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Epstein-Barr virus from Burkitt Lymphoma biopsies from Africa and South America share novel LMP-1 promoter and gene variations
Epstein Barr virus (EBV) sequence variation is thought to contribute to Burkitt lymphoma (BL), but lack of data from primary BL tumors hampers efforts to test this hypothesis. We directly sequenced EBV from 12 BL biopsies from Ghana, Brazil, and Argentina, aligned the obtained reads to the wild-type...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4655394/ https://www.ncbi.nlm.nih.gov/pubmed/26593963 http://dx.doi.org/10.1038/srep16706 |
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author | Lei, Haiyan Li, Tianwei Li, Bingjie Tsai, Shien Biggar, Robert J. Nkrumah, Francis Neequaye, Janet Gutierrez, Marina Epelman, Sidnei Mbulaiteye, Sam M. Bhatia, Kishor Lo, Shyh-Ching |
author_facet | Lei, Haiyan Li, Tianwei Li, Bingjie Tsai, Shien Biggar, Robert J. Nkrumah, Francis Neequaye, Janet Gutierrez, Marina Epelman, Sidnei Mbulaiteye, Sam M. Bhatia, Kishor Lo, Shyh-Ching |
author_sort | Lei, Haiyan |
collection | PubMed |
description | Epstein Barr virus (EBV) sequence variation is thought to contribute to Burkitt lymphoma (BL), but lack of data from primary BL tumors hampers efforts to test this hypothesis. We directly sequenced EBV from 12 BL biopsies from Ghana, Brazil, and Argentina, aligned the obtained reads to the wild-type (WT) EBV reference sequence, and compared them with 100 published EBV genomes from normal and diseased people from around the world. The 12 BL EBVs were Type 1. Eleven clustered close to each other and to EBV from Raji BL cell line, but away from 12 EBVs reported from other BL-derived cell lines and away from EBV from NPC and healthy people from Asia. We discovered 23 shared novel nucleotide-base changes in the latent membrane protein (LMP)-1 promoter and gene (associated with 9 novel amino acid changes in the LMP-1 protein) of the 11 BL EBVs. Alignment of this region for the 112 EBV genomes revealed four distinct patterns, tentatively termed patterns A to D. The distribution of BL EBVs was 48%, 8%, 24% and 20% for patterns A to D, respectively; the NPC EBV’s were Pattern B, and EBV-WT was pattern D. Further work is needed to investigate the association between EBV LMP-1 patterns with BL. |
format | Online Article Text |
id | pubmed-4655394 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-46553942015-11-27 Epstein-Barr virus from Burkitt Lymphoma biopsies from Africa and South America share novel LMP-1 promoter and gene variations Lei, Haiyan Li, Tianwei Li, Bingjie Tsai, Shien Biggar, Robert J. Nkrumah, Francis Neequaye, Janet Gutierrez, Marina Epelman, Sidnei Mbulaiteye, Sam M. Bhatia, Kishor Lo, Shyh-Ching Sci Rep Article Epstein Barr virus (EBV) sequence variation is thought to contribute to Burkitt lymphoma (BL), but lack of data from primary BL tumors hampers efforts to test this hypothesis. We directly sequenced EBV from 12 BL biopsies from Ghana, Brazil, and Argentina, aligned the obtained reads to the wild-type (WT) EBV reference sequence, and compared them with 100 published EBV genomes from normal and diseased people from around the world. The 12 BL EBVs were Type 1. Eleven clustered close to each other and to EBV from Raji BL cell line, but away from 12 EBVs reported from other BL-derived cell lines and away from EBV from NPC and healthy people from Asia. We discovered 23 shared novel nucleotide-base changes in the latent membrane protein (LMP)-1 promoter and gene (associated with 9 novel amino acid changes in the LMP-1 protein) of the 11 BL EBVs. Alignment of this region for the 112 EBV genomes revealed four distinct patterns, tentatively termed patterns A to D. The distribution of BL EBVs was 48%, 8%, 24% and 20% for patterns A to D, respectively; the NPC EBV’s were Pattern B, and EBV-WT was pattern D. Further work is needed to investigate the association between EBV LMP-1 patterns with BL. Nature Publishing Group 2015-11-23 /pmc/articles/PMC4655394/ /pubmed/26593963 http://dx.doi.org/10.1038/srep16706 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Lei, Haiyan Li, Tianwei Li, Bingjie Tsai, Shien Biggar, Robert J. Nkrumah, Francis Neequaye, Janet Gutierrez, Marina Epelman, Sidnei Mbulaiteye, Sam M. Bhatia, Kishor Lo, Shyh-Ching Epstein-Barr virus from Burkitt Lymphoma biopsies from Africa and South America share novel LMP-1 promoter and gene variations |
title | Epstein-Barr virus from Burkitt Lymphoma biopsies from Africa and South America share novel LMP-1 promoter and gene variations |
title_full | Epstein-Barr virus from Burkitt Lymphoma biopsies from Africa and South America share novel LMP-1 promoter and gene variations |
title_fullStr | Epstein-Barr virus from Burkitt Lymphoma biopsies from Africa and South America share novel LMP-1 promoter and gene variations |
title_full_unstemmed | Epstein-Barr virus from Burkitt Lymphoma biopsies from Africa and South America share novel LMP-1 promoter and gene variations |
title_short | Epstein-Barr virus from Burkitt Lymphoma biopsies from Africa and South America share novel LMP-1 promoter and gene variations |
title_sort | epstein-barr virus from burkitt lymphoma biopsies from africa and south america share novel lmp-1 promoter and gene variations |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4655394/ https://www.ncbi.nlm.nih.gov/pubmed/26593963 http://dx.doi.org/10.1038/srep16706 |
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