Dna2-intrinsic condensation regulates DNA end resection and reveals evolutionary redistribution of condensate grammar
- 1University of Toronto
Abstract
Eukaryotic cells commonly use biomolecular condensation of DNA double-strand break (DSB) repair scaffolds and signaling assemblies to organize repair reactions in space and time. Yet whether DSB end-processing enzymes themselves encode tunable phase separation that potentiates resection remains unclear. Here we show that the long-range resection enzyme Dna2 forms liquid-like condensates through an intrinsically disordered region that is necessary and sufficient for phase separation and catalytic enhancement in Saccharomyces cerevisiae. Dna2 condensates concentrate DNA substrates and enhance end processing, whereas disrupting condensate formation impairs repair kinetics, checkpoint signaling, and chromosome stability. Grafting of the heterologous intrinsically disordered region of human FUS partly rescues condensate formation and function, and Cdk1-dependent phosphorylation sites tune condensate stability and enzymatic output in cis and in trans. Machine-learning-based analysis reveals that condensation-promoting features of fungal Dna2 are shared with a restricted set of human DNA2-associated resection regulators. Together, these findings define phosphorylation-tuned, enzyme-intrinsic phase separation as an organizational principle of DSB end resection while supporting a model in which condensation-promoting features are redistributed among factors operating within conserved genome maintenance pathways.
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BibTeX
@misc{jordan2026dna2intrinsic,
title = {{Dna2-intrinsic condensation regulates DNA end resection and reveals evolutionary redistribution of condensate grammar}},
author = {C. A. Jordan and J. Lehar and B. J. Payliss and G. Laflamme and Z. Liu and J. The and J. N. Y. Chan and T. Chkuaseli and R. Hakem and L. E. Cowen and H. D. M. Wyatt and K. Mekhail},
howpublished = {bioRxiv},
year = {2026},
month = sep,
doi = {10.64898/2026.09.16.751900},
url = {https://www.biorxiv.org/content/10.64898/2026.09.16.751900v1},
note = {CC BY-NC-ND},
}
RIS
TY - UNPB
TI - Dna2-intrinsic condensation regulates DNA end resection and reveals evolutionary redistribution of condensate grammar
AU - C. A. Jordan
AU - J. Lehar
AU - B. J. Payliss
AU - G. Laflamme
AU - Z. Liu
AU - J. The
AU - J. N. Y. Chan
AU - T. Chkuaseli
AU - R. Hakem
AU - L. E. Cowen
AU - H. D. M. Wyatt
AU - K. Mekhail
PY - 2026
DA - 2026/09/16
PB - bioRxiv
DO - 10.64898/2026.09.16.751900
UR - https://www.biorxiv.org/content/10.64898/2026.09.16.751900v1
AB - Eukaryotic cells commonly use biomolecular condensation of DNA double-strand break (DSB) repair scaffolds and signaling assemblies to organize repair reactions in space and time. Yet whether DSB end-processing enzymes themselves encode tunable phase separation that potentiates resection remains unclear. Here we show that the long-range resection enzyme Dna2 forms liquid-like condensates through an intrinsically disordered region that is necessary and sufficient for phase separation and catalytic enhancement in Saccharomyces cerevisiae. Dna2 condensates concentrate DNA substrates and enhance end processing, whereas disrupting condensate formation impairs repair kinetics, checkpoint signaling, and chromosome stability. Grafting of the heterologous intrinsically disordered region of human FUS partly rescues condensate formation and function, and Cdk1-dependent phosphorylation sites tune condensate stability and enzymatic output in cis and in trans. Machine-learning-based analysis reveals that condensation-promoting features of fungal Dna2 are shared with a restricted set of human DNA2-associated resection regulators. Together, these findings define phosphorylation-tuned, enzyme-intrinsic phase separation as an organizational principle of DSB end resection while supporting a model in which condensation-promoting features are redistributed among factors operating within conserved genome maintenance pathways.
ER -