Phylogenetic resolution of complex mutational features at Y-STR DYS390 in Aboriginal Australians and Papuans

被引:49
作者
Forster, P
Kayser, M
Meyer, E
Roewer, L
Pfeiffer, H
Benkmann, H
Brinkmann, B
机构
[1] Univ Munster, Inst Med Legale, D-48149 Munster, Germany
[2] Humboldt Univ, Inst Legal Med, Berlin, Germany
[3] Univ Jena, Inst Legal Med, D-6900 Jena, Germany
[4] Univ Hamburg, Inst Human Genet, D-2000 Hamburg, Germany
关键词
human; Y chromosome; evolution; Australia; Papua New Guinea;
D O I
10.1093/oxfordjournals.molbev.a026018
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Y-chromosomal short tandem repeats (STRs) are used for the study of male aspects of human evolution as well as for forensic applications and paternity testing. Both applications require an understanding of the underlying mutational mechanisms that create variability. We describe complex mutations at the substructured DYS390 STR locus in 97 natives of the New Guinea/Australian region. Sequencing of short alleles in these populations indicates multirepeat deletions. All samples are further characterized using the five additional Y-STR loci DYS19, DXYS156-Y, DYS391, DYS392, and DYS393. Phylogenetic analysis of the resulting haplotypes yields ethnically specific clusters predating the settlement of Australia and Papua New Guinea (although archaic Home sapiens or Homo erectus lineages are absent). The phylogeny confirms that DYS390 violates the stepwise mutation model and demonstrates that the DYS390 locus mutates relatively rapidly and retains its variability after structural change.
引用
收藏
页码:1108 / 1114
页数:7
相关论文
共 21 条
  • [1] ALLEN RC, 1989, BIOTECHNIQUES, V7, P736
  • [2] BANDELT HJ, 1995, GENETICS, V141, P743
  • [3] Mutation rate in human microsatellites:: Influence of the structure and length of the tandem repeat
    Brinkmann, B
    Klintschar, M
    Neuhuber, F
    Hühne, J
    Rolf, B
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 62 (06) : 1408 - 1415
  • [4] Complex mutational events at the HumD21S11 locus
    Brinkmann, B
    Meyer, E
    Junge, A
    [J]. HUMAN GENETICS, 1996, 98 (01) : 60 - 64
  • [5] STRUCTURE OF NEW MUTATIONS IN 2 STR SYSTEMS
    BRINKMANN, B
    MOLLER, A
    WIEGAND, P
    [J]. INTERNATIONAL JOURNAL OF LEGAL MEDICINE, 1995, 107 (04) : 201 - 203
  • [6] BUDOWLE B, 1991, AM J HUM GENET, V48, P137
  • [7] HLA-DR RFLP DISTRIBUTIONS IN 2 GROUPS OF ABORIGINAL AUSTRALIANS
    DAVIES, R
    PACE, R
    JAZWINSKA, EC
    SERJEANTSON, SW
    [J]. AUSTRALIAN AND NEW ZEALAND JOURNAL OF MEDICINE, 1990, 20 (06): : 790 - 793
  • [8] Dispersion of human Y chromosome haplotypes based on five microsatellites in global populations
    Deka, R
    Jin, L
    Shriver, MD
    Yu, LM
    Saha, N
    Barrantes, R
    Chakraborty, R
    Ferrell, RE
    [J]. GENOME RESEARCH, 1996, 6 (12): : 1177 - 1184
  • [9] 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
  • [10] GOEDDE HW, 1992, HUM GENET, V88, P344