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Ontogenetic Distribution of the Transcription Factor Nkx2.2 in the Developing Forebrain of Xenopus Laevis

The expression of the Nkx2.2 gene is involved in the organization of the alar-basal boundary in the forebrain of vertebrates. Its expression in different diencephalic and telencephalic regions, helped to define distinct progenitor domains in mouse and chick. Here we investigated the pattern of Nkx2....

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Autores principales: Domínguez, Laura, González, Agustín, Moreno, Nerea
Formato: Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3049246/
https://www.ncbi.nlm.nih.gov/pubmed/21415915
http://dx.doi.org/10.3389/fnana.2011.00011
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author Domínguez, Laura
González, Agustín
Moreno, Nerea
author_facet Domínguez, Laura
González, Agustín
Moreno, Nerea
author_sort Domínguez, Laura
collection PubMed
description The expression of the Nkx2.2 gene is involved in the organization of the alar-basal boundary in the forebrain of vertebrates. Its expression in different diencephalic and telencephalic regions, helped to define distinct progenitor domains in mouse and chick. Here we investigated the pattern of Nkx2.2 protein distribution throughout the development of the forebrain of the anuran amphibian, Xenopus laevis. We used immunohistochemical and in situ hybridization techniques for its detection in combination with other essential territorial markers in the forebrain. No expression was observed in the telencephalon. In the alar hypothalamus, Nkx2.2 positive cells were scattered in the suprachiasmatic territory, but also in the supraopto-paraventricular area, as defined by the expression of the transcription factor Orthopedia (Otp) and the lack of xDll4. In the basal hypothalamus Nkx2.2 expressing cells were localized in the tuberal region, with the exception of the arcuate nucleus, rich in Otp expressing cells. In the diencephalon it was expressed in all three prosomeres (P1–P3) and not in the zona limitans intrathalamica. The presence of Nkx2.2 expressing cells in P3 was restricted to the alar portion, as well as in prosomere P2, whereas in P1 the Nkx2.2 expressing cells were located in the basal plate and identified the alar/basal boundary. These results showed that Nkx2.2 and Sonic hedgehog are expressed in parallel adjacent stripes along the anterior–posterior axis. The results of this study showed a conserved distribution pattern of Nkx2.2 among vertebrates, crucial to recognize subdivisions that are otherwise indistinct, and supported the relevance of this transcription factor in the organization of the forebrain, particularly in the delineation of the alar/basal boundary of the forebrain.
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spelling pubmed-30492462011-03-17 Ontogenetic Distribution of the Transcription Factor Nkx2.2 in the Developing Forebrain of Xenopus Laevis Domínguez, Laura González, Agustín Moreno, Nerea Front Neuroanat Neuroscience The expression of the Nkx2.2 gene is involved in the organization of the alar-basal boundary in the forebrain of vertebrates. Its expression in different diencephalic and telencephalic regions, helped to define distinct progenitor domains in mouse and chick. Here we investigated the pattern of Nkx2.2 protein distribution throughout the development of the forebrain of the anuran amphibian, Xenopus laevis. We used immunohistochemical and in situ hybridization techniques for its detection in combination with other essential territorial markers in the forebrain. No expression was observed in the telencephalon. In the alar hypothalamus, Nkx2.2 positive cells were scattered in the suprachiasmatic territory, but also in the supraopto-paraventricular area, as defined by the expression of the transcription factor Orthopedia (Otp) and the lack of xDll4. In the basal hypothalamus Nkx2.2 expressing cells were localized in the tuberal region, with the exception of the arcuate nucleus, rich in Otp expressing cells. In the diencephalon it was expressed in all three prosomeres (P1–P3) and not in the zona limitans intrathalamica. The presence of Nkx2.2 expressing cells in P3 was restricted to the alar portion, as well as in prosomere P2, whereas in P1 the Nkx2.2 expressing cells were located in the basal plate and identified the alar/basal boundary. These results showed that Nkx2.2 and Sonic hedgehog are expressed in parallel adjacent stripes along the anterior–posterior axis. The results of this study showed a conserved distribution pattern of Nkx2.2 among vertebrates, crucial to recognize subdivisions that are otherwise indistinct, and supported the relevance of this transcription factor in the organization of the forebrain, particularly in the delineation of the alar/basal boundary of the forebrain. Frontiers Research Foundation 2011-03-02 /pmc/articles/PMC3049246/ /pubmed/21415915 http://dx.doi.org/10.3389/fnana.2011.00011 Text en Copyright © 2011 Domínguez, González and Moreno. http://www.frontiersin.org/licenseagreement This is an open-access article subject to an exclusive license agreement between the authors and Frontiers Media SA, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are credited.
spellingShingle Neuroscience
Domínguez, Laura
González, Agustín
Moreno, Nerea
Ontogenetic Distribution of the Transcription Factor Nkx2.2 in the Developing Forebrain of Xenopus Laevis
title Ontogenetic Distribution of the Transcription Factor Nkx2.2 in the Developing Forebrain of Xenopus Laevis
title_full Ontogenetic Distribution of the Transcription Factor Nkx2.2 in the Developing Forebrain of Xenopus Laevis
title_fullStr Ontogenetic Distribution of the Transcription Factor Nkx2.2 in the Developing Forebrain of Xenopus Laevis
title_full_unstemmed Ontogenetic Distribution of the Transcription Factor Nkx2.2 in the Developing Forebrain of Xenopus Laevis
title_short Ontogenetic Distribution of the Transcription Factor Nkx2.2 in the Developing Forebrain of Xenopus Laevis
title_sort ontogenetic distribution of the transcription factor nkx2.2 in the developing forebrain of xenopus laevis
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3049246/
https://www.ncbi.nlm.nih.gov/pubmed/21415915
http://dx.doi.org/10.3389/fnana.2011.00011
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