Y chromosome STR haplotypes in four populations from northwest Africa

被引:27
作者
Bosch, E
Calafell, F
Pérez-Lezaun, A
Comas, D
Izaabel, H
Akhayat, O
Sefiani, A
Hariti, G
Dugoujon, JM
Bertranpetit, J
机构
[1] Univ Pompeu Fabra, Fac Ciencies Salut & Vida, Unit Biol Evolut, Barcelona 08003, Spain
[2] Univ Ibnou Zohr, Fac Sci, Cellular & Mol Biol Lab, Agadir, Morocco
[3] Natl Inst Hyg, Rabat, Morocco
[4] CHU Alger Ctr, Hop Mustapha, Alger, Algeria
[5] CHU Purpan, CNRS, ERS 1590, Toulouse, France
关键词
Y chromosome; short tandem repeats (STRs); haplotypes; northwest African populations;
D O I
10.1007/s004140000136
中图分类号
DF [法律]; D9 [法律]; R [医药、卫生];
学科分类号
0301 ; 10 ;
摘要
The eight short tandem repeat (STR) polymorphic systems mapping on the male-specific region of the human Y chromosome, DYS19, DYS388, DYS389I, DYS389II, DYS390, DYS391, DYS392 and DYS393, were typed in four populations from northwest (NW) Africa (Moroccan Arabs, southern Moroccan Berbers, Saharawis and Mozabites). Allele frequency distributions showed statistically significant differences for ail loci among all the populations except for DYS19. Complete typing was obtained for 185 chromosomes, which showed 74 different haplotypes. The two most frequent haplotypes were found in 16.2% and 15.1% of the individuals, although the latter was almost exclusively found in the Mozabites. Locus and haplotype informativeness were measured by means of the gene diversity (D). The haplotype diversity ranged from 0.856 (Mozabites) to 0.967 (southern Moroccan Berbers). For some loci, allele frequencies in NW Africans were clearly different from those in Europeans. The most common NW African haplotype was found only in one individual out of a total of 494 Europeans typed for the whole STR set. Thus, NW African and European Y chromosomes are clearly differentiated.
引用
收藏
页码:36 / 40
页数:5
相关论文
共 21 条
  • [1] Novel mutation processes in the evolution of a haploid minisatellite, MSY1: array homogenization without homogenization
    Bouzekri, N
    Taylor, PG
    Hammer, MF
    Jobling, MA
    [J]. HUMAN MOLECULAR GENETICS, 1998, 7 (04) : 655 - 659
  • [2] Increased forensic efficiency of a STR-based Y-specific haplotype by addition of the highly polymorphic: DYS385 locus
    Caglia, A
    Dobosz, M
    Boschi, I
    d'Aloja, E
    Pascali, VL
    [J]. INTERNATIONAL JOURNAL OF LEGAL MEDICINE, 1998, 111 (03) : 142 - 146
  • [3] Genetic diversity in the Iberian Peninsula determined from mitochondrial sequence analysis
    CorteReal, HBSM
    Macaulay, VA
    Richards, MB
    Hariti, G
    Issad, MS
    CambonThomsen, A
    Papiha, S
    Bertranpetit, J
    Sykes, BC
    [J]. ANNALS OF HUMAN GENETICS, 1996, 60 : 331 - 350
  • [4] Chromosome Y microsatellites: Population genetic and evolutionary aspects
    deKnijff, P
    Kayser, M
    Caglia, A
    Corach, D
    Fretwell, N
    Gehrig, C
    Graziosi, G
    Heidorn, F
    Herrmann, S
    Herzog, B
    Hidding, M
    Honda, K
    Jobling, M
    Krawczak, M
    Leim, K
    Meuser, S
    Meyer, E
    Oesterreich, W
    Pandya, A
    Parson, W
    Penacino, G
    PerezLezaun, A
    Piccinini, A
    Prinz, M
    Schmitt, C
    Schneider, PM
    Szibor, R
    TeifelGreding, J
    Weichhold, G
    Roewer, L
    [J]. INTERNATIONAL JOURNAL OF LEGAL MEDICINE, 1997, 110 (03) : 134 - 149
  • [5] HLA class II DNA polymorphism in a Moroccan population from the Souss, Agadir area
    Izaabel, H
    Garchon, HJ
    Caillat-Zucman, S
    Beaurain, G
    Akhayat, O
    Bach, JF
    Sanchez-Mazas, A
    [J]. TISSUE ANTIGENS, 1998, 51 (01): : 106 - 110
  • [6] The Y chromosome in forensic analysis and paternity testing
    Jobling, MA
    Pandya, A
    TylerSmith, C
    [J]. INTERNATIONAL JOURNAL OF LEGAL MEDICINE, 1997, 110 (03) : 118 - 124
  • [7] Hypervariable digital DNA codes for human paternal lineages:: MVR-PCR at the Y-specific minisatellite, MSY1 (DYF155S1)
    Jobling, MA
    Bouzekri, N
    Taylor, PG
    [J]. HUMAN MOLECULAR GENETICS, 1998, 7 (04) : 643 - 653
  • [8] FATHERS AND SONS - THE Y-CHROMOSOME AND HUMAN-EVOLUTION
    JOBLING, MA
    TYLERSMITH, C
    [J]. TRENDS IN GENETICS, 1995, 11 (11) : 449 - 456
  • [9] Evaluation of Y-chromosomal STRs: A multicenter study
    Kayser, M
    Caglia, A
    Corach, D
    Fretwell, N
    Gehrig, C
    Graziosi, G
    Heidorn, F
    Herrmann, S
    Herzog, B
    Hidding, M
    Honda, K
    Jobling, M
    Krawczak, M
    Leim, K
    Meuser, S
    Meyer, E
    Oesterreich, W
    Pandya, A
    Parson, W
    Penacino, G
    PerezLezaun, A
    Piccinini, A
    Prinz, M
    Schmitt, C
    Schneider, PM
    Szibor, R
    TeifelGreding, J
    Weichold, G
    deKnijff, P
    Roewer, L
    [J]. INTERNATIONAL JOURNAL OF LEGAL MEDICINE, 1997, 110 (03) : 125 - +
  • [10] Dual origins of Finns revealed by Y chromosome haplotype variation
    Kittles, RA
    Perola, M
    Peltonen, L
    Bergen, AW
    Aragon, RA
    Virkkunen, M
    Linnoila, M
    Goldman, D
    Long, JC
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 62 (05) : 1171 - 1179