Adeno-associated virus and adenovirus coinfection induces a cellular DNA damage and repair response via redundant phosphatidylinositol 3-like kinase pathways

被引:26
作者
Collaco, Roy F. [1 ]
Bevington, Joyce M. [1 ]
Bhrigu, Vipul [1 ]
Kalman-Maltese, Vivian [1 ]
Trempe, James P. [1 ]
机构
[1] Univ Toledo, Dept Biochem & Canc Biol, Coll Med, Toledo, OH 43614 USA
关键词
AAV infection; DNA damage responses; DOUBLE-STRAND BREAKS; MRE11; COMPLEX; BINDING PROTEIN; REP78; PROTEIN; NONDIVIDING CELLS; IN-VITRO; S-PHASE; TRANSDUCTION; REPLICATION; ATM;
D O I
10.1016/j.virol.2009.06.005
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
During adeno-associated Virus and adenovirus (AAV/Ad) coinfection, accumulation of viral genomes and proteins can alter cellular stress responses. To determine how AAV/Ad coinfection affects the host we screened over 60 cellular Proteins for their responses. AAV/Ad coinfections induce a robust DNA damage response (DDR) that is distinct from that induced by Ad infection alone. Using chemical inhibitors, deficient cell lines and siRNA knockdowns of the DDR kinases, ATM, ATR and DNA-PK, we determined that DNA-PK and ATM kinases are the initial transducers of this response. AAV/Ad coinfection induces ATM- and DNA-PK mediated phosphorylation of RPA2, NBS1, H2AX and the checkpoint kinases CHK1/2. Inhibition of one or more of the DDR kinases reduces the level of phosphorylation of downstream targets but does not dramatically reduce Ad or AAV protein expression. However, AAV DNA levels are moderately affected by kinase inhibition. These experiments provide new insights into the cellular responses to AAV/Ad coinfections. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:24 / 33
页数:10
相关论文
共 61 条
[11]   ADENO-ASSOCIATED VIRUS AUTOINTERFERENCE [J].
CARTER, BJ ;
LAUGHLIN, CA ;
DELAMAZA, LM ;
MYERS, M .
VIROLOGY, 1979, 92 (02) :449-462
[12]   Identification of an adeno-associated virus rep protein binding site in the adenovirus E2a promoter [J].
Casper, JM ;
Timpe, JM ;
Dignam, JD ;
Trempe, JP .
JOURNAL OF VIROLOGY, 2005, 79 (01) :28-38
[13]   THE ADENOVIRUS DNA-BINDING PROTEIN STIMULATES THE RATE OF TRANSCRIPTION DIRECTED BY ADENOVIRUS AND ADENOASSOCIATED VIRUS PROMOTERS [J].
CHANG, LS ;
SHENK, T .
JOURNAL OF VIROLOGY, 1990, 64 (05) :2103-2109
[14]   ADENO-ASSOCIATED VIRUS P5 PROMOTER CONTAINS AN ADENOVIRUS E1A-INDUCIBLE ELEMENT AND A BINDING-SITE FOR THE MAJOR LATE TRANSCRIPTION FACTOR [J].
CHANG, LS ;
SHI, Y ;
SHENK, T .
JOURNAL OF VIROLOGY, 1989, 63 (08) :3479-3488
[15]   Host cell DNA repair pathways in adeno-associated viral genome processing [J].
Choi, Vivian W. ;
McCarty, Douglas M. ;
Samulski, R. Jude .
JOURNAL OF VIROLOGY, 2006, 80 (21) :10346-10356
[16]   The life and death of DNA-PK [J].
Collis, SJ ;
DeWeese, TL ;
Jeggo, PA ;
Parker, AR .
ONCOGENE, 2005, 24 (06) :949-961
[17]   ATR and ATRIP: Partners in checkpoint signaling [J].
Cortez, D ;
Guntuku, S ;
Qin, J ;
Elledge, SJ .
SCIENCE, 2001, 294 (5547) :1713-1716
[18]   Consequences of DNA-dependent protein kinase catalytic subunit deficiency on recombinant adeno-associated virus genome circularization and heterodimerization in muscle tissue [J].
Duan, DS ;
Yue, YP ;
Engelhardt, JF .
JOURNAL OF VIROLOGY, 2003, 77 (08) :4751-4759
[19]   Relocalization of the Mre11-Rad50-Nbs1 complex by the adenovirus E4 ORF3 protein is required for viral replication [J].
Evans, JD ;
Hearing, P .
JOURNAL OF VIROLOGY, 2005, 79 (10) :6207-6215
[20]  
FERRARI EK, 1996, J VIROL, V70, P3227