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TSG101 Associates with PARP1 and is Essential for PARylation and DNA Damage-induced NF-κB Activation

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Journal EMBO J
Date 2022 Sep 20
PMID 36124865
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Abstract

In a genome-wide screening for components of the dsDNA-break-induced IKK-NF-κB pathway, we identified scores of regulators, including tumor susceptibility gene TSG101. TSG101 is essential for DNA damage-induced formation of cellular poly(ADP-ribose) (PAR). TSG101 binds to PARP1 and is required for PARP1 activation. This function of TSG101 is independent of its role in the ESCRT-I endosomal sorting complex. In the absence of TSG101, the PAR-dependent formation of a nuclear PARP1-IKKγ signalosome, which triggers IKK activation, is impaired. According to its requirement for PARP1 and NF-κB activation, TSG101-deficient cells are defective in DNA repair and apoptosis protection. Loss of TSG101 results in PARP1 trapping at damage sites and mimics the effect of pharmacological PARP inhibition. We also show that the loss of TSG101 in connection with inactivated tumor suppressors BRCA1/2 in breast cancer cells is lethal. Our results imply TSG101 as a therapeutic target to achieve synthetic lethality in cancer treatment.

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References
1.
Ruland J, Sirard C, Elia A, Macpherson D, Wakeham A, Li L . p53 accumulation, defective cell proliferation, and early embryonic lethality in mice lacking tsg101. Proc Natl Acad Sci U S A. 2001; 98(4):1859-64. PMC: 29347. DOI: 10.1073/pnas.98.4.1859. View

2.
Wang W, Mani A, Wu Z . DNA damage-induced nuclear factor-kappa B activation and its roles in cancer progression. J Cancer Metastasis Treat. 2017; 3:45-59. PMC: 5472228. DOI: 10.20517/2394-4722.2017.03. View

3.
Jungmichel S, Rosenthal F, Altmeyer M, Lukas J, Hottiger M, Nielsen M . Proteome-wide identification of poly(ADP-Ribosyl)ation targets in different genotoxic stress responses. Mol Cell. 2013; 52(2):272-85. DOI: 10.1016/j.molcel.2013.08.026. View

4.
Kolmus K, Erdenebat P, Szymanska E, Stewig B, Goryca K, Derezinska-Wolek E . Concurrent depletion of Vps37 proteins evokes ESCRT-I destabilization and profound cellular stress responses. J Cell Sci. 2021; 134(1). DOI: 10.1242/jcs.250951. View

5.
Szklarczyk D, Gable A, Lyon D, Junge A, Wyder S, Huerta-Cepas J . STRING v11: protein-protein association networks with increased coverage, supporting functional discovery in genome-wide experimental datasets. Nucleic Acids Res. 2018; 47(D1):D607-D613. PMC: 6323986. DOI: 10.1093/nar/gky1131. View