Terry Fox Molecular Oncology Group and Segal Cancer Center, Bloomfield Center for Research on Aging, Lady Davis Institute for Medical Research and Departments of Oncology and Medicine, McGill University, Montréal, Québec, H3T 1E2, Canada.
Terry Fox Molecular Oncology Group and Segal Cancer Center, Bloomfield Center for Research on Aging, Lady Davis Institute for Medical Research and Departments of Oncology and Medicine, McGill University, Montréal, Québec, H3T 1E2, Canada.
Trends Biochem Sci. 2015 Nov;40(11):662-672. doi: 10.1016/j.tibs.2015.08.012. Epub 2015 Oct 15.
RNA-binding proteins (RBPs) maintain RNA metabolism homeostasis in the cell by regulating temporal, spatial, and functional dynamics of RNAs. RBPs achieve RNA binding not only through classical structured RNA-binding domains but also with sequences that are intrinsically disordered and often of low amino acid complexity. RBP-RNA interactions form ribonucleoprotein (RNP) complexes and emerging evidence indicates that RNPs form higher structures or lattices, promoting territories of phase transitions. Herein, we discuss the role of disordered sequences in RBPs, their function in RNPs and protein networks, as well as their regulation by post-translational modifications and how RBP deregulation leads to disease.
RNA 结合蛋白 (RBPs) 通过调节 RNA 的时间、空间和功能动态来维持细胞内的 RNA 代谢平衡。RBPs 不仅通过经典的结构 RNA 结合域,还通过内在无序且通常氨基酸复杂度低的序列来实现 RNA 结合。RBP-RNA 相互作用形成核糖核蛋白 (RNP) 复合物,并有新的证据表明 RNP 形成更高的结构或晶格,促进相变区域的形成。本文讨论了无序序列在 RBPs 中的作用、它们在 RNP 和蛋白质网络中的功能,以及它们受翻译后修饰的调节方式,以及 RBP 失调如何导致疾病。