Literature DB >> 19369398

Short- and long-range functions of Goosecoid in zebrafish axis formation are independent of Chordin, Noggin 1 and Follistatin-like 1b.

Monica Dixon Fox1, Ashley E E Bruce.   

Abstract

The organizer is essential for dorsal-ventral (DV) patterning in vertebrates. Goosecoid (Gsc), a transcriptional repressor found in the organizer, elicits partial secondary axes when expressed ventrally in Xenopus, similar to an organizer transplant. Although gsc is expressed in all vertebrate organizers examined, knockout studies in mouse suggested that it is not required for DV patterning. Moreover, experiments in Xenopus and zebrafish suggest a role in head formation, although a function in axial mesoderm formation is less clear. To clarify the role of Gsc in vertebrate development, we used gain- and loss-of-function approaches in zebrafish. Ventral injection of low doses of gsc produced incomplete secondary axes, which we propose results from short-range repression of BMP signaling. Higher gsc doses resulted in complete secondary axes and long-range signaling, correlating with repression of BMP and Wnt signals. In striking contrast to Xenopus, the BMP inhibitor Chordin (Chd) is not required for Gsc function. Gsc produced complete secondary axes in chd null mutant embryos and gsc-morpholino knockdown in chd mutants enhanced the mutant phenotype, suggesting that Gsc has Chd-independent functions in DV patterning. Even more striking was that Gsc elicited complete secondary axes in the absence of three secreted BMP antagonists, Chd, Follistatin-like 1b and Noggin 1, suggesting that Gsc functions in parallel with secreted BMP inhibitors. Our findings suggest that Gsc has dose dependent effects on axis induction and provide new insights into molecularly distinct short- and long-range signaling activities of the organizer.

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Year:  2009        PMID: 19369398     DOI: 10.1242/dev.031161

Source DB:  PubMed          Journal:  Development        ISSN: 0950-1991            Impact factor:   6.868


  8 in total

Review 1.  Temporally coordinated signals progressively pattern the anteroposterior and dorsoventral body axes.

Authors:  Francesca B Tuazon; Mary C Mullins
Journal:  Semin Cell Dev Biol       Date:  2015-06-27       Impact factor: 7.727

2.  Split top: a maternal cathepsin B that regulates dorsoventral patterning and morphogenesis.

Authors:  Yvette G Langdon; Ricardo Fuentes; Hong Zhang; Elliott W Abrams; Florence L Marlow; Mary C Mullins
Journal:  Development       Date:  2016-02-18       Impact factor: 6.868

3.  Correct anteroposterior patterning of the zebrafish neurectoderm in the absence of the early dorsal organizer.

Authors:  Máté Varga; Shingo Maegawa; Eric S Weinberg
Journal:  BMC Dev Biol       Date:  2011-05-16       Impact factor: 1.978

4.  A novel role of the organizer gene Goosecoid as an inhibitor of Wnt/PCP-mediated convergent extension in Xenopus and mouse.

Authors:  Bärbel Ulmer; Melanie Tingler; Sabrina Kurz; Markus Maerker; Philipp Andre; Dina Mönch; Marina Campione; Kirsten Deißler; Mark Lewandoski; Thomas Thumberger; Axel Schweickert; Abraham Fainsod; Herbert Steinbeißer; Martin Blum
Journal:  Sci Rep       Date:  2017-02-21       Impact factor: 4.379

5.  march5 Governs the Convergence and Extension Movement for Organization of the Telencephalon and Diencephalon in Zebrafish Embryos.

Authors:  Jangham Jung; Issac Choi; Hyunju Ro; Tae-Lin Huh; Joonho Choe; Myungchull Rhee
Journal:  Mol Cells       Date:  2020-01-31       Impact factor: 5.034

Review 6.  BMP Signaling: Lighting up the Way for Embryonic Dorsoventral Patterning.

Authors:  Yifang Yan; Qiang Wang
Journal:  Front Cell Dev Biol       Date:  2021-12-23

7.  Goosecoid Controls Neuroectoderm Specification via Dual Circuits of Direct Repression and Indirect Stimulation in Xenopus Embryos.

Authors:  Zobia Umair; Vijay Kumar; Ravi Shankar Goutam; Shiv Kumar; Unjoo Lee; Jaebong Kim
Journal:  Mol Cells       Date:  2021-10-31       Impact factor: 5.034

8.  Formation of the embryonic organizer is restricted by the competitive influences of Fgf signaling and the SoxB1 transcription factors.

Authors:  Cheng-Liang Kuo; Chi Man Lam; Jane E Hewitt; Paul J Scotting
Journal:  PLoS One       Date:  2013-02-28       Impact factor: 3.240

  8 in total

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