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转录起始需要人类线粒体转录因子A和启动子间距完整性。

Human mitochondrial transcription factor A and promoter spacing integrity are required for transcription initiation.

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

Biochim Biophys Acta. 1995 May 24;1271(1):127-34. doi: 10.1016/0925-4439(95)00019-z.

Abstract

The two major promoters for transcription of the human mitochondrial genome are located near each other in the displacement-loop region of the molecule. Previous work has localized these promoters to regions of < 100 nucleotides each; the DNA sequence at the transcription start site is stringently required, as is the region from -10 to -40 base pairs upstream of each respective start site. Each upstream site is recognized and bound by human mitochondrial transcription factor A (h-mtTFA), an event previously shown to be important for transcriptional activation. We report here results using recombinant h-mtTFA that demonstrate the dependence of transcription initiation of h-mtTFA. In addition, altering the distance between the h-mtTFA binding site and the transcription start site greatly impairs transcription initiation efficiency. The decrease in transcription initiation efficiency was shown to be a consequence of altering the position of h-mtTFA binding as opposed to the strength of h-mtTFA binding, as judged by DNA footprinting ability. Analysis of a chimeric yeast-human promoter revealed that the yeast mtTFA homologue cannot substitute for the human protein, even when bound at an appropriate position upstream of the human transcription start site.

摘要

人类线粒体基因组转录的两个主要启动子在分子的置换环区域彼此相邻。先前的研究已将这些启动子定位到各自长度小于100个核苷酸的区域;转录起始位点的DNA序列以及每个起始位点上游-10至-40碱基对的区域都是严格必需的。每个上游位点都由人类线粒体转录因子A(h-mtTFA)识别并结合,这一事件先前已证明对转录激活很重要。我们在此报告使用重组h-mtTFA的结果,这些结果证明了h-mtTFA转录起始的依赖性。此外,改变h-mtTFA结合位点与转录起始位点之间的距离会极大地损害转录起始效率。通过DNA足迹分析判断,转录起始效率的降低被证明是改变h-mtTFA结合位置而非h-mtTFA结合强度的结果。对嵌合酵母-人类启动子的分析表明,酵母mtTFA同源物不能替代人类蛋白,即使它结合在人类转录起始位点上游的适当位置。

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