Beyond RNA-binding domains: determinants of protein–RNA binding
- 1Department of Molecular Genetics, Weizmann Institute of Science, Rehovot 76100, Israel
- 2School of Science, Constructor University, 28759 Bremen, Germany
- Corresponding authors: naama.barkai{at}weizmann.ac.il, fjonas{at}constructor.university
-
Handling editor: Mihaela Zavolan
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.
Keywords
- intrinsically disordered regions (IDRs)
- RNA binding domains (RBDs)
- RNA binding proteins (RBPs)
- S. cerevisiae
- mRNA binding proteins (mRBPs)
Footnotes
-
Article is online at http://www.rnajournal.org/cgi/doi/10.1261/rna.080026.124.
-
Freely available online through the RNA Open Access option.
- Received March 17, 2024.
- Accepted September 12, 2024.
This article, published in RNA, is available under a Creative Commons License (Attribution 4.0 International), as described at http://creativecommons.org/licenses/by/4.0/.










