Nematodes join the family of chondroitin sulfate-synthesizing organisms: Identification of an active chondroitin sulfotransferase in Caenorhabditis elegans Show others and affiliations
2016 (English) In: Scientific Reports, E-ISSN 2045-2322, Vol. 6, no 1, article id 34662Article in journal (Refereed) Published
Abstract [en]
Proteoglycans are proteins that carry sulfated glycosaminoglycans (GAGs). They help form and maintain morphogen gradients, guiding cell migration and differentiation during animal development. While no sulfated GAGs have been found in marine sponges, chondroitin sulfate (CS) and heparan sulfate (HS) have been identified in Cnidarians, Lophotrocozoans and Ecdysozoans. The general view that nematodes such as Caenorhabditis elegans , which belong to Ecdysozoa, produce HS but only chondroitin without sulfation has therefore been puzzling. We have analyzed GAGs in C. elegans using reversed-phase ion-pairing HPLC, mass spectrometry and immunohistochemistry. Our analyses included wild type C. elegans but also a mutant lacking two HS sulfotransferases (hst-6 hst-2 ), as we suspected that the altered HS structure could boost CS sulfation. We could indeed detect sulfated CS in both wild type and mutant nematodes. While 4-O-sulfation of galactosamine dominated, we also detected 6-O-sulfated galactosamine residues. Finally, we identified the product of the gene C41C4.1 as a C. elegans CS-sulfotransferase and renamed it chst-1 (CarboHydrate SulfoTransferase) based on loss of CS-4-O-sulfation in a C41C4.1 mutant and in vitro sulfotransferase activity of recombinant C41C4.1 protein. We conclude that C. elegans indeed manufactures CS, making this widely used nematode an interesting model for developmental studies involving CS.
Place, publisher, year, edition, pages Springer Nature, 2016. Vol. 6, no 1, article id 34662
National Category
Molecular Biology Cell and Molecular Biology
Identifiers URN: urn:nbn:se:his:diva-25806 DOI: 10.1038/srep34662 ISI: 000384654100001 PubMedID: 27703236 Scopus ID: 2-s2.0-84989856164 OAI: oai:DiVA.org:his-25806 DiVA, id: diva2:1995376
Funder Swedish Research Council NIH (National Institutes of Health), P41GM104603
Note CC BY 4.0
Funding was provided by the Swedish Research Council (to L.K.), by the German Academic Exchange Service (to T.D.), by Stiftelsen för Proteoglykanforskning (to L.K.) and the U.S. National Institutes for Health grant number P41GM104603 (to J. Z). The authors thank Inger Eriksson and Anders Lundequist for their support with cell culture work, as well as Anders Malmström for providing the K4 polysaccharide enzyme substrate.
2025-09-052025-09-052025-11-12 Bibliographically approved