Viral Oncogenes, Noncoding RNAs, and RNA Splicing in Human Tumor Viruses

<p>Viral oncogenes are responsible for oncogenesis resulting from persistent virus infection. Although different human tumor viruses express different viral oncogenes and induce different tumors, their oncoproteins often target similar sets of cellular tumor suppressors or signal pathways to i...

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Main Author: Zhi-Ming Zheng
Format: Article
Language:English
Published: Ivyspring International Publisher 2010-01-01
Series:International Journal of Biological Sciences
Online Access:http://www.biolsci.org/v06p0730.htm
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spelling doaj-2d41455708024547a68e3cfe04ce01572020-11-24T23:45:01ZengIvyspring International PublisherInternational Journal of Biological Sciences1449-22882010-01-0167730755Viral Oncogenes, Noncoding RNAs, and RNA Splicing in Human Tumor VirusesZhi-Ming Zheng<p>Viral oncogenes are responsible for oncogenesis resulting from persistent virus infection. Although different human tumor viruses express different viral oncogenes and induce different tumors, their oncoproteins often target similar sets of cellular tumor suppressors or signal pathways to immortalize and/or transform infected cells. Expression of the viral E6 and E7 oncogenes in papillomavirus, E1A and E1B oncogenes in adenovirus, large T and small t antigen in polyomavirus, and Tax oncogene in HTLV-1 are regulated by alternative RNA splicing. However, this regulation is only partially understood. DNA tumor viruses also encode noncoding RNAs, including viral microRNAs, that disturb normal cell functions. Among the determined viral microRNA precursors, EBV encodes 25 from two major clusters (BART and BHRF1), KSHV encodes 12 from a latent region, human polyomavirus MCV produce only one microRNA from the late region antisense to early transcripts, but HPVs appears to produce no viral microRNAs.</p>http://www.biolsci.org/v06p0730.htm
collection DOAJ
language English
format Article
sources DOAJ
author Zhi-Ming Zheng
spellingShingle Zhi-Ming Zheng
Viral Oncogenes, Noncoding RNAs, and RNA Splicing in Human Tumor Viruses
International Journal of Biological Sciences
author_facet Zhi-Ming Zheng
author_sort Zhi-Ming Zheng
title Viral Oncogenes, Noncoding RNAs, and RNA Splicing in Human Tumor Viruses
title_short Viral Oncogenes, Noncoding RNAs, and RNA Splicing in Human Tumor Viruses
title_full Viral Oncogenes, Noncoding RNAs, and RNA Splicing in Human Tumor Viruses
title_fullStr Viral Oncogenes, Noncoding RNAs, and RNA Splicing in Human Tumor Viruses
title_full_unstemmed Viral Oncogenes, Noncoding RNAs, and RNA Splicing in Human Tumor Viruses
title_sort viral oncogenes, noncoding rnas, and rna splicing in human tumor viruses
publisher Ivyspring International Publisher
series International Journal of Biological Sciences
issn 1449-2288
publishDate 2010-01-01
description <p>Viral oncogenes are responsible for oncogenesis resulting from persistent virus infection. Although different human tumor viruses express different viral oncogenes and induce different tumors, their oncoproteins often target similar sets of cellular tumor suppressors or signal pathways to immortalize and/or transform infected cells. Expression of the viral E6 and E7 oncogenes in papillomavirus, E1A and E1B oncogenes in adenovirus, large T and small t antigen in polyomavirus, and Tax oncogene in HTLV-1 are regulated by alternative RNA splicing. However, this regulation is only partially understood. DNA tumor viruses also encode noncoding RNAs, including viral microRNAs, that disturb normal cell functions. Among the determined viral microRNA precursors, EBV encodes 25 from two major clusters (BART and BHRF1), KSHV encodes 12 from a latent region, human polyomavirus MCV produce only one microRNA from the late region antisense to early transcripts, but HPVs appears to produce no viral microRNAs.</p>
url http://www.biolsci.org/v06p0730.htm
work_keys_str_mv AT zhimingzheng viraloncogenesnoncodingrnasandrnasplicinginhumantumorviruses
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