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载脂蛋白B mRNA编辑酶1与载脂蛋白B mRNA编辑

Apobec-1 and apolipoprotein B mRNA editing.

作者信息

Chan L, Chang B H, Nakamuta M, Li W H, Smith L C

机构信息

Department of Cell Biology, Baylor College of Medicine, Houston, TX 77030, USA.

出版信息

Biochim Biophys Acta. 1997 Mar 10;1345(1):11-26. doi: 10.1016/s0005-2760(96)00156-7.

Abstract

Apolipoprotein (apo)B mRNA editing is a novel mechanism for the post-transcriptional regulation of gene expression in mammals. It consists of a C-->U conversion of the first base of the codon CAA, encoding glutamine-2153, to UAA, an in-frame stop codon, in apoB mRNA. Since its initial description in 1987, substantial progress has been made in the last few years on the mechanism of editing. Apobec-1, the catalytic component of the apoB mRNA editing enzyme complex, has been cloned. This article begins with an overview of the general biology of apoB mRNA editing. It then provides an in-depth analysis of the structure, evolution and possible mechanism of action of apobec-1. ApoB mRNA editing is the prototype of RNA editing in mammals. What we learn from apoB mRNA editing will be useful in our understanding of other examples of RNA editing in vertebrates which are being described with increasing frequency.

摘要

载脂蛋白(apo)B信使核糖核酸(mRNA)编辑是哺乳动物基因表达转录后调控的一种新机制。它包括将编码谷氨酰胺-2153的密码子CAA的第一个碱基由C转换为U,变为UAA,即载脂蛋白B信使核糖核酸中的一个框内终止密码子。自1987年首次描述以来,在过去几年中,编辑机制方面取得了重大进展。载脂蛋白B信使核糖核酸编辑酶复合体的催化成分载脂蛋白B信使核糖核酸编辑酶催化多肽1(Apobec-1)已被克隆。本文首先概述载脂蛋白B信使核糖核酸编辑的一般生物学特性。然后深入分析载脂蛋白B信使核糖核酸编辑酶催化多肽1的结构、进化及可能的作用机制。载脂蛋白B信使核糖核酸编辑是哺乳动物RNA编辑的原型。我们从载脂蛋白B信使核糖核酸编辑中学到的知识,将有助于我们理解脊椎动物中越来越频繁被描述的其他RNA编辑实例。

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