Mapping of mouse obesity genes: A generic approach to a complex trait

被引:25
作者
Fisler, JS
Warden, CH
机构
[1] UNIV CALIF LOS ANGELES, DEPT MED, DIV CARDIOL, LOS ANGELES, CA 90095 USA
[2] UNIV CALIF DAVIS, DEPT PEDIAT, DAVIS, CA 95616 USA
[3] UNIV CALIF DAVIS, ROWE PROGRAM GENET, DAVIS, CA 95616 USA
关键词
genetics; percentage body fat;
D O I
10.1093/jn/127.9.1909S
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Identification of genes underlying any complex trait such as obesity is an important and difficult problem in genetics. Traditional candidate gene approaches cannot be relied on to identify all of the genes influencing a complex trait, and positional cloning is very laborious. With the advent of new tools and methods, however, comprehensive approaches to the identification of any genes underlying complex traits are now available. Quantitative trait locus (QTL) mapping is a general technique to map Mendelian factors influencing complex traits. The QTL approach involves the crossing of two strains that differ in the trait of interest to produce F2 or backcross progeny, individually phenotyping and genotyping each progeny, and statistically associating the typed markers and the phenotype. QTL mapping has been used in the last 4 years to map genes for;a wide variety of traits, including body weight and growth, obesity, atherosclerosis and susceptibility to cancer in the mouse, and hypertension, hyperactivity and arthritis in the rat. QTL mapping has also been used to map genes in pigs, poultry, cows, fish and plants. Once a trait has been located in a chromosomal subregion, identifying the underlying gene remains a significant problem. A monogenic model must be developed, isolating one gene influencing a trait from other genes affecting the same phenotype. Then the positional candidate strategy, which relies on a combination of mapping to a chromosomal subregion followed by a survey of the interval to see if attractive candidates reside there, becomes practical.
引用
收藏
页码:S1909 / S1916
页数:8
相关论文
共 77 条
[1]   GENETIC-MAPPING OF QUANTITATIVE TRAIT LOCI FOR GROWTH AND FATNESS IN PIGS [J].
ANDERSSON, L ;
HALEY, CS ;
ELLEGREN, H ;
KNOTT, SA ;
JOHANSSON, M ;
ANDERSSON, K ;
ANDERSSONEKLUND, L ;
EDFORSLILJA, I ;
FREDHOLM, M ;
HANSSON, I ;
HAKANSSON, J ;
LUNDSTROM, K .
SCIENCE, 1994, 263 (5154) :1771-1774
[2]   GENETICS OF HISTOCOMPATIBILITY IN MICE .1. NEW LOCI AND CONGENIC LINES [J].
BAILEY, DW .
IMMUNOGENETICS, 1975, 2 (03) :249-256
[3]   MOLECULAR CHARACTERIZATION OF THE MOUSE AGOUTI LOCUS [J].
BULTMAN, SJ ;
MICHAUD, EJ ;
WOYCHIK, RP .
CELL, 1992, 71 (07) :1195-1204
[4]  
Cheverud JM, 1996, GENETICS, V142, P1305
[5]   DETECTION OF LINKAGE BETWEEN GENETIC-MARKERS AND GENES THAT AFFECT GROWTH AND CARCASS TRAITS IN PIGS [J].
CLAMP, PA ;
BEEVER, JE ;
FERNANDO, RL ;
MCLAREN, DG ;
SCHOOK, LB .
JOURNAL OF ANIMAL SCIENCE, 1992, 70 (09) :2695-2706
[6]   Quantitative trait loci in genetically hypertensive rats - Possible sex specificity [J].
Clark, JS ;
Jeffs, B ;
Davidson, AO ;
Lee, WK ;
Anderson, NH ;
Bihoreau, MT ;
Brosnan, MJ ;
Devlin, AM ;
Kelman, AW ;
Lindpaintner, K ;
Dominiczak, AF .
HYPERTENSION, 1996, 28 (05) :898-906
[7]   GENETIC-VARIATION IN THE BETA(3)-ADRENERGIC RECEPTOR AND AN INCREASED CAPACITY TO GAIN WEIGHT IN PATIENTS WITH MORBID-OBESITY [J].
CLEMENT, K ;
VAISSE, C ;
MANNING, BS ;
BASDEVANT, A ;
GUYGRAND, B ;
RUIZ, J ;
SILVER, KD ;
SHULDINER, AR ;
FROGUEL, P ;
STROSBERG, AD .
NEW ENGLAND JOURNAL OF MEDICINE, 1995, 333 (06) :352-354
[8]   FAT (FAT) AND TUBBY (TUB) - 2 AUTOSOMAL RECESSIVE MUTATIONS CAUSING OBESITY SYNDROMES IN THE MOUSE [J].
COLEMAN, DL ;
EICHER, EM .
JOURNAL OF HEREDITY, 1990, 81 (06) :424-427
[9]   GROWTH QUANTITATIVE TRAIT LOCI (QTL) ON MOUSE CHROMOSOME-10 IN A QUACKENBUSH-SWISS X C57BL/6J BACKCROSS [J].
COLLINS, AC ;
MARTIN, ICA ;
KIRKPATRICK, BW .
MAMMALIAN GENOME, 1993, 4 (08) :454-458
[10]   A GENETIC-LINKAGE MAP OF THE MOUSE - CURRENT APPLICATIONS AND FUTURE-PROSPECTS [J].
COPELAND, NG ;
JENKINS, NA ;
GILBERT, DJ ;
EPPIG, JT ;
MALTAIS, LJ ;
MILLER, JC ;
DIETRICH, WF ;
WEAVER, A ;
LINCOLN, SE ;
STEEN, RG ;
STEIN, LD ;
NADEAU, JH ;
LANDER, ES .
SCIENCE, 1993, 262 (5130) :57-66