Genetic loci controlling body fat, lipoprotein metabolism, and insulin levels in a multifactorial mouse model

被引:111
作者
Mehrabian, M
Wen, PZ
Fisler, J
Davis, RC
Lusis, AJ
机构
[1] Univ Calif Los Angeles, Dept Med, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Inst Mol Biol, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, Dept Microbiol & Mol Genet, Los Angeles, CA 90095 USA
关键词
genetics; obesity; mouse; insulin; lipoproteins;
D O I
10.1172/JCI1748
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
We analyzed the inheritance of body fat, leptin levels, plasma lipoprotein levels, insulin levels, and related traits in an intercross between inbred mouse strains CAST/Ei and C57BL/6J. CAST/Ei mice are unusually lean, with only similar to 8% of body weight as fat, whereas C57BL/6J mice have similar to 18% body fat. Quantitative trait locus analysis using > 200 F2 mice revealed highly significant loci (lod scores > 4.3) on chromosomes 2 (three separate loci) and 9 that contribute to mouse fat-pad mass for mice on a high-fat diet. Some loci also influenced plasma lipoprotein levels and insulin levels either on chow or high-fat diets. Two loci for body fat and lipoprotein levels ton central and distal chromosome 2) coincided with a locus having strong effects on hepatic lipase activity, an activity associated with visceral obesity and lipoprotein levels in humans. A locus contributing to plasma leptin levels (lod score 5.3) but not obesity was identified on chromosome 4, near the leptin receptor gene. These data identify candidate regions and candidate genes for studies of human obesity and diabetes, and suggest obesity is highly complex in terms of the number of genetic factors involved. Finally, they support the existence of specific genetic interactions between body fat, insulin metabolism, and lipoprotein metabolism.
引用
收藏
页码:2485 / 2496
页数:12
相关论文
共 47 条
[1]  
BOUCHARD C, 1995, INT J OBESITY, V19, pS10
[2]   THE RESPONSE TO LONG-TERM OVERFEEDING IN IDENTICAL-TWINS [J].
BOUCHARD, C ;
TREMBLAY, A ;
DESPRES, JP ;
NADEAU, A ;
LUPIEN, PJ ;
THERIAULT, G ;
DUSSAULT, J ;
MOORJANI, S ;
PINAULT, S ;
FOURNIER, G .
NEW ENGLAND JOURNAL OF MEDICINE, 1990, 322 (21) :1477-1482
[3]  
BRAY GA, 1990, FRONT NEUROENDOCRIN, V11, P128
[4]   Genetics of obesity: Advances from rodent studies [J].
Chagnon, YC ;
Bouchard, C .
TRENDS IN GENETICS, 1996, 12 (11) :441-444
[5]   Evidence that the diabetes gene encodes the leptin receptor: Identification of a mutation in the leptin receptor gene in db/db mice [J].
Chen, H ;
Charlat, O ;
Tartaglia, LA ;
Woolf, EA ;
Weng, X ;
Ellis, SJ ;
Lakey, ND ;
Culpepper, J ;
Moore, KJ ;
Breitbart, RE ;
Duyk, GM ;
Tepper, RI ;
Morgenstern, JP .
CELL, 1996, 84 (03) :491-495
[6]   Indication for linkage of the human OB gene region with extreme obesity [J].
Clement, K ;
Garner, C ;
Hager, J ;
Philippi, A ;
LeDuc, C ;
Carey, A ;
Harris, TJR ;
Jury, C ;
Cardon, LR ;
Basdevant, A ;
Demenais, F ;
GuyGrand, B ;
North, M ;
Froguel, P .
DIABETES, 1996, 45 (05) :687-690
[7]   BODY-FAT DISTRIBUTION IS A DETERMINANT OF THE HIGH-DENSITY-LIPOPROTEIN RESPONSE TO DIETARY-FAT AND CHOLESTEROL IN WOMEN [J].
CLIFTON, PM ;
ABBEY, M ;
NOAKES, M ;
BELTRAME, S ;
RUMBELOW, N ;
NESTEL, PJ .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1995, 15 (08) :1070-1078
[8]   A major quantitative trait locus determining serum leptin levels and fat mass is located on human chromosome 2 [J].
Comuzzie, AG ;
Hixson, JE ;
Almasy, L ;
Mitchell, BD ;
Mahaney, MC ;
Dyer, TD ;
Stern, MP ;
MacCluer, JW ;
Blangero, J .
NATURE GENETICS, 1997, 15 (03) :273-276
[9]   EVIDENCE AGAINST EITHER A PREMATURE STOP CODON OR THE ABSENCE OF OBESE GENE MESSENGER-RNA IN HUMAN OBESITY [J].
CONSIDINE, RV ;
CONSIDINE, EL ;
WILLIAMS, CJ ;
NYCE, MR ;
MAGOSIN, SA ;
BAUER, TL ;
ROSATO, EL ;
COLBERG, J ;
CARO, JF .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 95 (06) :2986-2988
[10]   Experimental strategies for the genetic dissection of complex traits in animal models [J].
Darvasi, A .
NATURE GENETICS, 1998, 18 (01) :19-24