High-risk human papillomaviruses (HPV) are the causative agents of cervical cancer. The life cycle of HPV Is tied to the differentiation status of its host cell, the keratinocyte. Differentiation triggers the productive phase of the life cycle, which includes viral genome amplification, late gene expression and virion production. In contrast to normal cells, which exit the cell cycle upon differentiation, expression of the HPV E6 and E7 proteins maintain a subset of cells active in the cell cycle largely through degradation of p53 and pRb, respectively The long-term goal of this project is to understand the mechanisms that regulate the activation of differentiation-dependent viral events. Toward this end, I have demonstrated that HPV31 stimulates a low level of caspase activation upon differentiation that is characteristic of the mitochondrial apoptotic pathway and necessary for amplification of viral genomes through cleavage of the viral replication protein El. In addition, I have recently found that HPV induces an ATM-dependent DNA damage response in differentiating cells, which is necessary for efficient viral genome amplification, as well as caspase activation through the ATM target Chk2. Based on the finding that caspase activation, as well as Chk2 activation, can be stimulated by both E6 and E7, and the identification of caspase cleavage sites in several HPV proteins, I hypothesize that the HPV proteins E6 and E7 induce caspase activation through a DNA damage response to activate late viral events.
Specific aims to test this hypothesis are: 1) Identify the mechanism(s) by which HPV activates caspases In differentiating cells by examining the effect of E6 and E7 on the DNA damage response and alteration of mitochondrial membrane integrity, as well as by performing a mutational analysis of E6 and E7 to identify domains that are necessary for Chk2 activation and caspase activation;2) Determine how caspase cleavage of HPV proteins contributes to differentiation-dependent events In the life cycle by using in vitro and in vivo studies. Delineating the pathway by which E6 and E7 mediate activation of a DNA damage response to lead to caspase activation will offer insight as to how HPV modulates apoptotic machinery to facilitate not only the viral life cycle, but possibly transformation as well.

Public Health Relevance

Human papillomaviruses are the causative agents of cervical cancer. Understanding how the viral oncoproteins contribute to the regulation of the viral life cycle will ultimately offer insight into how HPV causes disease, and provide potential therapeutic targets.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Transition Award (R00)
Project #
5R00CA137160-05
Application #
8307447
Study Section
Special Emphasis Panel (NSS)
Program Officer
Read-Connole, Elizabeth Lee
Project Start
2008-09-20
Project End
2013-08-31
Budget Start
2012-09-01
Budget End
2013-08-31
Support Year
5
Fiscal Year
2012
Total Cost
$241,530
Indirect Cost
$78,334
Name
University of North Carolina Chapel Hill
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
608195277
City
Chapel Hill
State
NC
Country
United States
Zip Code
27599
Gillespie, Kenric A; Mehta, Kavi P; Laimins, Laimonis A et al. (2012) Human papillomaviruses recruit cellular DNA repair and homologous recombination factors to viral replication centers. J Virol 86:9520-6
Anacker, Daniel; Moody, Cary (2012) Generation of organotypic raft cultures from primary human keratinocytes. J Vis Exp :
Fradet-Turcotte, Amelie; Bergeron-Labrecque, Fanny; Moody, Cary A et al. (2011) Nuclear accumulation of the papillomavirus E1 helicase blocks S-phase progression and triggers an ATM-dependent DNA damage response. J Virol 85:8996-9012