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核糖体释放因子RF4和终止因子RF3参与肽基tRNA从核糖体上的解离。

Ribosome release factor RF4 and termination factor RF3 are involved in dissociation of peptidyl-tRNA from the ribosome.

作者信息

Heurgué-Hamard V, Karimi R, Mora L, MacDougall J, Leboeuf C, Grentzmann G, Ehrenberg M, Buckingham R H

机构信息

UPR9073 du CNRS, Institut de Biologie Physico-Chimique, 13 rue Pierre et Marie Curie, F-75005 Paris, France.

出版信息

EMBO J. 1998 Feb 2;17(3):808-16. doi: 10.1093/emboj/17.3.808.

Abstract

Peptidyl-tRNA dissociation from ribosomes is an energetically costly but apparently inevitable process that accompanies normal protein synthesis. The drop-off products of these events are hydrolysed by peptidyl-tRNA hydrolase. Mutant selections have been made to identify genes involved in the drop-off of peptidyl-tRNA, using a thermosensitive peptidyl-tRNA hydrolase mutant in Escherichia coli. Transposon insertions upstream of the frr gene, which encodes RF4 (ribosome release or recycling factor), restored growth to this mutant. The insertions impaired expression of the frr gene. Mutations inactivating prfC, encoding RF3 (release factor 3), displayed a similar phenotype. Conversely, production of RF4 from a plasmid increased the thermosensitivity of the peptidyl-tRNA hydrolase mutant. In vitro measurements of peptidyl-tRNA release from ribosomes paused at stop signals or sense codons confirmed that RF3 and RF4 were able to stimulate peptidyl-tRNA release from ribosomes, and showed that this action of RF4 required the presence of translocation factor EF2, known to be needed for the function of RF4 in ribosome recycling. When present together, the three factors were able to stimulate release up to 12-fold. It is suggested that RF4 may displace peptidyl-tRNA from the ribosome in a manner related to its proposed function in removing deacylated tRNA during ribosome recycling.

摘要

肽基 - tRNA从核糖体上解离是一个能量消耗大但显然不可避免的过程,它伴随着正常的蛋白质合成。这些事件的脱落产物由肽基 - tRNA水解酶水解。利用大肠杆菌中的温度敏感型肽基 - tRNA水解酶突变体进行了突变体筛选,以鉴定参与肽基 - tRNA脱落的基因。在编码RF4(核糖体释放或循环因子)的frr基因上游的转座子插入恢复了该突变体的生长。这些插入损害了frr基因的表达。使编码RF3(释放因子3)的prfC失活的突变表现出类似的表型。相反,从质粒产生RF4增加了肽基 - tRNA水解酶突变体的温度敏感性。对在终止信号或有义密码子处暂停的核糖体上肽基 - tRNA释放的体外测量证实,RF3和RF4能够刺激肽基 - tRNA从核糖体上释放,并表明RF4的这种作用需要转位因子EF2的存在,已知EF2是RF4在核糖体循环中发挥功能所必需的。当这三种因子同时存在时,它们能够将释放刺激高达12倍。有人提出,RF4可能以与其在核糖体循环过程中去除脱酰基tRNA的拟议功能相关的方式将肽基 - tRNA从核糖体上置换下来。

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