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PCIF1, the only methyltransferase of N6,2-O-dimethyladenosine

N6-methyladenosine(m6A), is the most abundant post-transcriptional modification of mRNA in biology. When the first nucleotide after the m7G cap is adenosine, it is methylated at the N6 position to form N6,2-O-dimethyladenosine (m6Am). m6Am is a reversible modification located at the first transcribe...

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Autores principales: Wu, Yuting, Pu, Xi, Wu, Sihui, Zhang, Yiran, Fu, Shengqiao, Tang, Haowen, Wang, Xu, Xu, Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10544176/
https://www.ncbi.nlm.nih.gov/pubmed/37779183
http://dx.doi.org/10.1186/s12935-023-03066-7
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author Wu, Yuting
Pu, Xi
Wu, Sihui
Zhang, Yiran
Fu, Shengqiao
Tang, Haowen
Wang, Xu
Xu, Min
author_facet Wu, Yuting
Pu, Xi
Wu, Sihui
Zhang, Yiran
Fu, Shengqiao
Tang, Haowen
Wang, Xu
Xu, Min
author_sort Wu, Yuting
collection PubMed
description N6-methyladenosine(m6A), is the most abundant post-transcriptional modification of mRNA in biology. When the first nucleotide after the m7G cap is adenosine, it is methylated at the N6 position to form N6,2-O-dimethyladenosine (m6Am). m6Am is a reversible modification located at the first transcribed nucleotide, which is present in about 30% of cellular mRNAs, thus m6Am can have a significant impact on gene expression in the transcriptome. Phosphorylated CTD interaction factor 1(PCIF1), the unique and specific methyltransferase of m6Am, has been shown to affect mRNA stability, transcription, and translation. Several studies have shown that PCIF1 is clearly associated with tumor, viral, and endocrine diseases. Moreover, PCIF1 may be related to the tumor microenvironment, immune cell typing, and programmed cell death protein 1(PD-1) drug resistance. Here, we summarize the mechanism of PCIF1 involvement in mRNA modifications, and outline m6Am modifications and diseases in which PCIF1 is involved. We also summarized the role of PCIF1 in immune and immune checkpoint blockade(ICB) treatment, and predicted the possibility of PCIF1 as a biomarker and therapeutic target.
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spelling pubmed-105441762023-10-03 PCIF1, the only methyltransferase of N6,2-O-dimethyladenosine Wu, Yuting Pu, Xi Wu, Sihui Zhang, Yiran Fu, Shengqiao Tang, Haowen Wang, Xu Xu, Min Cancer Cell Int Review N6-methyladenosine(m6A), is the most abundant post-transcriptional modification of mRNA in biology. When the first nucleotide after the m7G cap is adenosine, it is methylated at the N6 position to form N6,2-O-dimethyladenosine (m6Am). m6Am is a reversible modification located at the first transcribed nucleotide, which is present in about 30% of cellular mRNAs, thus m6Am can have a significant impact on gene expression in the transcriptome. Phosphorylated CTD interaction factor 1(PCIF1), the unique and specific methyltransferase of m6Am, has been shown to affect mRNA stability, transcription, and translation. Several studies have shown that PCIF1 is clearly associated with tumor, viral, and endocrine diseases. Moreover, PCIF1 may be related to the tumor microenvironment, immune cell typing, and programmed cell death protein 1(PD-1) drug resistance. Here, we summarize the mechanism of PCIF1 involvement in mRNA modifications, and outline m6Am modifications and diseases in which PCIF1 is involved. We also summarized the role of PCIF1 in immune and immune checkpoint blockade(ICB) treatment, and predicted the possibility of PCIF1 as a biomarker and therapeutic target. BioMed Central 2023-10-01 /pmc/articles/PMC10544176/ /pubmed/37779183 http://dx.doi.org/10.1186/s12935-023-03066-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Review
Wu, Yuting
Pu, Xi
Wu, Sihui
Zhang, Yiran
Fu, Shengqiao
Tang, Haowen
Wang, Xu
Xu, Min
PCIF1, the only methyltransferase of N6,2-O-dimethyladenosine
title PCIF1, the only methyltransferase of N6,2-O-dimethyladenosine
title_full PCIF1, the only methyltransferase of N6,2-O-dimethyladenosine
title_fullStr PCIF1, the only methyltransferase of N6,2-O-dimethyladenosine
title_full_unstemmed PCIF1, the only methyltransferase of N6,2-O-dimethyladenosine
title_short PCIF1, the only methyltransferase of N6,2-O-dimethyladenosine
title_sort pcif1, the only methyltransferase of n6,2-o-dimethyladenosine
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10544176/
https://www.ncbi.nlm.nih.gov/pubmed/37779183
http://dx.doi.org/10.1186/s12935-023-03066-7
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