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首页> 外文期刊>Chromosome research: An international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology >The nucleolar transcriptome regulates Piwi shuttling between the nucleolus and the nucleoplasm
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The nucleolar transcriptome regulates Piwi shuttling between the nucleolus and the nucleoplasm

机译:核仁转录组体调节核仁和核仁之间的PIWI梭

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The nucleolus contains a lot of proteins unrelated to ribosome biogenesis. Some of these proteins shuttle between the nucleolus and the nucleoplasm regulating the cell cycle and stress response. The piRNA binding protein Piwi is involved in silencing of transposable elements (TEs) in the Drosophila gonads. Here we used cultured ovarian somatic cells (OSC) to characterize Piwi as a visitor to the nucleolus. Dynamic Piwi localization was shown to vary from its uniform distribution between the nucleoplasm and the nucleolus to pronounced nucleolar immobilization. We were intrigued by this localization behavior and revealed that nascent nucleolar transcripts recruit Piwi for nucleolar retention. Piwi eviction from the nucleolus was observed upon RNase treatment and after RNA polymerase (Pol) I inhibition, but not after Pol II inactivation. On the contrary, heat shock caused drastic Piwi redistribution from the nucleoplasm to the nucleolus, which occurred only in the presence of Pol I-mediated transcription. These results allow us to hypothesizethat specific stress-induced transcripts made by Pol I promote the nucleolar sequestration of proteins in Drosophila, similar to previous observations in mammalian cells. We also found that in OSC, Piwi partially restricts expression of the rDNA copies containing R1 and R2 retrotransposon insertions especially upon heat shock-induced activation of these copies. Therefore, we suggest that Piwi intranuclear shuttling may have a functional role in ensuring a balance between silencing of rDNA-specific TEs under stress and the canonical Piwi function in non-nucleolar TE repression.
机译:核仁含有许多与核糖体生物发生不相关的蛋白质。其中一些蛋白质梭在核仁和核细胞中调节细胞周期和应力反应之间的梭菌。 PiRNA结合蛋白PIWI涉及在果蝇性腺中的转移元素(TES)的沉默中。在这里,我们使用培养的卵巢体细胞(OSC)将PIWI作为核仁的游客表征。动态PIWI定位被证明从核状和核仁之间的均匀分布而变化,以发音核仁固定化。我们呼吁这种本地化行为,并揭示了新生的核仁转录物募集核仁潴留的PIWI。在RNase治疗和RNA聚合酶(POL)I抑制后观察到来自核仁的PIWI驱逐,但在POL II灭活后没有。相反,热冲击引起从核状到核仁的核开中的剧烈PIWI再分布,该核仁仅在Pol I介导的转录存在下发生。这些结果允许我们揭示由Pol I促进果蝇中蛋白质的核仁封存的特异性应激诱导的转录物,类似于哺乳动物细胞中先前的观察结果。我们还发现,在OSC中,PIWI部分限制含有R1和R2回复横向插入的RDNA拷贝的表达,特别是在热冲击诱导的这些拷贝的激活时。因此,我们建议PIWI核心穿梭在确保在rDNA特异性TES下的沉默和非核油TE抑制中的规范PIWI功能下的沉默之间具有功能作用。

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