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首页> 外文期刊>Nucleic acids research >Successful transformation of yeast mitochondria with RPM1: an approach for in vivo studies of mitochondrial RNase P RNA structure, function and biosynthesis
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Successful transformation of yeast mitochondria with RPM1: an approach for in vivo studies of mitochondrial RNase P RNA structure, function and biosynthesis

机译:用RPM1成功转化酵母线粒体:体内研究线粒体RNase P RNA结构,功能和生物合成的方法

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摘要

ABSTRACT Mitochondrial RNase P RNA (Rpm1r) is coded by the RPM1 gene of mitochondrial DNA in many yeasts. As aninitial step to developing a genetic approach to the structure and biogenesis of yeast mitochondrial RNase P, biollstlc transformation has been used to introduce wild type and altered RPM1 genes into strains containing no mitochondrial DNA. The introduced wild type gene does support RNase P activity demonstrating that pre-existing RNase P activityis not necessary for the biosynthesis of the enzyme. Mutations Introduced Into RPM1 in vitro result in reduced accumulation of mature tRNA and in an alteration of the processing of Rpm1r In vivo.
机译:摘要线粒体RNase P RNA(Rpm1r)由许多酵母中的线粒体DNA的RPM1基因编码。作为开发遗传方法来构建酵母线粒体RNase P的遗传方法的第一步,已使用biollstlc转化将野生型和改变的RPM1基因引入不含线粒体DNA的菌株中。引入的野生型基因确实支持RNase P活性,表明该酶的生物合成不需要预先存在的RNase P活性。体外引入RPM1的突变导致减少了成熟tRNA的积累并改变了Rpm1r在体内的加工过程。

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