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Evolutionarily conserved regulation of hypocretin neuron specification by Lhx9.
Liu, Justin; Merkle, Florian T; Gandhi, Avni V; Gagnon, James A; Woods, Ian G; Chiu, Cindy N; Shimogori, Tomomi; Schier, Alexander F; Prober, David A.
Afiliação
  • Liu J; Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
  • Merkle FT; Departments of Molecular and Cellular Biology, and Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA 02138, USA Harvard Stem Cell Institute, Harvard University, Cambridge, MA 02138, USA.
  • Gandhi AV; Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
  • Gagnon JA; Departments of Molecular and Cellular Biology, and Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA 02138, USA.
  • Woods IG; Departments of Molecular and Cellular Biology, and Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA 02138, USA.
  • Chiu CN; Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
  • Shimogori T; Brain Science Institute, RIKEN, Saitama 351-0198, Japan.
  • Schier AF; Departments of Molecular and Cellular Biology, and Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA 02138, USA Harvard Stem Cell Institute, Harvard University, Cambridge, MA 02138, USA Division of Sleep Medicine, Harvard University, Cambridge, MA 02115, USA.
  • Prober DA; Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA dprober@caltech.edu.
Development ; 142(6): 1113-24, 2015 Mar 15.
Article em En | MEDLINE | ID: mdl-25725064
Loss of neurons that express the neuropeptide hypocretin (Hcrt) has been implicated in narcolepsy, a debilitating disorder characterized by excessive daytime sleepiness and cataplexy. Cell replacement therapy, using Hcrt-expressing neurons generated in vitro, is a potentially useful therapeutic approach, but factors sufficient to specify Hcrt neurons are unknown. Using zebrafish as a high-throughput system to screen for factors that can specify Hcrt neurons in vivo, we identified the LIM homeobox transcription factor Lhx9 as necessary and sufficient to specify Hcrt neurons. We found that Lhx9 can directly induce hcrt expression and we identified two potential Lhx9 binding sites in the zebrafish hcrt promoter. Akin to its function in zebrafish, we found that Lhx9 is sufficient to specify Hcrt-expressing neurons in the developing mouse hypothalamus. Our results elucidate an evolutionarily conserved role for Lhx9 in Hcrt neuron specification that improves our understanding of Hcrt neuron development.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fatores de Transcrição / Neuropeptídeos / Separação Celular / Regulação da Expressão Gênica / Proteínas de Peixe-Zebra / Peptídeos e Proteínas de Sinalização Intracelular / Hipotálamo / Neurônios Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fatores de Transcrição / Neuropeptídeos / Separação Celular / Regulação da Expressão Gênica / Proteínas de Peixe-Zebra / Peptídeos e Proteínas de Sinalização Intracelular / Hipotálamo / Neurônios Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2015 Tipo de documento: Article