Conserved protein Seb1 that interacts with RNA polymerase II and RNA is an antipausing transcription elongation factor
- 1Department of Biochemistry, University of Oxford, Oxford OX1 3QU, United Kingdom
- 2Centre for Bacterial Cell Biology, Biosciences Institute, Newcastle University, Newcastle upon Tyne NE2 4AX, United Kingdom
- Corresponding authors: lidia.vasilieva{at}bioch.ox.ac.uk; krzysztof.kus{at}bioch.ox.ac.uk
-
Handling editor: Javier Caceres
Abstract
Maturation of protein-coding precursor messenger RNA (pre-mRNA) is closely linked to RNA polymerase II (Pol II) transcription. However, the mechanistic understanding of how pre-mRNA processing is coordinated with transcription remains incomplete. Conserved proteins interacting with the C-terminal domain of the largest catalytic subunit of Pol II and nascent RNA (CID-RRM factors) were demonstrated to play a role in pre-mRNA 3′-end processing and termination of Pol II transcription. Here, we use a fully reconstituted system to demonstrate that the fission yeast CID-RRM factor Seb1 acts as a bona fide elongation factor. Our analyses show that Seb1 exhibits context-dependent regulation of Pol II pausing, capable of either promoting or inhibiting pause site entry. We propose that CID–RRM factors coordinate Pol II transcription and pre-mRNA 3′-end processing by modulating the rate of Pol II transcription.
Keywords
Footnotes
-
Article is online at http://www.rnajournal.org/cgi/doi/10.1261/rna.080765.125.
-
Freely available online through the RNA Open Access option.
- Received September 12, 2025.
- Accepted October 4, 2025.
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/.










