The NDST gene family in zebrafish: role of NDST1B in pharyngeal arch formation

PLoS One. 2015 Mar 13;10(3):e0119040. doi: 10.1371/journal.pone.0119040. eCollection 2015.

Abstract

Heparan sulfate (HS) proteoglycans are ubiquitous components of the extracellular matrix and plasma membrane of metazoans. The sulfation pattern of the HS glycosaminoglycan chain is characteristic for each tissue and changes during development. The glucosaminyl N-deacetylase/N-sulfotransferase (NDST) enzymes catalyze N-deacetylation and N-sulfation during HS biosynthesis and have a key role in designing the sulfation pattern. We here report on the presence of five NDST genes in zebrafish. Zebrafish ndst1a, ndst1b, ndst2a and ndst2b represent duplicated mammalian orthologues of NDST1 and NDST2 that arose through teleost specific genome duplication. Interestingly, the single zebrafish orthologue ndst3, is equally similar to tetrapod Ndst3 and Ndst4. It is likely that a local duplication in the common ancestor of lobe-finned fish and tetrapods gave rise to these two genes. All zebrafish Ndst genes showed distinct but partially overlapping expression patterns during embryonic development. Morpholino knockdown of ndst1b resulted in delayed development, craniofacial cartilage abnormalities, shortened body and pectoral fin length, resembling some of the features of the Ndst1 mouse knockout.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amidohydrolases / metabolism
  • Animals
  • Branchial Region / metabolism
  • Branchial Region / physiology*
  • Fish Proteins / genetics*
  • Fish Proteins / metabolism
  • Glycosaminoglycans / metabolism
  • Heparitin Sulfate / metabolism
  • Mice
  • Mice, Knockout
  • Phylogeny
  • Sulfotransferases / genetics*
  • Sulfotransferases / metabolism
  • Zebrafish / genetics*
  • Zebrafish / metabolism

Substances

  • Fish Proteins
  • Glycosaminoglycans
  • Heparitin Sulfate
  • Sulfotransferases
  • Amidohydrolases
  • N-acetylglucosamine deacetylase

Grants and funding

This work was supported by grants from the Knut and Alice Wallenberg Foundation (to J.L.), the Swedish Research Council (to T.H., J.L., L.K.), the Linnaeus Framework Grant “Genomics of Phenotypic Diversity in Natural Populations” (to J.L.), the Swedish Cancer Society (L.K.), Stiftelsen för Proteoglykanforskning (L.K.), and Uppsala University (to J.L. and L.K.). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.