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Mechanisms of NAT10 as ac4C writer in diseases

In the early stage, N4-acetylcytidine (ac4C) was regarded as a conservative nucleoside present on tRNA and rRNA. Recently, studies have shown that ac4C also exists in human and yeast mRNA. N-Acetyltransferase-like protein 10 (NAT10) is the first enzyme to be found to catalyze ac4C production in euka...

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Autores principales: Xie, Lihua, Zhong, Xiaolin, Cao, Wenyu, Liu, Jianghua, Zu, Xuyu, Chen, Ling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Gene & Cell Therapy 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10148080/
https://www.ncbi.nlm.nih.gov/pubmed/37128278
http://dx.doi.org/10.1016/j.omtn.2023.03.023
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author Xie, Lihua
Zhong, Xiaolin
Cao, Wenyu
Liu, Jianghua
Zu, Xuyu
Chen, Ling
author_facet Xie, Lihua
Zhong, Xiaolin
Cao, Wenyu
Liu, Jianghua
Zu, Xuyu
Chen, Ling
author_sort Xie, Lihua
collection PubMed
description In the early stage, N4-acetylcytidine (ac4C) was regarded as a conservative nucleoside present on tRNA and rRNA. Recently, studies have shown that ac4C also exists in human and yeast mRNA. N-Acetyltransferase-like protein 10 (NAT10) is the first enzyme to be found to catalyze ac4C production in eukaryotic RNA and has acetyltransferase activity and RNA-binding activity. Here, we first describe the structure and cellular localization of NAT10. Then, we conclude the active roles of NAT10 as the ac4C “writer” in mRNA stability and translation efficiency, oocyte maturation, bone remodeling, and fatty acid metabolism. With respect to disease, we focused on the promoting functions of NAT10 in proliferation, metastasis, and apoptosis in multiple tumors. The immune regulatory role of NAT10 in systemic lupus erythematosus and the maintenance role of NAT10 in virus RNA stability and replication in influenza A virus are also introduced. This review identifies NAT10 as a potential target for diagnosis, therapy, and prognosis in clinical application.
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spelling pubmed-101480802023-04-30 Mechanisms of NAT10 as ac4C writer in diseases Xie, Lihua Zhong, Xiaolin Cao, Wenyu Liu, Jianghua Zu, Xuyu Chen, Ling Mol Ther Nucleic Acids Review In the early stage, N4-acetylcytidine (ac4C) was regarded as a conservative nucleoside present on tRNA and rRNA. Recently, studies have shown that ac4C also exists in human and yeast mRNA. N-Acetyltransferase-like protein 10 (NAT10) is the first enzyme to be found to catalyze ac4C production in eukaryotic RNA and has acetyltransferase activity and RNA-binding activity. Here, we first describe the structure and cellular localization of NAT10. Then, we conclude the active roles of NAT10 as the ac4C “writer” in mRNA stability and translation efficiency, oocyte maturation, bone remodeling, and fatty acid metabolism. With respect to disease, we focused on the promoting functions of NAT10 in proliferation, metastasis, and apoptosis in multiple tumors. The immune regulatory role of NAT10 in systemic lupus erythematosus and the maintenance role of NAT10 in virus RNA stability and replication in influenza A virus are also introduced. This review identifies NAT10 as a potential target for diagnosis, therapy, and prognosis in clinical application. American Society of Gene & Cell Therapy 2023-04-03 /pmc/articles/PMC10148080/ /pubmed/37128278 http://dx.doi.org/10.1016/j.omtn.2023.03.023 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Review
Xie, Lihua
Zhong, Xiaolin
Cao, Wenyu
Liu, Jianghua
Zu, Xuyu
Chen, Ling
Mechanisms of NAT10 as ac4C writer in diseases
title Mechanisms of NAT10 as ac4C writer in diseases
title_full Mechanisms of NAT10 as ac4C writer in diseases
title_fullStr Mechanisms of NAT10 as ac4C writer in diseases
title_full_unstemmed Mechanisms of NAT10 as ac4C writer in diseases
title_short Mechanisms of NAT10 as ac4C writer in diseases
title_sort mechanisms of nat10 as ac4c writer in diseases
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10148080/
https://www.ncbi.nlm.nih.gov/pubmed/37128278
http://dx.doi.org/10.1016/j.omtn.2023.03.023
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