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线粒体聚腺苷酸聚合酶与聚腺苷酸化

Mitochondrial poly(A) polymerase and polyadenylation.

作者信息

Chang Jeong Ho, Tong Liang

机构信息

Department of Biological Sciences, Columbia University, New York, NY 10027, USA.

出版信息

Biochim Biophys Acta. 2012 Sep-Oct;1819(9-10):992-7. doi: 10.1016/j.bbagrm.2011.10.012. Epub 2011 Dec 7.

Abstract

Polyadenylation of mitochondrial RNAs in higher eukaryotic organisms have diverse effects on their function and metabolism. Polyadenylation completes the UAA stop codon of a majority of mitochondrial mRNAs in mammals, regulates the translation of the mRNAs, and has diverse effects on their stability. In contrast, polyadenylation of most mitochondrial mRNAs in plants leads to their degradation, consistent with the bacterial origin of this organelle. PAPD1 (mtPAP, TUTase1), a noncanonical poly(A) polymerase (ncPAP), is responsible for producing the poly(A) tails in mammalian mitochondria. The crystal structure of human PAPD1 was reported recently, offering molecular insights into its catalysis. This article is part of a Special Issue entitled: Mitochondrial Gene Expression.

摘要

高等真核生物中线粒体RNA的多聚腺苷酸化对其功能和代谢具有多种影响。在哺乳动物中,多聚腺苷酸化完成了大多数线粒体mRNA的UAA终止密码子,调节mRNA的翻译,并对其稳定性产生多种影响。相比之下,植物中大多数线粒体mRNA的多聚腺苷酸化会导致其降解,这与该细胞器的细菌起源一致。PAPD1(线粒体多聚腺苷酸聚合酶,TUTase1),一种非典型的多聚(A)聚合酶(ncPAP),负责在哺乳动物线粒体中产生多聚(A)尾。最近报道了人类PAPD1的晶体结构,为其催化作用提供了分子层面的见解。本文是名为“线粒体基因表达”的特刊的一部分。

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