Literature DB >> 9811573

XBF-1, a winged helix transcription factor with dual activity, has a role in positioning neurogenesis in Xenopus competent ectoderm.

C Bourguignon1, J Li, N Papalopulu.   

Abstract

Neuronal differentiation in the vertebrate nervous system is temporally and spatially controlled by mechanisms which are largely unknown. Here we investigate the role of XBF-1, an anterior neural plate-specific winged helix transcription factor, in controlling the pattern of neurogenesis in Xenopus ectoderm. We show that, in the anterior neural plate of normal embryos, prospective neurogenesis is positioned at the anterior boundary of the XBF-1 expression domain. By misexpressing XBF-1 in the posterior neural plate we show that a high dose of XBF-1 has a dual effect; it suppresses endogenous neuronal differentiation in high expressing cells and induces ectopic neuronal differentiation in adjacent cells. In contrast, a low dose of XBF-1 does not suppress but instead, expands the domain of neuronal differentiation in the lateral and ventral sides of the embryo. XBF-1 regulates the expression of XSox3, X-ngnr-1, X-Myt-1 and X-&Dgr;-1 suggesting that it acts early in the cascade leading to neuronal differentiation. A fusion of XBF-1 to a strong repressor domain (EnR) mimics most of the XBF-1 effects suggesting that the wild type XBF-1 is a transcriptional repressor. However, fusion of XBF-1 to a strong activation domain (E1A) specifically suppresses neuronal differentiation suggesting that XBF-1 may also work as a transcriptional activator. Based on these findings, we propose that XBF-1 is involved in positioning neuronal differentiation by virtue of its concentration dependent, dual activity, as a suppressor and an activator of neurogenesis.

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Year:  1998        PMID: 9811573     DOI: 10.1242/dev.125.24.4889

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


  37 in total

1.  Complementary expression of AP-2 and AP-2rep in ectodermal derivatives of Xenopus embryos.

Authors:  Masanori Gotoh; Yumi Izutsu; Mitsugu Maéno
Journal:  Dev Genes Evol       Date:  2003-05-17       Impact factor: 0.900

2.  Transducin-like enhancer of Split-1 (TLE1) combines with Forkhead box protein G1 (FoxG1) to promote neuronal survival.

Authors:  Somasish Ghosh Dastidar; Sriram Narayanan; Stefano Stifani; Santosh R D'Mello
Journal:  J Biol Chem       Date:  2012-02-21       Impact factor: 5.157

3.  FoxG1 and TLE2 act cooperatively to regulate ventral telencephalon formation.

Authors:  Martin Roth; Boyan Bonev; Jennefer Lindsay; Robert Lea; Niki Panagiotaki; Corinne Houart; Nancy Papalopulu
Journal:  Development       Date:  2010-03-31       Impact factor: 6.868

4.  FoxG1 promotes the survival of postmitotic neurons.

Authors:  Somasish Ghosh Dastidar; Paul Michael Zagala Landrieu; Santosh R D'Mello
Journal:  J Neurosci       Date:  2011-01-12       Impact factor: 6.167

5.  Endogenous gradients of resting potential instructively pattern embryonic neural tissue via Notch signaling and regulation of proliferation.

Authors:  Vaibhav P Pai; Joan M Lemire; Jean-François Paré; Gufa Lin; Ying Chen; Michael Levin
Journal:  J Neurosci       Date:  2015-03-11       Impact factor: 6.167

6.  The winged-helix protein brain factor 1 interacts with groucho and hes proteins to repress transcription.

Authors:  J Yao; E Lai; S Stifani
Journal:  Mol Cell Biol       Date:  2001-03       Impact factor: 4.272

7.  The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis.

Authors:  Fanny Kortüm; Soma Das; Max Flindt; Deborah J Morris-Rosendahl; Irina Stefanova; Amy Goldstein; Denise Horn; Eva Klopocki; Gerhard Kluger; Peter Martin; Anita Rauch; Agathe Roumer; Sulagna Saitta; Laurence E Walsh; Dagmar Wieczorek; Gökhan Uyanik; Kerstin Kutsche; William B Dobyns
Journal:  J Med Genet       Date:  2011-03-25       Impact factor: 6.318

8.  Choice of either beta-catenin or Groucho/TLE as a co-factor for Xtcf-3 determines dorsal-ventral cell fate of diencephalon during Xenopus development.

Authors:  Saori Tsuji; Chikara Hashimoto
Journal:  Dev Genes Evol       Date:  2005-03-04       Impact factor: 0.900

9.  The transcription factor Foxg1 regulates the competence of telencephalic cells to adopt subpallial fates in mice.

Authors:  Martine Manuel; Ben Martynoga; Tian Yu; John D West; John O Mason; David J Price
Journal:  Development       Date:  2010-02       Impact factor: 6.868

10.  Anxa4 Genes are Expressed in Distinct Organ Systems in Xenopus laevis and tropicalis But are Functionally Conserved.

Authors:  Karine L Massé; Robert J Collins; Surinder Bhamra; Rachel A Seville; Elizabeth A Jones
Journal:  Organogenesis       Date:  2007-10       Impact factor: 2.500

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