Uncoupling of mTORC1 from E2F activity maintains DNA damage and senescence

Leighton H. Daigh, Debarya Saha, David L. Rosenthal, Katherine R. Ferrick and Tobias Meyer ()
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Leighton H. Daigh: Stanford University School of Medicine
Debarya Saha: Weill Cornell Medical College
David L. Rosenthal: Weill Cornell Medical College
Katherine R. Ferrick: Stanford University School of Medicine
Tobias Meyer: Stanford University School of Medicine

Nature Communications, 2024, vol. 15, issue 1, 1-16

Abstract: Abstract DNA damage is a primary trigger for cellular senescence, which in turn causes organismal aging and is a promising target of anti-aging therapies. Most DNA damage occurs when DNA is fragile during DNA replication in S phase, but senescent cells maintain DNA damage long-after DNA replication has stopped. How senescent cells induce DNA damage and why senescent cells fail to repair damaged DNA remain open questions. Here, we combine reversible expression of the senescence-inducing CDK4/6 inhibitory protein p16INK4 (p16) with live single-cell analysis and show that sustained mTORC1 signaling triggers senescence in non-proliferating cells by increasing transcriptional DNA damage and inflammation signaling that persists after p16 is degraded. Strikingly, we show that activation of E2F transcriptional program, which is regulated by CDK4/6 activity and promotes expression of DNA repair proteins, repairs transcriptionally damaged DNA without requiring DNA replication. Together, our study suggests that senescence can be maintained by ongoing mTORC1-induced transcriptional DNA damage that cannot be sufficiently repaired without induction of protective E2F target genes.

Date: 2024
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DOI: 10.1038/s41467-024-52820-6

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