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Viral trans-factor independent replication of human papillomavirus genomes

BACKGROUND: Papillomaviruses (PVs) establish a persistent infection in the proliferating basal cells of the epithelium. The viral genome is replicated and maintained as a low-copy nuclear plasmid in basal keratinocytes. Bovine and human papillomaviruses (BPV and HPV) are known to utilize two viral p...

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Autores principales: Pittayakhajonwut, Daraporn, Angeletti, Peter C
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2893153/
https://www.ncbi.nlm.nih.gov/pubmed/20537170
http://dx.doi.org/10.1186/1743-422X-7-123
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author Pittayakhajonwut, Daraporn
Angeletti, Peter C
author_facet Pittayakhajonwut, Daraporn
Angeletti, Peter C
author_sort Pittayakhajonwut, Daraporn
collection PubMed
description BACKGROUND: Papillomaviruses (PVs) establish a persistent infection in the proliferating basal cells of the epithelium. The viral genome is replicated and maintained as a low-copy nuclear plasmid in basal keratinocytes. Bovine and human papillomaviruses (BPV and HPV) are known to utilize two viral proteins; E1, a DNA helicase, and E2, a transcription factor, which have been considered essential for viral DNA replication. However, growing evidence suggests that E1 and E2 are not entirely essential for stable replication of HPV. RESULTS: Here we report that multiple HPV16 mutants, lacking either or both E1 and E2 open reading frame (ORFs) and the long control region (LCR), still support extrachromosomal replication. Our data clearly indicate that HPV16 has a mode of replication, independent of viral trans-factors, E1 and E2, which is achieved by origin activity located outside of the LCR.
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spelling pubmed-28931532010-06-29 Viral trans-factor independent replication of human papillomavirus genomes Pittayakhajonwut, Daraporn Angeletti, Peter C Virol J Research BACKGROUND: Papillomaviruses (PVs) establish a persistent infection in the proliferating basal cells of the epithelium. The viral genome is replicated and maintained as a low-copy nuclear plasmid in basal keratinocytes. Bovine and human papillomaviruses (BPV and HPV) are known to utilize two viral proteins; E1, a DNA helicase, and E2, a transcription factor, which have been considered essential for viral DNA replication. However, growing evidence suggests that E1 and E2 are not entirely essential for stable replication of HPV. RESULTS: Here we report that multiple HPV16 mutants, lacking either or both E1 and E2 open reading frame (ORFs) and the long control region (LCR), still support extrachromosomal replication. Our data clearly indicate that HPV16 has a mode of replication, independent of viral trans-factors, E1 and E2, which is achieved by origin activity located outside of the LCR. BioMed Central 2010-06-10 /pmc/articles/PMC2893153/ /pubmed/20537170 http://dx.doi.org/10.1186/1743-422X-7-123 Text en Copyright ©2010 Pittayakhajonwut and Angeletti; 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
Pittayakhajonwut, Daraporn
Angeletti, Peter C
Viral trans-factor independent replication of human papillomavirus genomes
title Viral trans-factor independent replication of human papillomavirus genomes
title_full Viral trans-factor independent replication of human papillomavirus genomes
title_fullStr Viral trans-factor independent replication of human papillomavirus genomes
title_full_unstemmed Viral trans-factor independent replication of human papillomavirus genomes
title_short Viral trans-factor independent replication of human papillomavirus genomes
title_sort viral trans-factor independent replication of human papillomavirus genomes
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2893153/
https://www.ncbi.nlm.nih.gov/pubmed/20537170
http://dx.doi.org/10.1186/1743-422X-7-123
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