The role of disorder in RNA binding affinity and specificity. Issue 12 (23rd December 2020)

• Record Type: Journal Article
• Authors: Ottoz, Diana S. M.; Berchowitz, Luke E.
• Is Part Of: Open biology. Volume 10:Issue 12(2020)
• Publication Date: 2020-12-23
• Subjects: RNA-binding proteins -- RNA-binding modules -- RNA-binding domains -- intrinsically disordered regions -- linkers -- assemblies -- amyloids; Biology -- Periodicals; 570
• DOI: 10.1098/rsob.200328
• Languages: English
• ISSNs: 2046-2441

Abstract

Abstract : Abstract : Most RNA-binding modules are small and bind few nucleotides. RNA-binding proteins typically attain the physiological specificity and affinity for their RNA targets by combining several RNA-binding modules. Here, we review how disordered linkers connecting RNA-binding modules govern the specificity and affinity of RNA–protein interactions by regulating the effective concentration of these modules and their relative orientation. RNA-binding proteins also often contain extended intrinsically disordered regions that mediate protein–protein and RNA–protein interactions with multiple partners. We discuss how these regions can connect proteins and RNA resulting in heterogeneous higher-order assemblies such as membrane-less compartments and amyloid-like structures that have the characteristics of multi-modular entities. The assembled state generates additional RNA-binding specificity and affinity properties that contribute to further the function of RNA-binding proteins within the cellular environment.