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超越 RNA 结合结构域:蛋白与 RNA 结合的决定因素。

Beyond RNA-binding domains: determinants of protein-RNA binding.

机构信息

Department of Molecular Genetics, Weizmann Institute of Science, Rehovot 76100, Israel.

Department of Molecular Genetics, Weizmann Institute of Science, Rehovot 76100, Israel

出版信息

RNA. 2024 Nov 18;30(12):1620-1633. doi: 10.1261/rna.080026.124.

Abstract

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.

摘要

RNA 结合蛋白 (RBPs) 由 RNA 结合域 (RBDs) 组成,这些 RBDs 通常通过固有无序区域 (IDRs) 连接。结构和生化分析表明,无序连接子通过定向相邻的 RBDs 来促进 RNA 结合,并且还鉴定了某些直接与 RNA 接触的无序重复序列。然而,IDRs 和预测的 RBDs 对体内结合模式的相对贡献还没有得到很好的探索。在这里,我们扩大了 RNA 标记方法的规模,以绘制出酿酒酵母中 16 种 RBPs 的全转录组结合图谱。然后,我们对其中的 8 种进行了广泛的序列突变,以区分预测的 RBD 内和周围 IDRs 的结合决定因素。测试的大多数预测的 RBD 并不单独对 mRNA 结合是必需的。然而,缺乏预测的 RNA 结合潜力的多个 IDRs 似乎对结合亲和力或特异性是必需的。我们的结果为研究较少的 RBPs 的功能提供了新的见解,并强调了体内 RBP-RNA 相互作用的复杂和分布式编码。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9f8/11571813/ef9abb3f4882/1620f01.jpg

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