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小鼠D1Pas1是一种DEAD盒RNA解旋酶,是雄性生殖细胞第一次减数分裂前期完成所必需的。

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

作者信息

Inoue Hiroki, Ogonuki Narumi, Hirose Michiko, Hatanaka Yuki, Matoba Shogo, Chuma Shinichiro, Kobayashi Kimio, Wakana Shigeharu, Noguchi Junko, Inoue Kimiko, Tanemura Kentaro, Ogura Atsuo

机构信息

RIKEN BioResource Center, Tsukuba, Ibaraki, 305-0074, Japan; Laboratory of Animal Reproduction and Development, Graduate School of Agricultural Science, Tohoku University, Miyagi, 981-8555, Japan.

RIKEN BioResource Center, Tsukuba, Ibaraki, 305-0074, Japan.

出版信息

Biochem Biophys Res Commun. 2016 Sep 16;478(2):592-8. doi: 10.1016/j.bbrc.2016.07.109. Epub 2016 Jul 27.

Abstract

D1Pas1 is a mouse autosomal DEAD-box RNA helicase expressed predominantly in the testis. To assess its possible function, we generated D1Pas1-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.

摘要

D1Pas1是一种主要在睾丸中表达的小鼠常染色体DEAD盒RNA解旋酶。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了D1Pas1缺陷型小鼠。D1Pas1的缺失并未导致明显的胚胎缺陷或死亡,这表明D1Pas1对于胚胎发育并非必不可少。虽然纯合敲除雌性小鼠表现出正常的生殖性能,但纯合敲除雄性小鼠完全不育。由于在粗线期后期精子发生停滞,D1Pas1缺陷型雄性小鼠的生精上皮中没有精子细胞或精子。与缺乏另一种睾丸DEAD盒RNA解旋酶Mvh的雄性小鼠不同,在D1Pas1缺陷型雄性小鼠中未发现LINE-1等逆转座子的上调。至少在联会复合体形成之前,D1Pas1缺陷型雄性小鼠发育中的精母细胞的减数分裂染色体行为与野生型雄性小鼠的无异。因此,小鼠D1Pas1是第一个被鉴定出的在雄性生殖细胞第一次减数分裂前期的最后步骤中起关键作用的DEAD盒RNA解旋酶。

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