• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

核糖体移码和转录滑动:从基因隐写术和密码学到偶然用途。

Ribosomal frameshifting and transcriptional slippage: From genetic steganography and cryptography to adventitious use.

作者信息

Atkins John F, Loughran Gary, Bhatt Pramod R, Firth Andrew E, Baranov Pavel V

机构信息

School of Biochemistry and Cell Biology, University College Cork, Cork, Ireland School of Microbiology, University College Cork, Cork, Ireland Department of Human Genetics, University of Utah, Salt Lake City, UT 84112, USA

School of Biochemistry and Cell Biology, University College Cork, Cork, Ireland.

出版信息

Nucleic Acids Res. 2016 Sep 6;44(15):7007-78. doi: 10.1093/nar/gkw530. Epub 2016 Jul 19.

DOI:10.1093/nar/gkw530
PMID:27436286
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5009743/
Abstract

Genetic decoding is not 'frozen' as was earlier thought, but dynamic. One facet of this is frameshifting that often results in synthesis of a C-terminal region encoded by a new frame. Ribosomal frameshifting is utilized for the synthesis of additional products, for regulatory purposes and for translational 'correction' of problem or 'savior' indels. Utilization for synthesis of additional products occurs prominently in the decoding of mobile chromosomal element and viral genomes. One class of regulatory frameshifting of stable chromosomal genes governs cellular polyamine levels from yeasts to humans. In many cases of productively utilized frameshifting, the proportion of ribosomes that frameshift at a shift-prone site is enhanced by specific nascent peptide or mRNA context features. Such mRNA signals, which can be 5' or 3' of the shift site or both, can act by pairing with ribosomal RNA or as stem loops or pseudoknots even with one component being 4 kb 3' from the shift site. Transcriptional realignment at slippage-prone sequences also generates productively utilized products encoded trans-frame with respect to the genomic sequence. This too can be enhanced by nucleic acid structure. Together with dynamic codon redefinition, frameshifting is one of the forms of recoding that enriches gene expression.

摘要

基因解码并非如之前所认为的那样是“固定不变的”,而是动态的。其中一个方面是移码,这通常会导致由新的读码框编码的C末端区域的合成。核糖体移码被用于合成额外的产物、用于调控目的以及对问题插入缺失或“挽救性”插入缺失进行翻译“校正”。用于合成额外产物在移动染色体元件和病毒基因组的解码中尤为突出。稳定染色体基因的一类调控性移码控制着从酵母到人类的细胞多胺水平。在许多有效利用移码的情况下,在易发生移码的位点发生移码的核糖体比例会因特定的新生肽或mRNA上下文特征而增加。这样的mRNA信号,可以在移码位点的5'端或3'端,或者两端都有,它可以通过与核糖体RNA配对起作用,或者作为茎环或假结起作用,甚至其中一个元件在离移码位点3'端4 kb处。在易发生滑动的序列处的转录重排也会产生相对于基因组序列以反式读码框编码的有效利用的产物。这同样可以通过核酸结构得到增强。与动态密码子重新定义一起,移码是丰富基因表达的重新编码形式之一。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5bd/5009743/a2ab25889d79/gkw530fig20.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5bd/5009743/83f0e2f24b28/gkw530fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5bd/5009743/f88f9627528f/gkw530fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5bd/5009743/fb69244c2144/gkw530fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5bd/5009743/e702f975b523/gkw530fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5bd/5009743/0bd07588a56b/gkw530fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5bd/5009743/d535e023de1c/gkw530fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5bd/5009743/cbd2f781c99d/gkw530fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5bd/5009743/d133fcd06033/gkw530fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5bd/5009743/7bca5e027afc/gkw530fig9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5bd/5009743/b9637824df4c/gkw530fig10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5bd/5009743/e83c4afd1e91/gkw530fig11.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5bd/5009743/136ba4c779f6/gkw530fig12.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5bd/5009743/1a34ae8eb741/gkw530fig13.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5bd/5009743/7cbbc1b51656/gkw530fig14.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5bd/5009743/6be18d5facc5/gkw530fig15.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5bd/5009743/695e994cb3d5/gkw530fig16.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5bd/5009743/8839deeba64c/gkw530fig17.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5bd/5009743/320bb21da2c5/gkw530fig18.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5bd/5009743/051f65075a06/gkw530fig19.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5bd/5009743/a2ab25889d79/gkw530fig20.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5bd/5009743/83f0e2f24b28/gkw530fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5bd/5009743/f88f9627528f/gkw530fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5bd/5009743/fb69244c2144/gkw530fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5bd/5009743/e702f975b523/gkw530fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5bd/5009743/0bd07588a56b/gkw530fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5bd/5009743/d535e023de1c/gkw530fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5bd/5009743/cbd2f781c99d/gkw530fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5bd/5009743/d133fcd06033/gkw530fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5bd/5009743/7bca5e027afc/gkw530fig9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5bd/5009743/b9637824df4c/gkw530fig10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5bd/5009743/e83c4afd1e91/gkw530fig11.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5bd/5009743/136ba4c779f6/gkw530fig12.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5bd/5009743/1a34ae8eb741/gkw530fig13.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5bd/5009743/7cbbc1b51656/gkw530fig14.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5bd/5009743/6be18d5facc5/gkw530fig15.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5bd/5009743/695e994cb3d5/gkw530fig16.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5bd/5009743/8839deeba64c/gkw530fig17.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5bd/5009743/320bb21da2c5/gkw530fig18.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5bd/5009743/051f65075a06/gkw530fig19.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5bd/5009743/a2ab25889d79/gkw530fig20.jpg

