Recurrent mutations in topoisomerase IIα cause a previously undescribed mutator phenotype in human cancers

Topoisomerases nick and reseal DNA to relieve torsional stress associated with transcription and replication and to resolve structures such as knots and catenanes. Stabilization of the yeast Top2 cleavage intermediates is mutagenic in yeast, but whether this extends to higher eukaryotes is less clear. Chemotherapeutic topoisomerase poisons also elevate cleavage, resulting in mutagenesis. Here, we describe p.K743N mutations in human topoisomerase hTOP2 alpha and link them to a previously undescribed mutator phenotype in cancer. Overexpression of the orthologous mutant protein in yeast generated a characteristic pattern of 2- to 4-base pair (bp) duplications resembling those in tumors with p.K743N. Using mutant strains and biochemical analysis, we determined the genetic requirements of this mutagenic process and showed that it results from trapping of the mutant yeast yTop2 cleavage complex. In addition to 2- to 4-bp duplications, hTOP2 alpha p.K743N is also associated with deletions that are absent in yeast. We call the combined pattern of duplications and deletions ID_TOP2 alpha. All seven tumors carrying the hTOP2a p.K743N mutation showed ID_TOP2 alpha, while it was absent from all other tumors examined (n = 12,269). Each tumor with the ID_TOP2 alpha signature had indels in several known cancer genes, which included frameshift mutations in tumor suppressors PTEN and TP53 and an activating insertion in BRAF. Sequence motifs found at ID_TOP2 alpha mutations were present at 80% of indels in cancer-driver genes, suggesting that ID_TOP2 alpha mutagenesis may contribute to tumorigenesis. The results reported here shed further light on the role of topoisomerase II in genome instability.

Automated summary

This study identified a mutation in human topoisomerase hTOP2 alpha (p.K743N) and linked it to a previously undescribed mutator phenotype in cancer. The research determined the genetic requirements and mechanisms of this mutagenic process and showed that it may contribute to tumorigenesis. The results shed further light on the role of topoisomerase II in genome instability.