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Journal of Virology, March 2004, p. 2984-2993, Vol. 78, No. 6
0022-538X/04/$08.00+0     DOI: 10.1128/JVI.78.6.2984-2993.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.

US11 of Herpes Simplex Virus Type 1 Interacts with HIPK2 and Antagonizes HIPK2-Induced Cell Growth Arrest

Stéphane Giraud,{dagger} Chantal Diaz-Latoud,{dagger} Sabine Hacot,{dagger} Julien Textoris,{dagger} Roland P. Bourette,{dagger} and Jean-Jacques Diaz*

INSERM U369, Faculté de Médecine Lyon-RTH Laennec, 69372 Lyon Cedex 08, France

Received 5 August 2003/ Accepted 13 November 2003

Homeodomain-interacting protein kinase 2 (HIPK2) is a nuclear serine/threonine kinase of the subfamily of dual-specificity Yak1-related kinase proteins. HIPK2 was first described as a homeodomain-interacting protein kinase acting as a corepressor for homeodomain transcription factors. More recently, it was reported that HIPK2 plays a role in p53-mediated cellular apoptosis and could also participate in the regulation of the cell cycle. US11 protein of herpes simplex virus type 1 is a multifunctional protein involved in the regulation of several processes related to the survival of cells submitted to environmental stresses by mechanisms that are not fully elucidated. In an attempt to better understand the multiple functions of US11, we identified cellular binding partners of this protein by using the yeast two-hybrid system. We report that US11 interacts with HIPK2 through the PEST domain of HIPK2 and that this interaction occurs also in human cells. This interaction modifies the subcellular distribution of HIPK2 and protects the cell against the HIPK2-induced cell growth arrest.


* Corresponding author. Present address: Centre de Génétique Moléculaire et Cellulaire (CGMC), CNRS-UMR 5534, Domaine Scientifique de la DOUA, BÂt Gregor Mendel, 43 Bd du 11 Novembre 1918, 69622 Villeurbanne Cedex, France. Phone: 33 4 72 44 79 26. Fax: 33 4 72 44 05 55. E-mail: diaz{at}cgmc.univ-lyon1.fr.

{dagger} Present address: Centre de Génétique Moléculaire et Cellulaire, CNRS UMR 5534, Université Claude Bernard Lyon 1, 69622 Villeurbanne Cedex, France.


Journal of Virology, March 2004, p. 2984-2993, Vol. 78, No. 6
0022-538X/04/$08.00+0     DOI: 10.1128/JVI.78.6.2984-2993.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.




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