help button home button Endocrine Society JCEM
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

This Article
Right arrow Full Text (PDF)
Right arrow Submit a related Letter to the Editor
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow Request Copyright Permission
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Lee, Y.-S.
Right arrow Articles by Loke, K.-Y.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Lee, Y.-S.
Right arrow Articles by Loke, K.-Y.
The Journal of Clinical Endocrinology & Metabolism Vol. 87, No. 3 1423-1426
Copyright © 2002 by The Endocrine Society


Other Original Articles

A Novel Melanocortin 3 Receptor Gene (MC3R) Mutation Associated with Severe Obesity

Yung-Seng Lee, Larry Kok-Seng Poh and Kah-Yin Loke

Paediatric Endocrine Section, Department of Paediatrics, National University of Singapore, Singapore

Abstract

The melanocortin 3 receptor (MC3R) plays a critical role in weight regulation as demonstrated in mouse models. We describe a novel mutation Ile183Asn (T548A) found in heterozygosity in a 13-year-old obese girl and her father. Methods: The MC3R gene was sequenced in 41 unrelated obese children, and 121 DNA samples from non-obese individuals were analysed for this novel sequence variant by allele-specific polymerase chain reaction (PCR). The genotypes of four family members of the pedigree were also analysed by allele-specific PCR. Results: Ile183Asn was found in the proband and her father, though all four family members were obese. The sequence variant was not founf in 121 control samples. The proband has high percentage body fat (49%), but the father’s percentage body fat was only 30%. There were no distinguishing phenotypic features. Insulin sensitivity was significantly higher compared to the 40 other obese subjects without MC3R gene mutations. Discussion: The difference in phenotypes between the two related heterozygotes, and the observation of obesity in other family members without the mutation suggests that obesity results from a varying combination of environmental, behavioural and multiple genetic factors (other than MC3R), even within the same family.




This article has been cited by other articles:


Home page
Am. J. Clin. Nutr.Home page
D. M Savastano, M. Tanofsky-Kraff, J. C Han, C. Ning, R. A Sorg, C. A Roza, L. E Wolkoff, K. Anandalingam, K. S Jefferson-George, R. E Figueroa, et al.
Energy intake and energy expenditure among children with polymorphisms of the melanocortin-3 receptor
Am. J. Clinical Nutrition, October 1, 2009; 90(4): 912 - 920.
[Abstract] [Full Text] [PDF]


Home page
Hum Mol GenetHome page
M. A. Calton, B. A. Ersoy, S. Zhang, J. P. Kane, M. J. Malloy, C. R. Pullinger, Y. Bromberg, L. A. Pennacchio, R. Dent, R. McPherson, et al.
Association of functionally significant Melanocortin-4 but not Melanocortin-3 receptor mutations with severe adult obesity in a large North American case-control study
Hum. Mol. Genet., March 15, 2009; 18(6): 1140 - 1147.
[Abstract] [Full Text] [PDF]


Home page
J EndocrinolHome page
Z.-C. Fan, J. L Sartin, and Y.-X. Tao
Molecular cloning and pharmacological characterization of porcine melanocortin-3 receptor
J. Endocrinol., January 1, 2008; 196(1): 139 - 148.
[Abstract] [Full Text] [PDF]


Home page
DiabetesHome page
Y. Seng Lee, L. Kok Seng Poh, B. Lay Kee Kek, and K. Yin Loke
The Role of Melanocortin 3 Receptor Gene in Childhood Obesity
Diabetes, October 1, 2007; 56(10): 2622 - 2630.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Clin. Nutr.Home page
N. Santoro, L. Perrone, G. Cirillo, P. Raimondo, A. Amato, C. Brienza, and E. M. del Giudice
Effect of the melanocortin-3 receptor C17A and G241A variants on weight loss in childhood obesity
Am. J. Clinical Nutrition, April 1, 2007; 85(4): 950 - 953.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Endocrinol. Metab.Home page
J. Rutanen, J. Pihlajamaki, M. Vanttinen, U. Salmenniemi, E. Ruotsalainen, T. Kuulasmaa, S. Kainulainen, and M. Laakso
Single Nucleotide Polymorphisms of the Melanocortin-3 Receptor Gene Are Associated with Substrate Oxidation and First-Phase Insulin Secretion in Offspring of Type 2 Diabetic Subjects
J. Clin. Endocrinol. Metab., March 1, 2007; 92(3): 1112 - 1117.
[Abstract] [Full Text] [PDF]


Home page
Physiol. GenomicsHome page
J. Grosse, P. Tarnow, H. Rompler, B. Schneider, R. Sedlmeier, U. Huffstadt, D. Korthaus, M. Nehls, S. Wattler, T. Schoneberg, et al.
N-ethyl-N-nitrosourea-based generation of mouse models for mutant G protein-coupled receptors
Physiol Genomics, September 14, 2006; 26(3): 209 - 217.
[Abstract] [Full Text] [PDF]


Home page
Hum Mol GenetHome page
D. J. Lloyd, S. Bohan, and N. Gekakis
Obesity, hyperphagia and increased metabolic efficiency in Pc1 mutant mice
Hum. Mol. Genet., June 1, 2006; 15(11): 1884 - 1893.
[Abstract] [Full Text] [PDF]


Home page
DiabetesHome page
N. Feng, S. F. Young, G. Aguilera, E. Puricelli, D. C. Adler-Wailes, N. G. Sebring, and J. A. Yanovski
Co-occurrence of Two Partially Inactivating Polymorphisms of MC3R Is Associated With Pediatric-Onset Obesity
Diabetes, September 1, 2005; 54(9): 2663 - 2667.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Endocrinol. Metab.Home page
C. S. Fox, N. L. Heard-Costa, R. S. Vasan, J. M. Murabito, R. B. D'Agostino Sr., and L. D. Atwood
Genomewide Linkage Analysis of Weight Change in the Framingham Heart Study
J. Clin. Endocrinol. Metab., June 1, 2005; 90(6): 3197 - 3201.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Endocrinol. Metab.Home page
Y.-X. Tao and D. L. Segaloff
Functional Characterization of Melanocortin-3 Receptor Variants Identify a Loss-of-Function Mutation Involving an Amino Acid Critical for G Protein-Coupled Receptor Activation
J. Clin. Endocrinol. Metab., August 1, 2004; 89(8): 3936 - 3942.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Regul. Integr. Comp. Physiol.Home page
M. H. Humphreys
{gamma}-MSH, sodium metabolism, and salt-sensitive hypertension
Am J Physiol Regulatory Integrative Comp Physiol, March 1, 2004; 286(3): R417 - R430.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
C. Liu, E. Goshu, A. Wells, and C.-M. Fan
Identification of the Downstream Targets of SIM1 and ARNT2, a Pair of Transcription Factors Essential for Neuroendocrine Cell Differentiation
J. Biol. Chem., November 7, 2003; 278(45): 44857 - 44867.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Endocrinology Endocrine Reviews J. Clin. End. & Metab.
Molecular Endocrinology Recent Prog. Horm. Res. All Endocrine Journals
Copyright © 2002 by The Endocrine Society