Donnelly Centre, University of Toronto, Toronto M5S 3E1, Canada.
Nature. 2013 Jul 11;499(7457):172-7. doi: 10.1038/nature12311.
RNA-binding proteins are key regulators of gene expression, yet only a small fraction have been functionally characterized. Here we report a systematic analysis of the RNA motifs recognized by RNA-binding proteins, encompassing 205 distinct genes from 24 diverse eukaryotes. The sequence specificities of RNA-binding proteins display deep evolutionary conservation, and the recognition preferences for a large fraction of metazoan RNA-binding proteins can thus be inferred from their RNA-binding domain sequence. The motifs that we identify in vitro correlate well with in vivo RNA-binding data. Moreover, we can associate them with distinct functional roles in diverse types of post-transcriptional regulation, enabling new insights into the functions of RNA-binding proteins both in normal physiology and in human disease. These data provide an unprecedented overview of RNA-binding proteins and their targets, and constitute an invaluable resource for determining post-transcriptional regulatory mechanisms in eukaryotes.
RNA 结合蛋白是基因表达的关键调节因子,但只有一小部分具有功能特征。在这里,我们报告了对 RNA 结合蛋白识别的 RNA 基序的系统分析,涵盖了来自 24 个不同真核生物的 205 个不同基因。RNA 结合蛋白的序列特异性显示出深度的进化保守性,因此可以从它们的 RNA 结合域序列推断出大量后生动物 RNA 结合蛋白的识别偏好。我们在体外鉴定的基序与体内 RNA 结合数据很好地相关。此外,我们可以将它们与不同类型的转录后调控中的不同功能作用相关联,从而深入了解 RNA 结合蛋白在正常生理和人类疾病中的功能。这些数据提供了 RNA 结合蛋白及其靶标的空前概述,并为确定真核生物的转录后调控机制构成了宝贵的资源。