double-strand break repair protein MRE11A; meiotic recombination 11 homolog A; MRE11 homolog A; meiotic recombination 11 homolog 1; MRE11 homolog 1 (MRE11A, HNGS1, MRE11)
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Function
- component of the MRN complex, thus role in DND double-strand break repair
- nuclease activity
- phosphorylated upon DNA damage, probably by ATM or ATR
- component of the BASC complex
- interacts with DCLRE1C/Artemis
Structure
belongs to the MRE11/RAD32 family
Compartment
Alternative splicing
named isoforms=2
Pathology
- defects in MRE11A are a cause of ataxia telangiectasia-like disorder
- defects in MRE11A may be a cause of breast cancer
Notes
- in case of infection by adenovirus E4, the MRN complex is inactivated & degraded by viral oncoproteins
More general terms
Component of
References
- ↑ UniProt http://www.uniprot.org/uniprot/P49959.html
- ↑ Atlas of Genetics & Cytogenetics in Oncology & Haematology http://atlasgeneticsoncology.org/genes/MRE11ID247.html
- ↑ MRE11base; Note: MRE11A mutation db http://bioinf.uta.fi/MRE11Abase/
- ↑ NIEHS-SNPs http://egp.gs.washington.edu/data/mre11a/