ISG15 conjugation to proteins on nascent DNA mitigates DNA replication stress.

Autor: Wardlaw CP; Molecular Biology Program, Memorial Sloan-Kettering Cancer Center, New York, NY, USA., Petrini JHJ; Molecular Biology Program, Memorial Sloan-Kettering Cancer Center, New York, NY, USA. petrinij@mskcc.org.
Jazyk: angličtina
Zdroj: Nature communications [Nat Commun] 2022 Oct 10; Vol. 13 (1), pp. 5971. Date of Electronic Publication: 2022 Oct 10.
DOI: 10.1038/s41467-022-33535-y
Abstrakt: The pathways involved in suppressing DNA replication stress and the associated DNA damage are critical to maintaining genome integrity. The Mre11 complex is unique among double strand break (DSB) repair proteins for its association with the DNA replication fork. Here we show that Mre11 complex inactivation causes DNA replication stress and changes in the abundance of proteins associated with nascent DNA. One of the most highly enriched proteins at the DNA replication fork upon Mre11 complex inactivation was the ubiquitin like protein ISG15. Mre11 complex deficiency and drug induced replication stress both led to the accumulation of cytoplasmic DNA and the subsequent activation of innate immune signaling via cGAS-STING-Tbk1. This led to ISG15 induction and protein ISGylation, including constituents of the replication fork. ISG15 plays a direct role in preventing replication stress. Deletion of ISG15 was associated with replication fork stalling, tonic ATR activation, genomic aberrations, and sensitivity to aphidicolin. These data reveal a previously unrecognized role for ISG15 in mitigating DNA replication stress and promoting genomic stability.
(© 2022. The Author(s).)
Databáze: MEDLINE
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