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副黏病毒P mRNA编辑的口吃模型。

A stuttering model for paramyxovirus P mRNA editing.

作者信息

Vidal S, Curran J, Kolakofsky D

机构信息

Department of Microbiology, University of Geneva School of Medicine, Switzerland.

出版信息

EMBO J. 1990 Jun;9(6):2017-22. doi: 10.1002/j.1460-2075.1990.tb08330.x.

Abstract

Paramyxovirus P genes are transcribed into two mRNAs which differ from each other by either one (measles and Sendai virus) or two (SV5 and mumps virus) G insertions, and which code for either the P or V proteins. The G insertions always occur within a short run of Gs, and a stuttering mechanism for the insertions has been suggested in which the viral polymerase reiteratively copies a template C residue during mRNA synthesis. Support for this mechanism was obtained by varying the reaction conditions during Sendai virus mRNA synthesis in vitro. A stuttering model is proposed which accounts for how the ratio of inserted to uninserted mRNAs is controlled, and why some paramyxoviruses insert one G and others two Gs when insertions occur.

摘要

副黏病毒P基因被转录为两种mRNA,它们因一个(麻疹病毒和仙台病毒)或两个(SV5和腮腺炎病毒)G插入而彼此不同,并且分别编码P或V蛋白。G插入总是发生在一段短的G序列中,有人提出了一种滑读机制来解释这种插入,即病毒聚合酶在mRNA合成过程中反复复制模板C残基。通过在体外改变仙台病毒mRNA合成过程中的反应条件,获得了对该机制的支持。本文提出了一种滑读模型,该模型解释了插入型与未插入型mRNA的比例是如何被控制的,以及当发生插入时,为什么有些副黏病毒插入一个G,而有些则插入两个G。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d74/551911/6f25b3ace4f8/emboj00233-0327-a.jpg

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