The Human Adenovirus Type 5 E4orf6/E1B55K E3 Ubiquitin Ligase Complex Can Mimic E1A Effects on E2F

Author:

Dallaire Frédéric1,Schreiner Sabrina2,Blair G. Eric3,Dobner Thomas4,Branton Philip E.156,Blanchette Paola1

Affiliation:

1. Department of Biochemistry, McGill University, Montreal, Québec, Canada

2. Institute of Virology, Technische Universität München/Helmholtz Zentrum München, Munich, Germany

3. School of Molecular and Cellular Biology, University of Leeds, Leeds, United Kingdom

4. Heinrich Pette Institute, Leibniz Institute for Experimental Virology, Hamburg, Germany

5. Department of Oncology, McGill University, Montreal, Québec, Canada

6. Goodman Cancer Research Centre, McGill University, Montreal, Québec, Canada

Abstract

During the course of work on the adenovirus E3 ubiquitin ligase formed by the viral E4orf6 and E1B55K proteins, we found, very surprisingly, that expression of these species was sufficient to permit low levels of replication of an adenovirus vector lacking E1A, the central regulator of infection. E1A products uncouple E2F transcription factors from Rb repression complexes, thus stimulating viral gene expression and cell and viral DNA synthesis. We found that the E4orf6/E1B55K ligase mimics these functions. This finding is of significance because it represents an entirely new function for the ligase in regulating adenovirus replication.

Funder

Gouvernement du Canada | CIHR | Institute of Infection and Immunity

Else Kröner-Fresenius-Stiftung

Dräger-Stiftung

Deutsche Krebshilfe e.V.

Deutsche Forschungsgemeinschaft

Wilhelm Sander-Stiftung

Freie und Hansestadt Hamburg

Bundesministerium fur Gesundheit

Yorkshire Cancer Research

Publisher

American Society for Microbiology

Subject

Molecular Biology,Microbiology

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