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1
Ribosome release factor RF4 and termination factor RF3 are involved in dissociation of peptidyl-tRNA from the ribosome.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。
EMBO J. 1998 Feb 2;17(3):808-16. doi: 10.1093/emboj/17.3.808.
2
Ribosome recycling factor and release factor 3 action promotes TnaC-peptidyl-tRNA Dropoff and relieves ribosome stalling during tryptophan induction of tna operon expression in Escherichia coli.核糖体循环因子和释放因子3的作用促进TnaC-肽基-tRNA脱落,并在大肠杆菌色氨酸诱导tna操纵子表达过程中缓解核糖体停滞。
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3
Release factor RF3 abolishes competition between release factor RF1 and ribosome recycling factor (RRF) for a ribosome binding site.释放因子RF3消除了释放因子RF1与核糖体循环因子(RRF)之间对核糖体结合位点的竞争。
J Mol Biol. 1997 Oct 24;273(2):389-401. doi: 10.1006/jmbi.1997.1324.
4
Shutdown in protein synthesis due to the expression of mini-genes in bacteria.由于细菌中微型基因的表达导致蛋白质合成停止。
J Mol Biol. 1999 Aug 27;291(4):745-59. doi: 10.1006/jmbi.1999.3028.
5
Protein synthesis factors (RF1, RF2, RF3, RRF, and tmRNA) and peptidyl-tRNA hydrolase rescue stalled ribosomes at sense codons.蛋白质合成因子(RF1、RF2、RF3、RRF 和 tmRNA)和肽基-tRNA 水解酶在有义密码子处拯救停滞的核糖体。
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6
Release factor RF3 in E.coli accelerates the dissociation of release factors RF1 and RF2 from the ribosome in a GTP-dependent manner.大肠杆菌中的释放因子RF3以GTP依赖的方式加速释放因子RF1和RF2从核糖体上的解离。
EMBO J. 1997 Jul 1;16(13):4126-33. doi: 10.1093/emboj/16.13.4126.
7
Fast recycling of Escherichia coli ribosomes requires both ribosome recycling factor (RRF) and release factor RF3.大肠杆菌核糖体的快速循环需要核糖体循环因子(RRF)和释放因子RF3。
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8
Functional interaction between release factor one and P-site peptidyl-tRNA on the ribosome.释放因子1与核糖体P位点肽基-tRNA之间的功能相互作用。
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9
Initiation factors IF1 and IF2 synergistically remove peptidyl-tRNAs with short polypeptides from the P-site of translating Escherichia coli ribosomes.起始因子IF1和IF2协同作用,从正在翻译的大肠杆菌核糖体的P位点去除带有短多肽的肽基-tRNA。
J Mol Biol. 1998 Aug 14;281(2):241-52. doi: 10.1006/jmbi.1998.1953.
10
A novel class of bacterial translation factor RF3 mutations suggests specific structural domains for premature peptidyl-tRNA drop-off.一种新型细菌翻译因子 RF3 突变提示了特定的结构域用于过早的肽酰-tRNA 脱落。
FEBS Lett. 2010 Feb 19;584(4):790-4. doi: 10.1016/j.febslet.2009.12.048. Epub 2009 Dec 30.

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6
Drop-off-reinitiation triggered by EF-G-driven mistranslocation and its alleviation by EF-P.EF-G 驱动的翻译错误引发的起始因子脱落-再起始及其被 EF-P 缓解。
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Nascent polypeptide within the exit tunnel stabilizes the ribosome to counteract risky translation.新生多肽在出口隧道内稳定核糖体以抵消危险的翻译。
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Mechanistic insights into translation inhibition by aminoglycoside antibiotic arbekacin.对氨基糖苷类抗生素阿贝卡星抑制翻译作用的机制性见解。
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10
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Acetylornithinase of Escherichia coli: partial purification and some properties.大肠杆菌的乙酰鸟氨酸酶:部分纯化及某些性质
J Biol Chem. 1956 Jan;218(1):97-106.
2
Release factor RF3 abolishes competition between release factor RF1 and ribosome recycling factor (RRF) for a ribosome binding site.释放因子RF3消除了释放因子RF1与核糖体循环因子(RRF)之间对核糖体结合位点的竞争。
J Mol Biol. 1997 Oct 24;273(2):389-401. doi: 10.1006/jmbi.1997.1324.
3
Purification of active Escherichia coli ribosome recycling factor (RRF) from an osmo-regulated expression system.从渗透调节表达系统中纯化活性大肠杆菌核糖体循环因子(RRF)。
Biochimie. 1997 May;79(5):243-6. doi: 10.1016/s0300-9084(97)83511-0.
4
Fast recycling of Escherichia coli ribosomes requires both ribosome recycling factor (RRF) and release factor RF3.大肠杆菌核糖体的快速循环需要核糖体循环因子(RRF)和释放因子RF3。
EMBO J. 1997 Jul 1;16(13):4134-41. doi: 10.1093/emboj/16.13.4134.
5
Release factor RF3 in E.coli accelerates the dissociation of release factors RF1 and RF2 from the ribosome in a GTP-dependent manner.大肠杆菌中的释放因子RF3以GTP依赖的方式加速释放因子RF1和RF2从核糖体上的解离。
EMBO J. 1997 Jul 1;16(13):4126-33. doi: 10.1093/emboj/16.13.4126.
6
Prokaryotic and eukaryotic translation factors. Ad Hoc Nomenclature Subcommittee Report.原核生物和真核生物翻译因子。特设命名小组委员会报告。
Biochimie. 1996;78(11-12):1119-22.
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Cotranslational folding of globin.珠蛋白的共翻译折叠
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8
Unconventional structure of tRNA(Lys)SUU anticodon explains tRNA's role in bacterial and mammalian ribosomal frameshifting and primer selection by HIV-1.tRNA(Lys)SUU反密码子的非常规结构解释了tRNA在细菌和哺乳动物核糖体移码以及HIV-1引物选择中的作用。
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9
BEE95: a novel sequence family related to IRU/ERIC dispersed enterobacterial intergenic elements.BEE95:一个与IRU/ERIC分散型肠杆菌基因间元件相关的新序列家族。
Mol Microbiol. 1995 Dec;18(5):987-9. doi: 10.1111/j.1365-2958.1995.18050987.x.
10
Ribosome recycling by ribosome recycling factor (RRF)--an important but overlooked step of protein biosynthesis.核糖体循环因子(RRF)介导的核糖体循环——蛋白质生物合成中一个重要但被忽视的步骤。
Adv Biophys. 1996;32:121-201. doi: 10.1016/0065-227x(96)84743-5.

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.

DOI:10.1093/emboj/17.3.808
PMID:9451005
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1170429/
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。