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A more recent version of this article appeared on March 15, 2002
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Papers In Press, published online ahead of print January 11, 2002
J. Biol. Chem, 10.1074/jbc.M106955200
Submitted on July 23, 2001
Revised on January 11, 2002
Accepted on January 10, 2002

YB-1 relocates to the nucleus in adenovirus infected cells and facilitates viral replication by inducing E2 gene expression through the E2 late promoter

Per S. Holm, Stephan Bergamnn, Karsten Juerchott, Hermann Lage, Karsten Brand, Axel Ladhoff, Klaus Mantwill, David T. Curiel, Matthias Dobbelstein, Manfred Dietel, Bernd Gaensbacher, and Hans D. Royer

Klinikum Rechts der Isar, Exp Oncology and Therapy, Munich 81675

Corresponding Author: per.s.holm{at}lrz.tum.de

The adenovirus early proteins E1A and E1B-55KDa are key regulators of viral DNA replication and it was thought that targeting of p53 by E1B-55KDa is essential for this process. Here we have indentified a previously unrecognized function of E1B for adenovirus replication. We found that E1B-55KDa is involved in targeting the transcription factor YB-1 to the nuclei of adenovirus type 5 infected cells where it is associated with viral inclusion bodies believed to be sites of viral transcription and replication. We show that YB-1 facilitates E2 gene expression through the E2 late promoter thus controlling E2 gene activity at later stages of infection. The role of YB-1 for adenovirus replication was demonstrated with an E1-minus adenovirus vector containing a YB-1 transgene. In infected cells, AdYB-1 efficiently replicated and produced infectious progeny particles. Thus adenovirus E1B-55KDa protein and the host cell factor YB-1 act jointly to facilitate adenovirus replication.


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