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Publication : De novo deletions and duplications at recombination hotspots in mouse germlines.

First Author  Lukaszewicz A Year  2021
Journal  Cell Volume  184
Issue  24 Pages  5970-5984.e18
PubMed ID  34793701 Mgi Jnum  J:328637
Mgi Id  MGI:6833912 Doi  10.1016/j.cell.2021.10.025
Citation  Lukaszewicz A, et al. (2021) De novo deletions and duplications at recombination hotspots in mouse germlines. Cell 184(24):5970-5984.e18
abstractText  Numerous DNA double-strand breaks (DSBs) arise during meiosis to initiate homologous recombination. These DSBs are usually repaired faithfully, but here, we uncover a distinct type of mutational event in which deletions form via joining of ends from two closely spaced DSBs (double cuts) within a single hotspot or at adjacent hotspots on the same or different chromatids. Deletions occur in normal meiosis but are much more frequent when DSB formation is dysregulated in the absence of the ATM kinase. Events between chromosome homologs point to multi-chromatid damage and aborted gap repair. Some deletions contain DNA from other hotspots, indicating that double cutting at distant sites creates substrates for insertional mutagenesis. End joining at double cuts can also yield tandem duplications or extrachromosomal circles. Our findings highlight the importance of DSB regulation and reveal a previously hidden potential for meiotic mutagenesis that is likely to affect human health and genome evolution.
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