Clément K, Dina C, Basdevant A, Chastang N, Pelloux V, Lahlou N, Berlan M, Langin D, Guy-Grand B, Froguel P
Nutrition Department, Hôtel-Dieu Hospital, Paris, France.
Diabetes. 1999 Feb;48(2):398-402. doi: 10.2337/diabetes.48.2.398.
As part of an ongoing search for susceptibility genes in obese families, we performed linkage analyses in 101 French families between qualitative and quantitative traits related to morbid obesity and polymorphisms located in or near 15 candidate genes whose products are involved in body weight regulation. These included cholecystokinin A and B receptors (CCK-AR and CCK-BR), glucagon-like peptide 1 receptor (GLP-1R), the LIM/homeodomain islet-1 gene (Isl-1), the caudal-type homeodomain 3 (CDX-3), the uncoupling protein 1 (UCP-1), the beta3-adrenoceptor (beta3-AR), the fatty acid-binding protein 2 (FABP-2), the hormone-sensitive lipase (HSL), the lipoprotein lipase (LPL), the apoprotein-C2 (apo-C2), the insulin receptor substrate-1 (IRS-1), the peroxisome proliferator-activated receptor-gamma (PPAR-gamma), tumor necrosis factor-alpha (TNF-alpha), and the liver carnitine palmitoyltransferase-1 (CPT-1). Phenotypes related to obesity such as BMI, adult life body weight gain, fasting leptin, insulin, fasting glycerol, and free fatty acids were used for nonparametric sib-pair analyses. A weak indication for linkage was obtained between the Isl-1 locus and obesity status defined by a z score over one SD of BMI (n = 226 sib pairs, pi = 0.54 +/- 0.02, P = 0.03). Moreover, a suggestive indication for linkage was found between the Isl-1 locus and BMI and leptin values (P = 0.001 and 0.0003, respectively) and leptin adjusted for BMI (P = 0.0001). Multipoint analyses for leptin trait with Isl-1 and two flanking markers (D5S418 and D5S407) showed that the logarithm of odds (LOD) score is 1.73, coinciding with the Isl-1 locus. Although marginally positive indications for linkage in subgroups of families were found with IRS-1, CPT-1, and HSL loci, our data suggested that these genes are not major contributors to obesity. Whether an obesity susceptibility gene (Isl-1 itself or another nearby gene) lies on chromosome 5q should be determined by further analyses.
作为对肥胖家族中易感基因持续研究的一部分,我们对101个法国家庭进行了连锁分析,研究与病态肥胖相关的定性和定量性状,以及位于15个候选基因内部或附近的多态性,这些基因的产物参与体重调节。这些基因包括胆囊收缩素A和B受体(CCK-AR和CCK-BR)、胰高血糖素样肽1受体(GLP-1R)、LIM/同源结构域胰岛-1基因(Isl-1)、尾型同源结构域3(CDX-3)、解偶联蛋白1(UCP-1)、β3-肾上腺素能受体(β3-AR)、脂肪酸结合蛋白2(FABP-2)、激素敏感性脂肪酶(HSL)、脂蛋白脂肪酶(LPL)、载脂蛋白C2(apo-C2)、胰岛素受体底物-1(IRS-1)、过氧化物酶体增殖物激活受体γ(PPAR-γ)、肿瘤坏死因子-α(TNF-α)以及肝脏肉碱棕榈酰转移酶-1(CPT-1)。与肥胖相关的表型,如体重指数(BMI)、成年期体重增加、空腹瘦素、胰岛素、空腹甘油和游离脂肪酸,用于非参数同胞对分析。在Isl-1基因座与由BMI超过一个标准差的z评分定义的肥胖状态之间获得了微弱的连锁迹象(n = 226对同胞,pi = 0.54 +/- 0.02,P = 0.03)。此外,在Isl-1基因座与BMI和瘦素值之间发现了提示性的连锁迹象(分别为P = 0.001和0.0003),以及经BMI校正的瘦素(P = 0.0001)。对瘦素性状与Isl-1以及两个侧翼标记(D5S418和D5S407)进行的多点分析表明,优势对数(LOD)分数为1.73,与Isl-1基因座一致。虽然在家族亚组中发现IRS-1、CPT-1和HSL基因座有微弱的正向连锁迹象,但我们的数据表明这些基因并非肥胖的主要促成因素。5号染色体q臂上是否存在肥胖易感基因(Isl-1本身或附近的另一个基因)应通过进一步分析来确定。