RAD1
Gene Ontology Biological Process
- DNA amplification [IMP]
- double-strand break repair via homologous recombination [IBA]
- double-strand break repair via single-strand annealing, removal of nonhomologous ends [IMP]
- meiotic mismatch repair [IMP]
- mitotic recombination [IMP]
- nucleotide-excision repair, DNA incision, 5'-to lesion [IDA]
- removal of nonhomologous ends [IMP]
- resolution of meiotic recombination intermediates [IBA]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
MSH3
Gene Ontology Biological Process
Gene Ontology Molecular Function
Gene Ontology Cellular Component
Dosage Lethality
A genetic interaction is inferred when over expression or increased dosage of one gene causes lethality in a strain that is mutated or deleted for another gene.
Publication
Coordination of Rad1-Rad10 interactions with Msh2-Msh3, Saw1 and RPA is essential for functional 3' non-homologous tail removal.
Double strand DNA break repair (DSBR) comprises multiple pathways. A subset of DSBR pathways, including single strand annealing, involve intermediates with 3' non-homologous tails that must be removed to complete repair. In Saccharomyces cerevisiae, Rad1-Rad10 is the structure-specific endonuclease that cleaves the tails in 3' non-homologous tail removal (3' NHTR). Rad1-Rad10 is also an essential component of the nucleotide excision ... [more]
Throughput
- Low Throughput
Ontology Terms
- phenotype: inviable (APO:0000112)
Additional Notes
- overespressing Msh3 in a rad1R218A background decreases survival
Related interactions
Interaction | Experimental Evidence Code | Dataset | Throughput | Score | Curated By | Notes |
---|---|---|---|---|---|---|
MSH3 RAD1 | Far Western Far Western An interaction is detected between a protein immobilized on a membrane and a purified protein probe. | Low | - | BioGRID | - | |
MSH3 RAD1 | Phenotypic Enhancement Phenotypic Enhancement A genetic interaction is inferred when mutation or overexpression of one gene results in enhancement of any phenotype (other than lethality/growth defect) associated with mutation or over expression of another gene. | Low | - | BioGRID | 156427 |
Curated By
- BioGRID