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. 1997 Sep 1;100(5):1240–1247. doi: 10.1172/JCI119637

Identification of an obesity quantitative trait locus on mouse chromosome 2 and evidence of linkage to body fat and insulin on the human homologous region 20q.

A V Lembertas 1, L Pérusse 1, Y C Chagnon 1, J S Fisler 1, C H Warden 1, D A Purcell-Huynh 1, F T Dionne 1, J Gagnon 1, A Nadeau 1, A J Lusis 1, C Bouchard 1
PMCID: PMC508301  PMID: 9276742

Abstract

Chromosomal synteny between the mouse model and humans was used to map a gene for the complex trait of obesity. Analysis of NZB/BINJ x SM/J intercross mice located a quantitative trait locus (QTL) for obesity on distal mouse chromosome 2, in a region syntenic with a large region of human chromosome 20, showing linkage to percent body fat (likelihood of the odds [LOD] score 3.6) and fat mass (LOD score 4.3). The QTL was confirmed in a congenic mouse strain. To test whether the QTL contributes to human obesity, we studied linkage between markers located within a 52-cM region extending from 20p12 to 20q13.3 and measures of obesity in 650 French Canadian subjects from 152 pedigrees participating in the Quebec Family Study. Sib-pair analysis based on a maximum of 258 sib pairs revealed suggestive linkages between the percentage of body fat (P < 0.004), body mass index (P < 0.008), and fasting insulin (P < 0.0005) and a locus extending approximately from ADA (the adenosine deaminase gene) to MC3R (the melanocortin 3 receptor gene). These data provide evidence that a locus on human chromosome 20q contributes to body fat and insulin in a human population, and demonstrate the utility of using interspecies syntenic relationships to find relevant disease loci in humans.

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Selected References

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  1. Borecki I. B., Rice T., Pérusse L., Bouchard C., Rao D. C. An exploratory investigation of genetic linkage with body composition and fatness phenotypes: the Québec Family Study. Obes Res. 1994 May;2(3):213–219. doi: 10.1002/j.1550-8528.1994.tb00050.x. [DOI] [PubMed] [Google Scholar]
  2. Bouchard C., Tremblay A., Després J. P., Nadeau A., Lupien P. J., Thériault G., Dussault J., Moorjani S., Pinault S., Fournier G. The response to long-term overfeeding in identical twins. N Engl J Med. 1990 May 24;322(21):1477–1482. doi: 10.1056/NEJM199005243222101. [DOI] [PubMed] [Google Scholar]
  3. Bray M. S., Boerwinkle E., Hanis C. L. OB gene not linked to human obesity in Mexican American affected sib pairs from Starr County, Texas. Hum Genet. 1996 Nov;98(5):590–595. doi: 10.1007/s004390050265. [DOI] [PubMed] [Google Scholar]
  4. Bultman S. J., Michaud E. J., Woychik R. P. Molecular characterization of the mouse agouti locus. Cell. 1992 Dec 24;71(7):1195–1204. doi: 10.1016/s0092-8674(05)80067-4. [DOI] [PubMed] [Google Scholar]
  5. Chagnon Y. C., Pérusse L., Lamothe M., Chagnon M., Nadeau A., Dionne F. T., Gagnon J., Chung W. K., Leibel R. L., Bouchard C. Suggestive linkages between markers on human 1p32-p22 and body fat and insulin levels in the Quebec Family Study. Obes Res. 1997 Mar;5(2):115–121. doi: 10.1002/j.1550-8528.1997.tb00651.x. [DOI] [PubMed] [Google Scholar]
  6. Chen H., Charlat O., Tartaglia L. A., Woolf E. A., Weng X., Ellis S. J., Lakey N. D., Culpepper J., Moore K. J., Breitbart R. E. Evidence that the diabetes gene encodes the leptin receptor: identification of a mutation in the leptin receptor gene in db/db mice. Cell. 1996 Feb 9;84(3):491–495. doi: 10.1016/s0092-8674(00)81294-5. [DOI] [PubMed] [Google Scholar]
