Cancer-associated 53BP1 mutations induce DNA damage repair defects

TP53 binding protein 1 (53BP1) plays an important role in DNA damage repair and maintaining genomic stability. However, the mutations of 53BP1 in human cancers have not been systematically examined. Here, we have analyzed 541 somatic mutations of 53BP1 across 34 types of human cancer from databases of The Cancer Genome Atlas, International Cancer Genome Consortium and Catalogue of Somatic Mutations in Cancer. Among these cancer-associated 53BP1 mutations, truncation mutations disrupt the nuclear localization of 53BP1 thus abolish its biological functions in DNA damage repair. Moreover, with biochemical analyses and structural modeling, we have examined the detailed molecular mechanism by which missense mutations in the key domains causes the DNA damage repair defects. Taken together, our results reveal the functional defects of a set of cancer-associated 53BP1 mutations. •541 somatic mutations of 53BP1 across 34 cancer types from three cancer databases were analyzed.•Truncation mutants of 53BP1 that abolish the C-terminal functional domains disrupt the repair activity of 53BP1.•Mutations of 53BP1 which abolish the correct folding of the key domains may cause the DNA damage repair defects.