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Journal of Virology, October 2008, p. 9917-9927, Vol. 82, No. 20
0022-538X/08/$08.00+0     doi:10.1128/JVI.00953-08
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

Ectromelia Virus Encodes a Novel Family of F-Box Proteins That Interact with the SCF Complex{triangledown}

Nick van Buuren,1 Brianne Couturier,1 Yue Xiong,2 and Michele Barry1*

Department of Medical Microbiology and Immunology, University of Alberta, Edmonton, Alberta, Canada,1 Department of Biochemistry and Biophysics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina2

Received 7 May 2008/ Accepted 21 July 2008

Poxviruses are notorious for encoding multiple proteins that regulate cellular signaling pathways, including the ubiquitin-proteasome system. Bioinformatics indicated that ectromelia virus, the causative agent of lethal mousepox, encoded four proteins, EVM002, EVM005, EVM154, and EVM165, containing putative F-box domains. In contrast to cellular F-box proteins, the ectromelia virus proteins contain C-terminal F-box domains in conjunction with N-terminal ankyrin repeats, a combination that has not been previously reported for cellular proteins. These observations suggested that the ectromelia virus F-box proteins interact with SCF (Skp1, cullin-1, and F-box) ubiquitin ligases. We focused our studies on EVM005, since this protein had only one ortholog in cowpox virus. Using mass spectrometry, we identified cullin-1 as a binding partner for EVM005, and this interaction was confirmed by overexpression of hemagglutinin (HA)-cullin-1. During infection, Flag-EVM005 and HA-cullin-1 colocalized to distinct cellular bodies. Significantly, EVM005 coprecipitated with endogenous Skp1, cullin-1, and Roc1 and associated with conjugated ubiquitin, suggesting that EVM005 interacted with the components of a functional ubiquitin ligase. Interaction of EVM005 with cullin-1 and Skp1 was abolished upon deletion of the F-box, indicating that the F-box played a crucial role in interaction with the SCF complex. Additionally, EVM002 and EVM154 interacted with Skp1 and conjugated ubiquitin, suggesting that ectromelia virus encodes multiple F-box-containing proteins that regulate the SCF complex. Our results indicate that ectromelia virus has evolved multiple proteins that interact with the SCF complex.


* Corresponding author. Mailing address: 621 HMRC, Department of Medical Microbiology and Immunology, University of Alberta, Edmonton, Alberta, Canada T6G 2S2. Phone: (780) 492-0702. Fax: (780) 492-9828. E-mail: michele.barry{at}ualberta.ca

{triangledown} Published ahead of print on 6 August 2008.


Journal of Virology, October 2008, p. 9917-9927, Vol. 82, No. 20
0022-538X/08/$08.00+0     doi:10.1128/JVI.00953-08
Copyright © 2008, American Society for Microbiology. All Rights Reserved.







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