A Dominant Mutation in Human RAD51 Reveals Its Function in DNA Interstrand Crosslink Repair Independent of Homologous Recombination

作者：Wang Anderson T; Kim Taeho; Wagner John E; Conti Brooke A; Lach Francis P; Huang Athena L; Molina Henrik; Sanborn Erica M; Zierhut Heather; Cornes Belinda K; Abhyankar Avinash; Sougnez Carrie; Gabriel Stacey B; Auerbach Arleen D; Kowalczykowski Stephen C; Smogorzewska Agata

来源：Molecular Cell, 2015, 59(3): 478-490.

DOI：10.1016/j.molcel.2015.07.009

Repair of DNA interstrand crosslinks requires action of multiple DNA repair pathways, including homologous recombination. Here, we report a de novo heterozygous T131P mutation in RAD51/FANCR, the key recombinase essential for homologous recombination, in a patient with Fanconi anemia-like phenotype. In vitro, RAD51-T131P displays DNA-independent ATPase activity, no DNA pairing capacity, and a co-dominant-negative effect on RAD51 recombinase function. However, the patient cells are homologous recombination proficient due to the low ratio of mutant to wild-type RAD51 in cells. Instead, patient cells are sensitive to crosslinking agents and display hyperphosphorylation of Replication Protein A due to increased activity of DNA2 and WRN at the DNA interstrand crosslinks. Thus, proper RAD51 function is important during DNA interstrand crosslink repair outside of homologous recombination. Our study provides a molecular basis for how RAD51 and its associated factors may operate in a homologous recombination-independent manner to maintain genomic integrity.

• 出版日期2015-8-6