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Adenosine methylation as a molecular imprint defining the fate of RNA

Multiple lines of evidence suggest the RNA modification N (6)‐methyladonsine (m(6)A), which is installed in the nucleus cotranscriptionally and, thereafter, serves as a reversible chemical imprint that influences several steps of mRNA metabolism. This includes but is not limited to RNA folding, spli...

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Detalles Bibliográficos
Autores principales: Knuckles, Philip, Bühler, Marc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6175371/
https://www.ncbi.nlm.nih.gov/pubmed/29782652
http://dx.doi.org/10.1002/1873-3468.13107
Descripción
Sumario:Multiple lines of evidence suggest the RNA modification N (6)‐methyladonsine (m(6)A), which is installed in the nucleus cotranscriptionally and, thereafter, serves as a reversible chemical imprint that influences several steps of mRNA metabolism. This includes but is not limited to RNA folding, splicing, stability, transport and translation. In this Review we focus on the current view of the nuclear installation of m(6)A as well as the molecular players involved, the so called m(6)A writers. We also explore the effector proteins, or m(6)A readers, that decode the imprint in different cellular contexts and compartments, and ultimately, the way the modification influences the lifecycle of an RNA molecule. The wide evolutionary conservation of m(6)A and its critical role in physiology and disease warrants further studies into this burgeoning and exciting field.