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Originally published In Press as doi:10.1074/jbc.M011028200 on March 13, 2001

J. Biol. Chem., Vol. 276, Issue 22, 19640-19647, June 1, 2001
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Features of the Parkin/Ariadne-like Ubiquitin Ligase, HHARI, That Regulate Its Interaction with the Ubiquitin-conjugating Enzyme, UbcH7*

Helen C. ArdleyDagger §, Nancy G. S. TanDagger , Stephen A. RoseDagger , Alexander F. MarkhamDagger , and Philip A. RobinsonDagger

From the Dagger  Molecular Medicine Unit and the  Leeds Dental Institute, University of Leeds, Clinical Sciences Building, St. James's University Hospital, Leeds LS9 7TF, United Kingdom

We recently reported the identification of a RING finger-containing protein, HHARI (human homologue of Drosophila ariadne), which binds to the human ubiquitin-conjugating enzyme UbcH7 in vitro. We now demonstrate that HHARI interacts and co-localizes with UbcH7 in mammalian cells, particularly in the perinuclear region. We have further defined a minimal interaction region of HHARI comprising residues 186-254, identified individual amino acid residues essential for the interaction, and determined that the distance between the RING1 finger and IBR (in between RING fingers) domains is critical to maintaining binding. We have also established that the RING1 finger of HHARI cannot be substituted for by the highly homologous RING finger domains of either of the ubiquitin-protein ligase components c-CBL or Parkin, despite their similarity in structure and their independent capabilities to bind UbcH7. Furthermore, mutation of the RING1 finger domain of HHARI from a RING-HC to a RING-H2 type abolishes interaction with UbcH7. These studies demonstrate that very subtle changes to the domains that regulate recognition between highly conserved components of the ubiquitin pathway can dramatically affect their ability to interact.

* This work was supported by the Wellcome Trust, the Royal Society, Yorkshire Cancer Research, and a Lloyds of London Tercentenary Foundation Fellowship (to H. C. A.).The costs of publication of this article were defrayed in part by the payment of page charges. The article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

§ To whom correspondence should be addressed: Molecular Medicine Unit, Level 6, Clinical Sciences Bldg., St. James's University Hospital, Leeds LS9 7TF, UK. Tel.: 44-113-2065682; Fax: 44-113-2444475; E-mail: rmrhca@stjames.leeds.ac.uk.

Copyright © 2001 by The American Society for Biochemistry and Molecular Biology, Inc.
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