The origin and evolution of human ampliconic gene families and ampliconic structure

被引:44
作者
Bhowmick, Bejon Kumar [1 ]
Satta, Yoko [1 ]
Takahata, Naoyuki [1 ]
机构
[1] Grad Univ Adv Studies, Dept Biosyst Sci, Sokendai, Kanagawa 2400193, Japan
关键词
D O I
10.1101/gr.5734907
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
Out of the nine male-specific gene families in the human Y chromosome amplicons, we investigate the origin and evolution of seven families for which gametologous and orthologous sequences are available. Proto-X/Y gene pairs in the original mammalian sex chromosomes played major roles in origins and gave rise to five gene families: XKRY, VCY, HSFY, RBMY, and TSPY. The divergence times between gametologous X- and Y-linked copies in these families are well correlated with the former X- chromosomal locations. The CDY and DAZ families originated exceptionally by retroposition and transposition of autosomal copies, respectively, but CDY possesses an X- linked copy of enigmatic origin. We also investigate the evolutionary relatedness among Y-linked copies of a gene family in light of their ampliconic locations ( palindromes, inverted repeats, and the TSPY array). Although any pair of copies located at the same arm positions within a palindrome is identical or nearly so by frequent gene conversion, copies located at different arm positions are distinctively different. Since these and other distinct copies in various gene families were amplified almost simultaneously in the stem lineage of Catarrhini, we take these simultaneous amplifications as evidence for the elaborate formation of Y ampliconic structure. Curiously, some copies in a gene family located at different palindromes exhibit high sequence similarity, and in most cases, such similarity greatly extends to repeat units that harbor these copies. It appears that such palindromic repeat units have evolved by and large en bloc, but they have undergone frequent exchanges between palindromes.
引用
收藏
页码:441 / 450
页数:10
相关论文
共 47 条
  • [11] An evolutionarily conserved germ cell-specific hnRNP is encoded by a retrotransposed gene
    Elliott, DJ
    Venables, JP
    Newton, CS
    Lawson, D
    Boyle, S
    Eperon, IC
    Cooke, HJ
    [J]. HUMAN MOLECULAR GENETICS, 2000, 9 (14) : 2117 - 2124
  • [12] A member of a gene family on Xp22.3, VCX-A, is deleted in patients with X-linked nonspecific mental retardation
    Fukami, M
    Kirsch, S
    Schiller, S
    Richter, A
    Benes, V
    Franco, B
    Muroya, K
    Rao, E
    Merker, S
    Niesler, B
    Ballabio, A
    Ansorge, W
    Ogata, T
    Rappold, GA
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 67 (03) : 563 - 573
  • [13] THE ORIGIN AND FUNCTION OF THE MAMMALIAN Y-CHROMOSOME AND Y-BORNE GENES - AN EVOLVING UNDERSTANDING
    GRAVES, JAM
    [J]. BIOESSAYS, 1995, 17 (04) : 311 - 320
  • [14] The rise and fall of SRY
    Graves, JAM
    [J]. TRENDS IN GENETICS, 2002, 18 (05) : 259 - 264
  • [15] The Old World monkey DAZ (Deleted in AZoospermia) gene yields insights into the evolution of the DAZ gene cluster on the human Y chromosome
    Gromoll, J
    Weinbauer, GF
    Skaletsky, H
    Schlatt, S
    Rocchietti-March, M
    Page, DC
    Nieschlag, E
    [J]. HUMAN MOLECULAR GENETICS, 1999, 8 (11) : 2017 - 2024
  • [16] Late Miocene hominids from the Middle Awash, Ethiopia
    Haile-Selassie, Y
    [J]. NATURE, 2001, 412 (6843) : 178 - 181
  • [17] Conservation of Y-linked genes during human evolution revealed by comparative sequencing in chimpanzee
    Hughes, JF
    Skaletsky, H
    Pyntikova, T
    Minx, PJ
    Graves, T
    Rozen, S
    Wilson, RK
    Page, DC
    [J]. NATURE, 2005, 437 (7055) : 101 - 104
  • [18] The amelogenin loci span an ancient pseudoautosomal boundary in diverse mammalian species
    Iwase, M
    Satta, Y
    Hirai, Y
    Hirai, H
    Imai, H
    Takahata, N
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (09) : 5258 - 5263
  • [19] A BOVINE HOMOLOG OF THE HUMAN TSPY GENE
    JAKUBICZKA, S
    SCHNIEDERS, F
    SCHMIDTKE, J
    [J]. GENOMICS, 1993, 17 (03) : 732 - 735
  • [20] JUKES T H, 1969, P21