超越 RNA 结合域:蛋白质与 RNA 结合的决定因素。

IF 4.2 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY RNA Pub Date : 2024-11-18 DOI:10.1261/rna.080026.124
Inbal Zigdon, Miri Carmi, Sagie Brodsky, Zohar Rosenwaser, Naama Barkai, Felix Jonas
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引用次数: 0

摘要

RNA 结合蛋白(RBPs)由 RNA 结合结构域(RBDs)组成,通常通过内在无序区(IDRs)连接。结构和生化分析表明,无序连接体通过确定相邻 RBDs 的方向来促进 RNA 结合,某些无序重复区还直接与 RNA 接触。然而,IDR 和预测的 RBD 对体内结合模式的相对贡献还没有得到充分探讨。在这里,我们提升了 RNA 标记方法,绘制了芽殖酵母中 16 个 RBPs 的全转录组结合图。然后,我们进行了大量的序列突变,以区分预测的 RBD 内的结合决定因子以及其中八个 RBPs 周围的 IDR。所测试的大多数预测的 RBD 对于 mRNA 结合并不是必不可少的,而缺乏预测的 RNA 结合潜力的多个 IDR 对于结合亲和力或特异性似乎是必不可少的。我们的研究结果为研究较少的 RBPs 的功能提供了新的见解,并强调了体内 RBP-RNA 相互作用编码的复杂性和分布性。
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Beyond RNA-binding domains: determinants of protein-RNA binding.

RNA-binding proteins (RBPs) are composed of RNA-binding domains (RBDs) often linked via intrinsically disordered regions (IDRs). Structural and biochemical analyses have shown that disordered linkers contribute to RNA binding by orienting the adjacent RBDs and also characterized certain disordered repeats that directly contact the RNA. However, the relative contribution of IDRs and predicted RBDs to the in vivo binding pattern is poorly explored. Here, we upscaled the RNA-tagging method to map the transcriptome-wide binding of 16 RBPs in budding yeast. We then performed extensive sequence mutations to distinguish binding determinants within predicted RBDs and the surrounding IDRs in eight of these. The majority of the predicted RBDs tested were not individually essential for mRNA binding. However, multiple IDRs that lacked predicted RNA-binding potential appeared essential for binding affinity or specificity. Our results provide new insights into the function of poorly studied RBPs and emphasize the complex and distributed encoding of RBP-RNA interaction in vivo.

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来源期刊
RNA
RNA 生物-生化与分子生物学
CiteScore
8.30
自引率
2.20%
发文量
101
审稿时长
2.6 months
期刊介绍: RNA is a monthly journal which provides rapid publication of significant original research in all areas of RNA structure and function in eukaryotic, prokaryotic, and viral systems. It covers a broad range of subjects in RNA research, including: structural analysis by biochemical or biophysical means; mRNA structure, function and biogenesis; alternative processing: cis-acting elements and trans-acting factors; ribosome structure and function; translational control; RNA catalysis; tRNA structure, function, biogenesis and identity; RNA editing; rRNA structure, function and biogenesis; RNA transport and localization; regulatory RNAs; large and small RNP structure, function and biogenesis; viral RNA metabolism; RNA stability and turnover; in vitro evolution; and RNA chemistry.
期刊最新文献
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