AbstractThe 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 ...
AbstractTo study DNA double-strand break (DSB) repair in mammalian cells, the Saccharomyces cerevisi...
Viruses manipulate the cellular environment to promote productive infection. Cells mount anti-viral ...
Adenovirus infection induces a cellular DNA damage response that can inhibit viral DNA replication a...
AbstractThe adenovirus oncoproteins E4 34k and E4 11k, the products of E4 open reading frames 6 and ...
AbstractAdenovirus mutants that lack the entire E4 region are severely defective for late gene expre...
AbstractThe ligase IV/XRCC4 complex plays a central role in DNA double-strand break repair by non-ho...
AbstractAdenovirus inundates the productively infected cell with linear, double-stranded DNA and an ...
AbstractAdenovirus mutants that lack the entire E4 region are severely defective for late gene expre...
Viruses are highly evolved entities that target key cellular pathways in order to promote their own ...
After induction of DNA double strand breaks (DSBs) the cellular DNA damage response (DDR) functions ...
Adenoviruses (Ad) with the early region E4 deleted (E4-deleted virus) are defective for DNA replicat...
Adenoviruses (Ad) with the early region E4 deleted (E4-deleted virus) are defective for DNA replicat...
Adenoviruses (Ad) with the early region E4 deleted (E4-deleted virus) are defective for DNA replicat...
It is well established that adenoviruses inactivate the host cell DNA damage response to enhance vir...
inhibits repair of double strand breaks in the cellular genome of a 293-based inducible cell lin
AbstractTo study DNA double-strand break (DSB) repair in mammalian cells, the Saccharomyces cerevisi...
Viruses manipulate the cellular environment to promote productive infection. Cells mount anti-viral ...
Adenovirus infection induces a cellular DNA damage response that can inhibit viral DNA replication a...
AbstractThe adenovirus oncoproteins E4 34k and E4 11k, the products of E4 open reading frames 6 and ...
AbstractAdenovirus mutants that lack the entire E4 region are severely defective for late gene expre...
AbstractThe ligase IV/XRCC4 complex plays a central role in DNA double-strand break repair by non-ho...
AbstractAdenovirus inundates the productively infected cell with linear, double-stranded DNA and an ...
AbstractAdenovirus mutants that lack the entire E4 region are severely defective for late gene expre...
Viruses are highly evolved entities that target key cellular pathways in order to promote their own ...
After induction of DNA double strand breaks (DSBs) the cellular DNA damage response (DDR) functions ...
Adenoviruses (Ad) with the early region E4 deleted (E4-deleted virus) are defective for DNA replicat...
Adenoviruses (Ad) with the early region E4 deleted (E4-deleted virus) are defective for DNA replicat...
Adenoviruses (Ad) with the early region E4 deleted (E4-deleted virus) are defective for DNA replicat...
It is well established that adenoviruses inactivate the host cell DNA damage response to enhance vir...
inhibits repair of double strand breaks in the cellular genome of a 293-based inducible cell lin
AbstractTo study DNA double-strand break (DSB) repair in mammalian cells, the Saccharomyces cerevisi...
Viruses manipulate the cellular environment to promote productive infection. Cells mount anti-viral ...
Adenovirus infection induces a cellular DNA damage response that can inhibit viral DNA replication a...