  7. Clement K., Garner C., Hager J., Philippi A., LeDuc C., Carey A., Harris T. J., Jury C., Cardon L. R., Basdevant A. Indication for linkage of the human OB gene region with extreme obesity. Diabetes. 1996 May;45(5):687–690. doi: 10.2337/diab.45.5.687. [DOI] [PubMed] [Google Scholar]
  8. Comuzzie A. G., Hixson J. E., Almasy L., Mitchell B. D., Mahaney M. C., Dyer T. D., Stern M. P., MacCluer J. W., Blangero J. A major quantitative trait locus determining serum leptin levels and fat mass is located on human chromosome 2. Nat Genet. 1997 Mar;15(3):273–276. doi: 10.1038/ng0397-273. [DOI] [PubMed] [Google Scholar]
  9. DeBry R. W., Seldin M. F. Human/mouse homology relationships. Genomics. 1996 May 1;33(3):337–351. doi: 10.1006/geno.1996.0209. [DOI] [PubMed] [Google Scholar]
  10. Desbuquois B., Aurbach G. D. Use of polyethylene glycol to separate free and antibody-bound peptide hormones in radioimmunoassays. J Clin Endocrinol Metab. 1971 Nov;33(5):732–738. doi: 10.1210/jcem-33-5-732. [DOI] [PubMed] [Google Scholar]
  11. Duggirala R., Stern M. P., Mitchell B. D., Reinhart L. J., Shipman P. A., Uresandi O. C., Chung W. K., Leibel R. L., Hales C. N., O'Connell P. Quantitative variation in obesity-related traits and insulin precursors linked to the OB gene region on human chromosome 7. Am J Hum Genet. 1996 Sep;59(3):694–703. [PMC free article] [PubMed] [Google Scholar]
  12. Frankel W. N., Johnson E. W., Lutz C. M. Congenic strains reveal effects of the epilepsy quantitative trait locus, El2, separate from other El loci. Mamm Genome. 1995 Dec;6(12):839–843. doi: 10.1007/BF00292432. [DOI] [PubMed] [Google Scholar]
  13. Gantz I., Tashiro T., Barcroft C., Konda Y., Shimoto Y., Miwa H., Glover T., Munzert G., Yamada T. Localization of the genes encoding the melanocortin-2 (adrenocorticotropic hormone) and melanocortin-3 receptors to chromosomes 18p11.2 and 20q13.2-q13.3 by fluorescence in situ hybridization. Genomics. 1993 Oct;18(1):166–167. doi: 10.1006/geno.1993.1448. [DOI] [PubMed] [Google Scholar]
  14. Ghosh S., Palmer S. M., Rodrigues N. R., Cordell H. J., Hearne C. M., Cornall R. J., Prins J. B., McShane P., Lathrop G. M., Peterson L. B. Polygenic control of autoimmune diabetes in nonobese diabetic mice. Nat Genet. 1993 Aug;4(4):404–409. doi: 10.1038/ng0893-404. [DOI] [PubMed] [Google Scholar]
  15. Graff R. J., Snell G. D. Histocompatibility genes of mce. 8. The alleles of the H-1 locus. Transplantation. 1968 Jul;6(4):598–617. doi: 10.1097/00007890-196807000-00013. [DOI] [PubMed] [Google Scholar]
  16. Haseman J. K., Elston R. C. The investigation of linkage between a quantitative trait and a marker locus. Behav Genet. 1972 Mar;2(1):3–19. doi: 10.1007/BF01066731. [DOI] [PubMed] [Google Scholar]
  17. Hyer R. N., Julier C., Buckley J. D., Trucco M., Rotter J., Spielman R., Barnett A., Bain S., Boitard C., Deschamps I. High-resolution linkage mapping for susceptibility genes in human polygenic disease: insulin-dependent diabetes mellitus and chromosome 11q. Am J Hum Genet. 1991 Feb;48(2):243–257. [PMC free article] [PubMed] [Google Scholar]
  18. Jacob H. J., Lindpaintner K., Lincoln S. E., Kusumi K., Bunker R. K., Mao Y. P., Ganten D., Dzau V. J., Lander E. S. Genetic mapping of a gene causing hypertension in the stroke-prone spontaneously hypertensive rat. Cell. 1991 Oct 4;67(1):213–224. doi: 10.1016/0092-8674(91)90584-l. [DOI] [PubMed] [Google Scholar]
  19. Kern P. A., Ong J. M., Goers J. W., Pedersen M. E. Regulation of lipoprotein lipase immunoreactive mass in isolated human adipocytes. J Clin Invest. 1988 Feb;81(2):398–406. doi: 10.1172/JCI113332. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Kuczmarski R. J., Flegal K. M., Campbell S. M., Johnson C. L. Increasing prevalence of overweight among US adults. The National Health and Nutrition Examination Surveys, 1960 to 1991. JAMA. 1994 Jul 20;272(3):205–211. doi: 10.1001/jama.272.3.205. [DOI] [PubMed] [Google Scholar]
