Dissection of multigenic obesity traits in congenic mouse strains

被引:30
作者
Estrada-Smith, D
Castellani, LW
Wong, H
Wen, PZ
Chui, A
Lusis, AJ
Davis, RC
机构
[1] Gonda Goldschmeid Ctr Neurosci & Human Genet Res, Dept Human Genet, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Dept Med, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, Dept Microbiol Mol Genet & Immunol, Los Angeles, CA 90095 USA
关键词
D O I
10.1007/s00335-003-2294-8
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
Previous quantitative trait locus mapping (QTL) identified multigenic obesity (MOB) loci on mouse Chromosome (Chr) 2 that influence the interrelated phenotypes of obesity, insulin resistance, and dyslipidemia. To better localize and characterize the MOB locus, three congenic mouse strains were created. Overlapping genomic intervals from the lean CAST/Ei (CAST) strain were introgressed onto an obesity-susceptible C57BL/6 (BL6) background to create proximal (15 Mb-73 Mb), middle (63 Mb-165 Mb), and distal (83 Mb-182 Mb) congenic strains. The congenic strains showed differences in obesity, insulin, and lipid traits consistent with the original QTL analysis for the locus. Importantly, characterization of the MOB congenics localized the effects of genes that underlie obesity-related traits to an introgressed interval (73-83 Mb) unique to the middle MOB congenic. Conversely, significant differences between the lipid and insulin profiles of the middle and distal MOB congenics implicated the presence of at least two genes that underlie these traits. When fed an atherogenic diet, several traits associated with metabolic syndrome were observed in the distal MOB congenic, while alterations in plasma lipoproteins were observed in the middle MOB congenic strain.
引用
收藏
页码:14 / 22
页数:9
相关论文
共 28 条
[1]   Identification of Cd36 (Fat) as an insulin-resistance gene causing defective fatty acid and glucose metabolism in hypertensive rats [J].
Aitman, TJ ;
Glazier, AM ;
Wallace, CA ;
Cooper, LD ;
Norsworthy, PJ ;
Wahid, FN ;
Al-Majali, KM ;
Trembling, PM ;
Mann, CJ ;
Shoulders, CC ;
Graf, D ;
St Lezin, E ;
Kurtz, TW ;
Kren, V ;
Pravenec, M ;
Ibrahimi, A ;
Abumrad, NA ;
Stanton, LW ;
Scott, J .
NATURE GENETICS, 1999, 21 (01) :76-83
[2]  
[Anonymous], 1999, ELS OCEAN ENGN BK S
[3]   Genetic and mutational analyses of a large multiethnic Bardet-Biedl cohort reveal a minor involvement of BBS6 and delineate the critical intervals of other loci [J].
Beales, PL ;
Katsanis, N ;
Lewis, RA ;
Ansley, SJ ;
Elcioglu, N ;
Raza, J ;
Woods, MO ;
Green, JS ;
Parfrey, PS ;
Davidson, WS ;
Lupski, JR .
AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 68 (03) :606-616
[4]   Linkage of genetic markers on human chromosomes 20 and 12 to NIDDM in Caucasian sib pairs with a history of diabetic nephropathy [J].
Bowden, DW ;
Sale, M ;
Howard, TD ;
Qadri, A ;
Spray, BJ ;
Rothschild, CB ;
Akots, G ;
Rich, SS ;
Freedman, BI .
DIABETES, 1997, 46 (05) :882-886
[5]  
Cheverud JM, 1996, GENETICS, V142, P1305
[6]   The Finland-United States Investigation of Non-Insulin-Dependent Diabetes Mellitus Genetics (FUSION) study.: I.: An autosomal genome scan for genes that predispose to type 2 diabetes [J].
Ghosh, S ;
Watanabe, RM ;
Valle, TT ;
Hauser, ER ;
Magnuson, VL ;
Langefeld, CD ;
Ally, DS ;
Mohlke, KL ;
Silander, K ;
Kohtamäki, K ;
Chines, P ;
Balow, J ;
Birznieks, G ;
Chang, J ;
Eldridge, W ;
Erdos, MR ;
Karanjawala, ZE ;
Knapp, JI ;
Kudelko, K ;
Martin, C ;
Morales-Mena, A ;
Musick, A ;
Musick, T ;
Pfahl, C ;
Porter, R ;
Rayman, JB ;
Rha, D ;
Segal, L ;
Shapiro, S ;
Sharaf, R ;
Shurtleff, B ;
So, A ;
Tannenbaum, J ;
Te, C ;
Tovar, J ;
Unni, A ;
Welch, C ;
Whiten, R ;
Witt, A ;
Blaschak-Harvan, J ;
Douglas, JA ;
Duren, WL ;
Epstein, MP ;
Fingerlin, TE ;
Kaleta, HS ;
Lange, EM ;
Li, C ;
McEachin, RC ;
Stringham, HM ;
Trager, E .
AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 67 (05) :1174-1185
[7]   A genome-wide scan for human obesity genes reveals a major susceptibility locus on chromosome 10 [J].
Hager, J ;
Dina, C ;
Francke, S ;
Dubois, S ;
Houari, M ;
Vatin, V ;
Vaillant, E ;
Lorentz, N ;
Basdevant, A ;
Clement, K ;
Guy-Grand, B ;
Froguel, P .
NATURE GENETICS, 1998, 20 (03) :304-308
[8]   A genome-wide search for human non-insulin dependent (type 2) diabetes genes reveals a major susceptibility locus on chromosome 2 [J].
Hanis, CL ;
Boerwinkle, E ;
Chakraborty, R ;
Ellsworth, DL ;
Concannon, P ;
Stirling, B ;
Morrison, VA ;
Wapelhorst, B ;
Spielman, RS ;
GogolinEwens, KJ ;
Shephard, JM ;
Williams, SR ;
Risch, N ;
Hinds, D ;
Iwasaki, N ;
Ogata, M ;
Omori, Y ;
Petzold, C ;
Rietzsch, H ;
Schroder, HE ;
Schulze, J ;
Cox, NJ ;
Menzel, S ;
Boriraj, VV ;
Chen, X ;
Lim, LR ;
Lindner, T ;
Mereu, LE ;
Wang, YQ ;
Xiang, K ;
Yamagata, K ;
Yang, Y ;
Bell, GI .
NATURE GENETICS, 1996, 13 (02) :161-166
[9]   Linkage of body mass index to chromosome 20 in Utah pedigrees [J].
Hunt, SC ;
Abkevich, V ;
Hensel, CH ;
Gutin, A ;
Neff, CD ;
Russell, DL ;
Tran, T ;
Hong, XK ;
Jammulapati, S ;
Riley, R ;
Weaver-Feldhaus, J ;
Macalma, T ;
Richards, MM ;
Gress, R ;
Francis, M ;
Thomas, A ;
Frech, GC ;
Adams, TD ;
Shattuck, D ;
Stone, S .
HUMAN GENETICS, 2001, 109 (03) :279-285
[10]   New susceptibility locus for NIDDM is localized to human chromosome 20q [J].
Ji, LN ;
Malecki, M ;
Warram, JH ;
Yang, YD ;
Rich, SS ;
Krolewski, AS .
DIABETES, 1997, 46 (05) :876-881