SLX4, a coordinator of structure-specific endonucleases, is mutated in a new Fanconi anemia subtype
- PMID: 21240277
- DOI: 10.1038/ng.751
SLX4, a coordinator of structure-specific endonucleases, is mutated in a new Fanconi anemia subtype
Abstract
DNA interstrand crosslink repair requires several classes of proteins, including structure-specific endonucleases and Fanconi anemia proteins. SLX4, which coordinates three separate endonucleases, was recently recognized as an important regulator of DNA repair. Here we report the first human individuals found to have biallelic mutations in SLX4. These individuals, who were previously diagnosed as having Fanconi anemia, add SLX4 as an essential component to the FA-BRCA genome maintenance pathway.
Comment in
-
Genomic instability: Expanding the reach of Fanconi anaemia.Nat Rev Cancer. 2011 Mar;11(3):158. doi: 10.1038/nrc3027. Epub 2011 Feb 17. Nat Rev Cancer. 2011. PMID: 21451554 No abstract available.
-
Cancel all Hollidays for SLX4 mutations: identification of a new Fanconi anemia subtype, FANCP.Clin Genet. 2011 Jul;80(1):28-30. doi: 10.1111/j.1399-0004.2011.01679.x. Epub 2011 Apr 25. Clin Genet. 2011. PMID: 21476996
References
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases
Research Materials
