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一种人类线粒体转录激活因子在体内和体外均可功能性替代酵母线粒体HMG盒蛋白。

A human mitochondrial transcriptional activator can functionally replace a yeast mitochondrial HMG-box protein both in vivo and in vitro.

作者信息

Parisi M A, Xu B, Clayton D A

机构信息

Department of Developmental Biology, Stanford University School of Medicine, California 94305-5427.

出版信息

Mol Cell Biol. 1993 Mar;13(3):1951-61. doi: 10.1128/mcb.13.3.1951-1961.1993.

Abstract

Human mitochondrial transcription factor A is a 25-kDa protein that binds immediately upstream of the two major mitochondrial promoters, thereby leading to correct and efficient initiation of transcription. Although the nature of yeast mitochondrial promoters is significantly different from that of human promoters, a potential functional homolog of the human transcriptional activator protein has been previously identified in yeast mitochondria. The importance of the yeast protein in yeast mitochondrial DNA function has been shown by inactivation of its nuclear gene (ABF2) in Saccharomyces cerevisiae cells resulting in loss of mitochondrial DNA. We report here that the nuclear gene for human mitochondrial transcription factor A can be stably expressed in yeast cells devoid of the yeast homolog protein. The human protein is imported efficiently into yeast mitochondria, is processed correctly, and rescues the loss-of-mitochondrial DNA phenotype in a yeast abf2 strain, thus functionally substituting for the yeast protein. Both human and yeast proteins affect yeast mitochondrial transcription initiation in vitro, suggesting that the two proteins may have a common role in this fundamental process.

摘要

人类线粒体转录因子A是一种25千道尔顿的蛋白质,它结合在两个主要线粒体启动子的紧邻上游位置,从而导致转录的正确且高效起始。尽管酵母线粒体启动子的性质与人类启动子有显著差异,但人类转录激活蛋白的潜在功能同源物此前已在酵母线粒体中被鉴定出来。通过在酿酒酵母细胞中使其核基因(ABF2)失活导致线粒体DNA丢失,已证明了酵母蛋白在酵母线粒体DNA功能中的重要性。我们在此报告,人类线粒体转录因子A的核基因可在缺乏酵母同源蛋白的酵母细胞中稳定表达。人类蛋白能高效导入酵母线粒体,被正确加工,并挽救酵母abf2菌株中线粒体DNA丢失的表型,从而在功能上替代酵母蛋白。人类和酵母蛋白在体外均影响酵母线粒体转录起始,这表明这两种蛋白在这一基本过程中可能具有共同作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d96/359509/439d2642b288/molcellb00015-0652-a.jpg

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