  21. Lander E. S., Green P., Abrahamson J., Barlow A., Daly M. J., Lincoln S. E., Newberg L. A., Newburg L. MAPMAKER: an interactive computer package for constructing primary genetic linkage maps of experimental and natural populations. Genomics. 1987 Oct;1(2):174–181. doi: 10.1016/0888-7543(87)90010-3. [DOI] [PubMed] [Google Scholar]
  22. Lander E. S., Schork N. J. Genetic dissection of complex traits. Science. 1994 Sep 30;265(5181):2037–2048. doi: 10.1126/science.8091226. [DOI] [PubMed] [Google Scholar]
  23. Lander E., Kruglyak L. Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results. Nat Genet. 1995 Nov;11(3):241–247. doi: 10.1038/ng1195-241. [DOI] [PubMed] [Google Scholar]
  24. Malas S., Peters J., Abbott C. The genes for endothelin 3, vitamin D 24-hydroxylase, and melanocortin 3 receptor map to distal mouse chromosome 2, in the region of conserved synteny with human chromosome 20. Mamm Genome. 1994 Sep;5(9):577–579. doi: 10.1007/BF00354934. [DOI] [PubMed] [Google Scholar]
  25. Miller M. W., Duhl D. M., Vrieling H., Cordes S. P., Ollmann M. M., Winkes B. M., Barsh G. S. Cloning of the mouse agouti gene predicts a secreted protein ubiquitously expressed in mice carrying the lethal yellow mutation. Genes Dev. 1993 Mar;7(3):454–467. doi: 10.1101/gad.7.3.454. [DOI] [PubMed] [Google Scholar]
  26. Miwa H., Gantz I., Konda Y., Shimoto Y., Yamada T. Structural determinants of the melanocortin peptides required for activation of melanocortin-3 and melanocortin-4 receptors. J Pharmacol Exp Ther. 1995 Apr;273(1):367–372. [PubMed] [Google Scholar]
  27. Morel L., Yu Y., Blenman K. R., Caldwell R. A., Wakeland E. K. Production of congenic mouse strains carrying genomic intervals containing SLE-susceptibility genes derived from the SLE-prone NZM2410 strain. Mamm Genome. 1996 May;7(5):335–339. doi: 10.1007/s003359900098. [DOI] [PubMed] [Google Scholar]
  28. Morton N. E., Collins A., Lawrence S., Shields D. C. Algorithms for a location database. Ann Hum Genet. 1992 Jul;56(Pt 3):223–232. doi: 10.1111/j.1469-1809.1992.tb01147.x. [DOI] [PubMed] [Google Scholar]
  29. Nadeau J. H. Maps of linkage and synteny homologies between mouse and man. Trends Genet. 1989 Mar;5(3):82–86. doi: 10.1016/0168-9525(89)90031-0. [DOI] [PubMed] [Google Scholar]
  30. Naggert J. K., Fricker L. D., Varlamov O., Nishina P. M., Rouille Y., Steiner D. F., Carroll R. J., Paigen B. J., Leiter E. H. Hyperproinsulinaemia in obese fat/fat mice associated with a carboxypeptidase E mutation which reduces enzyme activity. Nat Genet. 1995 Jun;10(2):135–142. doi: 10.1038/ng0695-135. [DOI] [PubMed] [Google Scholar]
  31. Norman R. A., Bogardus C., Ravussin E. Linkage between obesity and a marker near the tumor necrosis factor-alpha locus in Pima Indians. J Clin Invest. 1995 Jul;96(1):158–162. doi: 10.1172/JCI118016. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Norman R. A., Leibel R. L., Chung W. K., Power-Kehoe L., Chua S. C., Jr, Knowler W. C., Thompson D. B., Bogardus C., Ravussin E. Absence of linkage of obesity and energy metabolism to markers flanking homologues of rodent obesity genes in Pima Indians. Diabetes. 1996 Sep;45(9):1229–1232. doi: 10.2337/diab.45.9.1229. [DOI] [PubMed] [Google Scholar]
  33. Norman R. A., Thompson D. B., Foroud T., Garvey W. T., Bennett P. H., Bogardus C., Ravussin E. Genomewide search for genes influencing percent body fat in Pima Indians: suggestive linkage at chromosome 11q21-q22. Pima Diabetes Gene Group. Am J Hum Genet. 1997 Jan;60(1):166–173. [PMC free article] [PubMed] [Google Scholar]
