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Mammalian Fused is essential for sperm head shaping and periaxonemal structure formation during spermatogenesis

机译:哺乳动物融合对精子形成过程中精子头部的塑造和腹膜结构的形成至关重要

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摘要

During mammalian spermatogenesis, the diploid spermatogonia mature into haploid spermatozoa through a highly controlled process of mitosis, meiosis and post-meiotic morphological remodeling (spermiogenesis). Despite important progress made in this area, the molecular mechanisms underpinning this transformation are poorly understood. Our analysis of the expression and function of the putative serine-threonine kinase Fused (Fu) provides critical insight into key steps in spermatogenesis. In this report, we demonstrate that conditional inactivation of Fu in male germ cells results in infertility due to diminished sperm count, abnormal head shaping, decapitation and motility defects of the sperm. Interestingly, mutant flagellar axonemes are intact but exhibit altered periaxonemal structures that affect motility. These data suggest that Fu plays a central role in shaping the sperm head and controlling the organization of the periaxonemal structures in the flagellum. We show that Fu localizes to multiple tubulin-containing or microtubule-organizing structures, including the manchette and the acrosome-acroplaxome complex that are involved in spermatid head shaping. In addition, Fu interacts with the outer dense fiber protein Odf1, a major component of the periaxonemal structures in the sperm flagellum, and Kif27, which is detected in the manchette. We propose that disrupted Fu function in these structures underlies the head and flagellar defects in Fu-deficient sperm. Since a majority of human male infertility syndromes stem from reduced sperm motility and structural defects, uncovering Fu’s role in spermiogenesis provides new insight into the causes of sterility and the biology of reproduction.
机译:在哺乳动物的精子发生过程中,通过高度控制的有丝分裂,减数分裂和减数分裂后形态重塑(生精),二倍体精原细胞成熟为单倍体精子。尽管在该领域取得了重要进展,但对这种转化的分子机制知之甚少。我们对推定的丝氨酸-苏氨酸激酶融合(Fu)的表达和功能的分析为精子发生的关键步骤提供了关键的见识。在此报告中,我们证明,由于精子数量减少,畸形的头部畸形,断头术和精子运动缺陷,男性生殖细胞中Fu的条件失活导致不孕。有趣的是,突变鞭毛轴突完好无损,但表现出影响运动性的改变的腹膜周围结构。这些数据表明,Fu在塑造精子头部和控制鞭毛中腹膜周围结构的组织中起着核心作用。我们显示富本地化到多个包含微管蛋白或微管组织结构,包括涉及精子头部成形的manchette和顶体-顶体复杂。此外,Fu还与外部密集纤维蛋白Odf1和Kif27相互作用,而Odf1是精子鞭毛中腹膜结构的主要组成部分,而Kif27则在手杖中被检测到。我们提出,在这些结构中破坏的Fu功能是Fu缺乏精子的头部和鞭毛缺陷的基础。由于大多数人类男性不育综合症源于精子活动力降低和结构缺陷,因此揭示Fu在精子发生中的作用,可以为人们了解不育原因和生殖生物学提供新的见识。

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