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首页> 外文期刊>Human Molecular Genetics >A novel requirement in mammalian spermatid differentiation for the DAZ-family protein Boule
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A novel requirement in mammalian spermatid differentiation for the DAZ-family protein Boule

机译:DAZ家族蛋白球在哺乳动物精子分化中的新要求

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摘要

Reproduction is required for the survival of all animals, yet few reproductive genes have been shown to have a conserved requirement for fertility across the animal kingdom. Remarkably, the RNA binding protein BOULE, the oldest member of the DAZ (Deleted in AZoospermia) family of genes, appears to have maintained its conserved functional motif and spermatogenic expression from insects to humans. Boule mutations lead to a pachytene meiotic arrest before metaphase in Drosophila males and C. elegans females, and human BOULE can restore meiosis in the fly testis, suggesting a conserved meiotic function of human BOULE. However, the physiological function of BOULE in mammals is not yet known. We generated Boule knockout mice and found it to be required only for spermatogenesis, as in Drosophila. Interestingly, meiosis completed normally in the absence of Boule, and haploid round spermatids were readily detected. However, round spermatids did not progress beyond step 6, revealing a novel role for Boule in spermiogenesis, the differentiation of round spermatids into mature spermatozoa. Expression of key regulators of spermiogenesis was unaffected in Boule−/− mice, suggesting that Boule regulates germ-cell differentiation through a novel pathway.
机译:繁殖是所有动物生存所必需的,但很少有繁殖基因对整个动物界的繁殖力具有保守的要求。值得注意的是,RNA结合蛋白BOULE是DAZ(在无精子症中删除)家族中最古老的基因,它似乎从昆虫到人类都保持了其保守的功能基序和生精表达。果蝇突变导致果蝇雄性和秀丽隐杆线虫雌性中期过渡之前的粗线性减数分裂停滞,并且人的BOULE可以恢复苍蝇睾丸的减数分裂,表明人的BOULE具有保守的减数分裂功能。但是,BOULE在哺乳动物中的生理功能尚不清楚。我们产生了Boule基因敲除小鼠,发现它仅需要精子发生,如果蝇中那样。有趣的是,减数分裂在不存在布尔的情况下正常完成,并且容易检测到单倍体圆形精子。然而,圆形的精子并没有超过第6步,这揭示了Boule在精子发生中的新作用,即圆形的精子分化为成熟的精子。在Boule -/-小鼠中精子发生关键调控因子的表达不受影响,这表明Boule通过一种新途径调节生殖细胞的分化。

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  • 来源
    《Human Molecular Genetics》 |2010年第12期|p.2360-2369|共10页
  • 作者

    Michael J.W. VanGompel;

  • 作者单位

    Division of Reproductive Biology Research, Department of Obstetrics and Gynecology, Center for Genetic Medicine, and Robert H. Lurie Comprehensive Cancer Center, Northwestern University, Feinberg School of Medicine, 303 E Superior St., Room 7-250, Chicago, IL 60611, USA;

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