Large-scale variation among human and great ape genomes determined by array comparative genomic hybridization

被引:105
作者
Locke, DP
Segraves, R
Carbone, L
Archidiacono, N
Albertson, DG
Pinkel, D
Eichler, EE [1 ]
机构
[1] Case Western Reserve Univ, Sch Med, Ctr Computat Genom, Dept Genet, Cleveland, OH 44106 USA
[2] Case Western Reserve Univ, Sch Med, Ctr Human Genet, Cleveland, OH 44106 USA
[3] Univ Hosp Cleveland, Cleveland, OH 44106 USA
[4] Univ Calif San Francisco, Ctr Comprehens Canc, San Francisco, CA 94143 USA
[5] Univ Bari, Sez Genet, Dipartimento Anat Patol & Genet, Bari, Italy
关键词
D O I
10.1101/gr.1003303
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
Large-scale genomic rearrangements are a major force Of evolutionary change and the ascertainment of such events between the human and great ape genomes is fundamental to a complete understanding of the genetic history and evolution of our species. Here, we present the results of an evolutionary analysis utilizing array comparative genomic hybridization (array CGH), measuring copy-number gains and losses among these species. Using an array of 2460 human bacterial artificial chromosomes (BACs) (12% of the genome), we identified a total of 63 sites of putative DNA copy-number variation between humans and the great apes (chimpanzee, bonobo, gorilla, and orangutan). Detailed molecular characterization of a subset of these sites confirmed rearrangements ranging from 40 to at least 175 kb in size. Surprisingly, the majority of variant sites differentiating great ape and human genomes were found within interstitial euchromatin. These data suggest that such large-scale events are not restricted solely to subtelomeric or pericentromeric regions, but also occur within genic regions. In addition, 519 of the verified variant sites localized to areas of intrachromosomal segmental duplication within the human genome. On the basis of the frequency of duplication in humans, this represents a 14-fold positional bias. In contrast to previous cytogenetic and comparative mapping studies, these results indicate extensive local repatterning of hominoid chromosomes in euchromatic regions through a duplication-driven mechanism of genome evolution.
引用
收藏
页码:347 / 357
页数:11
相关论文
共 34 条
  • [11] Genome scanning with array CGH delineates regional alterations in mouse islet carcinomas
    Hodgson G.
    Hager J.H.
    Volik S.
    Hariono S.
    Wernick M.
    Moore D.
    Albertson D.G.
    Pinkel D.
    Collins C.
    Hanahan D.
    Gray J.W.
    [J]. Nature Genetics, 2001, 29 (4) : 459 - 464
  • [12] Molecular structure and evolution of an alpha satellite non-alpha satellite junction at 16p11
    Horvath, JE
    Viggiano, L
    Loftus, BJ
    Adams, MD
    Archidiacono, N
    Rocchi, M
    Eichler, EE
    [J]. HUMAN MOLECULAR GENETICS, 2000, 9 (01) : 113 - 123
  • [13] The mosaic structure of human pericentromeric DNA: A strategy for characterizing complex regions of the human genome
    Horvath, JE
    Schwartz, S
    Eichler, EE
    [J]. GENOME RESEARCH, 2000, 10 (06) : 839 - 852
  • [14] Fully automatic quantification of microarray image data
    Jain, AN
    Tokuyasu, TA
    Snijders, AM
    Segraves, R
    Albertson, DG
    Pinkel, D
    [J]. GENOME RESEARCH, 2002, 12 (02) : 325 - 332
  • [15] Structure of chromosomal duplicons and their role in mediating human genomic disorders
    Ji, YG
    Eichler, EE
    Schwartz, S
    Nicholls, RD
    [J]. GENOME RESEARCH, 2000, 10 (05) : 597 - 610
  • [16] Great ape DNA sequences reveal a reduced diversity and an expansion in humans
    Kaessmann, H
    Wiebe, V
    Weiss, G
    Pääbo, S
    [J]. NATURE GENETICS, 2001, 27 (02) : 155 - 156
  • [17] EVOLUTION AT 2 LEVELS IN HUMANS AND CHIMPANZEES
    KING, MC
    WILSON, AC
    [J]. SCIENCE, 1975, 188 (4184) : 107 - 116
  • [18] HIGH-RESOLUTION MAPPING OF HUMAN CHROMOSOME-11 BY INSITU HYBRIDIZATION WITH COSMID CLONES
    LICHTER, P
    TANG, CJC
    CALL, K
    HERMANSON, G
    EVANS, GA
    HOUSMAN, D
    WARD, DC
    [J]. SCIENCE, 1990, 247 (4938) : 64 - 69
  • [19] Genomic disorders: structural features of the genome can lead to DNA rearrangements and human disease traits
    Lupski, JR
    [J]. TRENDS IN GENETICS, 1998, 14 (10) : 417 - 422
  • [20] Pathological consequences of sequence duplications in the human genome
    Mazzarella, R
    Schlessinger, D
    [J]. GENOME RESEARCH, 1998, 8 (10) : 1007 - 1021