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
  • [1] High-resolution physical and transcriptional mapping of the autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy locus on chromosome 21q22.3 FISH
    Aaltonen, J
    HorelliKuitunen, N
    Fan, JB
    Bjorses, P
    Perheentupa, J
    Myers, R
    Palotie, A
    Peltonen, L
    [J]. GENOME RESEARCH, 1997, 7 (08) : 820 - 829
  • [2] AGUIRRE A, 1991, AM J HUM GENET, V49, P450
  • [3] MUTATION IN THE FOLLICLE-STIMULATING-HORMONE RECEPTOR GENE CAUSES HEREDITARY HYPERGONADOTROPIC OVARIAN FAILURE
    AITTOMAKI, K
    LUCENA, JLD
    PAKARINEN, P
    SISTONEN, P
    TAPANAINEN, J
    GROMOLL, J
    KASKIKARI, R
    SANKILA, EM
    LEHVASLAIHO, H
    ENGEL, AR
    NIESCHLAG, E
    HUHTANIEMI, I
    DELACHAPELLE, A
    [J]. CELL, 1995, 82 (06) : 959 - 968
  • [4] AMINOFF M, 1995, AM J HUM GENET, V57, P824
  • [5] Rheumatoid arthritis association in Colombian population is restricted to HLA-DRB1*04 QRRAA alleles
    Anaya, JM
    Correa, PA
    Mantilla, RD
    Arcos-Burgos, M
    [J]. GENES AND IMMUNITY, 2002, 3 (01) : 56 - 58
  • [6] ANAYA JM, 2002, IN PRESS SEMINARS AR
  • [7] Familial dysautonomia is caused by mutations of the IKAP gene
    Anderson, SL
    Coli, R
    Daly, IW
    Kichula, EA
    Rork, MJ
    Volpi, SA
    Ekstein, J
    Rubin, BY
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 68 (03) : 753 - 758
  • [8] Archival, demographic and genetic studies define a Sardinian sub-isolate as a suitable model for mapping complex traits
    Angius, A
    Melis, PM
    Morelli, L
    Petretto, E
    Casu, G
    Maestrale, GB
    Fraumene, C
    Bebbere, D
    Forabosco, P
    Pirastu, M
    [J]. HUMAN GENETICS, 2001, 109 (02) : 198 - 209
  • [9] Arcos-Burgos M, 1998, REV NEUROLOGIA, V26, P50
  • [10] Vitiligo: complex segregation and linkage disequilibrium analyses with respect to microsatellite loci spanning the HLA
    Arcos-Burgos, M
    Parodi, E
    Salgar, M
    Bedoya, E
    Builes, JJ
    Jaramillo, D
    Ceballos, G
    Uribe, A
    Rivera, N
    Rivera, D
    Fonseca, I
    Camargo, M
    Palacio, LG
    [J]. HUMAN GENETICS, 2002, 110 (04) : 334 - 342