QTL analysis of self-selected macronutrient diet intake: fat, carbohydrate, and total kilocalories

被引:49
作者
Richards, BKS
Belton, BN
Poole, AC
Mancuso, JJ
Churchill, GA
Li, R
Volaufova, J
Zuberi, A
York, B
机构
[1] Pennington Biomed Res Ctr, Baton Rouge, LA 70808 USA
[2] Jackson Lab, Bar Harbor, ME 04609 USA
关键词
genetics; mouse inbred strains; food intake; energy intake; diet selection; body weight; fat pad; obesity;
D O I
10.1152/physiolgenomics.00037.2002
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The present study investigated the inheritance of dietary fat, carbohydrate, and kilocalorie intake traits in an F-2 population derived from an intercross between C57BL/6J (fat-preferring) and CAST/EiJ (carbohydrate-preferring) mice. Mice were phenotyped for self-selected food intake in a paradigm which provided for 10 days a choice between two macronutrient diets containing 78/22% of energy as a composite of either fat/protein or carbohydrate/protein. Quantitative trait locus (QTL) analysis identified six significant loci for macronutrient intake: three for fat intake on chromosomes (Chrs) 8 (Mnif1), 18 (Mnif2), and X (Mnif3), and three for carbohydrate intake on Chrs 17 (Mnic1),6 (Mnic2), and X (Mnic3). An absence of interactions among these QTL suggests the existence of separate mechanisms controlling the intake of fat and carbohydrate. Two significant QTL for cumulative kilocalorie intake, adjusted for baseline body weight, were found on Chrs 17 (Kcal1) and 18 (Kcal2). Without body weight adjustment, another significant kcal locus appeared on distal Chr 2 (Kcal3). These macronutrient and kilocalorie QTL, with the exception of loci on Chrs 8 and X, encompassed chromosomal regions influencing body weight gain and adiposity in this F-2 population. These results provide new insight into the genetic basis of naturally occurring variation in nutrient intake phenotypes.
引用
收藏
页码:205 / 217
页数:13
相关论文
共 54 条
[1]   Sucrose consumption in mice: major influence of two genetic loci affecting peripheral sensory responses [J].
Bachmanov, AA ;
Reed, DR ;
Ninomiya, Y ;
Inoue, M ;
Tordoff, MG ;
Price, RA ;
Beauchamp, GK .
MAMMALIAN GENOME, 1997, 8 (08) :545-548
[2]   Positional cloning of the mouse saccharin preference (Sac) locus [J].
Bachmanov, AA ;
Li, X ;
Reed, DR ;
Ohmen, JD ;
Li, SR ;
Chen, ZY ;
Tordoff, MG ;
de Jong, PJ ;
Wu, CY ;
West, DB ;
Chatterjee, A ;
Ross, DA ;
Beauchamp, GK .
CHEMICAL SENSES, 2001, 26 (07) :925-933
[3]  
BERTHOUD HR, 2000, NEURAL METABOLIC CON, P361
[4]   Using mouse models to dissect the genetics of obesity [J].
Brockmann, GA ;
Bevova, MR .
TRENDS IN GENETICS, 2002, 18 (07) :367-376
[5]  
Cheverud JM, 1996, GENETICS, V142, P1305
[6]  
CHURCHILL GA, 1994, GENETICS, V138, P963
[7]   Molecular heterosis: A review [J].
Comings, DE ;
MacMurray, JP .
MOLECULAR GENETICS AND METABOLISM, 2000, 71 (1-2) :19-31
[8]   Quantitative trait loci affecting growth in high growth (hg) mice [J].
Corva, PM ;
Horvat, S ;
Medrano, JF .
MAMMALIAN GENOME, 2001, 12 (04) :284-290
[9]   Decreased postnatal survival and altered body weight regulation in procolipase-deficient mice [J].
D'Agostino, D ;
Cordle, RA ;
Kullman, J ;
Erlanson-Albertsson, C ;
Muglia, LJ ;
Lowe, ME .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (09) :7170-7177
[10]   The neural network that regulates energy balance is responsive to glucocorticoids and insulin and also regulates HPA axis responsivity at a site proximal to CRF neurons [J].
Dallman, MF ;
Akana, SF ;
Strack, AM ;
Hanson, ES ;
Sebastian, RJ .
STRESS: BASIC MECHANISMS AND CLINICAL IMPLICATIONS, 1995, 771 :730-742