Conserved protein Seb1 that interacts with RNA polymerase II and RNA is an antipausing transcription elongation factor

  1. Lidia Vasiljeva1
  1. 1Department of Biochemistry, University of Oxford, Oxford OX1 3QU, United Kingdom
  2. 2Centre for Bacterial Cell Biology, Biosciences Institute, Newcastle University, Newcastle upon Tyne NE2 4AX, United Kingdom
  1. Corresponding authors: lidia.vasilieva{at}bioch.ox.ac.uk; krzysztof.kus{at}bioch.ox.ac.uk
  1. 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

  • 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/.

| Table of Contents
OPEN ACCESS ARTICLE