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在体内和体外理解物种特异性和保守的 RNA-蛋白质相互作用。

Understanding species-specific and conserved RNA-protein interactions in vivo and in vitro.

机构信息

Department of Biochemistry and Biophysics, University of North Carolina, Chapel Hill, NC, USA.

Department of Pharmacology, University of North Carolina, Chapel Hill, NC, USA.

出版信息

Nat Commun. 2024 Sep 27;15(1):8400. doi: 10.1038/s41467-024-52231-7.

Abstract

While evolution is often considered from a DNA- and protein-centric view, RNA-based regulation can also impact gene expression and protein sequences. Here we examine interspecies differences in RNA-protein interactions using the conserved neuronal RNA-binding protein, Unkempt (UNK) as model. We find that roughly half of mRNAs bound in human are also bound in mouse. Unexpectedly, even when transcript-level binding was conserved across species differential motif usage was prevalent. To understand the biochemical basis of UNK-RNA interactions, we reconstitute the human and mouse UNK-RNA interactomes using a high-throughput biochemical assay. We uncover detailed features driving binding, show that in vivo patterns are captured in vitro, find that highly conserved sites are the strongest bound, and associate binding strength with downstream regulation. Furthermore, subtle sequence differences surrounding motifs are key determinants of species-specific binding. We highlight the complex features driving protein-RNA interactions and how these evolve to confer species-specific regulation.

摘要

虽然进化通常被认为是从 DNA 和蛋白质为中心的角度来看待的,但基于 RNA 的调控也可以影响基因表达和蛋白质序列。在这里,我们使用保守的神经元 RNA 结合蛋白 Unkempt(UNK)作为模型,研究了物种间 RNA-蛋白质相互作用的差异。我们发现,大约一半在人类中结合的 mRNA 在老鼠中也有结合。出乎意料的是,即使在跨物种的转录水平结合是保守的,差异基序的使用也很普遍。为了了解 UNK-RNA 相互作用的生化基础,我们使用高通量生化测定法重新构建了人类和老鼠的 UNK-RNA 相互作用组。我们揭示了驱动结合的详细特征,表明体内模式在体外被捕获,发现高度保守的位点结合最强,并将结合强度与下游调节联系起来。此外,基序周围的细微序列差异是决定物种特异性结合的关键因素。我们强调了驱动蛋白质-RNA 相互作用的复杂特征,以及这些特征如何进化以赋予物种特异性调节。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bfc4/11436793/13f3af904d1b/41467_2024_52231_Fig1_HTML.jpg

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