Browse > Article
http://dx.doi.org/10.5808/GI.2008.6.1.014

Inbreeding Coefficients in Two Isolated Mongolian Populations - GENDISCAN Study  

Sung, Joo-Hon (Department of Epidemiology, Seoul National University School of Public Health)
Lee, Mi-Kyeong (Ilchon Institute, Seoul National University College of Medicine)
Seo, Jeong-Sun (Ilchon Institute, Seoul National University College of Medicine)
Abstract
GENDISCAN study (Gene Discovery for Complex traits in Asian population of Northeast area) was designed to incorporate methodologies which enhance the power to identify genetic variations underlying complex disorders. Use of population isolates as the target population is a unique feather of this study. However, population isolates may have hidden inbreeding structures which can affect the validity of the study. To understand how this issue may affect results of GENDISCAN, we estimated inbreeding coefficients in two study populations in Mongolia. We analyzed the status of Hardy-Weinberg Equilibrium (HWE), polymorphism information contents (PIC), heterozygosity, allelic diversity, and inbreeding coefficients, using 317 and 1,044 STR (short tandem repeat) markers in Orkhontuul and Dashbalbar populations. HWE assumptions were generally met in most markers (88.6% and 94.2% respectively), and single marker PIC ranged between 0.2 and 0.9. Inbreeding coefficients were estimated to be 0.0023 and 0.0021, which are small enough to assure that conventional genetic analysis would work without any specific modification. We concluded that the population isolates used in GENDISCAN study would not present significant inflation of type I errors from inbreeding effects in its gene discovery analysis.
Keywords
inbreeding coefficient; Mengolian population; STR; HWE; PIC;
Citations & Related Records
연도 인용수 순위
  • Reference
1 Nomura, T. (2005). Joint effect of selection, linkage and partial inbreeding on additive genetic variance in an infinite population. Biom J. 47, 527-540.   DOI   ScienceOn
2 Zhang, W., Collins, A., Gibson, J., Tapper, W.J., Hunt, S., Deloukas, P., Bentley, D.R., and Morton, N.E. (2004). Impact of population structure, effective bottleneck time, and allele frequency on linkage disequilibrium maps. Proc Natl Acad Sci USA. 101, 18075-18080   DOI   ScienceOn
3 Grant, S.F., Thorleifsson, G., Reynisdottir, I., Benediktsson, R., Manolescu, A., Sainz, J., Helgason, A., Stefansson, H., Emilsson, V., Helgadottir, A., Styrkarsdottir, U., Magnusson, K.P., Walters, G.B., Palsdottir, E., Jonsdottir, T., Gudmundsdottir, T., Gylfason, A., Saemundsdottir, J., Wilensky, R.L., Reilly, M.P., Rader, D.J., Bagger, Y., Christiansen, C., Gudnason, V., Sigurdsson, G., Thorsteinsdottir, U., Gulcher, J.R., Kong, A., and Stefansson, K. (2006). Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes. Nat Genet. 38, 320-323.   DOI   ScienceOn
4 rcos-Burgos, M., and Muenke, M. (2002). Genetics of population isolates. Clin Genet. 61, 233-247.   DOI   ScienceOn
5 Escamilla, M.A. (2001). Population isolates: their special value for locating genes for bipolar disorder. Bipolar Disord. 3, 299-317.   DOI   ScienceOn
6 Jensen-Seaman, M.I., Deinard, A.S., and Kidd, K.K. (2001). Modern African ape populations as genetic and demographic models of the last common ancestor of humans, chimpanzees, and gorillas. J Hered. 92, 475-480.   DOI   ScienceOn
7 Peltonen, L., McKusick, V.A. (2001). Genomics and medicine. Dissecting human disease in the postgenomic era. Science 291,1224-1229.   DOI   ScienceOn
8 Gillespie, J.H. (2004). Population Genetics, A concise guide. 2nd Edition, The Johns Hopkins University Press, Baltimore MA, USA.
9 Hartl, D.L. (2000). Primer of population genetics 3 sub-Edition. Sinauer Associates, USA
10 Czika, W. (2005). SAS/Genetics 9.1.3 User's Guide. SAS Institute Inc., Cary, NC, USA.
11 Merikangas, K.R., Risch, N. (2003) Genomic priorities and public health. Science 302, 599-601.   DOI   ScienceOn
12 Hossjer, O. (2006). Modeling the effect of inbreeding among founders in linkage analysis. Theor Popul Biol. 70, 146-163.   DOI   ScienceOn
13 Pajukanta, P., Allayee, H., Krass, K.L., Kuraishy, A., Soro, A., Lilja, H.E., Mar, R., Taskinen, M.R., Nuotio, I., Laakso, M., Rotter, J.I., de Bruin, T.W., Cantor, R.M., Lusis, A.J., and Peltonen, L. (2003). Combined analysis of genome scans of dutch and finnish families reveals a susceptibility locus for high-density lipoprotein cholesterol on chromosome 16q. Am J Hum Genet. 72, 903-917.   DOI   ScienceOn
14 Santos-Lopes, S.S., Pereira, R.W., Wilson, I.J., and Pena ,S.D. (2007). A worldwide phylogeography for the human X chromosome. PLoS ONE. 2, e557.   DOI