Literature DB >> 12091302

The zebrafish T-box genes no tail and spadetail are required for development of trunk and tail mesoderm and medial floor plate.

Sharon L Amacher1, Bruce W Draper, Brian R Summers, Charles B Kimmel.   

Abstract

T-box genes encode transcriptional regulators that control many aspects of embryonic development. Here, we demonstrate that the mesodermally expressed zebrafish spadetail (spt)/VegT and no tail (ntl)/Brachyury T-box genes are semi-redundantly and cell-autonomously required for formation of all trunk and tail mesoderm. Despite the lack of posterior mesoderm in spt(-);ntl(-) embryos, dorsal-ventral neural tube patterning is relatively normal, with the notable exception that posterior medial floor plate is completely absent. This contrasts sharply with observations in single mutants, as mutations singly in ntl or spt enhance posterior medial floor plate development. We find that ntl function is required to repress medial floor plate and promote notochord fate in cells of the wild-type notochord domain and that spt and ntl together are required non cell-autonomously for medial floor plate formation, suggesting that an inducing signal present in wild-type mesoderm is lacking in spt(-);ntl(-) embryos.

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Year:  2002        PMID: 12091302     DOI: 10.1242/dev.129.14.3311

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


  55 in total

Review 1.  T-box genes in early embryogenesis.

Authors:  Chris Showell; Olav Binder; Frank L Conlon
Journal:  Dev Dyn       Date:  2004-01       Impact factor: 3.780

2.  An interacting network of T-box genes directs gene expression and fate in the zebrafish mesoderm.

Authors:  Lisa M Goering; Kazuyuki Hoshijima; Barbara Hug; Brent Bisgrove; Andreas Kispert; David Jonah Grunwald
Journal:  Proc Natl Acad Sci U S A       Date:  2003-07-25       Impact factor: 11.205

3.  Medial floor plate formation in zebrafish consists of two phases and requires trunk-derived Midkine-a.

Authors:  Matthias Schäfer; Martina Rembold; Joachim Wittbrodt; Manfred Schartl; Christoph Winkler
Journal:  Genes Dev       Date:  2005-04-15       Impact factor: 11.361

4.  nanos1 is required to maintain oocyte production in adult zebrafish.

Authors:  Bruce W Draper; Claire M McCallum; Cecilia B Moens
Journal:  Dev Biol       Date:  2007-03-13       Impact factor: 3.582

5.  Identification of direct T-box target genes in the developing zebrafish mesoderm.

Authors:  Aaron T Garnett; Tina M Han; Michael J Gilchrist; James C Smith; Michael B Eisen; Fiona C Wardle; Sharon L Amacher
Journal:  Development       Date:  2009-01-21       Impact factor: 6.868

6.  Wnt signaling and tbx16 form a bistable switch to commit bipotential progenitors to mesoderm.

Authors:  Cortney M Bouldin; Alyssa J Manning; Yu-Hsuan Peng; Gist H Farr; King L Hung; Alice Dong; David Kimelman
Journal:  Development       Date:  2015-06-10       Impact factor: 6.868

Review 7.  Kidney organogenesis in the zebrafish: insights into vertebrate nephrogenesis and regeneration.

Authors:  Gary F Gerlach; Rebecca A Wingert
Journal:  Wiley Interdiscip Rev Dev Biol       Date:  2012-10-16       Impact factor: 5.814

Review 8.  Using zebrafish to study podocyte genesis during kidney development and regeneration.

Authors:  Paul T Kroeger; Rebecca A Wingert
Journal:  Genesis       Date:  2014-06-25       Impact factor: 2.487

9.  No tail co-operates with non-canonical Wnt signaling to regulate posterior body morphogenesis in zebrafish.

Authors:  Florence Marlow; Encina M Gonzalez; Chunyue Yin; Concepcion Rojo; Lilianna Solnica-Krezel
Journal:  Development       Date:  2003-12-03       Impact factor: 6.868

10.  Versatile synthesis and rational design of caged morpholinos.

Authors:  Xiaohu Ouyang; Ilya A Shestopalov; Surajit Sinha; Genhua Zheng; Cameron L W Pitt; Wen-Hong Li; Andrew J Olson; James K Chen
Journal:  J Am Chem Soc       Date:  2009-09-23       Impact factor: 15.419

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