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Differential requirements for Gli2 and Gli3 in the regional specification of the mouse hypothalamus

Secreted protein Sonic hedgehog (Shh) ventralizes the neural tube by modulating the crucial balance between activating and repressing functions (GliA, GliR) of transcription factors Gli2 and Gli3. This balance—the Shh-Gli code—is species- and context-dependent and has been elucidated for the mouse s...

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Autores principales: Haddad-Tóvolli, Roberta, Paul, Fabian A., Zhang, Yuanfeng, Zhou, Xunlei, Theil, Thomas, Puelles, Luis, Blaess, Sandra, Alvarez-Bolado, Gonzalo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4373379/
https://www.ncbi.nlm.nih.gov/pubmed/25859185
http://dx.doi.org/10.3389/fnana.2015.00034
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author Haddad-Tóvolli, Roberta
Paul, Fabian A.
Zhang, Yuanfeng
Zhou, Xunlei
Theil, Thomas
Puelles, Luis
Blaess, Sandra
Alvarez-Bolado, Gonzalo
author_facet Haddad-Tóvolli, Roberta
Paul, Fabian A.
Zhang, Yuanfeng
Zhou, Xunlei
Theil, Thomas
Puelles, Luis
Blaess, Sandra
Alvarez-Bolado, Gonzalo
author_sort Haddad-Tóvolli, Roberta
collection PubMed
description Secreted protein Sonic hedgehog (Shh) ventralizes the neural tube by modulating the crucial balance between activating and repressing functions (GliA, GliR) of transcription factors Gli2 and Gli3. This balance—the Shh-Gli code—is species- and context-dependent and has been elucidated for the mouse spinal cord. The hypothalamus, a forebrain region regulating vital functions like homeostasis and hormone secretion, shows dynamic and intricate Shh expression as well as complex regional differentiation. Here we asked if particular combinations of Gli2 and Gli3 and of GliA and GliR functions contribute to the variety of hypothalamic regions, i.e., we wanted to approach the question of a possible hypothalamic version of the Shh-Gli code. Based on mouse mutant analysis, we show that: (1) hypothalamic regional heterogeneity is based in part on differentially stringent requirements for Gli2 or Gli3; (2) another source of diversity are differential requirements for Shh of neural vs. non-neural origin; (3) the medial progenitor domain known to depend on Gli2 for its development generates several essential hypothalamic nuclei plus the pituitary and median eminence; (4) the suppression of Gli3R by neural and non-neural Shh is essential for hypothalamic specification. Finally, we have mapped our results on a recent model which considers the hypothalamus as a transverse region with alar and basal portions. Our data confirm the model and are explained by it.
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spelling pubmed-43733792015-04-09 Differential requirements for Gli2 and Gli3 in the regional specification of the mouse hypothalamus Haddad-Tóvolli, Roberta Paul, Fabian A. Zhang, Yuanfeng Zhou, Xunlei Theil, Thomas Puelles, Luis Blaess, Sandra Alvarez-Bolado, Gonzalo Front Neuroanat Neuroanatomy Secreted protein Sonic hedgehog (Shh) ventralizes the neural tube by modulating the crucial balance between activating and repressing functions (GliA, GliR) of transcription factors Gli2 and Gli3. This balance—the Shh-Gli code—is species- and context-dependent and has been elucidated for the mouse spinal cord. The hypothalamus, a forebrain region regulating vital functions like homeostasis and hormone secretion, shows dynamic and intricate Shh expression as well as complex regional differentiation. Here we asked if particular combinations of Gli2 and Gli3 and of GliA and GliR functions contribute to the variety of hypothalamic regions, i.e., we wanted to approach the question of a possible hypothalamic version of the Shh-Gli code. Based on mouse mutant analysis, we show that: (1) hypothalamic regional heterogeneity is based in part on differentially stringent requirements for Gli2 or Gli3; (2) another source of diversity are differential requirements for Shh of neural vs. non-neural origin; (3) the medial progenitor domain known to depend on Gli2 for its development generates several essential hypothalamic nuclei plus the pituitary and median eminence; (4) the suppression of Gli3R by neural and non-neural Shh is essential for hypothalamic specification. Finally, we have mapped our results on a recent model which considers the hypothalamus as a transverse region with alar and basal portions. Our data confirm the model and are explained by it. Frontiers Media S.A. 2015-03-25 /pmc/articles/PMC4373379/ /pubmed/25859185 http://dx.doi.org/10.3389/fnana.2015.00034 Text en Copyright © 2015 Haddad-Tóvolli, Paul, Zhang, Zhou, Theil, Puelles, Blaess and Alvarez-Bolado. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroanatomy
Haddad-Tóvolli, Roberta
Paul, Fabian A.
Zhang, Yuanfeng
Zhou, Xunlei
Theil, Thomas
Puelles, Luis
Blaess, Sandra
Alvarez-Bolado, Gonzalo
Differential requirements for Gli2 and Gli3 in the regional specification of the mouse hypothalamus
title Differential requirements for Gli2 and Gli3 in the regional specification of the mouse hypothalamus
title_full Differential requirements for Gli2 and Gli3 in the regional specification of the mouse hypothalamus
title_fullStr Differential requirements for Gli2 and Gli3 in the regional specification of the mouse hypothalamus
title_full_unstemmed Differential requirements for Gli2 and Gli3 in the regional specification of the mouse hypothalamus
title_short Differential requirements for Gli2 and Gli3 in the regional specification of the mouse hypothalamus
title_sort differential requirements for gli2 and gli3 in the regional specification of the mouse hypothalamus
topic Neuroanatomy
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4373379/
https://www.ncbi.nlm.nih.gov/pubmed/25859185
http://dx.doi.org/10.3389/fnana.2015.00034
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