Production and purification of endogenously modified tRNA-derived small RNAs

被引:32
|
作者
Drino, Aleksej [1 ]
Oberbauer, Vera [1 ]
Troger, Conor [1 ]
Janisiw, Eva [1 ]
Anrather, Dorothea [2 ]
Hartl, Markus [2 ]
Kaiser, Steffen [3 ]
Kellner, Stefanie [3 ]
Schaefer, Matthias R. [1 ]
机构
[1] Med Univ Vienna, Ctr Anat & Cell Biol, Div Cell & Dev Biol, Schwarzspanierstr 17, A-1090 Vienna, Austria
[2] Vienna Bioctr VBC, Max Perutz Labs MPL, Mass Spectrometry Facil, Vienna, Austria
[3] Ludwig Maximilians Univ Munchen, Dept Chem, Munich, Germany
基金
奥地利科学基金会;
关键词
tRNA; tRNA fragments; RNA modifications; stress; BREAST-CANCER; SPERM TSRNAS; ANGIOGENIN; FRAGMENTS; STRESS; CLEAVAGE; 5-METHYLCYTOSINE; RIBONUCLEASE; METHYLATION; CONTRIBUTE;
D O I
10.1080/15476286.2020.1733798
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
During particular stress conditions, transfer RNAs (tRNAs) become substrates of stress-induced endonucleases, resulting in the production of distinct tRNA-derived small RNAs (tsRNAs). These small RNAs have been implicated in a wide range of biological processes, but how isoacceptor and even isodecoder-specific tsRNAs act at the molecular level is still poorly understood. Importantly, stress-induced tRNA cleavage affects only a few tRNAs of a given isoacceptor or isodecoder, raising the question as to how such limited molecule numbers could exert measurable biological impact. While the molecular function of individual tsRNAs is likely mediated through association with other molecules, addressing the interactome of specific tsRNAs has only been attempted by using synthetic RNA sequences. Since tRNAs carry post-transcriptional modifications, tsRNAs are likely modified but the extent of their modifications remains largely unknown. Here, we developed a biochemical framework for the production and purification of specific tsRNAs using human cells. Preparative scale purification of tsRNAs from biological sources should facilitate experimentally addressing as to how exactly these small RNAs mediate the multitude of reported molecular functions.
引用
收藏
页码:1104 / 1115
页数:12
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