Mutations in Melanocortin-3 Receptor Gene and Human Obesity

被引:25
作者
Yang, Z. [1 ]
Tao, Y. -X. [1 ]
机构
[1] Auburn Univ, Coll Vet Med, Dept Anat Physiol & Pharmacol, Auburn, AL 36849 USA
来源
GENETICS OF MONOGENIC AND SYNDROMIC OBESITY | 2016年 / 140卷
关键词
PROTEIN-COUPLED-RECEPTORS; EARLY-ONSET OBESITY; BODY-MASS INDEX; MESSENGER-RNA EXPRESSION; TYPE-2; DIABETES-MELLITUS; FUNCTIONAL-CHARACTERIZATION; LEPTIN RECEPTOR; FOOD-INTAKE; PROOPIOMELANOCORTIN NEURONS; SUBSTRATE OXIDATION;
D O I
10.1016/bs.pmbts.2016.01.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The prevalence of obesity calls for novel therapeutic targets. The melanocortin-3 receptor (MC3R) has been increasingly recognized as an important regulator of energy homeostasis and MC3R has been intensively analyzed in molecular genetic studies for obesity-related traits. Twenty-seven MC3R mutations and two common polymorphic variants have been identified so far in different cohorts. The mutant MC3Rs demonstrate multiple defects in functional analysis and can be cataloged into different classes according to receptor life cycle based classification system. Although the pathogenic role of MC3R in human obesity remains controversial, recent findings in the noncanonical signaling pathway of MC3R mutants have provided new insights. Potential therapeutic strategies for obesity related to MC3R mutations are highlighted.
引用
收藏
页码:97 / 129
页数:33
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