Replication stress induces POLQ-mediated structural variant formation throughout common fragile sites after entry into mitosis

Thomas E. Wilson (), Samreen Ahmed, Amanda Winningham and Thomas W. Glover ()
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Thomas E. Wilson: University of Michigan Medical School
Samreen Ahmed: University of Michigan Medical School
Amanda Winningham: University of Michigan Medical School
Thomas W. Glover: University of Michigan Medical School

Nature Communications, 2024, vol. 15, issue 1, 1-19

Abstract: Abstract Genomic structural variants (SVs) greatly impact human health, but much is unknown about the mechanisms that generate the largest class of nonrecurrent alterations. Common fragile sites (CFSs) are unstable loci that provide a model for SV formation, especially large deletions, under replication stress. We study SV junction formation as it occurs in human cell lines by applying error-minimized capture sequencing to CFS DNA harvested after low-dose aphidicolin treatment. SV junctions form throughout CFS genes at a 5-fold higher rate after cells pass from G2 into M-phase. Neither SV formation nor CFS expression depend on mitotic DNA synthesis (MiDAS), an error-prone form of replication active at CFSs. Instead, analysis of tens of thousands of de novo SV junctions combined with DNA repair pathway inhibition reveal a primary role for DNA polymerase theta (POLQ)-mediated end-joining (TMEJ). We propose an important role for mitotic TMEJ in nonrecurrent SV formation genome wide.

Date: 2024
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DOI: 10.1038/s41467-024-53917-8

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