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Updated: Apr 20, 2026

Capturing Common Fragile Site Breaks by Native γH2A.X ChIP
Published on: January 24, 2025
High-resolution breakpoint analysis provides evidence for the sequence-directed nature of genome rearrangements in
Michal B Kovac1, Monika Kovacova, Hynek Bachraty
1Research Group Human Genomics, Department of Biomedicine, University of Basel, Basel, Switzerland; Medical Genetics, University Hospital Basel, Basel, Switzerland; The Wellcome Trust Centre for Human Genetics, University of Oxford, Old Road Campus, Oxford, UK.
Abstract:
Although most of the pertinent data on the sequence-directed processes leading to genome rearrangements (GRs) have come from studies on somatic tissues, little is known about GRs in the germ line of patients with hereditary disorders. This study aims at identifying DNA motifs and higher order structures of genome architecture, which can result in losses and gains of genetic material in the germ line. We first identified candidate motifs by studying 112 pathogenic germ-line GRs in hereditary colorectal cancer patients, and subsequently created an algorithm, termed recombination type ratio, which correctly predicts the propensity of rearrangements with respect to homologous versus nonhomologous recombination events.
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