  34. Ohisalo J. J., Ranta S., Huhtaniemi I. T. Inhibition of adenosine 3',5'-monophosphate accumulation and lipolysis by adenosine analogs in human subcutaneous adipocytes. J Clin Endocrinol Metab. 1984 Jan;58(1):32–35. doi: 10.1210/jcem-58-1-32. [DOI] [PubMed] [Google Scholar]
  35. Patel P., Lo Y. M., Hattersley A., Bell G. I., Tybjaerg-Hansen A., Nerup J., Turner R. C., Wainscoat J. S. Linkage analysis of maturity-onset diabetes of the young with microsatellite polymorphisms. No linkage to ADA or GLUT2 genes in two families. Diabetes. 1992 Aug;41(8):962–967. doi: 10.2337/diab.41.8.962. [DOI] [PubMed] [Google Scholar]
  36. Price R. A., Ness R., Laskarzewski P. Common major gene inheritance of extreme overweight. Hum Biol. 1990 Dec;62(6):747–765. [PubMed] [Google Scholar]
  37. Purcell-Huynh D. A., Weinreb A., Castellani L. W., Mehrabian M., Doolittle M. H., Lusis A. J. Genetic factors in lipoprotein metabolism. Analysis of a genetic cross between inbred mouse strains NZB/BINJ and SM/J using a complete linkage map approach. J Clin Invest. 1995 Oct;96(4):1845–1858. doi: 10.1172/JCI118230. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Pérusse L., Chagnon Y. C., Dionne F. T., Bouchard C. The human obesity gene map: the 1996 update. Obes Res. 1997 Jan;5(1):49–61. doi: 10.1002/j.1550-8528.1997.tb00283.x. [DOI] [PubMed] [Google Scholar]
  39. Reed D. R., Ding Y., Xu W., Cather C., Green E. D., Price R. A. Extreme obesity may be linked to markers flanking the human OB gene. Diabetes. 1996 May;45(5):691–694. doi: 10.2337/diab.45.5.691. [DOI] [PubMed] [Google Scholar]
  40. Rice T., Borecki I. B., Bouchard C., Rao D. C. Segregation analysis of fat mass and other body composition measures derived from underwater weighing. Am J Hum Genet. 1993 May;52(5):967–973. [PMC free article] [PubMed] [Google Scholar]
  41. Rice T., Tremblay A., Dériaz O., Pérusse L., Rao D. C., Bouchard C. Genetic pleiotropy for resting metabolic rate with fat-free mass and fat mass: the Québec Family Study. Obes Res. 1996 Mar;4(2):125–131. doi: 10.1002/j.1550-8528.1996.tb00524.x. [DOI] [PubMed] [Google Scholar]
  42. Risch N., Ghosh S., Todd J. A. Statistical evaluation of multiple-locus linkage data in experimental species and its relevance to human studies: application to nonobese diabetic (NOD) mouse and human insulin-dependent diabetes mellitus (IDDM). Am J Hum Genet. 1993 Sep;53(3):702–714. [PMC free article] [PubMed] [Google Scholar]
  43. Roselli-Rehfuss L., Mountjoy K. G., Robbins L. S., Mortrud M. T., Low M. J., Tatro J. B., Entwistle M. L., Simerly R. B., Cone R. D. Identification of a receptor for gamma melanotropin and other proopiomelanocortin peptides in the hypothalamus and limbic system. Proc Natl Acad Sci U S A. 1993 Oct 1;90(19):8856–8860. doi: 10.1073/pnas.90.19.8856. [DOI] [PMC free article] [PubMed] [Google Scholar]
  44. SIRI W. E. The gross composition of the body. Adv Biol Med Phys. 1956;4:239–280. doi: 10.1016/b978-1-4832-3110-5.50011-x. [DOI] [PubMed] [Google Scholar]
  45. SNELL G. D. Histocompatibility genes of the mouse. I. Demonstration of weak histocompatibility differences by immunization and controlled tumor dosage. J Natl Cancer Inst. 1958 Apr;20(4):787–824. [PubMed] [Google Scholar]
  46. Stunkard A. J., Harris J. R., Pedersen N. L., McClearn G. E. The body-mass index of twins who have been reared apart. N Engl J Med. 1990 May 24;322(21):1483–1487. doi: 10.1056/NEJM199005243222102. [DOI] [PubMed] [Google Scholar]
