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Journal of Virology, June 2001, p. 5391-5397, Vol. 75, No. 11
Institut für Virologie,
Philipps-Universität Marburg, 35037 Marburg, Germany
Received 11 August 2000/Accepted 6 March 2001
Promyelocytic leukemia (PML) oncogenic domains (PODs) accumulate
the transcriptional cofactor named CREB binding protein (CBP) and have
been suggested to function as centers of transcription. Transcriptional
activation by nuclear hormones, such as glucocorticoids, is augmented
by the key constituent of PODs, the PML protein, and decreased by the
POD-associated Tax protein of human T-cell leukemia virus type 1 (HTLV-1). This led to the hypothesis that intact PODs might play a
positive role in the activation of these promoters. We report here that
transiently expressed E4orf3 protein of adenovirus type 5, immediate-early protein 1 of human cytomegalovirus, and the
PML-retinoic acid receptor fusion protein from leukemia cells each
redistribute CBP within the nucleus. However, unlike the Tax protein of
HTLV-1, these factors did not inhibit a glucocorticoid-inducible promoter but strongly enhanced its activity. Thus, at least
glucocorticoid-induced transcription does not depend on POD integrity.
0022-538X/01/$04.00+0 DOI: 10.1128/JVI.75.11.5391-5397.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Viral and Cellular Factors That Target the
Promyelocytic Leukemia Oncogenic Domains Strongly Activate a
Glucocorticoid-Responsive Promoter
*
Corresponding author. Mailing address: Institut
für Virologie, Philipps-Universität, Robert Koch Str. 17, 35037 Marburg, Germany. Phone: 49 6421 28 64318. Fax: 49 6421 28 68962. E-mail: dobbelst{at}mailer.uni-marburg.de.
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