Literature DB >> 21056656

Oral-aboral patterning and gastrulation of sea urchin embryos depend on sulfated glycosaminoglycans.

Karl-Frederik Bergeron1, Xing Xu, Bruce P Brandhorst.   

Abstract

Glycosaminoglycans (GAGs) are a heavily sulfated component of the extracellular matrix (ECM) implicated in a variety of cell signaling events involved in patterning of embryos. Embryos of the sea urchin Strongylocentrotus purpuratus were exposed to several inhibitors that disrupt GAG function during development. Treatment with chlorate, a general inhibitor of sulfation that leads to undersulfated GAGs, reduced sulfation of the urchin blastocoelar ECM. It also prevented correct specification of the oral-aboral axis and mouth formation, resulting in a radialized phenotype characterized by the lack of an oral field, incomplete gastrulation and formation of multiple skeletal spicule rudiments. Oral markers were initially expressed in most of the prospective ectoderm of chlorate-treated early blastulae, but then declined as aboral markers became expressed throughout most of the ectoderm. Nodal expression in the presumptive oral field is necessary and sufficient to specify the oral-aboral axis in urchins. Several lines of evidence suggest a deregulation of Nodal signaling is involved in the radialization caused by chlorate: (1) Radial embryos resemble those in which Nodal expression was knocked down. (2) Chlorate disrupted localized nodal expression in oral ectoderm, even when applied after the oral-aboral axis is specified and expression of other oral markers is resistant to treatment. (3) Inhibition with SB-431542 of ALK-4/5/7 receptors that mediate Nodal signaling causes defects in ectodermal patterning similar to those caused by chlorate. (4) Intriguingly, treatment of embryos with a sub-threshold dose of SB-431542 rescued the radialization caused by low concentrations of chlorate. Our results indicate important roles for sulfated GAGs in Nodal signaling and oral-aboral axial patterning, and in the cellular processes necessary for archenteron extension and mouth formation during gastrulation. We propose that interaction of the Nodal ligand with sulfated GAGs limits its diffusion, and is required to specify an oral field in the urchin embryo and organize the oral-aboral axis.
Copyright © 2010 Elsevier Ireland Ltd. All rights reserved.

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Year:  2010        PMID: 21056656     DOI: 10.1016/j.mod.2010.11.001

Source DB:  PubMed          Journal:  Mech Dev        ISSN: 0925-4773            Impact factor:   1.882


  10 in total

1.  Axial patterning interactions in the sea urchin embryo: suppression of nodal by Wnt1 signaling.

Authors:  Zheng Wei; Ryan Range; Robert Angerer; Lynne Angerer
Journal:  Development       Date:  2012-03-21       Impact factor: 6.868

2.  Direct and indirect control of oral ectoderm regulatory gene expression by Nodal signaling in the sea urchin embryo.

Authors:  Enhu Li; Stefan C Materna; Eric H Davidson
Journal:  Dev Biol       Date:  2012-07-06       Impact factor: 3.582

Review 3.  The evolution of nervous system patterning: insights from sea urchin development.

Authors:  Lynne M Angerer; Shunsuke Yaguchi; Robert C Angerer; Robert D Burke
Journal:  Development       Date:  2011-09       Impact factor: 6.868

4.  HpSumf1 is involved in the activation of sulfatases responsible for regulation of skeletogenesis during sea urchin development.

Authors:  Tetsushi Sakuma; Kazuya Ohnishi; Kazumasa Fujita; Hiroshi Ochiai; Naoaki Sakamoto; Takashi Yamamoto
Journal:  Dev Genes Evol       Date:  2011-06-27       Impact factor: 0.900

5.  A Proteoglycan-Like Molecule Offers Insights Into Ground Substance Changes During Holothurian Intestinal Regeneration.

Authors:  Gabriel E Vázquez-Vélez; José F Rodríguez-Molina; Mónica C Quiñones-Frías; María Pagán; José E García-Arrarás
Journal:  J Histochem Cytochem       Date:  2016-04-28       Impact factor: 2.479

6.  Brittlestars contain highly sulfated chondroitin sulfates/dermatan sulfates that promote fibroblast growth factor 2-induced cell signaling.

Authors:  Rashmi Ramachandra; Ramesh B Namburi; Olga Ortega-Martinez; Xiaofeng Shi; Joseph Zaia; Sam T Dupont; Michael C Thorndyke; Ulf Lindahl; Dorothe Spillmann
Journal:  Glycobiology       Date:  2013-11-18       Impact factor: 4.313

7.  Nodal-mediated epigenesis requires dynamin-mediated endocytosis.

Authors:  Robin P Ertl; Anthony J Robertson; Diane Saunders; James A Coffman
Journal:  Dev Dyn       Date:  2011-02-08       Impact factor: 3.780

8.  Early asymmetric cues triggering the dorsal/ventral gene regulatory network of the sea urchin embryo.

Authors:  Vincenzo Cavalieri; Giovanni Spinelli
Journal:  Elife       Date:  2014-12-02       Impact factor: 8.140

9.  A model-based approach to designing developmental toxicology experiments using sea urchin embryos.

Authors:  Michael D Collins; Elvis Han Cui; Seung Won Hyun; Weng Kee Wong
Journal:  Arch Toxicol       Date:  2022-01-13       Impact factor: 5.153

10.  Functional divergence of paralogous transcription factors supported the evolution of biomineralization in echinoderms.

Authors:  Jian Ming Khor; Charles A Ettensohn
Journal:  Elife       Date:  2017-11-20       Impact factor: 8.140

  10 in total

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