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N6-methyladenosine Modification of Hepatitis B Virus RNA in the Coding Region of HBx
N6-methyladenosine (m(6)A) is a post-transcriptional modification of RNA involved in transcript transport, degradation, translation, and splicing. We found that HBV RNA is modified by m(6)A predominantly in the coding region of HBx. The mutagenesis of methylation sites reduced the HBV mRNA and HBs p...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9917364/ https://www.ncbi.nlm.nih.gov/pubmed/36768585 http://dx.doi.org/10.3390/ijms24032265 |
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author | Murata, Takayuki Iwahori, Satoko Okuno, Yusuke Nishitsuji, Hironori Yanagi, Yusuke Watashi, Koichi Wakita, Takaji Kimura, Hiroshi Shimotohno, Kunitada |
author_facet | Murata, Takayuki Iwahori, Satoko Okuno, Yusuke Nishitsuji, Hironori Yanagi, Yusuke Watashi, Koichi Wakita, Takaji Kimura, Hiroshi Shimotohno, Kunitada |
author_sort | Murata, Takayuki |
collection | PubMed |
description | N6-methyladenosine (m(6)A) is a post-transcriptional modification of RNA involved in transcript transport, degradation, translation, and splicing. We found that HBV RNA is modified by m(6)A predominantly in the coding region of HBx. The mutagenesis of methylation sites reduced the HBV mRNA and HBs protein levels. The suppression of m(6)A by an inhibitor or knockdown in primary hepatocytes decreased the viral RNA and HBs protein levels in the medium. These results suggest that the m(6)A modification of HBV RNA is needed for the efficient replication of HBV in hepatocytes. |
format | Online Article Text |
id | pubmed-9917364 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-99173642023-02-11 N6-methyladenosine Modification of Hepatitis B Virus RNA in the Coding Region of HBx Murata, Takayuki Iwahori, Satoko Okuno, Yusuke Nishitsuji, Hironori Yanagi, Yusuke Watashi, Koichi Wakita, Takaji Kimura, Hiroshi Shimotohno, Kunitada Int J Mol Sci Article N6-methyladenosine (m(6)A) is a post-transcriptional modification of RNA involved in transcript transport, degradation, translation, and splicing. We found that HBV RNA is modified by m(6)A predominantly in the coding region of HBx. The mutagenesis of methylation sites reduced the HBV mRNA and HBs protein levels. The suppression of m(6)A by an inhibitor or knockdown in primary hepatocytes decreased the viral RNA and HBs protein levels in the medium. These results suggest that the m(6)A modification of HBV RNA is needed for the efficient replication of HBV in hepatocytes. MDPI 2023-01-23 /pmc/articles/PMC9917364/ /pubmed/36768585 http://dx.doi.org/10.3390/ijms24032265 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Murata, Takayuki Iwahori, Satoko Okuno, Yusuke Nishitsuji, Hironori Yanagi, Yusuke Watashi, Koichi Wakita, Takaji Kimura, Hiroshi Shimotohno, Kunitada N6-methyladenosine Modification of Hepatitis B Virus RNA in the Coding Region of HBx |
title | N6-methyladenosine Modification of Hepatitis B Virus RNA in the Coding Region of HBx |
title_full | N6-methyladenosine Modification of Hepatitis B Virus RNA in the Coding Region of HBx |
title_fullStr | N6-methyladenosine Modification of Hepatitis B Virus RNA in the Coding Region of HBx |
title_full_unstemmed | N6-methyladenosine Modification of Hepatitis B Virus RNA in the Coding Region of HBx |
title_short | N6-methyladenosine Modification of Hepatitis B Virus RNA in the Coding Region of HBx |
title_sort | n6-methyladenosine modification of hepatitis b virus rna in the coding region of hbx |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9917364/ https://www.ncbi.nlm.nih.gov/pubmed/36768585 http://dx.doi.org/10.3390/ijms24032265 |
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