The Homeodomain Transcription Factor NKX2.1 Is Essential for the Early Specification of Melanocortin Neuron Identity and Activates Pomc Expression in the Developing Hypothalamus
Food intake is tightly regulated by a group of neurons present in the arcuate nucleus of the hypothalamus, which release -encoded melanocortins, the absence of which induces marked hyperphagia and early-onset obesity. Although the relevance of hypothalamic POMC neurons in the regulation of body weig...
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| Published in: | The Journal of neuroscience Vol. 39; no. 21; pp. 4023 - 4035 |
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| Main Authors: | , , , , , |
| Format: | Journal Article |
| Language: | English |
| Published: |
United States
Society for Neuroscience
22-05-2019
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| Subjects: | |
| Online Access: | Get full text |
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| Summary: | Food intake is tightly regulated by a group of neurons present in the arcuate nucleus of the hypothalamus, which release
-encoded melanocortins, the absence of which induces marked hyperphagia and early-onset obesity. Although the relevance of hypothalamic POMC neurons in the regulation of body weight and energy balance is well appreciated, little is known about the transcription factors that establish the melanocortin neuron identity during brain development and its phenotypic maintenance in postnatal life. Here, we report that the transcription factor NKX2.1 is present in mouse hypothalamic POMC neurons from early development to adulthood. Electromobility shift assays showed that NKX2.1 binds
to NKX binding motifs present in the neuronal
enhancers nPE1 and nPE2 and chromatin immunoprecipitation assays detected
binding of NKX2.1 to nPE1 and nPE2 in mouse hypothalamic extracts. Transgenic and mutant studies performed in mouse embryos of either sex and adult males showed that the NKX motifs present in nPE1 and nPE2 are essential for their transcriptional enhancer activity. The conditional early inactivation of
in the ventral hypothalamus prevented the onset of
expression. Selective
ablation from POMC neurons decreased
expression in adult males and mildly increased their body weight and adiposity. Our results demonstrate that NKX2.1 is necessary to activate
expression by binding to conserved canonical NKX motifs present in nPE1 and nPE2. Therefore, NKX2.1 plays a critical role in the early establishment of hypothalamic melanocortin neuron identity and participates in the maintenance of
expression levels during adulthood.
Food intake and body weight regulation depend on hypothalamic neurons that release satiety-inducing neuropeptides, known as melanocortins. Central melanocortins are encoded by
, and
mutations may lead to hyperphagia and severe obesity. Although the importance of central melanocortins is well appreciated, the genetic program that establishes and maintains fully functional POMC neurons remains to be explored. Here, we combined molecular, genetic, developmental, and functional studies that led to the discovery of NKX2.1, a transcription factor that participates in the early morphogenesis of the developing hypothalamus, as a key player in establishing the early identity of melanocortin neurons by activating
expression. Thus,
adds to the growing list of genes that participate in body weight regulation and adiposity. |
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| Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 D.P.O. and M.B.T. contributed equally to this work. Author contributions: D.P.O., M.B.T., F.S.J.d.S., S.N., M.J.L., and M.R. designed research; D.P.O., M.B.T., F.S.J.d.S., S.N., and M.R. performed research; M.J.L. and M.R. contributed unpublished reagents/analytic tools; D.P.O., M.B.T., F.S.J.d.S., S.N., and M.R. analyzed data; M.R. wrote the paper. |
| ISSN: | 0270-6474 1529-2401 |
| DOI: | 10.1523/JNEUROSCI.2924-18.2019 |