TY - JOUR
AU1 - Tufan, Ahmet Buğra
AU2 - Lazarow, Katina
AU3 - Kolesnichenko, Marina
AU4 - Sporbert, Anje
AU5 - Kries, Jens Peter
AU6 - Scheidereit, Claus
AB - 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.
TI - TSG101 associates with PARP1 and is essential for PARylation and DNA damage‐induced NF‐κB activation
JF - The EMBO Journal
DO - 10.15252/embj.2021110372
DA - 2022-11-02
UR - https://www.deepdyve.com/lp/wiley/tsg101-associates-with-parp1-and-is-essential-for-parylation-and-dna-4Jv5R0btzT
VL - 41
IS - 21
DP - DeepDyve
ER -