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Messenger ribonucleoprotein complexes containing human ELAV proteins: interactions with cytoskeleton and translational apparatus

机译:含有人类ELAV蛋白的信使核糖核蛋白复合物:与细胞骨架和翻译装置的相互作用

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摘要

Mammalian ELAV proteins bind to polyadenylated messenger RNAs and have specificity for AU-rich sequences, Preferred binding sites in vitro include the AUUUA pentamer and related sequences present in the 3' untranslated regions of many growth regulatory mRNAs, Human ELAV (hELAV) proteins have been implicated in post-transcriptional regulation of gene expression by their effects on the stability and translatability of growth regulatory mRNAs. We have examined the intracellular localization of ELAV proteins in neurons and in tumor cells of neuronal origin using indirect immunofluorescence, confocal microscopy and biochemical separation, Mammalian neuronal ELAV proteins are found predominantly in the cytoplasm of cells in mRNP complexes termed alpha complexes which, when associated with polysomes, form large and high density beta complexes, as assayed by glycerol and accudenz gradients, respectively, Puromycin, cytochalasin or EDTA treatments disrupt beta complexes causing the release of alpha complexes, which then appear, by confocal microscopy, as large hELAV mRNP granules associated with microtubules, Association of partially purified hELAV mRNP alpha complexes with microtubules was confirmed by in vitro reconstitution assays, Furthermore, colchicine treatment of cells suggested that association of hELAV mRNP alpha complexes with microtubules is also necessary for the formation of beta complexes. Our data suggest a model in which a subset of mRNAs is associated with microtubules as ELAV mRNP particles (alpha complexes) which, in turn, associate with polysomes to form a translational apparatus (beta complex) that is, through polysomes, associated with the microfilament cytoskeletal network, hELAV proteins in these mRNP granules may affect post-transcriptional regulation of gene expression via the intracellular transport, localization and/or translation of growth regulatory mRNAs. [References: 46]
机译:哺乳动物ELAV蛋白与聚腺苷酸信使RNA结合并对富含AU的序列具有特异性。体外优选的结合位点包括AUUUA五聚体和存在于许多生长调节mRNA的3'非翻译区中的相关序列,人类ELAV(hELAV)蛋白已被它们对生长调节mRNA的稳定性和可翻译性的影响与基因表达的转录后调控有关。我们已经使用间接免疫荧光,共聚焦显微镜和生化分离检查了神经元和神经元起源的肿瘤细胞中ELAV蛋白的细胞内定位,哺乳动物神经元ELAV蛋白主要存在于细胞质中的mRNP复合物(称为α复合物)中。分别用甘油和Accudenz梯度测定,与多核糖体形成大和高密度β复合物,嘌呤霉素,细胞松弛素或EDTA处理破坏β复合物,导致α复合物释放,然后通过共聚焦显微镜观察,其显示为大的hELAV mRNP颗粒与微管相关,通过体外重组分析证实了部分纯化的hELAV mRNPα复合物与微管的结合。此外,秋水仙碱对细胞的处理表明,hELAV mRNPα复合物与微管的结合对于形成β复合物也是必要的。我们的数据提出了一个模型,其中mRNA的一个子集与微管相关联,如ELAV mRNP颗粒(α复合物),而后者又与多核糖体结合形成翻译装置(β复合物),即通过多核糖体与微丝结合在细胞骨架网络中,这些mRNP颗粒中的hELAV蛋白可能通过生长调节mRNA的细胞内转运,定位和/或翻译来影响基因表达的转录后调节。 [参考:46]

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