reactive to the yeast OSCP). The transcription products of the yeast gene have been characterized. There is a single major transcript from the ATP5 gene of 1.05 kilobases. The level of the transcription product is increased from 3-5-fold after growth in galactose medium as compared to cells grown in glucose medium. The transcriptional initiation sites were determined to occur at +68(G) and +69(T) at comparable frequency and were not dependent on the growth medium. These results suggest that transcription of the ATP5 gene is catabolite-repressed.

摘要

对编码酿酒酵母线粒体寡霉素敏感性赋予蛋白(OSCP)的基因进行了测序,并对该基因产物进行了表征。OSCP是线粒体ATP合酶的亚基5,线粒体ATP合酶是一种多聚体蛋白复合物。因此,这里将编码酵母OSCP的基因称为ATP5基因。根据预测的一级序列,未成熟酵母OSCP的计算分子量为22813,其氨基酸序列与牛OSCP的同源性为35%,相似性为65%。构建了一个缺失突变体。该突变菌株无法在甘油培养基上生长,没有可检测到的对寡霉素敏感的ATP酶活性,也没有可检测到的与OSCP相应分子量的免疫反应性蛋白(使用对酵母OSCP有反应的抗体)。对酵母基因的转录产物进行了表征。ATP5基因有一个1.05千碱基的主要转录本。与在葡萄糖培养基中生长的细胞相比,在半乳糖培养基中生长后,转录产物的水平增加了3至5倍。转录起始位点确定在+68(G)和+69(T)处,频率相当,且不依赖于生长培养基。这些结果表明,ATP5基因的转录受到分解代谢物阻遏。

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