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从精子发生或卵子发生生殖细胞的 FBF 结合景观中识别亚网络。

Toward Identifying Subnetworks from FBF Binding Landscapes in Spermatogenic or Oogenic Germlines.

机构信息

Department of Biochemistry, University of Wisconsin-Madison, Wisconsin 53706.

Howard Hughes Medical Institute, University of Wisconsin-Madison, Wisconsin 53706.

出版信息

G3 (Bethesda). 2019 Jan 9;9(1):153-165. doi: 10.1534/g3.118.200300.

Abstract

Metazoan PUF (Pumilio and FBF) RNA-binding proteins regulate various biological processes, but a common theme across phylogeny is stem cell regulation. In , FBF ( Binding Factor) maintains germline stem cells regardless of which gamete is made, but FBF also functions in the process of spermatogenesis. We have begun to "disentangle" these biological roles by asking which FBF targets are gamete-independent, as expected for stem cells, and which are gamete-specific. Specifically, we compared FBF iCLIP binding profiles in adults making sperm to those making oocytes. Normally, XX adults make oocytes. To generate XX adults making sperm, we used a mutant requiring growth at 25°; for comparison, wild-type oogenic hermaphrodites were also raised at 25°. Our FBF iCLIP data revealed FBF binding sites in 1522 RNAs from oogenic adults and 1704 RNAs from spermatogenic adults. More than half of these FBF targets were independent of germline gender. We next clustered RNAs by FBF-RNA complex frequencies and found four distinct blocks. Block I RNAs were enriched in spermatogenic germlines, and included validated target , while Block II and III RNAs were common to both genders, and Block IV RNAs were enriched in oogenic germlines. Block II (510 RNAs) included almost all validated FBF targets and was enriched for cell cycle regulators. Block III (21 RNAs) was enriched for RNA-binding proteins, including previously validated FBF targets and We suggest that Block I RNAs belong to the FBF network for spermatogenesis, and that Blocks II and III are associated with stem cell functions.

摘要

后生动物 PUF(Pumilio 和 FBF)RNA 结合蛋白调节各种生物过程,但贯穿整个进化过程的一个共同主题是干细胞调节。在,FBF(结合因子)维持生殖细胞干细胞,无论产生哪种配子,但 FBF 也在精子发生过程中发挥作用。我们已经开始通过询问哪些 FBF 靶标是配子独立的,这是干细胞所期望的,以及哪些是配子特异性的,来“解开”这些生物学作用。具体来说,我们比较了在产生精子的成年个体和产生卵子的成年个体中 FBF iCLIP 的结合谱。正常情况下,XX 个体产生卵子。为了产生 XX 个体产生精子,我们使用了一个需要在 25°C 下生长的突变体;作为对照,野生型的卵母细胞型雌雄同体也在 25°C 下培养。我们的 FBF iCLIP 数据显示,在产生卵子的成年个体中 1522 个 RNA 和产生精子的成年个体中 1704 个 RNA 中存在 FBF 结合位点。这些 FBF 靶标中有一半以上与生殖细胞性别无关。接下来,我们根据 FBF-RNA 复合物频率对 RNA 进行聚类,发现了四个不同的块。Block I RNA 在精子发生生殖细胞中富集,包括已验证的靶标,而 Block II 和 III RNA 存在于两性中,Block IV RNA 在卵母细胞生殖细胞中富集。Block II(510 个 RNA)包括几乎所有已验证的 FBF 靶标,并且富含细胞周期调节剂。Block III(21 个 RNA)富含 RNA 结合蛋白,包括先前验证的 FBF 靶标和。我们认为 Block I RNA 属于精子发生的 FBF 网络,而 Block II 和 III 与干细胞功能相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cea4/6325917/852d94e440d6/153f1.jpg

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