Högskolan i Skövde

his.sePublications
System disruptions
There are recurring service disruptions on some of the search portals due to high traffic. We are working to resolve the issue, you may temporarily encounter an error message.
Change search
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • apa-cv
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf
Nematodes join the family of chondroitin sulfate-synthesizing organisms: Identification of an active chondroitin sulfotransferase in Caenorhabditis elegans
Department of Medical Biochemistry and Microbiology, Science for Life Laboratory, Uppsala University, Sweden.ORCID iD: 0000-0003-1991-2723
Department of Biochemistry, Center for Biomedical Mass Spectrometry, Boston University Medical Campus, Boston, USA.
Department of Organismal Biology, Science for Life Laboratory, Uppsala University, Sweden.
Department of Biochemistry, Center for Biomedical Mass Spectrometry, Boston University Medical Campus, USA.
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-25806DOI: 10.1038/srep34662ISI: 000384654100001PubMedID: 27703236Scopus ID: 2-s2.0-84989856164OAI: oai:DiVA.org:his-25806DiVA, id: diva2:1995376
Funder
Swedish Research CouncilNIH (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.

Available from: 2025-09-05 Created: 2025-09-05 Last updated: 2025-11-12Bibliographically approved

Open Access in DiVA

fulltext(237 kB)129 downloads
File information
File name FULLTEXT01.pdfFile size 237 kBChecksum SHA-512
4110582ff21ab174ce1da7a9d141793167d3084a5f12ff2173fa7f454dbe8d5b2ab6d882dd22d5408da28cde2e3a0bf60206dc1d427ac5d8a7524bf1888f17d7
Type fulltextMimetype application/pdf

Other links

Publisher's full textPubMedScopus

Authority records

Dierker, Tabea

Search in DiVA

By author/editor
Dierker, Tabea
In the same journal
Scientific Reports
Molecular BiologyCell and Molecular Biology

Search outside of DiVA

GoogleGoogle Scholar
Total: 130 downloads
The number of downloads is the sum of all downloads of full texts. It may include eg previous versions that are now no longer available

doi
pubmed
urn-nbn

Altmetric score

doi
pubmed
urn-nbn
Total: 364 hits
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • apa-cv
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf