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Mechanistic Insights into RAD51-associated Protein 1 (RAD51AP1) Action in Homologous DNA Repair*
- Publication Year :
- 2012
- Publisher :
- American Society for Biochemistry and Molecular Biology, 2012.
-
Abstract
- Homologous recombination catalyzed by the RAD51 recombinase is essential for maintaining genome integrity upon the induction of DNA double strand breaks and other DNA lesions. By enhancing the recombinase activity of RAD51, RAD51AP1 (RAD51-associated protein 1) serves a key role in homologous recombination-mediated chromosome damage repair. We show here that RAD51AP1 harbors two distinct DNA binding domains that are both needed for maximal protein activity under physiological conditions. We have finely mapped the two DNA binding domains in RAD51AP1 and generated mutant variants that are impaired in either or both of the DNA binding domains. Examination of these mutants reveals that both domains are indispensable for RAD51AP1 function in cells. These and other results illuminate the mechanistic basis of RAD51AP1 action in homologous DNA repair.
- Subjects :
- HMG-box
DNA Repair
DNA repair
genetic processes
RAD51
Biology
Biochemistry
Peptide Mapping
Homology directed repair
Humans
Amino Acid Sequence
Molecular Biology
Replication protein A
Conserved Sequence
Sequence Deletion
chemistry.chemical_classification
Genetics
DNA ligase
Recombinase activity
RNA-Binding Proteins
Cell Biology
DNA
DNA repair protein XRCC4
Peptide Fragments
Recombinant Proteins
Cell biology
Protein Structure, Tertiary
DNA-Binding Proteins
enzymes and coenzymes (carbohydrates)
Phenotype
chemistry
Amino Acid Substitution
health occupations
Mutagenesis, Site-Directed
biological phenomena, cell phenomena, and immunity
Reports
HeLa Cells
Protein Binding
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Accession number :
- edsair.doi.dedup.....c7232efb9195dd6ef1dfc539c88c39fe