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Staufen Recruitment into Stress Granules Does Not Affect Early mRNA Transport in Oligodendrocytes

机译:Staufen募集进入应激颗粒不会影响少突胶质细胞中的早期mRNA转运。

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摘要

Staufen is a conserved double-stranded RNA-binding protein required for mRNA localization in Drosophila oocytes and embryos. The mammalian homologues Staufen 1 and Staufen 2 have been implicated in dendritic RNA targeting in neurons. Here we show that in rodent oligodendrocytes, these two proteins are present in two independent sets of RNA granules located at the distal myelinating processes. A third kind of RNA granules lacks Staufen and contains major myelin mRNAs. Myelin Staufen granules associate with microfilaments and microtubules, and their subcellular distribution is affected by polysome-disrupting drugs. Under oxidative stress, both Staufen 1 and Staufen 2 are recruited into stress granules (SGs), which are stress-induced organelles containing transiently silenced messengers. Staufen SGs contain the poly(A)-binding protein (PABP), the RNA-binding proteins HuR and TIAR, and small but not large ribosomal subunits. Staufen recruitment into perinuclear SGs is paralleled by a similar change in the overall localization of polyadenylated RNA. Under the same conditions, the distribution of recently transcribed and exported mRNAs is not affected. Our results indicate that Staufen 1 and Staufen 2 are novel and ubiquitous SG components and suggest that Staufen RNPs are involved in repositioning of most polysomal mRNAs, but not of recently synthesized transcripts, during the stress response.
机译:Staufen是保守的双链RNA结合蛋白,用于果蝇卵母细胞和胚胎中的mRNA定位。哺乳动物同系物Staufen 1和Staufen 2与神经元中树突状RNA靶向有关。在这里,我们显示在啮齿动物少突胶质细胞中,这两种蛋白质存在于位于远端髓鞘形成过程的两组独立的RNA颗粒中。第三种RNA颗粒缺少Staufen,并且含有主要的髓磷脂mRNA。髓磷脂Staufen颗粒与微丝和微管相关联,其亚细胞分布受到破坏多核糖体的药物的影响。在氧化压力下,Staufen 1和Staufen 2均被募集到应力颗粒(SGs​​)中,它们是应力诱导的细胞器,包含短暂沉默的信使。 Staufen SGs包含多聚(A)结合蛋白(PABP),RNA结合蛋白HuR和TIAR,以及小的但不大的核糖体亚基。将Staufen募集到核周SG中,同时在聚腺苷酸化RNA的整体定位中发生类似的变化。在相同条件下,最近转录和输出的mRNA的分布不受影响。我们的结果表明,Staufen 1和Staufen 2是新颖且无处不在的SG组件,并表明Staufen RNP在应激反应过程中参与了大多数多体mRNA的重新定位,但不参与最近合成的转录本的重新定位。

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