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Research Progress of m(6)A RNA Methylation in Skin Diseases

N(6)-Methyladenosine (m(6)A) is the most common mRNA modification in eukaryotes and is a dynamically reversible posttranscriptional modification. The enzymes involved in m(6)A modification mainly include methyltransferases (writers), demethylases (erasers), and methylated readers (Readers). m(6)A mo...

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Detalles Bibliográficos
Autores principales: Liu, Chang, Wang, Xin, Yang, Shengju, Cao, Shuanglin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10132905/
https://www.ncbi.nlm.nih.gov/pubmed/37124930
http://dx.doi.org/10.1155/2023/3091204
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author Liu, Chang
Wang, Xin
Yang, Shengju
Cao, Shuanglin
author_facet Liu, Chang
Wang, Xin
Yang, Shengju
Cao, Shuanglin
author_sort Liu, Chang
collection PubMed
description N(6)-Methyladenosine (m(6)A) is the most common mRNA modification in eukaryotes and is a dynamically reversible posttranscriptional modification. The enzymes involved in m(6)A modification mainly include methyltransferases (writers), demethylases (erasers), and methylated readers (Readers). m(6)A modification is mainly catalyzed by m(6)A methyltransferase and removed by m(6)A demethylase. The modified RNA can be specifically recognized and bound by m(6)A recognition protein. This protein complex then mediates RNA splicing, maturation, nucleation, degradation, and translation. m(6)A also alters gene expression and regulates cellular processes such as self-renewal, differentiation, invasion, and apoptosis. An increasing body of evidence indicates that the m(6)A methylation modification process is closely related to the occurrence of various skin diseases. In this review, we discuss the role of m(6)A methylation in skin development and skin diseases including psoriasis, melanoma, and cutaneous squamous cell carcinoma.
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spelling pubmed-101329052023-04-27 Research Progress of m(6)A RNA Methylation in Skin Diseases Liu, Chang Wang, Xin Yang, Shengju Cao, Shuanglin Biomed Res Int Review Article N(6)-Methyladenosine (m(6)A) is the most common mRNA modification in eukaryotes and is a dynamically reversible posttranscriptional modification. The enzymes involved in m(6)A modification mainly include methyltransferases (writers), demethylases (erasers), and methylated readers (Readers). m(6)A modification is mainly catalyzed by m(6)A methyltransferase and removed by m(6)A demethylase. The modified RNA can be specifically recognized and bound by m(6)A recognition protein. This protein complex then mediates RNA splicing, maturation, nucleation, degradation, and translation. m(6)A also alters gene expression and regulates cellular processes such as self-renewal, differentiation, invasion, and apoptosis. An increasing body of evidence indicates that the m(6)A methylation modification process is closely related to the occurrence of various skin diseases. In this review, we discuss the role of m(6)A methylation in skin development and skin diseases including psoriasis, melanoma, and cutaneous squamous cell carcinoma. Hindawi 2023-04-19 /pmc/articles/PMC10132905/ /pubmed/37124930 http://dx.doi.org/10.1155/2023/3091204 Text en Copyright © 2023 Chang Liu et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Liu, Chang
Wang, Xin
Yang, Shengju
Cao, Shuanglin
Research Progress of m(6)A RNA Methylation in Skin Diseases
title Research Progress of m(6)A RNA Methylation in Skin Diseases
title_full Research Progress of m(6)A RNA Methylation in Skin Diseases
title_fullStr Research Progress of m(6)A RNA Methylation in Skin Diseases
title_full_unstemmed Research Progress of m(6)A RNA Methylation in Skin Diseases
title_short Research Progress of m(6)A RNA Methylation in Skin Diseases
title_sort research progress of m(6)a rna methylation in skin diseases
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10132905/
https://www.ncbi.nlm.nih.gov/pubmed/37124930
http://dx.doi.org/10.1155/2023/3091204
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