Skip to main content

Advertisement

Log in

GOAT links dietary lipids with the endocrine control of energy balance

  • Brief Communication
  • Published:

From Nature Medicine

View current issue Submit your manuscript

An Erratum to this article was published on 01 September 2009

This article has been updated

Abstract

Central nervous system nutrient sensing and afferent endocrine signaling have been established as parallel systems communicating metabolic status and energy availability in vertebrates. The only afferent endocrine signal known to require modification with a fatty acid side chain is the orexigenic hormone ghrelin. We find that the ghrelin O-acyl transferase (GOAT), which is essential for ghrelin acylation, is regulated by nutrient availability, depends on specific dietary lipids as acylation substrates and links ingested lipids to energy expenditure and body fat mass. These data implicate the ghrelin-GOAT system as a signaling pathway that alerts the central nervous system to the presence of dietary calories, rather than to their absence as is commonly accepted.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Figure 1: Long-term fasting decreases Mboat4 expression and does not increase ghrelin acylation.
Figure 2: GOAT regulates energy homeostasis.

Similar content being viewed by others

Change history

  • 04 September 2009

    In the version of this article initially published, the fourth condition from the top in the key to the bar graphs in Figure 2c was mislabeled as ‘mC8’. The correct label is ‘hC8’. The error has been corrected in the HTML and PDF versions of the article.

References

  1. Obici, S. et al. J. Clin. Invest. 108, 1079–1085 (2001).

    Article  CAS  Google Scholar 

  2. Schwartz, M.W., Woods, S.C., Porte, D. Jr., Seeley, R.J. & Baskin, D.G. Nature 404, 661–671 (2000).

    Article  CAS  Google Scholar 

  3. Cao, H. et al. Cell 134, 933–944 (2008).

    Article  CAS  Google Scholar 

  4. Gillum, M.P. et al. Cell 135, 813–824 (2008).

    Article  CAS  Google Scholar 

  5. Kojima, M. et al. Nature 402, 656–660 (1999).

    Article  CAS  Google Scholar 

  6. López, M. et al. Cell Metab. 7, 389–399 (2008).

    Article  Google Scholar 

  7. Tschöp, M., Smiley, D.L. & Heiman, M.L. Nature 407, 908–913 (2000).

    Article  Google Scholar 

  8. Kamegai, J. et al. Diabetes 50, 2438–2443 (2001).

    Article  CAS  Google Scholar 

  9. Tschöp, M. et al. J. Endocrinol. Invest. 24, RC19–RC21 (2001).

    Article  Google Scholar 

  10. Gutierrez, J.A. et al. Proc. Natl. Acad. Sci. USA 105, 6320–6325 (2008).

    Article  CAS  Google Scholar 

  11. Yang, J., Brown, M.S., Liang, G., Grishin, N.V. & Goldstein, J.L. Cell 132, 387–396 (2008).

    Article  CAS  Google Scholar 

  12. Nishi, Y. et al. Endocrinology 146, 2255–2264 (2005).

    Article  CAS  Google Scholar 

  13. Drazen, D.L., Vahl, T.P., D'Alessio, D.A., Seeley, R.J. & Woods, S.C. Endocrinology 147, 23–30 (2006).

    Article  CAS  Google Scholar 

  14. Liu, J. et al. J. Clin. Endocrinol. Metab. 93, 1980–1987 (2008).

    Article  CAS  Google Scholar 

  15. Dole, V.P. & Rizack, M.A. J. Lipid Res. 2, 90–91 (1961).

    CAS  Google Scholar 

  16. Schwartz, G.J. et al. Cell Metab. 8, 281–288 (2008).

    Article  CAS  Google Scholar 

  17. Zurier, R.B., Campbell, R.G., Hashim, S.A. & Van Itallie, T.B. N. Engl. J. Med. 274, 490–493 (1966).

    Article  CAS  Google Scholar 

  18. Prior, I.A., Davidson, F., Salmond, C.E. & Czochanska, Z. Am. J. Clin. Nutr. 34, 1552–1561 (1981).

    Article  CAS  Google Scholar 

  19. Pfluger, P.T. et al. Am. J. Physiol. Gastrointest. Liver Physiol. 294, G610–G618 (2008).

    Article  CAS  Google Scholar 

  20. Gauna, C. et al. Am. J. Physiol. Endocrinol. Metab. 293, E697–E704 (2007).

    Article  CAS  Google Scholar 

Download references

Acknowledgements

We would like to thank J.E. Baker, B. Berger and J. Holland for their outstanding technical support. This manuscript was supported by the Leibniz Graduate College (H.K.) and by the US National Institutes of Health/National Institute of Diabetes and Digestive and Kidney Diseases Grant R01-DK069987 (to M.H.T.).

Author information

Authors and Affiliations

Authors

Contributions

H.K., P.T.P. and J.A.G. designed and performed most of the experiments and wrote the manuscript; P.J.S. generated mouse models; J.A.W. performed and interpreted mass spectrometry analyses; T.A.C. performed gene expression analyses; A.S., H.-G.J., R.J.J. and J.E.H. designed experiments, interpreted data and wrote the manuscript; and M.L.H. and M.H.T. conceptualized, analyzed and interpreted all studies and wrote the manuscript.

Corresponding author

Correspondence to Matthias H Tschöp.

Ethics declarations

Competing interests

J.A.G., P.J.S., T.A.C., J.A.W., J.E.H. and M.L.H. are employees and stock holders of the Eli Lilly Company.

Supplementary information

Supplementary Text and Figures

Supplementary Methods and Supplementary Figs. 1–7 (PDF 424 kb)

Rights and permissions

Reprints and permissions

About this article

Cite this article

Kirchner, H., Gutierrez, J., Solenberg, P. et al. GOAT links dietary lipids with the endocrine control of energy balance. Nat Med 15, 741–745 (2009). https://doi.org/10.1038/nm.1997

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/nm.1997

  • Springer Nature America, Inc.

This article is cited by

Navigation