Genetics of population isolates

被引:202
作者
Arcos-Burgos, M
Muenke, M
机构
[1] Natl Ctr Human Genome Res, Med Genet Branch, NIH, Bethesda, MD 20892 USA
[2] Univ Antioquia, Mutacarcinogenesis & Genet Epidemiol Grp, Medellin, Colombia
关键词
population genetics; complex disorder; Columbia;
D O I
10.1034/j.1399-0004.2002.610401.x
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Genetic isolates, as shown empirically by the Finnish, Old Order Amish, Hutterites, Sardinian and Jewish communities among others, represent a most important and powerful tool in genetically mapping inherited disorders. The main features associated with that genetic power are the existence of multigenerational pedigrees which are mostly descended from a small number of founders a short number of generations ago, environmental and phenotypic homogeneity, restricted geographical distribution, the presence of exhaustive and detailed records correlating individuals in very well ascertained pedigrees, and inbreeding as a norm. On the other hand, the presence of a multifounder effect or admixture among divergent populations in the founder time (e.g. the Finnish and the Paisa community from Colombia) will theoretically result in increased linkage disequilibrium among adjacent loci. The present review evaluates the historical context and features of some genetic isolates with emphasis on the basic population genetic concepts of inbreeding and genetic drift, and also the state-of-the-art in mapping traits, both Mendelian and complex, on genetic isolates.
引用
收藏
页码:233 / 247
页数:15
相关论文
共 202 条
  • [91] A putative vulnerability locus to multiple sclerosis maps to 5p14-p12 in a region syntenic to the murine locus Eae2
    Kuokkanen, S
    Sundvall, M
    Terwilliger, JD
    Tienari, PJ
    Wikstrom, J
    Holmdahl, R
    Pettersson, U
    Peltonen, L
    [J]. NATURE GENETICS, 1996, 13 (04) : 477 - 480
  • [92] IDENTIFICATION OF A COMMON MUTATION IN FINNISH PATIENTS WITH NONKETOTIC HYPERGLYCINEMIA
    KURE, S
    TAKAYANAGI, M
    NARISAWA, K
    TADA, K
    LEISTI, J
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1992, 90 (01) : 160 - 164
  • [93] LaBuda MC, 1996, AM J HUM GENET, V59, P1343
  • [94] Lahermo P, 1996, AM J HUM GENET, V58, P1309
  • [95] Fine mapping of a gene responsible for regulating dietary cholesterol absorption; founder effects underlie cases of phytosterolaemia in multiple communities
    Lee, MH
    Gordon, D
    Ott, J
    Lu, KM
    Ose, L
    Miettinen, T
    Gylling, H
    Stalenhoef, AF
    Pandya, A
    Hidaka, H
    Brewer, B
    Kojima, H
    Sakuma, N
    Pegoraro, R
    Salen, G
    Patel, SB
    [J]. EUROPEAN JOURNAL OF HUMAN GENETICS, 2001, 9 (05) : 375 - 384
  • [96] Lendon CL, 1997, HUM MUTAT, V10, P186
  • [97] Genome scan for predisposing loci for distal interphalangeal joint osteoarthritis:: Evidence for a locus on 2q
    Leppävuori, J
    Kujala, U
    Kinnunen, J
    Kaprio, J
    Nissilä, M
    Heliövaara, M
    Klinger, N
    Partanen, J
    Terwilliger, JD
    Peltonen, L
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 65 (04) : 1060 - 1067
  • [98] MUTATION IN GELSOLIN GENE IN FINNISH HEREDITARY AMYLOIDOSIS
    LEVY, E
    HALTIA, M
    FERNANDEZMADRID, I
    KOIVUNEN, O
    GHISO, J
    PRELLI, F
    FRANGIONE, B
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1990, 172 (06) : 1865 - 1867
  • [99] Genetic architecture of temperament
    Lichtermann, D
    Ekelund, J
    Peltonen, L
    Järvelin, MR
    [J]. AMERICAN JOURNAL OF PSYCHIATRY, 2001, 158 (08) : 1339 - 1339
  • [100] BETA-SARCOGLYCAN - CHARACTERIZATION AND ROLE IN LIMB-GIRDLE MUSCULAR-DYSTROPHY LINKED TO 4Q12
    LIM, LE
    DUCLOS, F
    BROUX, O
    BOURG, N
    SUNADA, Y
    ALLAMAND, V
    MEYER, J
    RICHARD, IZ
    MOOMAW, C
    SLAUGHTER, C
    TOME, FMS
    FARDEAU, M
    JACKSON, CE
    BECKMANN, JS
    CAMPBELL, KP
    [J]. NATURE GENETICS, 1995, 11 (03) : 257 - 265