Explosive mutation accumulation triggered by heterozygous human Pol ? proofreading-deficiency is driven by suppression of mismatch repair.

ABSTRACT: Tumors defective for DNA polymerase (Pol) ? proofreading have the highest tumor mutation burden identified. A major unanswered question is whether loss of Pol ? proofreading by itself is sufficient to drive this mutagenesis, or whether additional factors are necessary. To address this, we used a combination of next generation sequencing and in vitro biochemistry on human cell lines engineered to have defects in Pol ? proofreading and mismatch repair. Absent mismatch repair, monoallelic Pol ? proofreading deficiency caused a rapid increase in a unique mutation signature, similar to that observed in tumors from patients with biallelic mismatch repair deficiency and heterozygous Pol ? mutations. Restoring mismatch repair was sufficient to suppress the explosive mutation accumulation. These results strongly suggest that concomitant suppression of mismatch repair, a hallmark of colorectal and other aggressive cancers, is a critical force for driving the explosive mutagenesis seen in tumors expressing exonuclease-deficient Pol ?.

SUBMITTER: Hodel KP 

PROVIDER: S-EPMC5829921 | biostudies-literature | 2018 Feb

REPOSITORIES: biostudies-literature