4.4 Article

Increased IP3/Ca2+ signaling compensates depletion of LET-413/DLG-1 in C. elegans epithelial junction assembly

Journal

DEVELOPMENTAL BIOLOGY
Volume 327, Issue 1, Pages 34-47

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ydbio.2008.11.025

Keywords

Cell polarity; Junction; Epithelia; Spermatheca; Ovulation; Gonadogenesis; IP3/Ca2+ signaling; Caenorhabditis elegans

Funding

  1. NIH National Center for Research Resources (NCRR)
  2. Jurgen Manchot Stiftung
  3. Deutsche Forschungsgemeinschaft
  4. Agence National de la Recherche
  5. Association pour la Recherche contre le Cancer

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The let-413/scribble and dlg-1/discs large genes are key regulators of epithelial cell polarity in C. elegans and other systems but the mechanism how they organize a circumferential junctional belt around the apex of epithelial cells is not well understood. We report here that IP3/Ca2+ signaling is involved in the let-413/dlg-1 pathway for the establishment of epithelial cell polarity during the development in C elegans. Using RNAi to interfere with let-413 and dlg-1 gene functions during post-embryogenesis, we discovered a requirement for LET-413 and DLG-1 in the polarization of the spermathecal cells. The spermatheca forms an accordion-like organ through which eggs must enter to complete the ovulation process. LET-413- and DLG-1-depleted animals exhibit failure of ovulation. Consistent with this phenotype, the assembly of the apical junction into a continuous belt fails and the PAR-3 protein and microfilaments are no longer localized asymmetrically. All these defects can be suppressed by mutations in IPP-5, an inositol polyphosphate 5-phosphatase and in ITR-1, an inositol triphosphate receptor, which both are supposed to increase the intracellular Ca2+ level. Analysis of embryogenesis revealed that IP3/Ca2+ signaling is also required during junction assembly in embryonic epithelia. (C) 2008 Elsevier Inc. All rights reserved.

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