Papillomavirus Genomes Associate with BRD4 to Replicate at Fragile Sites in the Host Genome

PLoS Pathogens

Kui Shen¹  Alison A. McBride²  Moon Kyoo Jang² 

[1] Bioinformatics and Computational Biosciences Branch, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, United States of America;Laboratory of Viral Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, United States of America

关键词: Chromatin;    Viral replication;    DNA replication;    Cell binding;    HPV-1;    Binding analysis;    HPV-16;    BAC cloning;   

DOI  :  10.1371/journal.ppat.1004117

学科分类：生物科学（综合）

来源: Public Library of Science

【 摘 要 】

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.

【 授权许可】

CC BY