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Global identification of conserved post-transcriptional regulatory programs in trypanosomatids

机译:锥虫的保守的转录后调控程序的全球鉴定

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摘要

While regulatory programs are extensively studied at the level of transcription, elements that are involved in regulation of post-transcriptional processes are largely unknown, and methods for systematic identification of these elements are in early stages. Here, using a novel computational framework, we have integrated sequence information with several functional genomics data sets to characterize conserved regulatory programs of trypanosomatids, a group of eukaryotes that almost entirely rely on post-transcriptional processes for regulation of mRNA abundance. This analysis revealed a complex network of linear and structural RNA elements that potentially govern mRNA abundance across different life stages and environmental conditions. Furthermore, we show that the conserved regulatory network that we have identified is responsive to chemical perturbation of several biological functions in trypanosomatids. We have further characterized one of the most abundant regulatory RNA elements that we discovered, an AU-rich element (ARE) that can be found in 3' untranslated region of many trypanosomatid genes. Using bioinformatics approaches as well as in vitro and in vivo experiments, we have identified three ELAV-like homologs, including the developmentally critical protein TbRBP6, which regulate abundance of a large number of trypanosomatid ARE-containing transcripts. Together, these studies lay out a roadmap for characterization of mechanisms that modulate development and metabolic pathways in trypanosomatids.
机译:尽管在转录水平上对调控程序进行了广泛的研究,但转录后过程调控中涉及的元件尚不清楚,并且系统鉴定这些元件的方法尚处于早期阶段。在这里,使用新颖的计算框架,我们将序列信息与几个功能基因组学数据集集成在一起,以表征锥虫的保守调控程序,锥虫是一组真核生物,几乎完全依赖于转录后过程来调控mRNA丰度。这项分析揭示了线性和结构性RNA元件的复杂网络,这些网络可能控制着不同生命阶段和环境条件下的mRNA丰度。此外,我们表明,我们已经确定的保守的监管网络对锥虫的几种生物学功能的化学扰动有反应。我们进一步表征了我们发现的最丰富的调控RNA元件之一,一种富含AU的元件(ARE),可以在许多锥虫基因的3'非翻译区中发现。使用生物信息学方法以及体外和体内实验,我们已经鉴定出三个类似ELAV的同源物,包括发育关键蛋白TbRBP6,它调节大量含有锥虫的ARE转录物的丰度。总之,这些研究为调节锥虫的发育和代谢途径的机制提供了路线图。

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