Cdk1 gates cell cycle-dependent tRNA synthesis by regulating RNA polymerase III activity. Issue 22 (22nd September 2018)

• Record Type: Journal Article
• Authors: Herrera, Maria C; Chymkowitch, Pierre; Robertson, Joseph M; Eriksson, Jens; Bøe, Stig Ove; Alseth, Ingrun; Enserink, Jorrit M
• Is Part Of: Nucleic acids research. Volume 46:Issue 22(2018)
• Page Start: 11698
• Page End: 11711
• Publication Date: 2018-09-22
• Subjects: Nucleic acids -- Periodicals; Molecular biology -- Periodicals; 572.805
• DOI: 10.1093/nar/gky846
• Languages: English
• ISSNs: 0305-1048

Abstract

Abstract: tRNA genes are transcribed by RNA polymerase III (RNAPIII). During recent years it has become clear that RNAPIII activity is strictly regulated by the cell in response to environmental cues and the homeostatic status of the cell. However, the molecular mechanisms that control RNAPIII activity to regulate the amplitude of tDNA transcription in normally cycling cells are not well understood. Here, we show that tRNA levels fluctuate during the cell cycle and reveal an underlying molecular mechanism. The cyclin Clb5 recruits the cyclin dependent kinase Cdk1 to tRNA genes to boost tDNA transcription during late S phase. At tDNA genes, Cdk1 promotes the recruitment of TFIIIC, stimulates the interaction between TFIIIB and TFIIIC, and increases the dynamics of RNA polymerase III in vivo . Furthermore, we identified Bdp1 as a putative Cdk1 substrate in this process. Preventing Bdp1 phosphorylation prevented cell cycle-dependent recruitment of TFIIIC and abolished the cell cycle-dependent increase in tDNA transcription. Our findings demonstrate that under optimal growth conditions Cdk1 gates tRNA synthesis in S phase by regulating the RNAPIII machinery, revealing a direct link between the cell cycle and RNAPIII activity.