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Lack of Spem1 causes aberrant cytoplasm removal sperm deformation and male infertility

机译:Spem1缺乏会导致异常的细胞质去除精子变形和男性不育

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摘要

We identified a previously uncharacterized gene, spermatid maturation 1 (Spem1), encoding a protein exclusively expressed in the cytoplasm of steps 14–16 elongated spermatids in the mouse testis. This protein contains no known functional domains and is highly conserved across mammalian species. Male mice deficient in Spem1 were completely infertile because of deformed sperm characterized by a bent head wrapped around by the neck and the middle piece of the tail. We show that lack of Spem1 causes failure of the cytoplasm to become loose and detach from the head and the neck region of the developing spermatozoa. Retained cytoplasmic components mechanically obstruct the straightening of the sperm head and the stretching of the growing tail, leading to the bending of the head in the neck, followed by the wrapping of the head by the neck or the middle piece of the sperm tail. Our study reveals that proper cytoplasm removal is a genetically regulated process requiring the participation of Spem1 and that lack of Spem1 causes sperm deformation and male infertility.
机译:我们鉴定出一个以前未鉴定的基因,精子成熟1(Spem1),编码一种在小鼠睾丸中第14-16步伸长的精子的细胞质中专门表达的蛋白质。该蛋白质不包含已知的功能域,在整个哺乳动物物种中高度保守。缺乏Spem1的雄性小鼠由于精子畸形而完全不育,精子畸形的特征是头部弯曲,颈部和尾巴中间部分缠绕。我们显示缺乏Spem1会导致细胞质失败,并从发育中的精子的头部和颈部脱落并脱离。保留的细胞质成分机械性阻碍精子头的伸直和生长中的尾巴的拉伸,导致头部在颈部弯曲,随后将头部包裹在颈部或精子尾部的中间部分。我们的研究表明,正确去除细胞质是一个遗传调控的过程,需要Spem1的参与,而Spem1的缺乏会导致精子变形和男性不育。

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