Sequence determinants of <scp>RNA</scp> G‐quadruplex unfolding by Arg‐rich regions
RNA sequences with the potential to form G-quadruplexes (rGQs) are widespread but largely unfolded in cells by unknown mechanisms. rGQ folding status is a critical regulator of RNA splicing and translation. We show that rGQs can be unfolded by SR proteins, SR-related proteins, and other Arg-rich proteins, including SRSF1, SRSF3, SRSF9, U1-70K, and U2AF1. The length and composition of Arg-rich regions are key determinants of this activity: Arg residues are the primary drivers, while acidic residues attenuate the unfolding activity. To unfold ARPC2 rGQ, at least 13 Arg residues are required. Our findings identify Arg-rich proteins as previously unrecognized, helicase-independent regulators of rGQ structures, with potential broad impacts on RNA processing that merit further investigation.
Authors
- Nicholas L. Truex (ORCID: https://orcid.org/0000-0002-7369-685X)
- Joanna Koryo Kwao (ORCID: https://orcid.org/0000-0003-0538-160X)
- Trenton Paul (ORCID: https://orcid.org/0009-0000-0931-3888)
- Puspa Kunwar
- Naiduwadura Ivon Upekala De Silva (ORCID: https://orcid.org/0000-0002-5937-0271)
- Nathan Lehman
- Zihan Zhang
- Md Ibnul Rifat Rahman
- Jun Zhang
- Claire Cheng
- Hui‐Ting Lee
Institutions
- University of South Carolina (US)
- University of Alabama at Birmingham (US)
- Livingston Public Schools (US)
Publication Details
- Journal
- FEBS Letters
- Published
- 2026-01-09
- DOI
- https://doi.org/10.1002/1873-3468.70274
- Citations
- 1
- Primary Topic
- RNA Research and Splicing
- Type
- article
- Field-Weighted Citation Impact
- 22.24