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编辑后的载脂蛋白B转录本中单碱基替换的特征分析。

Characterization of single base substitutions in edited apolipoprotein B transcripts.

作者信息

Tennyson G E, Sabatos C A, Eggerman T L, Brewer H B

机构信息

Molecular Disease Branch, National Heart, Lung and Blood Institute, Bethesda, MD 20892.

出版信息

Nucleic Acids Res. 1989 Jan 25;17(2):691-8. doi: 10.1093/nar/17.2.691.

Abstract

Mature RNA transcripts from a single eukaryotic gene may contain different nucleotide sequences, ranging from alternately spliced exons to transcripts from separate alleles differing by only one base. Our laboratory and others have recently reported another class of RNA sequence differences, occurring in transcripts from the single copy apolipoprotein B (apoB) gene. A unique RNA editing mechanism allows expression of the CAA glutamine codon encoded by the apoB gene at nucleotide 6666, or terminates translation by the introduction of a premature UAA translational stop codon. In this study, we used the polymerase chain reaction (PCR) to amplify and characterize edited apoB RNA transcripts differing by a single nucleotide. Amplification and sequence analysis from small quantities of total RNA will facilitate the study of RNA editing and transcription in general.

摘要

来自单个真核基因的成熟RNA转录本可能包含不同的核苷酸序列,范围从交替剪接的外显子到仅相差一个碱基的不同等位基因的转录本。我们实验室和其他机构最近报道了另一类RNA序列差异,发生在单拷贝载脂蛋白B(apoB)基因的转录本中。一种独特的RNA编辑机制允许apoB基因在核苷酸6666处编码的CAA谷氨酰胺密码子表达,或者通过引入过早的UAA翻译终止密码子来终止翻译。在本研究中,我们使用聚合酶链反应(PCR)扩增并鉴定相差单个核苷酸的编辑后apoB RNA转录本。从少量总RNA进行扩增和序列分析将总体上促进RNA编辑和转录的研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03ff/331612/0ab41a4a65e3/nar00211-0224-a.jpg

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