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Mouse D1Pas1, a DEAD-box RNA helicase, is required for the completion of first meiotic prophase in male germ cells

机译:小鼠D1PAS1,一个死箱RNA螺旋酶,以完成第一个减数分子预先在雄性生殖细胞中

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摘要

D1Pas1 is a mouse autosomal DEAD-box RNA helicase expressed predominantly in the testis. To assess its possible function, we generated D1Pasl-deficient mice using embryonic stem cells with a targeted D1Pas1 allele. Deletion of D1Pas1 did not cause noticeable embryonic defects or death, indicating that D1Pas1 is not essential for embryogenesis. Whereas homozygous knockout female mice showed normal reproductive performance, homozygous knockout male mice were completely sterile. The seminiferous epithelium of D1Pas1-deficient males contained no spermatids or spermatozoa because of spermatogenic arrest at the late pachytene stage. Upregulation of retrotransposons such as LINE-1 was not found in D1Pas1-deficient males, unlike males lacking Mvh, another testicular DEAD-box RNA helicase. Meiotic chromosome behavior in developing spermatocytes of D1Pas1-deficient males was indistinguishable from that in wild-type males, at least until synaptonemal complex formation. Thus, mouse D1Pas1 is the first-identified DEAD-box RNA helicase that plays critical roles in the final step of the first meiotic prophase in male germ cells. (C) 2016 Elsevier Inc. All rights reserved.
机译:D1PAS1是小鼠常染色体死箱RNA螺旋酶,主要在睾丸中表达。为了评估其可能的功能,我们使用具有靶向D1PAS1等位基因的胚胎干细胞生成D1PASL缺陷小鼠。 D1PAS1的缺失没有引起明显的胚胎缺陷或死亡,表明D1PAS1对胚胎发生不是必需的。虽然纯合的敲除雌性小鼠表现出正常的生殖性能,但纯合的敲除雄性小鼠是完全无菌的。由于在晚期嗜孢子阶段的晚期抑制,D1Pas1缺陷型雄性的血管上皮不含精子或精子。在D1PAS1缺陷型男性中未发现诸如线-1等重转回转储的上调,与缺乏MVH的雄性,另一个睾丸死箱RNA螺旋酶。在野生型男性中,发育D1PAS1缺陷型雄性的生长细胞的减数分子染色体行为难以区别,至少直到Synaponemal复合体形成。因此,小鼠D1PAS1是第一个鉴定的死箱RNA螺旋酶,其在雄性生殖细胞中的第一减数分裂原版的最后步骤中起重要作用。 (c)2016年Elsevier Inc.保留所有权利。

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