Role of the nucleotide excision repair endonuclease XPF in the kinetoplastid parasite Trypanosoma brucei.

ABSTRACT: The nucleotide excision repair (NER) mechanism is responsible for removing bulky DNA damage, such as pyrimidine dimers induced by ultraviolet (UV) light. The NER pathway excises the damaged strand through incisions at the 5' and 3' ends of the damage, with the 5' incision catalyzed by the XPF-ERCC1 endonuclease complex. Here, we identify an XPF ortholog in Trypanosoma brucei, the causative agent of human African trypanosomiasis (sleeping sickness). XPF-deficient parasites exhibit hypersensitivity to UV irradiation and a slower rate of DNA damage repair. Consistent with its role in DNA repair, XPF localizes to the nucleus, associating with nucleoplasmic and nucleolar regions. Additionally, we demonstrate that TbXPF protects against intra- and inter-strand crosslinks induced by cisplatin and

SUBMITTER: Gomez-Linan C 

PROVIDER: S-EPMC12222486 | biostudies-literature | 2025 Jul

REPOSITORIES: biostudies-literature