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The Creb1 coactivator Crtc1 is required for energy balance and fertility.

Nature medicine | Oct 8, 2008

The adipocyte-derived hormone leptin maintains energy balance by acting on hypothalamic leptin receptors (Leprs) that act on the signal transducer and activator of transcription 3 (Stat3). Although disruption of Lepr-Stat3 signaling promotes obesity in mice, other features of Lepr function, such as fertility, seem normal, pointing to the involvement of additional regulators. Here we show that the cyclic AMP responsive element-binding protein-1 (Creb1)-regulated transcription coactivator-1 (Crtc1) is required for energy balance and reproduction-Crtc1(-/-) mice are hyperphagic, obese and infertile. Hypothalamic Crtc1 was phosphorylated and inactive in leptin-deficient ob/ob mice, while leptin administration increased amounts of dephosphorylated nuclear Crtc1. Dephosphorylated Crtc1 stimulated expression of the Cartpt and Kiss1 genes, which encode hypothalamic neuropeptides that mediate leptin's effects on satiety and fertility. Crtc1 overexpression in hypothalamic cells increased Cartpt and Kiss1 gene expression, whereas Crtc1 depletion decreased it. Indeed, leptin enhanced Crtc1 activity over the Cartpt and Kiss1 promoters in cells overexpressing Lepr, and these effects were disrupted by expression of a dominant-negative Creb1 polypeptide. As leptin administration increased recruitment of hypothalamic Crtc1 to Cartpt and Kiss1 promoters, our results indicate that the Creb1-Crtc1 pathway mediates the central effects of hormones and nutrients on energy balance and fertility.

Pubmed ID: 18758446 RIS Download

Mesh terms: Animals | Cells, Cultured | Cyclic AMP Response Element-Binding Protein | Energy Metabolism | Female | Fertility | Kisspeptins | Leptin | Male | Mice | Mice, Inbred C57BL | Mice, Obese | Nerve Tissue Proteins | Phosphorylation | Proteins | Transcription Factors

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Associated grants

  • Agency: NIDDK NIH HHS, Id: R01 DK049777-12
  • Agency: NIDDK NIH HHS, Id: R01 DK049777-15
  • Agency: NIDDK NIH HHS, Id: R01 DK049777-11
  • Agency: NIDDK NIH HHS, Id: R01 DK049777-13
  • Agency: NIDDK NIH HHS, Id: DK049777
  • Agency: NIDDK NIH HHS, Id: R01 DK049777-14
  • Agency: NIDDK NIH HHS, Id: R01 DK049777

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