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细胞核编码的真核生物tRNA生物合成及亚细胞运输的质量控制途径

Quality Control Pathways for Nucleus-Encoded Eukaryotic tRNA Biosynthesis and Subcellular Trafficking.

作者信息

Hopper Anita K, Huang Hsiao-Yun

机构信息

Department of Molecular Genetics and Center for RNA Biology, The Ohio State University, Columbus, Ohio, USA

Department of Molecular Genetics and Center for RNA Biology, The Ohio State University, Columbus, Ohio, USA.

出版信息

Mol Cell Biol. 2015 Jun;35(12):2052-8. doi: 10.1128/MCB.00131-15. Epub 2015 Apr 6.

DOI:10.1128/MCB.00131-15
PMID:25848089
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4438251/
Abstract

tRNAs perform an essential role in translating the genetic code. They are long-lived RNAs that are generated via numerous posttranscriptional steps. Eukaryotic cells have evolved numerous layers of quality control mechanisms to ensure that the tRNAs are appropriately structured, processed, and modified. We describe the known tRNA quality control processes that check tRNAs and correct or destroy aberrant tRNAs. These mechanisms employ two types of exonucleases, CCA end addition, tRNA nuclear aminoacylation, and tRNA subcellular traffic. We arrange these processes in order of the steps that occur from generation of precursor tRNAs by RNA polymerase (Pol) III transcription to end maturation and modification in the nucleus to splicing and additional modifications in the cytoplasm. Finally, we discuss the tRNA retrograde pathway, which allows tRNA reimport into the nucleus for degradation or repair.

摘要

转运RNA(tRNA)在遗传密码翻译过程中发挥着至关重要的作用。它们是通过众多转录后步骤产生的长寿RNA。真核细胞已经进化出多层质量控制机制,以确保tRNA具有适当的结构、加工和修饰。我们描述了已知的tRNA质量控制过程,这些过程会检查tRNA并纠正或破坏异常的tRNA。这些机制采用了两种类型的核酸外切酶、CCA末端添加、tRNA核氨基酰化和tRNA亚细胞运输。我们按照从RNA聚合酶(Pol)III转录产生前体tRNA,到在细胞核中进行末端成熟和修饰,再到在细胞质中进行剪接和其他修饰的步骤顺序来排列这些过程。最后,我们讨论了tRNA逆向途径,该途径允许tRNA重新导入细胞核进行降解或修复。

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本文引用的文献

1
In vivo biochemical analyses reveal distinct roles of β-importins and eEF1A in tRNA subcellular traffic.体内生化分析揭示了β-输入蛋白和延伸因子1A在转运RNA亚细胞运输中的不同作用。
Genes Dev. 2015 Apr 1;29(7):772-83. doi: 10.1101/gad.258293.115.
2
Yeast Kre33 and human NAT10 are conserved 18S rRNA cytosine acetyltransferases that modify tRNAs assisted by the adaptor Tan1/THUMPD1.酵母Kre33和人类NAT10是保守的18S rRNA胞嘧啶乙酰转移酶,它们在衔接蛋白Tan1/THUMPD1的协助下修饰tRNA。
Nucleic Acids Res. 2015 Feb 27;43(4):2242-58. doi: 10.1093/nar/gkv075. Epub 2015 Feb 4.
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On-enzyme refolding permits small RNA and tRNA surveillance by the CCA-adding enzyme.酶上重折叠允许添加CCA酶对小RNA和tRNA进行监测。
Cell. 2015 Feb 12;160(4):644-658. doi: 10.1016/j.cell.2015.01.005. Epub 2015 Jan 29.
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Surveillance and cleavage of eukaryotic tRNAs.真核生物转运RNA的监测与切割
Int J Mol Sci. 2015 Jan 15;16(1):1873-93. doi: 10.3390/ijms16011873.
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An evolutionary approach uncovers a diverse response of tRNA 2-thiolation to elevated temperatures in yeast.进化方法揭示了酵母中 tRNA 2-巯基化对高温的多样化响应。
RNA. 2015 Feb;21(2):202-12. doi: 10.1261/rna.048199.114. Epub 2014 Dec 12.
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tRNA thiolation links translation to stress responses in Saccharomyces cerevisiae.转运RNA硫醇化将酿酒酵母中的翻译与应激反应联系起来。
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