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Identification of Epstein-Barr Virus Replication Proteins in Burkitt’s Lymphoma Cells
The working model to describe the mechanisms used to replicate the cancer-associated virus Epstein-Barr virus (EBV) is partly derived from comparisons with other members of the Herpes virus family. Many genes within the EBV genome are homologous across the herpes virus family. Published transcriptom...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4693162/ https://www.ncbi.nlm.nih.gov/pubmed/26529022 http://dx.doi.org/10.3390/pathogens4040739 |
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author | Traylen, Chris Ramasubramanyan, Sharada Zuo, Jianmin Rowe, Martin Almohammad, Rajaei Heesom, Kate Sweet, Steve M. M. Matthews, David A. Sinclair, Alison J. |
author_facet | Traylen, Chris Ramasubramanyan, Sharada Zuo, Jianmin Rowe, Martin Almohammad, Rajaei Heesom, Kate Sweet, Steve M. M. Matthews, David A. Sinclair, Alison J. |
author_sort | Traylen, Chris |
collection | PubMed |
description | The working model to describe the mechanisms used to replicate the cancer-associated virus Epstein-Barr virus (EBV) is partly derived from comparisons with other members of the Herpes virus family. Many genes within the EBV genome are homologous across the herpes virus family. Published transcriptome data for the EBV genome during its lytic replication cycle show extensive transcription, but the identification of the proteins is limited. We have taken a global proteomics approach to identify viral proteins that are expressed during the EBV lytic replication cycle. We combined an enrichment method to isolate cells undergoing EBV lytic replication with SILAC-labeling coupled to mass-spectrometry and identified viral and host proteins expressed during the EBV lytic replication cycle. Amongst the most frequently identified viral proteins are two components of the DNA replication machinery, the single strand DNA binding protein BALF2, DNA polymerase accessory protein BMRF1 and both subunits of the viral ribonucleoside-diphosphate reductase enzyme (BORF2 and BaRF1). An additional 42 EBV lytic cycle proteins were also detected. This provides proteomic identification for many EBV lytic replication cycle proteins and also identifies post-translational modifications. |
format | Online Article Text |
id | pubmed-4693162 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-46931622016-01-06 Identification of Epstein-Barr Virus Replication Proteins in Burkitt’s Lymphoma Cells Traylen, Chris Ramasubramanyan, Sharada Zuo, Jianmin Rowe, Martin Almohammad, Rajaei Heesom, Kate Sweet, Steve M. M. Matthews, David A. Sinclair, Alison J. Pathogens Communication The working model to describe the mechanisms used to replicate the cancer-associated virus Epstein-Barr virus (EBV) is partly derived from comparisons with other members of the Herpes virus family. Many genes within the EBV genome are homologous across the herpes virus family. Published transcriptome data for the EBV genome during its lytic replication cycle show extensive transcription, but the identification of the proteins is limited. We have taken a global proteomics approach to identify viral proteins that are expressed during the EBV lytic replication cycle. We combined an enrichment method to isolate cells undergoing EBV lytic replication with SILAC-labeling coupled to mass-spectrometry and identified viral and host proteins expressed during the EBV lytic replication cycle. Amongst the most frequently identified viral proteins are two components of the DNA replication machinery, the single strand DNA binding protein BALF2, DNA polymerase accessory protein BMRF1 and both subunits of the viral ribonucleoside-diphosphate reductase enzyme (BORF2 and BaRF1). An additional 42 EBV lytic cycle proteins were also detected. This provides proteomic identification for many EBV lytic replication cycle proteins and also identifies post-translational modifications. MDPI 2015-10-30 /pmc/articles/PMC4693162/ /pubmed/26529022 http://dx.doi.org/10.3390/pathogens4040739 Text en © 2015 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Communication Traylen, Chris Ramasubramanyan, Sharada Zuo, Jianmin Rowe, Martin Almohammad, Rajaei Heesom, Kate Sweet, Steve M. M. Matthews, David A. Sinclair, Alison J. Identification of Epstein-Barr Virus Replication Proteins in Burkitt’s Lymphoma Cells |
title | Identification of Epstein-Barr Virus Replication Proteins in Burkitt’s Lymphoma Cells |
title_full | Identification of Epstein-Barr Virus Replication Proteins in Burkitt’s Lymphoma Cells |
title_fullStr | Identification of Epstein-Barr Virus Replication Proteins in Burkitt’s Lymphoma Cells |
title_full_unstemmed | Identification of Epstein-Barr Virus Replication Proteins in Burkitt’s Lymphoma Cells |
title_short | Identification of Epstein-Barr Virus Replication Proteins in Burkitt’s Lymphoma Cells |
title_sort | identification of epstein-barr virus replication proteins in burkitt’s lymphoma cells |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4693162/ https://www.ncbi.nlm.nih.gov/pubmed/26529022 http://dx.doi.org/10.3390/pathogens4040739 |
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