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1
A rare tRNA-Arg(CCU) that regulates Ty1 element ribosomal frameshifting is essential for Ty1 retrotransposition in Saccharomyces cerevisiae.一种调控Ty1元件核糖体移码的罕见tRNA-Arg(CCU)对酿酒酵母中的Ty1逆转录转座至关重要。
Genetics. 1993 Oct;135(2):309-20. doi: 10.1093/genetics/135.2.309.
2
Host genes that influence transposition in yeast: the abundance of a rare tRNA regulates Ty1 transposition frequency.影响酵母转座的宿主基因:一种稀有tRNA的丰度调节Ty1转座频率。
Proc Natl Acad Sci U S A. 1990 Nov;87(21):8360-4. doi: 10.1073/pnas.87.21.8360.
3
Posttranslational control of Ty1 retrotransposition occurs at the level of protein processing.Ty1逆转录转座的翻译后调控发生在蛋白质加工水平。
Mol Cell Biol. 1992 Jun;12(6):2813-25. doi: 10.1128/mcb.12.6.2813-2825.1992.
4
Initiator methionine tRNA is essential for Ty1 transposition in yeast.起始甲硫氨酸tRNA对酵母中Ty1转座至关重要。
Proc Natl Acad Sci U S A. 1992 Apr 15;89(8):3236-40. doi: 10.1073/pnas.89.8.3236.
5
Ribosomal frameshifting in the yeast retrotransposon Ty: tRNAs induce slippage on a 7 nucleotide minimal site.酵母逆转录转座子Ty中的核糖体移码:tRNA诱导在一个7核苷酸最小位点上的滑动。
Cell. 1990 Jul 27;62(2):339-52. doi: 10.1016/0092-8674(90)90371-k.
6
Proteolytic processing of pol-TYB proteins from the yeast retrotransposon Ty1.酵母逆转录转座子Ty1的pol-TYB蛋白的蛋白水解加工
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7
Single-step selection for Ty1 element retrotransposition.针对Ty1元件逆转录转座的单步筛选。
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8
Spermidine deficiency increases +1 ribosomal frameshifting efficiency and inhibits Ty1 retrotransposition in Saccharomyces cerevisiae.亚精胺缺乏会提高酿酒酵母中的 +1 核糖体移码效率并抑制 Ty1 逆转录转座。
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9
The pokeweed antiviral protein specifically inhibits Ty1-directed +1 ribosomal frameshifting and retrotransposition in Saccharomyces cerevisiae.商陆抗病毒蛋白可特异性抑制酿酒酵母中Ty1介导的+1核糖体移码和逆转座作用。
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Yeast Ty1 retrotransposon: the minus-strand primer binding site and a cis-acting domain of the Ty1 RNA are both important for packaging of primer tRNA inside virus-like particles.酵母Ty1逆转座子:Ty1 RNA的负链引物结合位点和顺式作用结构域对于引物tRNA包装到病毒样颗粒中均很重要。
Nucleic Acids Res. 1994 Nov 11;22(22):4560-5. doi: 10.1093/nar/22.22.4560.

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Ribosome Collisions Result in +1 Frameshifting in the Absence of No-Go Decay.核糖体碰撞导致在没有无意义衰变的情况下+1 移码。
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Translational recoding signals: Expanding the synthetic biology toolbox.翻译后文本:翻译重编码信号:拓展合成生物学工具包。
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本文引用的文献

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Proteolytic processing of Ty3 proteins is required for transposition.Ty3蛋白的蛋白水解加工是转座所必需的。
J Virol. 1993 Jan;67(1):19-28. doi: 10.1128/JVI.67.1.19-28.1993.
2
5' untranslated sequences are required for the translational control of a yeast regulatory gene.酵母调控基因的翻译控制需要5'非翻译序列。
Proc Natl Acad Sci U S A. 1984 Aug;81(16):5096-100. doi: 10.1073/pnas.81.16.5096.
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Transformation of intact yeast cells treated with alkali cations.经碱金属阳离子处理的完整酵母细胞的转化
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Molecular mechanism of codon recognition by tRNA species with modified uridine in the first position of the anticodon.反密码子第一位带有修饰尿苷的tRNA物种识别密码子的分子机制。
Proc Natl Acad Sci U S A. 1985 Aug;82(15):4905-9. doi: 10.1073/pnas.82.15.4905.
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Oligonucleotide-directed double-strand break repair in plasmids of Escherichia coli: a method for site-specific mutagenesis.大肠杆菌质粒中寡核苷酸定向双链断裂修复:一种位点特异性诱变方法。
Proc Natl Acad Sci U S A. 1986 Oct;83(19):7177-81. doi: 10.1073/pnas.83.19.7177.
6
Systematic alterations in the anticodon arm make tRNA(Glu)-Suoc a more efficient suppressor.反密码子臂的系统性改变使tRNA(Glu)-Suoc成为一种更有效的抑制子。
EMBO J. 1987 May;6(5):1499-506. doi: 10.1002/j.1460-2075.1987.tb02392.x.
7
Processing of TY1 proteins and formation of Ty1 virus-like particles in Saccharomyces cerevisiae.酿酒酵母中TY1蛋白的加工及Ty1病毒样颗粒的形成。
Mol Gen Genet. 1987 May;207(2-3):421-9. doi: 10.1007/BF00331610.
8
Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia.用于镰状细胞贫血诊断的β-珠蛋白基因组序列的酶促扩增及限制性酶切位点分析。
Science. 1985 Dec 20;230(4732):1350-4. doi: 10.1126/science.2999980.
9
Ty elements transpose through an RNA intermediate.Ty 元件通过 RNA 中间体进行转座。
Cell. 1985 Mar;40(3):491-500. doi: 10.1016/0092-8674(85)90197-7.
10
The DNA intermediate in yeast Ty1 element transposition copurifies with virus-like particles: cell-free Ty1 transposition.酵母Ty1元件转座过程中的DNA中间体与病毒样颗粒共纯化:无细胞Ty1转座。
Cell. 1988 Sep 23;54(7):955-66. doi: 10.1016/0092-8674(88)90110-9.