  47. Tartaglia L. A., Dembski M., Weng X., Deng N., Culpepper J., Devos R., Richards G. J., Campfield L. A., Clark F. T., Deeds J. Identification and expression cloning of a leptin receptor, OB-R. Cell. 1995 Dec 29;83(7):1263–1271. doi: 10.1016/0092-8674(95)90151-5. [DOI] [PubMed] [Google Scholar]
  48. Todd J. A., Aitman T. J., Cornall R. J., Ghosh S., Hall J., Hearne C. M., Knight A., Love J., McAleer M. A., Prins J. B. Genetic analysis of a complex, multifactorial disease, autoimmune type 1 (insulin-dependent) diabetes. Res Immunol. 1991 Jun-Aug;142(5-6):483–483. doi: 10.1016/0923-2494(91)90051-j. [DOI] [PubMed] [Google Scholar]
  49. Valera A., Pujol A., Pelegrin M., Bosch F. Transgenic mice overexpressing phosphoenolpyruvate carboxykinase develop non-insulin-dependent diabetes mellitus. Proc Natl Acad Sci U S A. 1994 Sep 13;91(19):9151–9154. doi: 10.1073/pnas.91.19.9151. [DOI] [PMC free article] [PubMed] [Google Scholar]
  50. Vogler G. P., Sørensen T. I., Stunkard A. J., Srinivasan M. R., Rao D. C. Influences of genes and shared family environment on adult body mass index assessed in an adoption study by a comprehensive path model. Int J Obes Relat Metab Disord. 1995 Jan;19(1):40–45. [PubMed] [Google Scholar]
  51. Warden C. H., Fisler J. S., Pace M. J., Svenson K. L., Lusis A. J. Coincidence of genetic loci for plasma cholesterol levels and obesity in a multifactorial mouse model. J Clin Invest. 1993 Aug;92(2):773–779. doi: 10.1172/JCI116649. [DOI] [PMC free article] [PubMed] [Google Scholar]
  52. Warden C. H., Fisler J. S., Shoemaker S. M., Wen P. Z., Svenson K. L., Pace M. J., Lusis A. J. Identification of four chromosomal loci determining obesity in a multifactorial mouse model. J Clin Invest. 1995 Apr;95(4):1545–1552. doi: 10.1172/JCI117827. [DOI] [PMC free article] [PubMed] [Google Scholar]
  53. West D. B., Boozer C. N., Moody D. L., Atkinson R. L. Dietary obesity in nine inbred mouse strains. Am J Physiol. 1992 Jun;262(6 Pt 2):R1025–R1032. doi: 10.1152/ajpregu.1992.262.6.R1025. [DOI] [PubMed] [Google Scholar]
  54. West D. B., Goudey-Lefevre J., York B., Truett G. E. Dietary obesity linked to genetic loci on chromosomes 9 and 15 in a polygenic mouse model. J Clin Invest. 1994 Oct;94(4):1410–1416. doi: 10.1172/JCI117477. [DOI] [PMC free article] [PubMed] [Google Scholar]
  55. West D. B., Waguespack J., York B., Goudey-Lefevre J., Price R. A. Genetics of dietary obesity in AKR/J x SWR/J mice: segregation of the trait and identification of a linked locus on chromosome 4. Mamm Genome. 1994 Sep;5(9):546–552. doi: 10.1007/BF00354928. [DOI] [PubMed] [Google Scholar]
  56. Wilson B. D., Ollmann M. M., Kang L., Stoffel M., Bell G. I., Barsh G. S. Structure and function of ASP, the human homolog of the mouse agouti gene. Hum Mol Genet. 1995 Feb;4(2):223–230. doi: 10.1093/hmg/4.2.223. [DOI] [PubMed] [Google Scholar]
  57. Xu W., Reed D. R., Ding Y., Price R. A. Absence of linkage between human obesity and the mouse agouti homologous region (20q11.2) or other markers spanning chromosome 20q. Obes Res. 1995 Nov;3(6):559–562. doi: 10.1002/j.1550-8528.1995.tb00190.x. [DOI] [PubMed] [Google Scholar]
  58. Yui M. A., Muralidharan K., Moreno-Altamirano B., Perrin G., Chestnut K., Wakeland E. K. Production of congenic mouse strains carrying NOD-derived diabetogenic genetic intervals: an approach for the genetic dissection of complex traits. Mamm Genome. 1996 May;7(5):331–334. doi: 10.1007/s003359900097. [DOI] [PubMed] [Google Scholar]
  59. Zhang Y., Proenca R., Maffei M., Barone M., Leopold L., Friedman J. M. Positional cloning of the mouse obese gene and its human homologue. Nature. 1994 Dec 1;372(6505):425–432. doi: 10.1038/372425a0. [DOI] [PubMed] [Google Scholar]

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