Literature DB >> 17724731

Tfap2 transcription factors in zebrafish neural crest development and ectodermal evolution.

Trevor L Hoffman1, Anna L Javier, Shelley A Campeau, Robert D Knight, Thomas F Schilling.   

Abstract

Transcription factor AP2 (Tfap2) genes play essential roles in development of the epidermis and migratory cells of the neural crest (NC) in vertebrate embryos. These transcriptional activators are among the earliest genes expressed in the ectoderm and specify fates within the epidermis/crest through both direct and indirect mechanisms. The Tfap2 family arose from a single ancestral gene in a chordate ancestor that underwent gene duplication to give up to five family members in living vertebrates. This coincided with the acquisition of important roles in NC development by Tfap2 genes suggesting that this gene family was important in ectodermal evolution and possibly in the origin of NC. Here, we show that a zebrafish tfap2c is expressed in the nonneural ectoderm during early development and functions redundantly with tfap2a in NC specification. In zebrafish embryos depleted of both tfap2a and tfap2c, NC cells are virtually eliminated. Cell transplantation experiments indicate that tfap2c functions cell-autonomously in NC specification. Cells of the enveloping layer, which forms a temporary skin layer surrounding the ectoderm, also fail to differentiate or to express appropriate keratins in tfap2c deficient embryos. The role of Tfap2 genes in epidermal and NC development is considered here in the broader context of ectodermal evolution. Distinct, tissue-specific functions for Tfap2 genes in different vertebrates may reflect subfunctionalisation of an ancestral gene that consequently led to the gain of novel roles for different subfamily members in patterning the epidermis and NC. Copyright 2007 Wiley-Liss, Inc.

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Year:  2007        PMID: 17724731     DOI: 10.1002/jez.b.21189

Source DB:  PubMed          Journal:  J Exp Zool B Mol Dev Evol        ISSN: 1552-5007            Impact factor:   2.656


  60 in total

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Review 3.  The role of foxi family transcription factors in the development of the ear and jaw.

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4.  Establishment of transgenic lines to monitor and manipulate Yap/Taz-Tead activity in zebrafish reveals both evolutionarily conserved and divergent functions of the Hippo pathway.

Authors:  Joel B Miesfeld; Brian A Link
Journal:  Mech Dev       Date:  2014-02-19       Impact factor: 1.882

Review 5.  Setting appropriate boundaries: fate, patterning and competence at the neural plate border.

Authors:  Andrew K Groves; Carole LaBonne
Journal:  Dev Biol       Date:  2013-12-07       Impact factor: 3.582

6.  Inhibition of neural crest formation by Kctd15 involves regulation of transcription factor AP-2.

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Journal:  Proc Natl Acad Sci U S A       Date:  2013-02-04       Impact factor: 11.205

7.  tp53-dependent and independent signaling underlies the pathogenesis and possible prevention of Acrofacial Dysostosis-Cincinnati type.

Authors:  Kristin E N Watt; Cynthia L Neben; Shawn Hall; Amy E Merrill; Paul A Trainor
Journal:  Hum Mol Genet       Date:  2018-08-01       Impact factor: 6.150

8.  Acrofacial Dysostosis, Cincinnati Type, a Mandibulofacial Dysostosis Syndrome with Limb Anomalies, Is Caused by POLR1A Dysfunction.

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Journal:  Am J Hum Genet       Date:  2015-04-23       Impact factor: 11.025

Review 9.  The molecular basis of craniofacial placode development.

Authors:  Sunita Singh; Andrew K Groves
Journal:  Wiley Interdiscip Rev Dev Biol       Date:  2016-03-07       Impact factor: 5.814

10.  Netrin-DCC, Robo-Slit, and heparan sulfate proteoglycans coordinate lateral positioning of longitudinal dopaminergic diencephalospinal axons.

Authors:  Edda Kastenhuber; Ursula Kern; Joshua L Bonkowsky; Chi-Bin Chien; Wolfgang Driever; Joern Schweitzer
Journal:  J Neurosci       Date:  2009-07-15       Impact factor: 6.167

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