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添加一个包含29个残基的羧基末端尾巴可将一个简单的含HMG盒蛋白转化为转录激活因子。

Addition of a 29 residue carboxyl-terminal tail converts a simple HMG box-containing protein into a transcriptional activator.

作者信息

Dairaghi D J, Shadel G S, Clayton D A

机构信息

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

出版信息

J Mol Biol. 1995 May 26;249(1):11-28. doi: 10.1006/jmbi.1995.9889.

Abstract

Human mitochondrial transcription factor A (h-mtTFA) is essential for initiation of transcription from the two promoters located in the displacement-loop region of human mitochondrial DNA. This 25 kDa protein contains two tandem, HMG box DNA-binding domains separated by a 27 amino acid residue linker region and followed by a 25 residue carboxyl-terminal tail; both the linker and tail are rich in basic amino acid residues. Mutational analysis of h-mtTFA revealed that the tail region is important for specific DNA recognition and essential for transcriptional activation. The critical role of the human tail in transcription was confirmed by constructing chimeric proteins that exchanged similar regions between h-mtTFA and its Saccharomyces cerevisiae homolog, sc-mtTFA. Wild-type sc-mtTFA is unable to activate transcription from the human mitochondrial light-strand promoter (LSP). Addition of the human tail region to sc-mtTFA conferred LSP-specific promoter activation. In all of the different h-mtTFA mutations tested, transcriptional activation was correlated with specific DNA-binding activity, suggesting that these two functions may be inseparable, a situation entirely consistent with previous mutational analyses of human mitochondrial promoters.

摘要

人类线粒体转录因子A(h-mtTFA)对于从位于人类线粒体DNA置换环区域的两个启动子起始转录至关重要。这种25 kDa的蛋白质包含两个串联的HMG盒DNA结合结构域,由一个27个氨基酸残基的连接区隔开,后面跟着一个25个残基的羧基末端尾巴;连接区和尾巴都富含碱性氨基酸残基。对h-mtTFA的突变分析表明,尾巴区域对于特异性DNA识别很重要,并且对于转录激活必不可少。通过构建在h-mtTFA与其酿酒酵母同源物sc-mtTFA之间交换相似区域的嵌合蛋白,证实了人类尾巴在转录中的关键作用。野生型sc-mtTFA无法激活人类线粒体轻链启动子(LSP)的转录。将人类尾巴区域添加到sc-mtTFA中可赋予LSP特异性启动子激活。在所有测试的不同h-mtTFA突变中,转录激活与特异性DNA结合活性相关,表明这两种功能可能不可分割,这种情况与先前对人类线粒体启动子的突变分析完全一致。

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