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Regulation and function of CMTR1‐dependent mRNA cap methylation
Author(s) -
InestaVaquera Francisco,
Cowling Victoria H
Publication year - 2017
Publication title -
wiley interdisciplinary reviews: rna
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.225
H-Index - 71
eISSN - 1757-7012
pISSN - 1757-7004
DOI - 10.1002/wrna.1450
Subject(s) - rna splicing , messenger rna , methylation , guanosine , methyltransferase , translation (biology) , biology , function (biology) , nucleotide , innate immune system , microbiology and biotechnology , rna , ribose , epigenetics , gene , genetics , immune system , biochemistry , enzyme
mRNA is modified co‐transcriptionally at the 5′ end by the addition of an inverted guanosine cap structure which can be methylated at several positions. The mRNA cap recruits proteins involved in gene expression and identifies the transcript as being cellular or ‘self’ in the innate immune response. Methylation of the first transcribed nucleotide on the ribose 2′‐O position is a prevalent cap modification which has roles in splicing, translation and provides protection against the innate immune response. In this review, we discuss the regulation and function of CMTR1, the first transcribed nucleotide ribose 2′‐O methyltransferase, and the molecular interactions which mediate methylated 2′‐O ribose function. WIREs RNA 2017, 8:e1450. doi: 10.1002/wrna.1450 This article is categorized under: RNA Interactions with Proteins and Other Molecules > Protein–RNA Interactions: Functional Implications RNA Processing > Capping and 5' End Modifications RNA in Disease and Development > RNA in Disease