TY - JOUR
T1 - Adenovirus E4 34k and E4 11k inhibit double strand break repair and are physically associated with the cellular DNA-dependent protein kinase
AU - Boyer, Julie
AU - Rohleder, Kent
AU - Ketner, Gary
N1 - Funding Information:
We thank C. S. H. Young for discussions critical in formulating the experiments presented here. We gratefully acknowledge gifts of antisera from Carl Anderson, Philip Branton, Patrick Hearing, and George Brush, and we thank Joan Allalunis-Turner for MO59J and MO59K cells. Patrick Swanson, Jinhak Lee, and Stephen Desiderio graciously provided plasmids, antisera, advice, and criticism of the V(D)J recombination experiments. We thank Stephen Desiderio, Marie Hardwick, Thomas Kelly, and Janice Clements for thoughtful criticism of the manuscript. J.B. is supported by NIH Grant 5 T32 AI 07417, and K.R. is supported by NIH Grant 5 T32 GM 07814. This work was supported by NIH Grant CA26239 and by ACS Grant VM-178.
PY - 1999/10/25
Y1 - 1999/10/25
N2 - The adenovirus oncoproteins E4 34k and E4 11k, the products of E4 open reading frames 6 and 3, respectively, individually prevent the formation of concatemers of the linear viral genome in infected cells. We show here that genome concatenation in E4 mutant-infected cells requires the cellular DNA- dependent protein kinase (DNA PK) and that E4 34k inhibits V(D)J recombination, a normal cellular process that is also dependent on DNA PK. We further show that both E4 34k and E4 11k coimmunoprecipitate with DNA PK. These observations indicate that E4 products block formation of concatemers of the viral genome by inhibiting DNA PK-dependent double strand break repair and suggest that they act by forming a physical complex with DNA PK. DNA PK also participates in activation of p53 DNA-binding activity by DNA damage. By inhibiting DNA PK function, E4 products may block p53 activation in response to the products of viral DNA replication and thus provide a new mechanism to prevent apoptosis of infected cells.
AB - The adenovirus oncoproteins E4 34k and E4 11k, the products of E4 open reading frames 6 and 3, respectively, individually prevent the formation of concatemers of the linear viral genome in infected cells. We show here that genome concatenation in E4 mutant-infected cells requires the cellular DNA- dependent protein kinase (DNA PK) and that E4 34k inhibits V(D)J recombination, a normal cellular process that is also dependent on DNA PK. We further show that both E4 34k and E4 11k coimmunoprecipitate with DNA PK. These observations indicate that E4 products block formation of concatemers of the viral genome by inhibiting DNA PK-dependent double strand break repair and suggest that they act by forming a physical complex with DNA PK. DNA PK also participates in activation of p53 DNA-binding activity by DNA damage. By inhibiting DNA PK function, E4 products may block p53 activation in response to the products of viral DNA replication and thus provide a new mechanism to prevent apoptosis of infected cells.
UR - http://www.scopus.com/inward/record.url?scp=0033604299&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0033604299&partnerID=8YFLogxK
U2 - 10.1006/viro.1999.9866
DO - 10.1006/viro.1999.9866
M3 - Article
C2 - 10544104
AN - SCOPUS:0033604299
SN - 0042-6822
VL - 263
SP - 307
EP - 312
JO - Virology
JF - Virology
IS - 2
ER -