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Yeast mitochondrial RNA polymerase primes mitochondrial DNA polymerase at origins of replication and promoter sequences

机译:酵母线粒体RNA聚合酶在复制起点和启动子序列中引发线粒体DNA聚合酶

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Three proteins phylogenetically grouped with proteins from the T7 replisome localize to yeast mitochondria: DNA polymerase gamma (Mip1), mitochondrial RNA polymerase (Rpo41), and a single-stranded binding protein (Rim1). Human and T7 bacteriophage RNA polymerases synthesize primers for their corresponding DNA polymerases. In contrast, DNA replication in yeast mitochondria is explained by two models: a transcription-dependent model in which Rpo41 primes Mip1 and a model in which double stranded breaks create free 3' OHs that are extended by Mip1. Herein we found that Rpo41 transcribes RNAs that can be extended by Mip1 on single and double-stranded DNA. In contrast to human mitochondrial RNA polymerase, which primes DNA polymerase gamma using transcripts from the light-strand and heavy-strand origins of replication, Rpo41 primes Mip1 at replication origins and promoter sequences in vitro. Our results suggest that in ori1, short transcripts serve as primers, whereas in ori5 an RNA transcript longer than 29 nucleotides is used as primer. (C) 2015 Elsevier B.V. and Mitochondria Research Society. All rights reserved.
机译:与来自T7复制体的蛋白质在系统发育上分组的三种蛋白质位于酵母线粒体中:DNA聚合酶γ(Mip1),线粒体RNA聚合酶(Rpo41)和单链结合蛋白(Rim1)。人和T7噬菌体RNA聚合酶为其相应的DNA聚合酶合成引物。相反,酵母线粒体中的DNA复制由两种模型解释:转录依赖性模型,其中Rpo41引发Mip1;双链断裂,产生游离的3'OH,该3'OH被Mip1延伸。在这里,我们发现Rpo41转录可通过Mip1在单链和双链DNA上延伸的RNA。与人类线粒体RNA聚合酶不同,后者使用来自轻链和重链复制起点的转录物引发DNA聚合酶gamma,而Rpo41在体外则以复制起点和启动子序列引发Mip1。我们的结果表明,在ori1中,短转录物用作引物,而在ori5中,长于29个核苷酸的RNA转录物被用作引物。 (C)2015 Elsevier B.V.和线粒体研究学会。版权所有。

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