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 inweight regulation as demonstrated in mouse models. We describe
anovel mutation Ile183Asn (T548A) found in heterozygosity ina
13-year-old obese girl and her father. Methods: The
MC3R genewas sequenced in 41 unrelated obese children,
and 121 DNA samplesfrom non-obese individuals were analysed for this
novel sequencevariant by allele-specific polymerase chain reaction
(PCR).The genotypes of four family members of the pedigree were also
analysedby allele-specific PCR. Results: Ile183Asn was
found in theproband and her father, though all four family members
wereobese. The sequence variant was not founf in 121 control samples.
Theproband has high percentage body fat (49%), but the fathers
percentagebody fat was only 30%. There were no distinguishing
phenotypicfeatures. Insulin sensitivity was significantly higher
comparedto the 40 other obese subjects without MC3R
gene mutations.Discussion: The difference in phenotypes
between the two relatedheterozygotes, and the observation of obesity
in other familymembers without the mutation suggests that obesity
results froma varying combination of environmental, behavioural and
multiplegenetic factors (other than MC3R), even within
the same family.
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