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核糖核酸酶线粒体RNA加工可在线粒体DNA前导链复制起点正确切割一个新的R环。

RNase mitochondrial RNA processing correctly cleaves a novel R loop at the mitochondrial DNA leading-strand origin of replication.

作者信息

Lee D Y, Clayton D A

机构信息

Department of Developmental Biology, Beckman Center for Molecular and Genetic Medicine, Stanford University School of Medicine, California 94305-5427, USA.

出版信息

Genes Dev. 1997 Mar 1;11(5):582-92. doi: 10.1101/gad.11.5.582.

Abstract

The precursor primer RNA for mammalian mitochondrial DNA leading-strand replication remains as a persistent R loop formed during transcription through the mitochondrial DNA control region. We have examined model R loops, which exist in a novel and physiologically accurate preprimer conformation, as potential substrates for mammalian RNase mitochondrial RNA processing (MRP). Mouse RNase MRP accurately cleaves an R loop containing the mouse mitochondrial DNA origin. The multiple cleavage sites on the R-loop substrate match the priming sites observed in vivo, suggesting that RNase MRP alone is capable of generating virtually all of the leading-strand replication primers.

摘要

哺乳动物线粒体DNA前导链复制的前体引物RNA,在转录通过线粒体DNA控制区的过程中,会以持续存在的R环形式保留下来。我们研究了模型R环,其以一种新颖且生理上准确的前引物构象存在,作为哺乳动物核糖核酸酶线粒体RNA加工(MRP)的潜在底物。小鼠核糖核酸酶MRP能准确切割包含小鼠线粒体DNA起始位点的R环。R环底物上的多个切割位点与体内观察到的引发位点相匹配,这表明仅核糖核酸酶MRP就能产生几乎所有的前导链复制引物。

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