| Literature DB >> 14992718 |
Muneesh Tewari1, Patrick J Hu, Jin Sook Ahn, Nono Ayivi-Guedehoussou, Pierre-Olivier Vidalain, Siming Li, Stuart Milstein, Chris M Armstrong, Mike Boxem, Maurice D Butler, Svetlana Busiguina, Jean-François Rual, Nieves Ibarrola, Sabrina T Chaklos, Nicolas Bertin, Philippe Vaglio, Mark L Edgley, Kevin V King, Patrice S Albert, Jean Vandenhaute, Akhilesh Pandey, Donald L Riddle, Gary Ruvkun, Marc Vidal.
Abstract
To initiate a system-level analysis of C. elegans DAF-7/TGF-beta signaling, we combined interactome mapping with single and double genetic perturbations. Yeast two-hybrid (Y2H) screens starting with known DAF-7/TGF-beta pathway components defined a network of 71 interactions among 59 proteins. Coaffinity purification (co-AP) assays in mammalian cells confirmed the overall quality of this network. Systematic perturbations of the network using RNAi, both in wild-type and daf-7/TGF-beta pathway mutant animals, identified nine DAF-7/TGF-beta signaling modifiers, seven of which are conserved in humans. We show that one of these has functional homology to human SNO/SKI oncoproteins and that mutations at the corresponding genetic locus daf-5 confer defects in DAF-7/TGF-beta signaling. Our results reveal substantial molecular complexity in DAF-7/TGF-beta signal transduction. Integrating interactome maps with systematic genetic perturbations may be useful for developing a systems biology approach to this and other signaling modules.Entities:
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Year: 2004 PMID: 14992718 DOI: 10.1016/s1097-2765(04)00033-4
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970