Cell-Cycle Modulation of Transcription Termination Factor Sen1

3Citations
Citations of this article
32Readers
Mendeley users who have this article in their library.

Abstract

Many non-coding transcripts (ncRNA) generated by RNA polymerase II in S. cerevisiae are terminated by the Nrd1-Nab3-Sen1 complex. However, Sen1 helicase levels are surprisingly low compared with Nrd1 and Nab3, raising questions regarding how ncRNA can be terminated in an efficient and timely manner. We show that Sen1 levels increase during the S and G2 phases of the cell cycle, leading to increased termination activity of NNS. Overexpression of Sen1 or failure to modulate its abundance by ubiquitin-proteasome-mediated degradation greatly decreases cell fitness. Sen1 toxicity is suppressed by mutations in other termination factors, and NET-seq analysis shows that its overexpression leads to a decrease in ncRNA production and altered mRNA termination. We conclude that Sen1 levels are carefully regulated to prevent aberrant termination. We suggest that ncRNA levels and coding gene transcription termination are modulated by Sen1 to fulfill critical cell cycle-specific functions. Transcription termination of noncoding RNAs by the Nrd1-Nab3-Sen1 (NNS) complex is affected by Sen1 protein levels. Controlled Sen1 degradation during the G1 phase of the cell cycle reduces NNS termination efficiency. In contrast, increased Sen1 levels lead to overactive noncoding RNA termination and reduced cell viability.

Cite

CITATION STYLE

APA

Mischo, H. E., Chun, Y., Harlen, K. M., Smalec, B. M., Dhir, S., Churchman, L. S., & Buratowski, S. (2018). Cell-Cycle Modulation of Transcription Termination Factor Sen1. Molecular Cell, 70(2), 312-326.e7. https://doi.org/10.1016/j.molcel.2018.03.010

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free