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Originally published as MBC in Press, 10.1091/mbc.E04-01-0039 on May 7, 2004

Vol. 15, Issue 7, 3073-3082, July 2004

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IRI-1, a LIN-15B Homologue, Interacts with Inositol-1,4,5-Triphosphate Receptors and Regulates Gonadogenesis, Defecation, and Pharyngeal Pumping in Caenorhabditis elegans

Denise S. Walker, Sung Ly, Nicholas J.D. Gower, and Howard A. Baylis *

Department of Zoology, University of Cambridge, Cambridge, CB2 3EJ, United Kingdom

Submitted January 16, 2004; Revised March 26, 2004; Accepted April 26, 2004
Monitoring Editor: Susan Strome

Inositol-1,4,5-triphosphate receptors (IP3Rs) are ligand-gated Ca2+ channels that control Ca2+ release from intracellular stores. They are central to a wide range of cellular responses. IP3Rs in Caenorhabditis elegans are encoded by a single gene, itr-1, and are widely expressed. Signaling through IP3 and IP3Rs is important in ovulation, control of the defecation cycle, modulation of pharyngeal pumping rate, and embryogenesis. To further elucidate the molecular basis of the diversity of IP3R function, we used a yeast two-hybrid screen to search for proteins that interact with ITR-1. We identified an interaction between ITR-1 and IRI-1, a previously uncharacterized protein with homology to LIN-15B. Iri-1 is widely expressed, and its expression overlaps significantly with that of itr-1. In agreement with this observation, iri-1 functions in known itr-1-mediated processes, namely, upregulation of pharyngeal pumping in response to food and control of the defecation cycle. Knockdown of iri-1 in an itr-1 loss-of-function mutant potentiates some of these effects and sheds light on the signaling pathways that control pharyngeal pumping rate. Knockdown of iri-1 expression also results in a sterile, evl phenotype, as a consequence of failures in early Z1/Z4 lineage divisions, such that gonadogenesis is severely disrupted.


Article published online ahead of print. Mol. Biol. Cell 10.1091/mbc.E04-01-0039. Article and publication date are available at www.molbiolcell.org/cgi/doi/10.1091/mbc.E04-01-0039.

* Corresponding author. E-mail address: hab{at}mole.bio.cam.ac.uk.




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