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噬菌体T4中的RNA加工与降解

RNA processing and decay in bacteriophage T4.

作者信息

Uzan Marc

机构信息

Institut Jacques Monod, CNRS-Universites Paris, Paris, France.

出版信息

Prog Mol Biol Transl Sci. 2009;85:43-89. doi: 10.1016/S0079-6603(08)00802-7.

Abstract

Bacteriophage T4 is the archetype of virulent phage. It has evolved very efficient strategies to subvert host functions to its benefit and to impose the expression of its genome. T4 utilizes a combination of host and phage-encoded RNases and factors to degrade its mRNAs in a stage-dependent manner. The host endonuclease RNase E is used throughout the phage development. The sequence-specific, T4-encoded RegB endoribonuclease functions in association with the ribosomal protein S1 to functionally inactivate early transcripts and expedite their degradation. T4 polynucleotide kinase plays a role in this process. Later, the viral factor Dmd protects middle and late mRNAs from degradation by the host RNase LS. T4 codes for a set of eight tRNAs and two small, stable RNA of unknown function that may contribute to phage virulence. Their maturation is assured by host enzymes, but one phage factor, Cef, is required for the biogenesis of some of them. The tRNA gene cluster also codes for a homing DNA endonuclease, SegB, responsible for spreading the tRNA genes to other T4-related phage.

摘要

噬菌体T4是烈性噬菌体的原型。它已经进化出非常有效的策略来颠覆宿主功能以使其自身受益,并强制表达其基因组。T4利用宿主和噬菌体编码的核糖核酸酶及因子的组合,以阶段依赖的方式降解其mRNA。宿主内切核酸酶核糖核酸酶E在噬菌体整个发育过程中都被使用。序列特异性的、由T4编码的RegB核糖核酸内切酶与核糖体蛋白S1协同作用,使早期转录本功能失活并加速其降解。T4多核苷酸激酶在这一过程中发挥作用。后来,病毒因子Dmd保护中期和晚期mRNA不被宿主核糖核酸酶LS降解。T4编码一组8种tRNA和两种功能未知的小的稳定RNA,它们可能有助于噬菌体的毒性。它们的成熟由宿主酶确保,但其中一些的生物合成需要一种噬菌体因子Cef。tRNA基因簇还编码一种归巢DNA内切核酸酶SegB,负责将tRNA基因传播到其他与T4相关的噬菌体。

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