Loci on chromosomes 2 (NIDDM1) and 15 interact to increase susceptibility to diabetes in Mexican Americans.

作者: Nancy J. Cox , Mike Frigge , Dan L. Nicolae , Patrick Concannon , Craig L. Hanis

DOI: 10.1038/6002

关键词:

摘要: Complex disorders such as diabetes, cardiovascular disease, asthma, hypertension and psychiatric illnesses account for a large disproportionate share of health care costs, but remain poorly characterized with respect to aetiology. The transmission is complex, reflecting the actions interactions multiple genetic environmental factors. Genetic analyses that allow simultaneous consideration susceptibility from regions may improve ability map genes complex disorders, are currently computationally intensive narrowly focused. We describe here an approach assessing evidence statistical between unlinked allows multipoint allele-sharing analysis take linkage at one region into in over rest genome. Using this method, we show interaction on chromosomes 2 (NIDDM1) 15 (near CYP19) makes contribution type diabetes Mexican Americans Starr County, Texas.

参考文章(21)
M Farrall, J A Todd, H J Cordell, Bennett, Y Kawaguchi, Two-locus maximum lod score analysis of a multifactorial trait: joint consideration of IDDM2 and IDDM4 with IDDM1 in type 1 diabetes. American Journal of Human Genetics. ,vol. 57, pp. 920- 934 ,(1995)
N J Schork, J Ott, M Boehnke, J D Terwilliger, Two-trait-locus linkage analysis: A powerful strategy for mapping complex genetic traits American Journal of Human Genetics. ,vol. 53, pp. 1127- 1136 ,(1993)
K S Kendler, P C Sham, C J MacLean, Joint linkage of multiple loci for a complex disorder. American Journal of Human Genetics. ,vol. 53, pp. 353- 366 ,(1993)
N Risch, Linkage strategies for genetically complex traits. II. The power of affected relative pairs. American Journal of Human Genetics. ,vol. 46, pp. 229- 241 ,(1990)
George Ebow Bonney, John M. Opitz, James F. Reynolds, On the statistical determination of major gene mechanisms in continuous human traits: Regressive models American Journal of Medical Genetics. ,vol. 18, pp. 731- 749 ,(1984) , 10.1002/AJMG.1320180420
Philippe Froguel, Habib Zouali, Nathalie Vionnet, Gilberto Velho, Martine Vaxillaire, Fang Sun, Suzanne Lesage, Markus Stoffel, Jun Takeda, Philippe Passa, M. Alan Permutt, Jacques S. Beckmann, Graeme I. Bell, Daniel Cohen, Familial Hyperglycemia Due to Mutations in Glucokinase -- Definition of a Subtype of Diabetes Mellitus The New England Journal of Medicine. ,vol. 328, pp. 697- 702 ,(1993) , 10.1056/NEJM199303113281005
Eric Lander, Leonid Kruglyak, Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results Nature Genetics. ,vol. 11, pp. 241- 247 ,(1995) , 10.1038/NG1195-241
Melanie M. Mahtani, Elisabeth Widén, Markku Lehto, Jeffrey Thomas, Mark McCarthy, James Brayer, Barbara Bryant, Gayun Chan, Mark Daly, Carol Forsblom, Timo Kanninen, Andrew Kirby, Leonid Kruglyak, Kevin Munnelly, Maikki Parkkonen, Mary Pat Reeve-Daly, Alix Weaver, Thomas Brettin, Geoffrey Duyk, Eric S. Lander, Leif C. Groop, Mapping of a gene for type 2 diabetes associated with an insulin secretion defect by a genome scan in Finnish families. Nature Genetics. ,vol. 14, pp. 90- 94 ,(1996) , 10.1038/NG0996-90
Doris A. Staffers, Jorge Ferrer, William L. Clarke, Joel F. Habener, Early-onset type-II diabetes mellitus (MODY4) linked to IPF1. Nature Genetics. ,vol. 17, pp. 138- 139 ,(1997) , 10.1038/NG1097-138
C.L. Hanis, E. Boerwinkle, R. Chakraborty, D.L. Ellsworth, P. Concannon, B. Stirling, V.A. Morrison, B. Wapelhorst, R.S. Spielman, K.J. Gogolin-Ewens, J.M. Shephard, S.R. Williams, N. Risch, D. Hinds, N. Iwasaki, M. Ogata, Y. Omori, C. Petzold, H. Rietzsch, H.-E. Schröder, J. Schulze, N.J. Cox, S. Menzel, V.V. Boriraj, X. Chen, L.R. Lim, T. Lindner, L.E. Mereu, Y.-Q. Wang, K. Xiang, K. Yamagata, Y. Yang, G.I. Bell, A genome–wide search for human non–insulin–dependent (type 2) diabetes genes reveals a major susceptibility locus on chromosome 2 Nature Genetics. ,vol. 13, pp. 161- 166 ,(1996) , 10.1038/NG0696-161