相似文献

1
Ribosomal frameshifting and transcriptional slippage: From genetic steganography and cryptography to adventitious use.核糖体移码和转录滑动:从基因隐写术和密码学到偶然用途。
Nucleic Acids Res. 2016 Sep 6;44(15):7007-78. doi: 10.1093/nar/gkw530. Epub 2016 Jul 19.
2
A sequence required for -1 ribosomal frameshifting located four kilobases downstream of the frameshift site.位于移码位点下游4千碱基处的-1核糖体移码所需序列。
J Mol Biol. 2001 Jul 27;310(5):987-99. doi: 10.1006/jmbi.2001.4801.
3
Polyamine sensing during antizyme mRNA programmed frameshifting.抗酶mRNA程序性移码过程中的多胺感知
Biochem Biophys Res Commun. 2005 Dec 23;338(3):1478-89. doi: 10.1016/j.bbrc.2005.10.115. Epub 2005 Oct 27.
4
Analysis of the roles of tRNA structure, ribosomal protein L9, and the bacteriophage T4 gene 60 bypassing signals during ribosome slippage on mRNA.在核糖体在信使核糖核酸(mRNA)上发生滑动期间,对转运核糖核酸(tRNA)结构、核糖体蛋白L9以及噬菌体T4基因60的通读信号所起作用的分析。
J Mol Biol. 2001 Jun 22;309(5):1029-48. doi: 10.1006/jmbi.2001.4717.
5
Programmed +1 frameshifting stimulated by complementarity between a downstream mRNA sequence and an error-correcting region of rRNA.由下游mRNA序列与rRNA的纠错区域之间的互补性刺激引发的程序性+1移码。
RNA. 2001 Feb;7(2):275-84. doi: 10.1017/s135583820100190x.
6
Programmed frameshifting in the synthesis of mammalian antizyme is +1 in mammals, predominantly +1 in fission yeast, but -2 in budding yeast.哺乳动物抗酶合成过程中的程序性移码在哺乳动物中为+1,在裂殖酵母中主要为+1,但在芽殖酵母中为-2。
RNA. 1998 Oct;4(10):1230-8. doi: 10.1017/s1355838298980864.
7
Antisense-induced ribosomal frameshifting.反义诱导的核糖体移码
Nucleic Acids Res. 2006;34(15):4302-10. doi: 10.1093/nar/gkl531. Epub 2006 Aug 18.
8
Productive mRNA stem loop-mediated transcriptional slippage: Crucial features in common with intrinsic terminators.有生产性的mRNA茎环介导的转录滑动:与内在终止子共有的关键特征。
Proc Natl Acad Sci U S A. 2015 Apr 21;112(16):E1984-93. doi: 10.1073/pnas.1418384112. Epub 2015 Apr 6.
9
Near-cognate peptidyl-tRNAs promote +1 programmed translational frameshifting in yeast.近同源肽基-tRNA促进酵母中的+1程序性翻译移码。
Mol Cell. 1999 Dec;4(6):1005-15. doi: 10.1016/s1097-2765(00)80229-4.
10
A genome-wide analysis of RNA pseudoknots that stimulate efficient -1 ribosomal frameshifting or readthrough in animal viruses.对刺激动物病毒中有效 -1 核糖体移码或通读的 RNA 假结进行全基因组分析。
Biomed Res Int. 2013;2013:984028. doi: 10.1155/2013/984028. Epub 2013 Nov 4.

