Literature DB >> 15030762

Nodal and BMP2/4 signaling organizes the oral-aboral axis of the sea urchin embryo.

Véronique Duboc1, Eric Röttinger, Lydia Besnardeau, Thierry Lepage.   

Abstract

In the sea urchin embryo, the oral-aboral axis is specified after fertilization by mechanisms that are largely unknown. We report that early sea urchin embryos express Nodal and Antivin in the presumptive oral ectoderm and demonstrate that these genes control formation of the oral-aboral axis. Overexpression of nodal converted the whole ectoderm into oral ectoderm and induced ectopic expression of the orally expressed genes goosecoid, brachyury, BMP2/4, and antivin. Conversely, when the function of Nodal was blocked, by injection of an antisense Morpholino oligonucleotide or by injection of antivin mRNA, neither the oral nor the aboral ectoderm were specified. Injection of nodal mRNA into Nodal-deficient embryos induced an oral-aboral axis in a largely non-cell-autonomous manner. These observations suggest that the mechanisms responsible for patterning the oral-aboral axis of the sea urchin embryo may share similarities with mechanisms that pattern the dorsoventral axis of other deuterostomes.

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Year:  2004        PMID: 15030762     DOI: 10.1016/s1534-5807(04)00056-5

Source DB:  PubMed          Journal:  Dev Cell        ISSN: 1534-5807            Impact factor:   12.270


  102 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

3.  Muscle development in Ciona intestinalis requires the b-HLH myogenic regulatory factor gene Ci-MRF.

Authors:  Thomas H Meedel; Patrick Chang; Hitoyoshi Yasuo
Journal:  Dev Biol       Date:  2006-09-29       Impact factor: 3.582

4.  ankAT-1 is a novel gene mediating the apical tuft formation in the sea urchin embryo.

Authors:  Shunsuke Yaguchi; Junko Yaguchi; Zheng Wei; Kogiku Shiba; Lynne M Angerer; Kazuo Inaba
Journal:  Dev Biol       Date:  2010-09-26       Impact factor: 3.582

5.  Cis-regulatory control of the nodal gene, initiator of the sea urchin oral ectoderm gene network.

Authors:  Jongmin Nam; Yi-Hsien Su; Pei Yun Lee; Anthony J Robertson; James A Coffman; Eric H Davidson
Journal:  Dev Biol       Date:  2007-03-28       Impact factor: 3.582

6.  The sea urchin animal pole domain is a Six3-dependent neurogenic patterning center.

Authors:  Zheng Wei; Junko Yaguchi; Shunsuke Yaguchi; Robert C Angerer; Lynne M Angerer
Journal:  Development       Date:  2009-04       Impact factor: 6.868

7.  Turing's theory of morphogenesis of 1952 and the subsequent discovery of the crucial role of local self-enhancement and long-range inhibition.

Authors:  Hans Meinhardt
Journal:  Interface Focus       Date:  2012-02-08       Impact factor: 3.906

8.  Oral-aboral identity displayed in the expression of HpHox3 and HpHox11/13 in the adult rudiment of the sea urchin Holopneustes purpurescens.

Authors:  Valerie B Morris; Maria Byrne
Journal:  Dev Genes Evol       Date:  2013-10-16       Impact factor: 0.900

9.  Short-range Wnt5 signaling initiates specification of sea urchin posterior ectoderm.

Authors:  Daniel C McIntyre; N Winn Seay; Jenifer C Croce; David R McClay
Journal:  Development       Date:  2013-11-13       Impact factor: 6.868

10.  Genetic basis for divergence in developmental gene expression in two closely related sea urchins.

Authors:  Lingyu Wang; Jennifer W Israel; Allison Edgar; Rudolf A Raff; Elizabeth C Raff; Maria Byrne; Gregory A Wray
Journal:  Nat Ecol Evol       Date:  2020-04-13       Impact factor: 15.460

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