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Journal of Virology, October 2004, p. 11439-11442, Vol. 78, No. 20
0022-538X/04/$08.00+0     DOI: 10.1128/JVI.78.20.11439-11442.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.

Four EBNA2 Domains Are Important for EBNALP Coactivation

Chih-Wen Peng, Bo Zhao, and Elliott Kieff*

Department of Medicine and Microbiology and Molecular Genetics, Channing Laboratory, Brigham and Women's Hospital, and Harvard Medical School, Boston, Massachusetts

Received 6 March 2004/ Accepted 28 May 2004

EBNA2 transcriptional activation and regulated EBNALP coactivation are critical for Epstein-Barr virus-infected primary B-lymphocyte growth transformation. EBNALP coactivation requires the EBNA2 acidic activation domain (E2AD); EBNALP can bind to E2AD. EBNALP has now been found to bind less well to EBNA2 amino acids 1 to 58, which has been identified to be a second transcriptional activation domain, E2AD2. E2AD2 was specifically coactivated by EBNALP. Moreover, E2AD, E2AD2, EBNA2 RG domain, and the intermediate domain between RG and E2AD had significant roles in EBNA2-mediated activation and EBNALP coactivation.


* Corresponding author. Mailing address: Department of Medicine and Microbiology and Molecular Genetics, Channing Laboratory, Brigham and Women's Hospital, and Harvard Medical School, 181 Longwood Ave., Boston, MA 02115. Phone: (617) 525-4252. Fax: (617) 525-4257. E-mail: ekieff{at}rics.bwh.harvard.edu.


Journal of Virology, October 2004, p. 11439-11442, Vol. 78, No. 20
0022-538X/04/$08.00+0     DOI: 10.1128/JVI.78.20.11439-11442.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.




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Copyright © 2004 by the American Society for Microbiology. All rights reserved.