Ward Monika A, Burgoyne Paul S
Institute for Biogenesis Research, John A. Burns School of Medicine, University of Hawaii, Honolulu, Hawaii 96822, USA.
Biol Reprod. 2006 Apr;74(4):652-8. doi: 10.1095/biolreprod.105.048090. Epub 2005 Dec 14.
In mouse and man, Y chromosome deletions are frequently associated with spermatogenic defects. XY(Tdy)(m1)qdelSry males have an extensive Yq deletion that almost completely abolishes the expression of two gene families, Ssty and Sly, located within the male-specific region of the mouse Y long arm. These males exhibit severe sperm defects and sterility. XY(RIII)qdel males have a smaller interstitial Yq deletion, removing approximately two thirds of Ssty/Sly gene copies, and display an increased incidence of mild sperm head anomalies with impairment of fertility and an intriguing distortion in the sex ratio of offspring in favor of females. Here we used intracytoplasmic sperm injection (ICSI) to investigate the functional capacity of sperm from these Yq deletion males. Any selection related to the ability of sperm to fertilize in vitro is removed by ICSI, and we obtained two generations of live offspring from the infertile males. Genotyping of ICSI-derived offspring revealed that the Y(Tdym1)qdel deletion does not interfere with production of Y chromosome-bearing gametes, as judged from the frequency of Y chromosome transmission to the offspring. ICSI results for XY(RIII)qdel males also indicate that there is no deficiency of Y sperm production in this genotype, although the data show an excess of females following in vitro fertilization and natural mating. Our findings suggest that 1) Yq deletions in mice do not bias the primary sex ratio and 2) Y(RIII)qdel spermatozoa have poorer fertilizing ability than their X-bearing counterparts. Thus, a normal complement of the Ssty and/or Sly gene families on mouse Yq appears necessary for normal sperm function.
ICSI was successfully used to reproduce infertile mice with Yq deletions, and the analysis of sperm function in obtained offspring demonstrated that gene families located within the deletion interval are necessary for normal sperm function.
在小鼠和人类中,Y染色体缺失常与精子发生缺陷相关。XY(Tdy)(m1)qdelSry雄性小鼠存在广泛的Yq缺失,几乎完全消除了位于小鼠Y长臂雄性特异性区域内的两个基因家族Ssty和Sly的表达。这些雄性小鼠表现出严重的精子缺陷和不育。XY(RIII)qdel雄性小鼠的Yq间质性缺失较小,约三分之二的Ssty/Sly基因拷贝被去除,表现出轻度精子头部异常的发生率增加,伴有生育能力受损,且后代性别比例出现有利于雌性的有趣偏差。在此,我们使用胞浆内精子注射(ICSI)来研究这些Yq缺失雄性小鼠精子的功能能力。ICSI消除了与精子体外受精能力相关的任何选择,我们从不育雄性小鼠获得了两代活后代。对ICSI衍生后代的基因分型显示,根据Y染色体传递给后代的频率判断,Y(Tdym1)qdel缺失并不干扰携带Y染色体配子的产生。XY(RIII)qdel雄性小鼠的ICSI结果也表明,该基因型中Y精子的产生不存在缺陷,尽管数据显示体外受精和自然交配后雌性过多。我们的研究结果表明:1)小鼠中的Yq缺失不会影响初级性别比例;2)XY(RIII)qdel精子的受精能力比携带X染色体的精子差。因此,小鼠Yq上Ssty和/或Sly基因家族的正常互补似乎是正常精子功能所必需的。
成功使用ICSI繁育出有Yq缺失的不育小鼠,对所获后代精子功能的分析表明,缺失区间内的基因家族是正常精子功能所必需的。