Loss of Function of the Melanocortin 2 Receptor Accessory Protein 2 Is Associated with Mammalian Obesity

Author:

Asai Masato12,Ramachandrappa Shwetha3,Joachim Maria1,Shen Yuan1,Zhang Rong1,Nuthalapati Nikhil1,Ramanathan Visali1,Strochlic David E.1,Ferket Peter4,Linhart Kirsten1,Ho Caroline1,Novoselova Tatiana V.5,Garg Sumedha3,Ridderstråle Martin6,Marcus Claude7,Hirschhorn Joel N.18,Keogh Julia M.3,O’Rahilly Stephen3,Chan Li F.5,Clark Adrian J.5,Farooqi I. Sadaf3,Majzoub Joseph A.1

Affiliation:

1. Division of Endocrinology, Department of Medicine, Boston Children’s Hospital, Harvard Medical School, 300 Longwood Avenue, Boston, MA 02115, USA.

2. Departments of Pathology, Endocrinology and Diabetes, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya 466-8550, Japan.

3. University of Cambridge Metabolic Research Laboratories and National Institute for Health Research (NIHR) Cambridge Biomedical Research Centre, Institute of Metabolic Science, Addenbrooke’s Hospital, Cambridge CB2 0QQ, UK.

4. Prestage Department of Poultry Science, North Carolina State University, Raleigh, NC 27695, USA.

5. William Harvey Research Institute, Centre for Endocrinology Queen Mary, University of London Barts and The London School of Medicine and Dentistry, London EC1M 6BQ, UK.

6. Department of Clinical Sciences, Lund University, Malmö, Sweden, and Steno Diabetes Center, DK-2820 Gentofte, Denmark.

7. Department for Clinical Science, Intervention and Technology, Karolinska Institute, Division of Pediatrics, National Childhood Obesity Centre, S-141 86 Stockholm, Sweden.

8. Department of Genetics, Harvard Medical School and Broad Institute, Cambridge, MA 02142, USA.

Abstract

Accessory to Obesity? Melanocortin receptors are a family of cell membrane receptors that control diverse physiological functions. Mutations in the gene encoding melanocortin 4 receptor (MC4R) are a cause of familial early-onset obesity. Asai et al. (p. 275 ) studied the function of an accessory protein for MC4R signaling, MRAP2, and found that mice genetically deficient in MRAP2 develop severe obesity. Sequencing of MRAP2 in unrelated, severely obese humans revealed one individual with a clearly disruptive genetic variant, suggesting that MRAP2 mutations might also be a rare cause of human obesity. In a zebrafish model, Sebag et al. (p. 278 ) studied two paralogs of the MRAP2 accessory protein, one of which enhanced MC4R responsiveness to α–melanocyte-stimulating hormone, which regulates feeding and growth.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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