Physiological consequences of defects in ERCC1-XPF DNA repair endonuclease.
DNA Repair (Amst)
; 10(7): 781-91, 2011 Jul 15.
Article
in En
| MEDLINE
| ID: mdl-21612988
ABSTRACT
ERCC1-XPF is a structure-specific endonuclease required for nucleotide excision repair, interstrand crosslink repair, and the repair of some double-strand breaks. Mutations in ERCC1 or XPF cause xeroderma pigmentosum, XFE progeroid syndrome or cerebro-oculo-facio-skeletal syndrome, characterized by increased risk of cancer, accelerated aging and severe developmental abnormalities, respectively. This review provides a comprehensive overview of the health impact of ERCC1-XPF deficiency, based on these rare diseases and mouse models of them. This offers an understanding of the tremendous health impact of DNA damage derived from environmental and endogenous sources.
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
DNA-Binding Proteins
/
DNA Repair
/
Endonucleases
/
DNA Repair-Deficiency Disorders
Limits:
Animals
/
Humans
Language:
En
Journal:
DNA Repair (Amst)
Journal subject:
BIOLOGIA MOLECULAR
/
BIOQUIMICA
Year:
2011
Document type:
Article
Affiliation country: