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Persistent broken chromosome inheritance drives genome instability

Pai, C.-C.; Durley, S. C.; Cheng, W.-C.; Chiang, N.-Y.; Wee, B.-Y.; Walker, C.; Kearsey, S. E.; Buffa, F.; Murray, J. M.; Humphrey, T. C.

2020-08-27 molecular biology
10.1101/2020.08.26.268565 bioRxiv
Show abstract

Persistent DNA damage arising from unrepaired broken chromosomes or telomere loss can promote DNA damage checkpoint adaptation, and cell cycle progression, thereby increasing cell survival but also genome instability. However, the nature and extent of such instability is unclear. We show, using Schizosaccharomyces pombe, that inherited broken chromosomes, arising from failed homologous recombination repair, are subject to cycles of segregation, DNA replication and extensive end-processing, termed here SERPent cycles, by daughter cells, over multiple generations. Following Chk1 loss these post-adaptive cycles continue until extensive processing through inverted repeats promotes annealing, fold-back inversion and a spectrum of chromosomal rearrangements, typically isochromosomes, or chromosome loss, in the resultant population. These findings explain how persistent DNA damage drives widespread genome instability, with implications for punctuated evolution, genetic disease and tumorigenesis. One Sentence SummaryReplication and processing of inherited broken chromosomes drives chromosomal instability.

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