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Functional analysis of hepatitis B virus pre-s deletion variants associated with hepatocellular carcinoma

BACKGROUND: Naturally occurring pre-S deletion mutants have been identified in hepatitis B carriers and shown to be associated with the development of hepatocellular carcinoma. The phenotypes of these pre-S deletion genomes remain unclear, and they were investigated in this study. METHODS: The pre-S...

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Autores principales: Lin, Chih-Ming, Wang, Gen-Ming, Jow, Guey-Mei, Chen, Bing-Fang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3323466/
https://www.ncbi.nlm.nih.gov/pubmed/22313590
http://dx.doi.org/10.1186/1423-0127-19-17
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author Lin, Chih-Ming
Wang, Gen-Ming
Jow, Guey-Mei
Chen, Bing-Fang
author_facet Lin, Chih-Ming
Wang, Gen-Ming
Jow, Guey-Mei
Chen, Bing-Fang
author_sort Lin, Chih-Ming
collection PubMed
description BACKGROUND: Naturally occurring pre-S deletion mutants have been identified in hepatitis B carriers and shown to be associated with the development of hepatocellular carcinoma. The phenotypes of these pre-S deletion genomes remain unclear, and they were investigated in this study. METHODS: The pre-S deletion genomes: (1) pre-S1 deletion, (2) deletion spanning pre-S1 and pre-S2, (3) pre-S2 N-terminal deletion, and (4) pre-S2 internal deletion were constructed and analyzed by transfection into Huh-7 cells. RESULTS: Functional analyses reveal that these mutants were divided into two groups: S promoter deletion and non-S promoter deletion variants. Compared with the wild-type genome, S promoter deletion variants led to an inverse ratio of pre-S1 mRNA and pre-S2/S mRNA, and intracellular accumulation of surface proteins. An interesting finding is that a small amount of L proteins was detected in the medium from S promoter deletion variant-transfected cells. Non-S promoter deletion variants conversely displayed a wild-type like mRNA and protein pattern. The secretion of surface proteins from non-S promoter deletion variants was inhibited less than from S promoter deletion variant. Immunofluorescence analysis showed mutant surface proteins colocalized with ER and exhibited an atypical distribution: granular staining pattern in the S-promoter deletion variants and perinuclear staining pattern in the non-S promoter deletion variants. CONCLUSION: This study shows that these pre-S deletion genomes exhibit two different phenotypes in mRNA transcription, surface protein expression and secretion. This diversity seems to result from the deletion of S promoter rather than result from the deletion of pre-S1 or pre-S2.
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spelling pubmed-33234662012-04-11 Functional analysis of hepatitis B virus pre-s deletion variants associated with hepatocellular carcinoma Lin, Chih-Ming Wang, Gen-Ming Jow, Guey-Mei Chen, Bing-Fang J Biomed Sci Research BACKGROUND: Naturally occurring pre-S deletion mutants have been identified in hepatitis B carriers and shown to be associated with the development of hepatocellular carcinoma. The phenotypes of these pre-S deletion genomes remain unclear, and they were investigated in this study. METHODS: The pre-S deletion genomes: (1) pre-S1 deletion, (2) deletion spanning pre-S1 and pre-S2, (3) pre-S2 N-terminal deletion, and (4) pre-S2 internal deletion were constructed and analyzed by transfection into Huh-7 cells. RESULTS: Functional analyses reveal that these mutants were divided into two groups: S promoter deletion and non-S promoter deletion variants. Compared with the wild-type genome, S promoter deletion variants led to an inverse ratio of pre-S1 mRNA and pre-S2/S mRNA, and intracellular accumulation of surface proteins. An interesting finding is that a small amount of L proteins was detected in the medium from S promoter deletion variant-transfected cells. Non-S promoter deletion variants conversely displayed a wild-type like mRNA and protein pattern. The secretion of surface proteins from non-S promoter deletion variants was inhibited less than from S promoter deletion variant. Immunofluorescence analysis showed mutant surface proteins colocalized with ER and exhibited an atypical distribution: granular staining pattern in the S-promoter deletion variants and perinuclear staining pattern in the non-S promoter deletion variants. CONCLUSION: This study shows that these pre-S deletion genomes exhibit two different phenotypes in mRNA transcription, surface protein expression and secretion. This diversity seems to result from the deletion of S promoter rather than result from the deletion of pre-S1 or pre-S2. BioMed Central 2012-02-07 /pmc/articles/PMC3323466/ /pubmed/22313590 http://dx.doi.org/10.1186/1423-0127-19-17 Text en Copyright ©2012 Lin et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Lin, Chih-Ming
Wang, Gen-Ming
Jow, Guey-Mei
Chen, Bing-Fang
Functional analysis of hepatitis B virus pre-s deletion variants associated with hepatocellular carcinoma
title Functional analysis of hepatitis B virus pre-s deletion variants associated with hepatocellular carcinoma
title_full Functional analysis of hepatitis B virus pre-s deletion variants associated with hepatocellular carcinoma
title_fullStr Functional analysis of hepatitis B virus pre-s deletion variants associated with hepatocellular carcinoma
title_full_unstemmed Functional analysis of hepatitis B virus pre-s deletion variants associated with hepatocellular carcinoma
title_short Functional analysis of hepatitis B virus pre-s deletion variants associated with hepatocellular carcinoma
title_sort functional analysis of hepatitis b virus pre-s deletion variants associated with hepatocellular carcinoma
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3323466/
https://www.ncbi.nlm.nih.gov/pubmed/22313590
http://dx.doi.org/10.1186/1423-0127-19-17
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