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本文引用的文献

1
Stimulation of stop codon readthrough: frequent presence of an extended 3' RNA structural element.终止密码子通读的刺激:扩展的 3' RNA 结构元件的频繁存在。
Nucleic Acids Res. 2011 Aug;39(15):6679-91. doi: 10.1093/nar/gkr224. Epub 2011 Apr 27.
2
Endogenous ribosomal frameshift signals operate as mRNA destabilizing elements through at least two molecular pathways in yeast.内源性核糖体移码信号通过至少两种分子途径在酵母中作为 mRNA 不稳定元件发挥作用。
Nucleic Acids Res. 2011 Apr;39(7):2799-808. doi: 10.1093/nar/gkq1220. Epub 2010 Nov 24.
3
RDP3: a flexible and fast computer program for analyzing recombination.RDP3:一个灵活快速的计算机程序,用于分析重组。
Bioinformatics. 2010 Oct 1;26(19):2462-3. doi: 10.1093/bioinformatics/btq467. Epub 2010 Aug 26.
4
Identification of a cellular factor that modulates HIV-1 programmed ribosomal frameshifting.鉴定一种可调节 HIV-1 程序性核糖体移码的细胞因子。
J Biol Chem. 2010 Jun 25;285(26):19776-84. doi: 10.1074/jbc.M109.085621. Epub 2010 Apr 23.
5
Processive selenocysteine incorporation during synthesis of eukaryotic selenoproteins.真核生物硒蛋白合成过程中的连续硒半胱氨酸掺入。
J Mol Biol. 2010 Jun 11;399(3):385-96. doi: 10.1016/j.jmb.2010.04.033. Epub 2010 Apr 24.
6
Frameshifting in alphaviruses: a diversity of 3' stimulatory structures.甲病毒中的移码框架:多样性的 3' 增强结构。
J Mol Biol. 2010 Mar 26;397(2):448-56. doi: 10.1016/j.jmb.2010.01.044. Epub 2010 Jan 28.
7
Evidence for ribosomal frameshifting and a novel overlapping gene in the genomes of insect-specific flaviviruses.昆虫特异性黄病毒基因组中核糖体移码和新重叠基因的证据。
Virology. 2010 Mar 30;399(1):153-166. doi: 10.1016/j.virol.2009.12.033. Epub 2010 Jan 25.
8
Theiler's murine encephalomyelitis virus L* amino acid position 93 is important for virus persistence and virus-induced demyelination.西勒氏鼠脑脊髓炎病毒 L* 氨基酸位置 93 对病毒持续存在和病毒诱导的脱髓鞘很重要。
J Virol. 2010 Feb;84(3):1348-54. doi: 10.1128/JVI.01585-09. Epub 2009 Nov 18.
9
NS1' of flaviviruses in the Japanese encephalitis virus serogroup is a product of ribosomal frameshifting and plays a role in viral neuroinvasiveness.黄病毒 NS1' 是日本脑炎病毒血清群的一种产物,是核糖体移码的结果,在病毒神经侵袭性方面发挥作用。
J Virol. 2010 Feb;84(3):1641-7. doi: 10.1128/JVI.01979-09. Epub 2009 Nov 11.
10
Saffold virus, a human Theiler's-like cardiovirus, is ubiquitous and causes infection early in life.萨福克病毒是一种类似泰勒病毒的人源嗜心性病毒,广泛存在,可在生命早期引起感染。
PLoS Pathog. 2009 May;5(5):e1000416. doi: 10.1371/journal.ppat.1000416. Epub 2009 May 1.

核糖体移码进入心脏病毒基因组 2B 编码区的重叠基因。

Ribosomal frameshifting into an overlapping gene in the 2B-encoding region of the cardiovirus genome.

机构信息

BioSciences Institute, University College Cork, Cork, Ireland.

出版信息

Proc Natl Acad Sci U S A. 2011 Nov 15;108(46):E1111-9. doi: 10.1073/pnas.1102932108. Epub 2011 Oct 24.

DOI:10.1073/pnas.1102932108
PMID:22025686
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3219106/
Abstract

The genus Cardiovirus (family Picornaviridae) currently comprises the species Encephalomyocarditis virus (EMCV) and Theilovirus. Cardioviruses have a positive-sense, single-stranded RNA genome that encodes a large polyprotein (L-1ABCD-2ABC-3ABCD) that is cleaved to produce approximately 12 mature proteins. We report on a conserved ORF that overlaps the 2B-encoding sequence of EMCV in the +2 reading frame. The ORF is translated as a 128-129 amino acid transframe fusion (2B*) with the N-terminal 11-12 amino acids of 2B, via ribosomal frameshifting at a conserved GGUUUUY motif. Mutations that knock out expression of 2B* result in a small-plaque phenotype. Curiously, although theilovirus sequences lack a long ORF in the +2 frame at this genomic location, they maintain a conserved GGUUUUU motif just downstream of the 2A-2B junction, and a highly localized peak in conservation at polyprotein-frame synonymous sites suggests that theiloviruses also utilize frameshifting here, albeit into a very short +2-frame ORF. Unlike previous cases of programmed -1 frameshifting, here frameshifting is modulated by virus infection, thus suggesting a novel regulatory role for frameshifting in these viruses.

摘要

该属心脏病毒(科小核糖核酸病毒科)目前包括脑炎心肌炎病毒(EMCV)和水疱性口炎病毒。心脏病毒具有正链、单链 RNA 基因组,编码一个大的多蛋白(L-1ABCD-2ABC-3ABCD),该多蛋白被切割产生约 12 个成熟蛋白。我们报告了一个在 +2 阅读框中与 EMCV 2B 编码序列重叠的保守 ORF。该 ORF 通过核糖体移码以翻译为 128-129 个氨基酸的跨框架融合(2B*),其 N 端为 2B 的 11-12 个氨基酸,移码发生在保守的 GGUUUUY 基序处。敲除 2B*表达的突变导致小斑块表型。奇怪的是,尽管水疱性口炎病毒序列在此基因组位置的 +2 框中缺少长 ORF,但它们在 2A-2B 连接处的下游保持保守的 GGUUUUU 基序,并且多蛋白框架同义位点的高度局部化保守峰表明水疱性口炎病毒也在此处利用移码,尽管移码进入非常短的 +2 框 ORF。与之前的 -1 框内移码不同,这里的移码受病毒感染的调节,因此表明移码在这些病毒中具有新的调节作用。