引用本文的文献

1
An RNA modification prevents extended codon-anticodon interactions from facilitating +1 frameshifting.一种RNA修饰可防止延长的密码子-反密码子相互作用促进+1移码。
Nat Commun. 2025 Aug 11;16(1):7392. doi: 10.1038/s41467-025-62342-4.
2
Statistical Methodology for Ribosomal Frameshift Detection.核糖体移码检测的统计方法
ACM BCB. 2022 Aug;2022. doi: 10.1145/3535508.3545529. Epub 2022 Aug 7.
3
Evolutionary origin of the frameshift sites in the ribosomal frameshifting genes of Euplotes.游仆虫核糖体移码基因中移码位点的进化起源。

本文引用的文献

1
Polyamines directly promote antizyme-mediated degradation of ornithine decarboxylase by the proteasome.多胺直接促进蛋白酶体介导的抗酶对鸟氨酸脱羧酶的降解。
Microb Cell. 2015 May 20;2(6):197-207. doi: 10.15698/mic2015.06.206.
2
Stability of HIV Frameshift Site RNA Correlates with Frameshift Efficiency and Decreased Virus Infectivity.HIV移码位点RNA的稳定性与移码效率及病毒感染性降低相关。
J Virol. 2016 Jul 11;90(15):6906-6917. doi: 10.1128/JVI.00149-16. Print 2016 Aug 1.
3
'2A-Like' Signal Sequences Mediating Translational Recoding: A Novel Form of Dual Protein Targeting.
BMC Genomics. 2025 Jul 19;26(1):676. doi: 10.1186/s12864-025-11870-w.
4
Conformational Analysis and Structure-Altering Mutations of the HIV-1 Frameshifting Element.HIV-1移码元件的构象分析与结构改变突变
Int J Mol Sci. 2025 Jun 30;26(13):6297. doi: 10.3390/ijms26136297.
5
RNA-DNA Differences: Mechanisms, Oxidative Stress, Transcriptional Fidelity, and Health Implications.RNA与DNA的差异:机制、氧化应激、转录保真度及其对健康的影响
Antioxidants (Basel). 2025 Apr 30;14(5):544. doi: 10.3390/antiox14050544.
6
Structural switching dynamically controls the doubly pseudoknotted Rous sarcoma virus-programmed ribosomal frameshifting element.结构转换动态控制双假结罗氏肉瘤病毒编程的核糖体移码元件。
Proc Natl Acad Sci U S A. 2025 Apr 8;122(14):e2418418122. doi: 10.1073/pnas.2418418122. Epub 2025 Apr 2.
7
Structural basis for aminoacylation of cellular modified tRNALys3 by human lysyl-tRNA synthetase.人赖氨酰 - tRNA合成酶对细胞修饰的tRNALys3进行氨酰化的结构基础。
Nucleic Acids Res. 2025 Feb 27;53(5). doi: 10.1093/nar/gkaf114.
8
Heterogeneous and multiple conformational transition pathways between pseudoknots of the SARS-CoV-2 frameshift element.严重急性呼吸综合征冠状病毒2型移码元件假结之间的异质性和多种构象转变途径。
Proc Natl Acad Sci U S A. 2025 Jan 28;122(4):e2417479122. doi: 10.1073/pnas.2417479122. Epub 2025 Jan 24.
