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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...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals
2020
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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. |
format | Online Article Text |
id | pubmed-7695415 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Impact Journals |
record_format | MEDLINE/PubMed |
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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