Chondroitin / dermatan sulfate modification enzymes in zebrafish development.

Chondroitin/dermatan sulfate (CS/DS) proteoglycans consist of unbranched sulfated polysaccharide chains of repeating GalNAc-GlcA/IdoA disaccharide units, attached to serine residues on specific proteins. The CS/DS proteoglycans are abundant in the extracellular matrix where they have essential funct...

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Main Authors: Judith Habicher, Tatjana Haitina, Inger Eriksson, Katarina Holmborn, Tabea Dierker, Per E Ahlberg, Johan Ledin
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4368567?pdf=render
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spelling doaj-2afd56c138f4412b83f708e1603897a02020-11-24T21:50:47ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-01103e012195710.1371/journal.pone.0121957Chondroitin / dermatan sulfate modification enzymes in zebrafish development.Judith HabicherTatjana HaitinaInger ErikssonKatarina HolmbornTabea DierkerPer E AhlbergJohan LedinChondroitin/dermatan sulfate (CS/DS) proteoglycans consist of unbranched sulfated polysaccharide chains of repeating GalNAc-GlcA/IdoA disaccharide units, attached to serine residues on specific proteins. The CS/DS proteoglycans are abundant in the extracellular matrix where they have essential functions in tissue development and homeostasis. In this report a phylogenetic analysis of vertebrate genes coding for the enzymes that modify CS/DS is presented. We identify single orthologous genes in the zebrafish genome for the sulfotransferases chst7, chst11, chst13, chst14, chst15 and ust and the epimerase dse. In contrast, two copies were found for mammalian sulfotransferases CHST3 and CHST12 and the epimerase DSEL, named chst3a and chst3b, chst12a and chst12b, dsela and dselb, respectively. Expression of CS/DS modification enzymes is spatially and temporally regulated with a large variation between different genes. We found that CS/DS 4-O-sulfotransferases and 6-O-sulfotransferases as well as CS/DS epimerases show a strong and partly overlapping expression, whereas the expression is restricted for enzymes with ability to synthesize di-sulfated disaccharides. A structural analysis further showed that CS/DS sulfation increases during embryonic development mainly due to synthesis of 4-O-sulfated GalNAc while the proportion of 6-O-sulfated GalNAc increases in later developmental stages. Di-sulfated GalNAc synthesized by Chst15 and 2-O-sulfated GlcA/IdoA synthesized by Ust are rare, in accordance with the restricted expression of these enzymes. We also compared CS/DS composition with that of heparan sulfate (HS). Notably, CS/DS biosynthesis in early zebrafish development is more dynamic than HS biosynthesis. Furthermore, HS contains disaccharides with more than one sulfate group, which are virtually absent in CS/DS.http://europepmc.org/articles/PMC4368567?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Judith Habicher
Tatjana Haitina
Inger Eriksson
Katarina Holmborn
Tabea Dierker
Per E Ahlberg
Johan Ledin
spellingShingle Judith Habicher
Tatjana Haitina
Inger Eriksson
Katarina Holmborn
Tabea Dierker
Per E Ahlberg
Johan Ledin
Chondroitin / dermatan sulfate modification enzymes in zebrafish development.
PLoS ONE
author_facet Judith Habicher
Tatjana Haitina
Inger Eriksson
Katarina Holmborn
Tabea Dierker
Per E Ahlberg
Johan Ledin
author_sort Judith Habicher
title Chondroitin / dermatan sulfate modification enzymes in zebrafish development.
title_short Chondroitin / dermatan sulfate modification enzymes in zebrafish development.
title_full Chondroitin / dermatan sulfate modification enzymes in zebrafish development.
title_fullStr Chondroitin / dermatan sulfate modification enzymes in zebrafish development.
title_full_unstemmed Chondroitin / dermatan sulfate modification enzymes in zebrafish development.
title_sort chondroitin / dermatan sulfate modification enzymes in zebrafish development.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2015-01-01
description Chondroitin/dermatan sulfate (CS/DS) proteoglycans consist of unbranched sulfated polysaccharide chains of repeating GalNAc-GlcA/IdoA disaccharide units, attached to serine residues on specific proteins. The CS/DS proteoglycans are abundant in the extracellular matrix where they have essential functions in tissue development and homeostasis. In this report a phylogenetic analysis of vertebrate genes coding for the enzymes that modify CS/DS is presented. We identify single orthologous genes in the zebrafish genome for the sulfotransferases chst7, chst11, chst13, chst14, chst15 and ust and the epimerase dse. In contrast, two copies were found for mammalian sulfotransferases CHST3 and CHST12 and the epimerase DSEL, named chst3a and chst3b, chst12a and chst12b, dsela and dselb, respectively. Expression of CS/DS modification enzymes is spatially and temporally regulated with a large variation between different genes. We found that CS/DS 4-O-sulfotransferases and 6-O-sulfotransferases as well as CS/DS epimerases show a strong and partly overlapping expression, whereas the expression is restricted for enzymes with ability to synthesize di-sulfated disaccharides. A structural analysis further showed that CS/DS sulfation increases during embryonic development mainly due to synthesis of 4-O-sulfated GalNAc while the proportion of 6-O-sulfated GalNAc increases in later developmental stages. Di-sulfated GalNAc synthesized by Chst15 and 2-O-sulfated GlcA/IdoA synthesized by Ust are rare, in accordance with the restricted expression of these enzymes. We also compared CS/DS composition with that of heparan sulfate (HS). Notably, CS/DS biosynthesis in early zebrafish development is more dynamic than HS biosynthesis. Furthermore, HS contains disaccharides with more than one sulfate group, which are virtually absent in CS/DS.
url http://europepmc.org/articles/PMC4368567?pdf=render
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