Literature DB >> 9584120

Combinatorial Gli gene function in floor plate and neuronal inductions by Sonic hedgehog.

A Ruiz i Altaba1.   

Abstract

Within the developing vertebrate nervous system, it is not known how progenitor cells interpret the positional information provided by inducing signals or how the domains in which distinct groups of neural cells differentiate are defined. Gli proteins may be involved in these processes. In the frog neural plate, we have previously shown that the zinc finger transcription factor Gli1 is expressed in midline cells and mediates the effects of Shh inducing floor plate differentiation. In contrast, Gli2 and Gli3 are expressed throughout the neural plate except for the midline. Here, it is shown that Gli3 and Shh repress each other whereas Gli2, like Gli1, is a target of Shh signaling. However, only Gli1 can induce the differentiation of floor plate cells. In addition, Gli2 and Gli3 repress the ectopic induction of floor plate cells by Gli1 in co-injection assays and inhibit endogenous floor plate differentiation. The definition of the floor plate domain, therefore, appears to be defined by the antagonizing activities of Gli2 and Gli3 on Gli1 function. Because both Gli1 and Gli2 are induced by Shh, these results establish a regulatory feedback loop triggered by Shh that restricts floor plate cells to the midline. We have also previously shown that the Gli genes induce neuronal differentiation and here it is shown that there is specificity to the types of neurons the Gli proteins induce. Only Gli1 induces Nkx2.1/TTF-1(+) ventral forebrain neurons. Moreover, Gli2 and Gli3 inhibit their differentiation. In contrast, the differentiation of spinal motor neurons can be induced by the two ventrally expressed Gli genes, Gli1 and Gli2, suggesting that Gli2 directly mediates induction of motor neurons by Shh. In addition, Gli3 inhibits motor neuron differentiation by Gli2. Thus, combinatorial Gli function may pattern the neural tube, integrating positional information and cell type differentiation.

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Year:  1998        PMID: 9584120     DOI: 10.1242/dev.125.12.2203

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


  77 in total

Review 1.  Molecular mechanisms regulating motor neuron development and degeneration.

Authors:  T J Kilpatrick; M Soilu-Hänninen
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Review 2.  The sonic hedgehog-patched-gli pathway in human development and disease.

Authors:  E H Villavicencio; D O Walterhouse; P M Iannaccone
Journal:  Am J Hum Genet       Date:  2000-09-21       Impact factor: 11.025

Review 3.  Patterning the limb before and after SHH signalling.

Authors:  Lia Panman; Rolf Zeller
Journal:  J Anat       Date:  2003-01       Impact factor: 2.610

Review 4.  Turning heads: development of vertebrate branchiomotor neurons.

Authors:  Anand Chandrasekhar
Journal:  Dev Dyn       Date:  2004-01       Impact factor: 3.780

Review 5.  Gli proteins and the control of spinal-cord patterning.

Authors:  John Jacob; James Briscoe
Journal:  EMBO Rep       Date:  2003-08       Impact factor: 8.807

6.  The sonic hedgehog signaling system as a bistable genetic switch.

Authors:  Karen Lai; Matthew J Robertson; David V Schaffer
Journal:  Biophys J       Date:  2004-05       Impact factor: 4.033

7.  Cooperative requirement of the Gli proteins in neurogenesis.

Authors:  Vân Nguyen; Ann L Chokas; Barbara Stecca; Ariel Ruiz i Altaba
Journal:  Development       Date:  2005-07       Impact factor: 6.868

8.  Nato3 integrates with the Shh-Foxa2 transcriptional network regulating the differentiation of midbrain dopaminergic neurons.

Authors:  Einat Nissim-Eliraz; Sophie Zisman; Omri Schatz; Nissim Ben-Arie
Journal:  J Mol Neurosci       Date:  2012-12-21       Impact factor: 3.444

Review 9.  Context-dependent regulation of the GLI code in cancer by HEDGEHOG and non-HEDGEHOG signals.

Authors:  Barbara Stecca; Ariel Ruiz i Altaba
Journal:  J Mol Cell Biol       Date:  2010-01-17       Impact factor: 6.216

10.  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

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