Retroposon Compensatory Mechanism hypothesis not supported:: Zfa knockout mice are fertile

被引:8
作者
Banks, KG
Johnson, KA
Lerner, CP
Mahaffey, CL
Bronson, RT
Simpson, EM
机构
[1] Univ British Columbia, Dept Med Genet, British Columbia Res Inst Childrens & Womens Hlth, Ctr Mol Med & Therapeut, Vancouver, BC V5Z 4H4, Canada
[2] Jackson Lab, Bar Harbor, ME 04609 USA
关键词
retroposon; sperm count; sex chromosome inactivation; X and Y chromosome; Retroposon Compensatory Mechanism; sex body;
D O I
10.1016/S0888-7543(03)00155-1
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
It is hypothesized that autosomal retroposons compensate for the loss of their inactivated essential X-chromosome progenitors during spermatogenesis. Here we test this Retroposon Compensatory Mechanism (RCM) hypothesis using the Zfy gene family. The mouse autosomal retroposon Zfa is expressed in testes at the same developmental time points at which Zfx levels decline, which correspond to the time of male sex chromosome inactivation, suggesting that Zfa may compensate for the loss of Zfx during spermatogenesis. We examined the effect of Zfa-targeted mutagenesis on spermatogenesis in three genetically distinct mouse strains. Surprisingly, Zfa knockout mice showed no detectable fertility, sperm count, or testes morphology defects. We therefore conclude that Zfa is not an essential gene for spermatogenesis and fertility. This surprising finding now challenges the RCM hypothesis at least for the Zfy gene family. It also forces us to reevaluate the original data underpinning the RCM hypothesis for this family and to propose alternative hypotheses. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:254 / 260
页数:7
相关论文
共 49 条
  • [1] INACTIVATION OF THE ZFX GENE ON THE MOUSE X-CHROMOSOME
    ADLER, DA
    BRESSLER, SL
    CHAPMAN, VM
    PAGE, DC
    DISTECHE, CM
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (11) : 4592 - 4595
  • [2] ZFA IS AN EXPRESSED RETROPOSON DERIVED FROM AN ALTERNATIVE TRANSCRIPT OF THE ZFX GENE
    ASHWORTH, A
    SKENE, B
    SWIFT, S
    LOVELLBADGE, R
    [J]. EMBO JOURNAL, 1990, 9 (05) : 1529 - 1534
  • [3] X-CHROMOSOME INACTIVATION MAY EXPLAIN THE DIFFERENCE IN VIABILITY OF XO HUMANS AND MICE
    ASHWORTH, A
    RASTAN, S
    LOVELLBADGE, R
    KAY, G
    [J]. NATURE, 1991, 351 (6325) : 406 - 408
  • [4] THE TESTIS-SPECIFIC PHOSPHOGLYCERATE KINASE GENE PGK-2 IS A RECRUITED RETROPOSON
    BOER, PH
    ADRA, CN
    LAU, YF
    MCBURNEY, MW
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1987, 7 (09) : 3107 - 3112
  • [5] DAGG CHARLES P., 1966, P309
  • [6] A TESTIS-SPECIFIC FORM OF THE HUMAN PYRUVATE-DEHYDROGENASE E1-ALPHA SUBUNIT IS CODED FOR BY AN INTRONLESS GENE ON CHROMOSOME-4
    DAHL, HHM
    BROWN, RM
    HUTCHISON, WM
    MARAGOS, C
    BROWN, GK
    [J]. GENOMICS, 1990, 8 (02) : 225 - 232
  • [7] 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
  • [8] Mice lacking mitochondrial uncoupling protein are cold-sensitive but not obese
    Enerback, S
    Jacobsson, A
    Simpson, EM
    Guerra, C
    Yamashita, H
    Harper, ME
    Kozak, LP
    [J]. NATURE, 1997, 387 (6628) : 90 - 94
  • [9] GENE-EXPRESSION, X-INACTIVATION, AND METHYLATION DURING SPERMATOGENESIS - THE CASE OF ZFA, ZFX AND ZFY IN MICE
    ERICKSON, RP
    ZWINGMAN, T
    AO, A
    [J]. MOLECULAR REPRODUCTION AND DEVELOPMENT, 1993, 35 (02) : 114 - 120
  • [10] Revised nomenclature for strain 129 mice
    Festing, MFW
    Simpson, EM
    Davisson, MT
    Mobraaten, LE
    [J]. MAMMALIAN GENOME, 1999, 10 (08) : 836 - 836