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Structural Insights into N(6)-methyladenosine (m(6)A) Modification in the Transcriptome

More than 100 types of chemical modifications in RNA have been well documented. Recently, several modifications, such as N(6)-methyladenosine (m(6)A), have been detected in mRNA, opening the window into the realm of epitranscriptomics. The m(6)A modification is the most abundant modification in mRNA...

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Detalles Bibliográficos
Autores principales: Huang, Jinbo, Yin, Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6112310/
https://www.ncbi.nlm.nih.gov/pubmed/29709557
http://dx.doi.org/10.1016/j.gpb.2018.03.001
Descripción
Sumario:More than 100 types of chemical modifications in RNA have been well documented. Recently, several modifications, such as N(6)-methyladenosine (m(6)A), have been detected in mRNA, opening the window into the realm of epitranscriptomics. The m(6)A modification is the most abundant modification in mRNA and non-coding RNA (ncRNA). At the molecular level, m(6)A affects almost all aspects of mRNA metabolism, including splicing, translation, and stability, as well as microRNA (miRNA) maturation, playing essential roles in a range of cellular processes. The m(6)A modification is regulated by three classes of proteins generally referred to as the “writer” (adenosine methyltransferase), “eraser” (m(6)A demethylating enzyme), and “reader” (m(6)A-binding protein). The m(6)A modification is reversibly installed and removed by writers and erasers, respectively. Readers, which are members of the YT521-B homology (YTH) family proteins, selectively bind to RNA and affect its fate in an m(6)A-dependent manner. In this review, we summarize the structures of the functional proteins that modulate the m(6)A modification, and provide our insights into the m(6)A-mediated gene regulation.