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Epitranscriptomics:Toward A Better Understanding of RNA Modifications 被引量:4

Epitranscriptomics:Toward A Better Understanding of RNA Modifications
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摘要 Ever since the first RNA nucleoside modification was charac- terized in 1957 [1], over 100 distinct chemical modifications have been identified in RNA to date [2]. Most of these modi- fications were characterized in non-coding RNAs (ncRNAs), including tRNA, rRNA, and small nuclear RNA (snRNA) [3]. Studies in the past few decades have located various mod- ifications in these ncRNAs and revealed their functional roles [3]. For instance, NLmethyladenosine (mlA), which is typically found at position 58 in the tRNA T-loop of eukaryotes, func- tions to stabilize tRNA tertiary structure [4] and affect transla- tion by regulating the associations between tRNA and polysome [5]. Pseudouridine (tp) in snRNA can fine-tune branch site interactions and affect mRNA splicing [6]. Ever since the first RNA nucleoside modification was charac- terized in 1957 [1], over 100 distinct chemical modifications have been identified in RNA to date [2]. Most of these modi- fications were characterized in non-coding RNAs (ncRNAs), including tRNA, rRNA, and small nuclear RNA (snRNA) [3]. Studies in the past few decades have located various mod- ifications in these ncRNAs and revealed their functional roles [3]. For instance, NLmethyladenosine (mlA), which is typically found at position 58 in the tRNA T-loop of eukaryotes, func- tions to stabilize tRNA tertiary structure [4] and affect transla- tion by regulating the associations between tRNA and polysome [5]. Pseudouridine (tp) in snRNA can fine-tune branch site interactions and affect mRNA splicing [6].
出处 《Genomics, Proteomics & Bioinformatics》 SCIE CAS CSCD 2017年第3期147-153,共7页 基因组蛋白质组与生物信息学报(英文版)
基金 supported by the National Key Research and Development Program from the Ministry of Science and Technology of China(Grant No.2016YFC0900300) the Beijing Natural Science Foundation(Grant No.5162012)of China awarded to CY
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