一种调控Ty1元件核糖体移码的罕见tRNA-Arg(CCU)对酿酒酵母中的Ty1逆转录转座至关重要。

A rare tRNA-Arg(CCU) that regulates Ty1 element ribosomal frameshifting is essential for Ty1 retrotransposition in Saccharomyces cerevisiae.

作者信息

Kawakami K, Pande S, Faiola B, Moore D P, Boeke J D, Farabaugh P J, Strathern J N, Nakamura Y, Garfinkel D J

机构信息

Department of Tumor Biology, University of Tokyo, Japan.

出版信息

Genetics. 1993 Oct;135(2):309-20. doi: 10.1093/genetics/135.2.309.

DOI:10.1093/genetics/135.2.309
PMID:8243996
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1205637/
Abstract

Translation of the yeast retrotransposon Ty1 TYA1(gag)-TYB1(pol) gene occurs by a +1 ribosomal frameshifting event at the sequence CUU AGG C. Because overexpression of a low abundance tRNA-Arg(CCU) encoded by the HSX1 gene resulted in a reduction in Ty1 frameshifting, it was suggested that a translational pause at the AGG-Arg codon is required for optimum frameshifting. The present work shows that the absence of tRNA-Arg(CCU) affects Ty1 transposition, translational frameshifting, and accumulation of mature TYB1 proteins. Transposition of genetically tagged Ty1 elements decreases at least 50-fold and translational frameshifting increases 3-17-fold in cells lacking tRNA-Arg(CCU). Accumulation of Ty1-integrase and Ty1-reverse transcriptase/ribonuclease H is defective in an hsx1 mutant. The defect in Ty1 transposition is complemented by the wild-type HSX1 gene or a mutant tRNA-Arg(UCU) gene containing a C for T substitution in the first position of the anticodon. Overexpression of TYA1 stimulates Ty1 transposition 50-fold above wild-type levels when the level of transposition is compared in isogenic hsx1 and HSX1 strains. Thus, the HSX1 gene determines the ratio of the TYA1 to TYA1-TYB1 precursors required for protein processing or stability, and keeps expression of TYB1 a rate-limiting step in the retrotransposition cycle.

摘要

酵母逆转录转座子Ty1的TYA1(gag)-TYB1(pol)基因的翻译是通过在序列CUU AGG C处发生的+1核糖体移码事件来实现的。由于HSX1基因编码的低丰度tRNA-Arg(CCU)的过表达导致Ty1移码减少,因此有人提出,在AGG-Arg密码子处的翻译暂停是实现最佳移码所必需的。目前的研究表明,tRNA-Arg(CCU)的缺失会影响Ty1转座、翻译移码以及成熟TYB1蛋白的积累。在缺乏tRNA-Arg(CCU)的细胞中,基因标记的Ty1元件的转座至少降低50倍,而翻译移码增加3至17倍。hsx1突变体中Ty1整合酶和Ty1逆转录酶/核糖核酸酶H的积累存在缺陷。Ty1转座的缺陷可由野生型HSX1基因或在反密码子第一位含有C到T替换的突变tRNA-Arg(UCU)基因来弥补。当在同基因的hsx1和HSX1菌株中比较转座水平时,TYA1的过表达会使Ty1转座比野生型水平高出50倍。因此,HSX1基因决定了蛋白质加工或稳定性所需的TYA1与TYA1-TYB1前体的比例,并使TYB1的表达成为逆转录转座循环中的限速步骤。