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RNA binding protein Musashi-1 directly targets Msi2 and Erh during early testis germ cell development and interacts with IPO5 upon translocation to the nucleus

机译:RNA结合蛋白Musashi-1在早期睾丸生殖细胞发育过程中直接靶向Msi2和Erh,并在易位至细胞核时与IPO5相互作用

摘要

Controlled gene regulation during gamete development is vital for maintaining reproductive potential. During the process of gamete development, male germ cells experience extended periods of inactive transcription despite requirements for continued growth and differentiation. Spermatogenesis therefore provides an ideal model to study the effects of posttranscriptional control on gene regulation. During spermatogenesis posttranscriptional regulation is orchestrated by abundantly expressed RNA-binding proteins. One such group of RNA-binding proteins is the Musashi family, previously identified as a critical regulator of testis germ cell development and meiosis in and also shown to be vital to sperm development and reproductive potential in the mouse. We focus in depth on the role and function of the vertebrate Musashi ortholog Musashi-1 (MSI1). Through detailed expression studies and utilizing our novel transgenic testis-specific overexpression model, we have identified 2 unique RNA-binding targets of MSI1 in spermatogonia, and , and have demonstrated a role for MSI1 in translational regulation. We have also provided evidence to suggest that nuclear import protein, IPO5, facilitates the nuclear translocation of MSI1 to the transcriptionally silenced XY chromatin domain in meiotic pachytene spermatocytes, resulting in the release of MSI1 RNA-binding targets. This firmly establishes MSI1 as a master regulator of posttranscriptional control during early spermatogenesis and highlights the significance of the subcellular localization of RNA binding proteins in relation to their function.
机译:配子发育过程中受控的基因调节对于维持生殖潜力至关重要。在配子发育过程中,尽管需要持续生长和分化,但雄性生殖细胞仍经历了较长时间的无活性转录。因此,精子发生提供了一个理想的模型来研究转录后控制对基因调控的影响。在精子发生过程中,转录后的调控是通过大量表达的RNA结合蛋白来进行的。这样的一组RNA结合蛋白是Musashi家族,该家族先前被确定为睾丸生殖细胞发育和减数分裂的关键调节剂,并且也显示出对小鼠精子发育和生殖潜力至关重要。我们深入研究脊椎动物武藏直系同源物武藏1(MSI1)的作用和功能。通过详细的表达研究和利用我们新颖的转基因睾丸特异性过表达模型,我们已经确定了精原细胞中MSI1的2个独特的RNA结合靶标,并且证明了MSI1在翻译调控中的作用。我们还提供了证据表明,核导入蛋白IPO5可以促进MSI1核易位到减数分裂的粗线精子细胞中转录沉默的XY染色质结构域,从而释放MSI1 RNA结合靶标。这牢固地将MSI1确立为早期精子发生过程中转录后控制的主要调节剂,并突出了RNA结合蛋白的亚细胞定位与其功能有关的重要性。

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