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MBC in Press, published online ahead of print August 25, 2004
Mol. Biol. Cell 10.1091/mbc.E04-03-0180

A more recent version of this article appeared on November 1, 2004
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Submitted on March 4, 2004
Revised on August 11, 2004
Accepted on August 17, 2004

Targeted Disruption of Drosophila Roc1b Reveals Functional Differences in the Roc Subunit of Cullin-dependent E3 Ubiquitin Ligases

Timothy D. Donaldson,*{dagger} Maher A. Noureddine,{dagger} Patrick J. Reynolds,{dagger} William Bradford,{dagger} and Robert J. Duronio*{dagger}{ddagger}{sect}||

*Lineberger Comprehensive Cancer Center, {dagger}Department of Biology, {ddagger}Curriculum in Genetics and Molecular Biology, {sect}Program in Molecular Biology and Biotechnology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599

Monitoring Editor: Mark Solomon

Cullin-dependent ubiquitin ligases regulate a variety of cellular and developmental processes by recruiting specific proteins for ubiquitin-mediated degradation. Cullin proteins form a scaffold for two functional modules: a catalytic module comprised of a small RING domain protein Roc1/Rbx1 and an ubiquitin conjugating enzyme (E2), and a substrate recruitment module containing one or more proteins that bind to and bring the substrate in proximity to the catalytic module. Here we present evidence that the three Drosophila Roc proteins are not functionally equivalent. Mutation of Roc1a causes lethality that cannot be rescued by expression of Roc1b or Roc2 using the Roc1a promoter. Roc1a mutant cells hyper-accumulate Cubitus interruptus, a transcription factor that mediates Hedgehog signaling. This phenotype is not rescued by expression of Roc2 and only partially by expression of Roc1b. Targeted disruption of Roc1b causes male sterility that is partially rescued by expression of Roc1a using the Roc1b promoter, but not by similar expression of Roc2. These data indicate that Roc proteins play nonredundant roles during development. Co-immunoprecipitation followed by Western or mass spectrometric analysis indicate that the three Roc proteins preferentially bind certain Cullins, providing a possible explanation for the distinct biological activities of each Drosophila Roc/Rbx.

||Corresponding author. E-mail: duronio{at}med.unc.edu




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