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微小转录起始事件表明,人类线粒体的两个启动子都具有双向功能。

Minor transcription initiation events indicate that both human mitochondrial promoters function bidirectionally.

作者信息

Chang D D, Hixson J E, Clayton D A

出版信息

Mol Cell Biol. 1986 Jan;6(1):294-301. doi: 10.1128/mcb.6.1.294-301.1986.

Abstract

Human mitochondrial DNA is transcribed from two distinct, strand-specific promoters located in the displacement loop region of the genome. The transcriptional control sequences identified by deletion mapping and site-directed mutagenesis studies span short regions surrounding the initiation sites and bear no obvious sequence homology to any nuclear or procaryotic promoters. In vitro transcription analyses also revealed several minor initiation sites that are characterized by a pyrimidine-rich region followed by a purine-rich region, a feature that is shared by the two major promoters. In this paper, we report a new class of minor promoters in human mitochondrial DNA. These minor promoters were localized to the same duplex DNA sequences that direct major transcriptional events, but they had transcriptional polarity opposite to that of the major promoters. Furthermore, nucleotide changes that affected the major form of transcription similarly affected transcription in the opposite direction. For one of these minor promoters, a corresponding in vivo RNA species initiating from the same site was identified. These observations indicate that the major transcriptional promoters in human mitochondria can function bidirectionally both in vivo and in vitro.

摘要

人类线粒体DNA是从位于基因组置换环区域的两个不同的、链特异性启动子转录而来的。通过缺失定位和定点诱变研究确定的转录控制序列跨越起始位点周围的短区域,与任何核或原核启动子没有明显的序列同源性。体外转录分析还揭示了几个次要起始位点,其特征是富含嘧啶的区域后接富含嘌呤的区域,这是两个主要启动子共有的特征。在本文中,我们报道了人类线粒体DNA中的一类新的次要启动子。这些次要启动子定位于指导主要转录事件的相同双链DNA序列,但它们的转录极性与主要启动子相反。此外,影响主要转录形式的核苷酸变化同样以相反的方向影响转录。对于其中一个次要启动子,鉴定出了从同一位点起始的相应体内RNA物种。这些观察结果表明,人类线粒体中的主要转录启动子在体内和体外都可以双向发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c93f/367510/3cee160ec02d/molcellb00085-0315-a.jpg

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