Document Detail

Prevalence and functionality of paucimorphic and private MC4R mutations in a large, unselected European British population, scanned by meltMADGE.
MedLine Citation:
PMID:  17072869     Owner:  NLM     Status:  MEDLINE    
Identification of unknown mutations has remained laborious, expensive, and only viable for studies of selected cases. Population-based "reference ranges" of rarer sequence diversity are not available. However, the research and diagnostic interpretation of sequence variants depends on such information. Additionally, this is the only way to determine prevalence of severe, moderate, and silent mutations and is also relevant to the development of screening programs. We previously described a system, meltMADGE, suitable for mutation scanning at the population level. Here we describe its application to a population-based study of MC4R (melanocortin 4 receptor) mutations, which are associated with obesity. We developed nine assays representing MC4R and examined a population sample of 1,100 subjects. Two "paucimorphisms" were identified (c.307G>A/p.Val103Ile in 27 subjects and c.-178A>C in 22 subjects). Neither exhibited any anthropometric effects, whereas there would have been >90% power to detect a body mass index (BMI) effect of 0.5 kg/m(2) at P=0.01. Two "private" variants were also identified. c.335C>T/p.Thr112Met has been previously described and appears to be silent. A novel variant, c.260C>A/p.Ala87Asp, was observed in a subject with a BMI of 31.5 kg/m(2) (i.e., clinically obese) but not on direct assay of a further 3,525 subjects. This mutation was predicted to be deleterious and analysis using a cyclic AMP (cAMP) responsive luciferase reporter assay showed substantial loss of function of the mutant receptor. This population-based mutation scan of MC4R suggests that there is no severe MC4R mutation with high prevalence in the United Kingdom, but that obesity-causing MC4R mutation at 1 in 1,100 might represent one of the commonest autosomal dominant disorders in man.
Khalid K Alharbi; Emmanuel Spanakis; Karen Tan; Matt J Smith; Mohammed A Aldahmesh; Sandra D O'Dell; Avan Aihie Sayer; Debbie A Lawlor; Shah Ebrahim; George Davey Smith; Stephen O'Rahilly; Sadaf Farooqi; Cyrus Cooper; David I W Phillips; Ian N M Day
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't; Validation Studies    
Journal Detail:
Title:  Human mutation     Volume:  28     ISSN:  1098-1004     ISO Abbreviation:  Hum. Mutat.     Publication Date:  2007 Mar 
Date Detail:
Created Date:  2007-02-05     Completed Date:  2007-03-16     Revised Date:  2014-02-19    
Medline Journal Info:
Nlm Unique ID:  9215429     Medline TA:  Hum Mutat     Country:  United States    
Other Details:
Languages:  eng     Pagination:  294-302     Citation Subset:  IM    
Copyright Information:
(c) 2006 Wiley-Liss, Inc.
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MeSH Terms
DNA Mutational Analysis
Genetic Testing / methods*
Great Britain
Middle Aged
Nucleic Acid Denaturation
Polymorphism, Single-Stranded Conformational*
Receptor, Melanocortin, Type 4 / genetics*
Grant Support
068086//Wellcome Trust; G9824984//Medical Research Council; MC_U147574213//Medical Research Council; MC_U147585824//Medical Research Council; MC_UP_A620_1014//Medical Research Council; U.1475.00.002.00001.01(74213)//Medical Research Council; //Wellcome Trust
Reg. No./Substance:
0/MC4R protein, human; 0/Receptor, Melanocortin, Type 4

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