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来自酿酒酵母的线粒体转录复合体。

Mitochondrial transcription complex from Saccharomyces cerevisiae.

作者信息

Levens D, Morimoto R, Rabinowitz M

出版信息

J Biol Chem. 1981 Feb 10;256(3):1466-72.

PMID:7005236
Abstract

A DNA protein complex has been isolated from the mitochondria of Saccharomyces cerevisiae. The complex transcribes RNA complementary to mtDNA in a nonrandom manner. The RNA polymerase activity contained in the transcription complex is not dependent on the addition of exogenous template. The activity is rendered template-dependent by autolysis and can be further purified by heparin-Sepharose 4B chromatography. The activity is inhibited by heparin, Mn2+, and increasing ionic strength. The activity requires Mg2+ and ribonucleotides. The preferred template for the template dependent activity is poly[d(AT)]. The majority of the RNA synthesized by the transcription complex from endogenous DNA is complementary to the DNA strands directing the synthesis of the large and small ribosomal RNA. In yeast the 21 S and 14S rRNA genes are widely separated, therefore the transcription of these two regions but not of the intervening regions by the transcription complex suggests the existence of at least two transcriptional promoters on the yeast mitochondrial genome.

摘要

已从酿酒酵母的线粒体中分离出一种DNA - 蛋白质复合物。该复合物以非随机方式转录与线粒体DNA互补的RNA。转录复合物中所含的RNA聚合酶活性不依赖于外源模板的添加。该活性通过自溶作用变为模板依赖性,并且可以通过肝素 - 琼脂糖4B层析进一步纯化。该活性受到肝素、Mn2 +和离子强度增加的抑制。该活性需要Mg2 +和核糖核苷酸。模板依赖性活性的首选模板是聚[d(AT)]。转录复合物从内源性DNA合成的大部分RNA与指导大、小核糖体RNA合成的DNA链互补。在酵母中,21S和14S rRNA基因相距很远,因此转录复合物对这两个区域而非中间区域的转录表明酵母线粒体基因组上至少存在两个转录启动子。

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