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N6-methyladenosine modification in mRNA: machinery, function and implications for health and diseases

期刊

FEBS JOURNAL
卷 283, 期 9, 页码 1607-1630

出版社

WILEY
DOI: 10.1111/febs.13614

关键词

epitranscriptomics; m(6)A effector; m(6)A methylation; m(6)A reader; m(6)A writer; mRNA modification

资金

  1. CSIR [38/1280/11/EMR-II]
  2. DST [SR/SO/BB/0066/2012]
  3. DBT [BT/PR6078/BRB/10/1114/2012]
  4. Jadavpur University

向作者/读者索取更多资源

N6-methyladenosine (m(6)A) modification in mRNA is extremely widespread, and functionally modulates the eukaryotic transcriptome to influence mRNA splicing, export, localization, translation, and stability. Methylated adenines are present in a large subset of mRNAs and long noncoding RNAs (lncRNAs). Methylation is reversible, and this is accomplished by the orchestrated action of highly conserved methyltransferase (m(6)A writer) and demethylase (m(6)A eraser) enzymes to shape the cellular 'epitranscriptome'. The engraved 'methyl code' is subsequently decoded and executed by a group of m(6)A reader/effector components, which, in turn, govern the fate of the modified transcripts, thereby dictating their potential for translation. Reversible mRNA methylation thus adds another layer of regulation at the post-transcriptional level in the gene expression programme of eukaryotes that finely sculpts a highly dynamic proteome in order to respond to diverse cues during cellular differentiation, immune tolerance, and neuronal signalling.

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