Identification of a second CtBP binding site in adenovirus type 5 E1A conserved region 3

被引:24
作者
Bruton, Rachel K. [1 ]
Pelka, Peter [2 ,3 ]
Mapp, Katie L. [1 ]
Fonseca, Gregory J. [2 ,3 ]
Torchia, Joseph [4 ,5 ]
Turnell, Andrew S. [1 ]
Mymryk, Joe S. [2 ,3 ]
Grand, Roger J. A. [1 ]
机构
[1] Univ Birmingham, Inst Canc Studies, Canc Res UK, Birmingham B15 2TT, W Midlands, England
[2] Univ Western Ontario, Dept Oncol, London, ON, Canada
[3] Univ Western Ontario, Dept Microbiol & Immunol, London, ON, Canada
[4] Univ Western Ontario, Dept Oncol, London Reg Canc Program, London, ON, Canada
[5] Univ Western Ontario, Dept Biochem, London Reg Canc Program, London, ON, Canada
关键词
D O I
10.1128/JVI.00248-08
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
C-terminal binding protein (CtBP) binds to adenovirus early region 1A (AdE1A) through a highly conserved PXDLS motif close to the C terminus. We now have demonstrated that CtBP1 also interacts directly with the transcriptional activation domain (conserved region 3 [CR3]) of adenovirus type 5 E1A (Ad5E1A) and requires the integrity of the entire CR3 region for optimal binding. The interaction appears to be at least partially mediated through a sequence ((161)RRNTGDP(167)) Very similar to a recently characterized novel CtBP binding motif in ZNF217 as well as other regions of CR3. Using reporter assays, we further demonstrated that CtBP1 represses Ad5E1A CR3-dependent transcriptional activation. Ad5E1A also appears to be recruited to the E-cadherin promoter through its interaction with CtBP. Significantly, Ad5E1A, CtBP1, and ZNF217 form a stable complex which requires CR3 and the PLDLS motif. It has been shown that Ad513SE1A, containing the CR3 region, is able to overcome the transcriptional repressor activity of a ZNF217 polypeptide fragment in a GAL4 reporter assay through recruitment of CtBP1. These results suggest a hitherto-unsuspected complexity in the association of Ad5E1A with CtBP, with the interaction resulting in transcriptional activation by recruitment of CR3-bound factors to CtBP1-containing complexes.
引用
收藏
页码:8476 / 8486
页数:11
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