Identification of novel chondroitin proteoglycans in Caenorhabditis elegans: embryonic cell division depends on CPG-1 and CPG-2

Author:

Olson Sara K.12,Bishop Joseph R.1,Yates John R.3,Oegema Karen14,Esko Jeffrey D.1

Affiliation:

1. Department of Cellular and Molecular Medicine, Glycobiology Research and Training Center

2. Biomedical Sciences Graduate Program, School of Medicine,

3. Department of Cell Biology, The Scripps Research Institute, La Jolla, CA 92037

4. Ludwig Institute for Cancer Research, University of California, San Diego, La Jolla, CA 92093

Abstract

Vertebrates produce multiple chondroitin sulfate proteoglycans that play important roles in development and tissue mechanics. In the nematode Caenorhabditis elegans, the chondroitin chains lack sulfate but nevertheless play essential roles in embryonic development and vulval morphogenesis. However, assignment of these functions to specific proteoglycans has been limited by the lack of identified core proteins. We used a combination of biochemical purification, Western blotting, and mass spectrometry to identify nine C. elegans chondroitin proteoglycan core proteins, none of which have homologues in vertebrates or other invertebrates such as Drosophila melanogaster or Hydra vulgaris. CPG-1/CEJ-1 and CPG-2 are expressed during embryonic development and bind chitin, suggesting a structural role in the egg. RNA interference (RNAi) depletion of individual CPGs had no effect on embryonic viability, but simultaneous depletion of CPG-1/CEJ-1 and CPG-2 resulted in multinucleated single-cell embryos. This embryonic lethality phenocopies RNAi depletion of the SQV-5 chondroitin synthase, suggesting that chondroitin chains on these two proteoglycans are required for cytokinesis.

Publisher

Rockefeller University Press

Subject

Cell Biology

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