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Analysis of METTL3 and METTL14 in hepatocellular carcinoma

N6-methyladenosine (m6A) RNA methylation is the most prevalent modification of messenger RNAs (mRNAs) and catalyzed by a multicomponent methyltransferase complex (MTC), among which methyltransferase-like 3 (METTL3) and METTL14 are two core molecules. However, METTL3 and METTL14 play opposite regulat...

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Autores principales: Liu, Xiangxiang, Qin, Jian, Gao, Tianyi, Li, Chenmeng, Chen, Xiaoxiang, Zeng, Kaixuan, Xu, Mu, He, Bangshun, Pan, Bei, Xu, Xueni, Pan, Yuqin, Sun, Huiling, Xu, Tao, Wang, Shukui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7695415/
https://www.ncbi.nlm.nih.gov/pubmed/33159022
http://dx.doi.org/10.18632/aging.103959
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author Liu, Xiangxiang
Qin, Jian
Gao, Tianyi
Li, Chenmeng
Chen, Xiaoxiang
Zeng, Kaixuan
Xu, Mu
He, Bangshun
Pan, Bei
Xu, Xueni
Pan, Yuqin
Sun, Huiling
Xu, Tao
Wang, Shukui
author_facet Liu, Xiangxiang
Qin, Jian
Gao, Tianyi
Li, Chenmeng
Chen, Xiaoxiang
Zeng, Kaixuan
Xu, Mu
He, Bangshun
Pan, Bei
Xu, Xueni
Pan, Yuqin
Sun, Huiling
Xu, Tao
Wang, Shukui
author_sort Liu, Xiangxiang
collection PubMed
description N6-methyladenosine (m6A) RNA methylation is the most prevalent modification of messenger RNAs (mRNAs) and catalyzed by a multicomponent methyltransferase complex (MTC), among which methyltransferase-like 3 (METTL3) and METTL14 are two core molecules. However, METTL3 and METTL14 play opposite regulatory roles in hepatocellular carcinoma (HCC). Based on The Cancer Genome Atlas (TCGA) database and Gene Expression Omnibus (GEO) database, we conducted a multi-omics analysis of METTL3 and METTL14 in HCC, including RNA-sequencing, m6ARIP-sequencing, and ribosome-sequencing profiles. We found that the expression and prognostic value of METTL3 and METTL14 are opposite in HCC. Besides, after METTL3 and METTL14 knockdown, most of the dysregulated mRNAs, signaling pathways and biological processes are distinct in HCC, which partly explains the contrary regulatory role of METTL3 and METTL14. Intriguingly, these mRNAs whose stability or translation efficiency are influenced by METTL3 or METTL14 in an m6A dependent manner, jointly regulate multiple signaling pathways and biological processes, which supports the cooperative role of METTL3 and METTL14 in catalyzing m6A modification. In conclusion, our study further clarified the contradictory role of METTL3 and METTL14 in HCC.
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spelling pubmed-76954152020-12-04 Analysis of METTL3 and METTL14 in hepatocellular carcinoma Liu, Xiangxiang Qin, Jian Gao, Tianyi Li, Chenmeng Chen, Xiaoxiang Zeng, Kaixuan Xu, Mu He, Bangshun Pan, Bei Xu, Xueni Pan, Yuqin Sun, Huiling Xu, Tao Wang, Shukui Aging (Albany NY) Research Paper N6-methyladenosine (m6A) RNA methylation is the most prevalent modification of messenger RNAs (mRNAs) and catalyzed by a multicomponent methyltransferase complex (MTC), among which methyltransferase-like 3 (METTL3) and METTL14 are two core molecules. However, METTL3 and METTL14 play opposite regulatory roles in hepatocellular carcinoma (HCC). Based on The Cancer Genome Atlas (TCGA) database and Gene Expression Omnibus (GEO) database, we conducted a multi-omics analysis of METTL3 and METTL14 in HCC, including RNA-sequencing, m6ARIP-sequencing, and ribosome-sequencing profiles. We found that the expression and prognostic value of METTL3 and METTL14 are opposite in HCC. Besides, after METTL3 and METTL14 knockdown, most of the dysregulated mRNAs, signaling pathways and biological processes are distinct in HCC, which partly explains the contrary regulatory role of METTL3 and METTL14. Intriguingly, these mRNAs whose stability or translation efficiency are influenced by METTL3 or METTL14 in an m6A dependent manner, jointly regulate multiple signaling pathways and biological processes, which supports the cooperative role of METTL3 and METTL14 in catalyzing m6A modification. In conclusion, our study further clarified the contradictory role of METTL3 and METTL14 in HCC. Impact Journals 2020-11-06 /pmc/articles/PMC7695415/ /pubmed/33159022 http://dx.doi.org/10.18632/aging.103959 Text en Copyright: © 2020 Liu et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Liu, Xiangxiang
Qin, Jian
Gao, Tianyi
Li, Chenmeng
Chen, Xiaoxiang
Zeng, Kaixuan
Xu, Mu
He, Bangshun
Pan, Bei
Xu, Xueni
Pan, Yuqin
Sun, Huiling
Xu, Tao
Wang, Shukui
Analysis of METTL3 and METTL14 in hepatocellular carcinoma
title Analysis of METTL3 and METTL14 in hepatocellular carcinoma
title_full Analysis of METTL3 and METTL14 in hepatocellular carcinoma
title_fullStr Analysis of METTL3 and METTL14 in hepatocellular carcinoma
title_full_unstemmed Analysis of METTL3 and METTL14 in hepatocellular carcinoma
title_short Analysis of METTL3 and METTL14 in hepatocellular carcinoma
title_sort analysis of mettl3 and mettl14 in hepatocellular carcinoma
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7695415/
https://www.ncbi.nlm.nih.gov/pubmed/33159022
http://dx.doi.org/10.18632/aging.103959
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