9
A Helicobacter pylori flagellar motor accessory is needed to maintain the barrier function of the outer membrane during flagellar rotation.幽门螺杆菌鞭毛运动辅助装置在鞭毛旋转过程中需要维持外膜的屏障功能。
PLoS Pathog. 2025 Jan 10;21(1):e1012860. doi: 10.1371/journal.ppat.1012860. eCollection 2025 Jan.
10
CParty: hierarchically constrained partition function of RNA pseudoknots.CParty:RNA假结的分层约束配分函数。
Bioinformatics. 2024 Dec 26;41(1). doi: 10.1093/bioinformatics/btae748.
介导翻译重编码的“类2A”信号序列:一种新型的双蛋白靶向形式
Traffic. 2016 Aug;17(8):923-39. doi: 10.1111/tra.12411. Epub 2016 Jun 2.
4
Reprogramming eukaryotic translation with ligand-responsive synthetic RNA switches.利用配体响应性合成RNA开关对真核生物翻译进行重编程。
Nat Methods. 2016 May;13(5):453-8. doi: 10.1038/nmeth.3807. Epub 2016 Mar 21.
5
Facile Recoding of Selenocysteine in Nature.自然界中硒代半胱氨酸的简易重编码
Angew Chem Int Ed Engl. 2016 Apr 18;55(17):5337-41. doi: 10.1002/anie.201511657. Epub 2016 Mar 16.
6
Rapidly Translated Polypeptides Are Preferred Substrates for Cotranslational Protein Degradation.快速翻译的多肽是共翻译蛋白质降解的优选底物。
J Biol Chem. 2016 Apr 29;291(18):9827-34. doi: 10.1074/jbc.M116.716175. Epub 2016 Mar 9.
7
Nucleotide sequence of Zygosaccharomyces bailii virus Z: Evidence for +1 programmed ribosomal frameshifting and for assignment to family Amalgaviridae.拜耳接合酵母病毒Z的核苷酸序列:存在+1程序性核糖体移码的证据及归属于融合病毒科的依据
Virus Res. 2016 Jun 2;217:115-24. doi: 10.1016/j.virusres.2016.02.008. Epub 2016 Mar 4.
8
Silencing quorum sensing and ICE mobility through antiactivation and ribosomal frameshifting.通过抗激活和核糖体移码来沉默群体感应和整合性接合元件的移动性。
Mob Genet Elements. 2015 Oct 20;5(6):103-108. doi: 10.1080/2159256X.2015.1107177. eCollection 2015 Nov-Dec.
9
High-Resolution Analysis of Coronavirus Gene Expression by RNA Sequencing and Ribosome Profiling.通过RNA测序和核糖体分析对冠状病毒基因表达进行高分辨率分析
PLoS Pathog. 2016 Feb 26;12(2):e1005473. doi: 10.1371/journal.ppat.1005473. eCollection 2016 Feb.
10
Polyamine regulating protein antizyme binds to ATP citrate lyase to accelerate acetyl-CoA production in cancer cells.多胺调节蛋白抗酶与ATP柠檬酸裂解酶结合以加速癌细胞中乙酰辅酶A的产生。
Biochem Biophys Res Commun. 2016 Mar 18;471(4):646-51. doi: 10.1016/j.bbrc.2016.02.084. Epub 2016 Feb 23.