一种驱动精原干细胞形成的翻译调节因子。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Kun Tan, Miles F Wilkinson
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引用次数: 0

摘要

背景:精原干细胞(SSC)是成人精子发生的关键。人们对驱动SSC生成的分子机制知之甚少:Zou等人报告说,产生SSCs-精原细胞(ProSG)的前体细胞需要RNA结合蛋白DDX20,以完成SSC形成过程中必须的增殖再激活步骤:结果与结论:我们总结了作者的发现,即 RNA 结合蛋白 DDX20 对于推动 ProSG 的增殖再激活至关重要,而 ProSG 的增殖再激活是体内 SSC 生成的关键步骤。他们提供的证据表明,DDX20通过促进编码已知对细胞周期和精原细胞稳态至关重要的蛋白质的mRNA的翻译能力来发挥这一作用。这一作用是否在人类中得到保留,还有待确定。此外,阐明其他转录后调节因子是否也在早期生殖细胞发育中发挥作用也很有意思。更广泛地说,确定转录后调节因子是否与转录调节因子协同作用以驱动生殖细胞发育将是非常有趣的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A translation regulator that drives spermatogonial stem cell formation.

Background: Spermatogonial stem cells (SSCs) are essential for adult spermatogenesis. Themolecular mechanisms driving SSC generation are poorly understood.

Objectives: Zou et al. reported that the precursor cells that give rise to SSCs-prospermatogonia (ProSG) require the RNA-binding protein, DDX20, in orderto undergo the obligatory proliferative re-activation step that proceeds SSC formation.

Materials and methods: Literature search.

Results and conclusion: We summarize the authors' discovery that the RNA-binding protein, DDX20, iscritical for driving the proliferative re-activation of ProSG, a key step that proceeds SSC generation in vivo. They provide evidence that DDX20 performs this role through its ability to promote the translation of mRNAs encoding proteins known to be essential for cell-cycle and spermatogonial homeostasis. It remains to be determined whether this role is conserved inhumans. It will also be interesting to elucidate whether other post-transcriptional regulators also have roles in early germ cell development. More broadly, it will be fascinating to determine whether post-transcriptional regulators workin concert with transcriptional regulators to drive germ-cell development.

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来源期刊
CiteScore
7.20
自引率
4.30%
发文量
567
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