Papillomavirus Genomes Associate with BRD4 to Replicate at Fragile Sites in the Host Genome
Identifieur interne : 000083 ( Main/Exploration ); précédent : 000082; suivant : 000084Papillomavirus Genomes Associate with BRD4 to Replicate at Fragile Sites in the Host Genome
Auteurs : Moon Kyoo Jang [États-Unis] ; Kui Shen [États-Unis] ; Alison A. Mcbride [États-Unis]Source :
- PLoS Pathogens [ 1553-7366 ] ; 2014.
Abstract
It has long been recognized that oncogenic viruses often integrate close to common fragile sites. The papillomavirus E2 protein, in complex with BRD4, tethers the viral genome to host chromatin to ensure persistent replication. Here, we map these targets to a number of large regions of the human genome and name them Persistent E2 and BRD4-Broad Localized Enrichments of Chromatin or PEB-BLOCs. PEB-BLOCs frequently contain deletions, have increased rates of asynchronous DNA replication, and are associated with many known common fragile sites. Cell specific fragile sites were mapped in human C-33 cervical cells by FANCD2 ChIP-chip, confirming the association with PEB-BLOCs. HPV-infected cells amplify viral DNA in nuclear replication foci and we show that these form adjacent to PEB-BLOCs. We propose that HPV replication, which hijacks host DNA damage responses, occurs adjacent to highly susceptible fragile sites, greatly increasing the chances of integration here, as is found in HPV-associated cancers.
Url:
DOI: 10.1371/journal.ppat.1004117
PubMed: 24832099
PubMed Central: 4022725
Affiliations:
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Mcbride</name><affiliation wicri:level="2"><nlm:aff id="aff1"><addr-line>Laboratory of Viral Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, United States of America</addr-line></nlm:aff><country xml:lang="fr">États-Unis</country><wicri:regionArea>Laboratory of Viral Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland</wicri:regionArea><placeName><region type="state">Maryland</region></placeName></affiliation></author></analytic><series><title level="j">PLoS Pathogens</title><idno type="ISSN">1553-7366</idno><idno type="eISSN">1553-7374</idno><imprint><date when="2014">2014</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p>It has long been recognized that oncogenic viruses often integrate close to common fragile sites. The papillomavirus E2 protein, in complex with BRD4, tethers the viral genome to host chromatin to ensure persistent replication. Here, we map these targets to a number of large regions of the human genome and name them Persistent E2 and BRD4-Broad Localized Enrichments of Chromatin or PEB-BLOCs. PEB-BLOCs frequently contain deletions, have increased rates of asynchronous DNA replication, and are associated with many known common fragile sites. Cell specific fragile sites were mapped in human C-33 cervical cells by FANCD2 ChIP-chip, confirming the association with PEB-BLOCs. HPV-infected cells amplify viral DNA in nuclear replication foci and we show that these form adjacent to PEB-BLOCs. We propose that HPV replication, which hijacks host DNA damage responses, occurs adjacent to highly susceptible fragile sites, greatly increasing the chances of integration here, as is found in HPV-associated cancers.</p></div></front><back><div1 type="bibliography"><listBibl><biblStruct><analytic><author><name sortKey="Skiadopoulos, Mh" uniqKey="Skiadopoulos M">MH Skiadopoulos</name></author><author><name sortKey="Mcbride, Aa" uniqKey="Mcbride A">AA McBride</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Ilves, I" uniqKey="Ilves I">I Ilves</name></author><author><name sortKey="Kivi, S" uniqKey="Kivi S">S Kivi</name></author><author><name sortKey="Ustav, M" uniqKey="Ustav M">M Ustav</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Lehman, Cw" uniqKey="Lehman C">CW Lehman</name></author><author><name sortKey="Botchan, Mr" uniqKey="Botchan M">MR 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uniqKey="Mcbride A" first="Alison A." last="Mcbride">Alison A. 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