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Role of EXO1 nuclease activity in genome maintenance, the immune response and tumor suppression in Exo1D173A mice

Shanzhi Wang, Kyeryoung Lee, Stephen Gray, Yongwei Zhang, Catherine Tang, Rikke B. Morrish, Elena Tosti, Johanna van Oers, Paula E. Cohen, Thomas MacCarthy, Sergio Roa, Matthew Scharff, Winfried Edelmann, View ORCID ProfileRichard Chahwan
doi: https://doi.org/10.1101/2021.10.05.463200
Shanzhi Wang
1Department of Cell Biology, Albert Einstein College of Medicine, 1300 Morris Park Avenue, NY 10461, USA
2Current position: Department of Chemistry, University of Arkansas at Little Rock, Little Rock, AR 72204, USA
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Kyeryoung Lee
1Department of Cell Biology, Albert Einstein College of Medicine, 1300 Morris Park Avenue, NY 10461, USA
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Stephen Gray
3Department of Biomedical Sciences, Cornell University, New York 14853, USA
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Yongwei Zhang
1Department of Cell Biology, Albert Einstein College of Medicine, 1300 Morris Park Avenue, NY 10461, USA
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Catherine Tang
4Department of Applied Mathematics and Statistics, Stony Brook University, Stony Brook, NY
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Rikke B. Morrish
5Current position: School of Physics and Astronomy, University of Exeter, Exeter EX4 4QD, UK
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Elena Tosti
1Department of Cell Biology, Albert Einstein College of Medicine, 1300 Morris Park Avenue, NY 10461, USA
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Johanna van Oers
1Department of Cell Biology, Albert Einstein College of Medicine, 1300 Morris Park Avenue, NY 10461, USA
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Paula E. Cohen
3Department of Biomedical Sciences, Cornell University, New York 14853, USA
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Thomas MacCarthy
4Department of Applied Mathematics and Statistics, Stony Brook University, Stony Brook, NY
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Sergio Roa
6Department of Biochemistry and Genetics, University of Navarra, 31008 Pamplona, Spain
7Centro de Investigacion Biomedica en Red de Cancer (CIBERONC), Instituto de Salud Carlos III, Madrid, Spain
8Navarra Institute for Health Research (IdiSNA), Pamplona, Spain
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Matthew Scharff
1Department of Cell Biology, Albert Einstein College of Medicine, 1300 Morris Park Avenue, NY 10461, USA
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Winfried Edelmann
1Department of Cell Biology, Albert Einstein College of Medicine, 1300 Morris Park Avenue, NY 10461, USA
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Richard Chahwan
9Institute of Experimental Immunology, University of Zurich, Zurich 8057, Switzerland
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  • ORCID record for Richard Chahwan
  • For correspondence: chahwan@immunology.uzh.ch
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ABSTRACT

DNA damage response pathways rely extensively on nuclease activity to process DNA intermediates. Exonuclease 1 (EXO1) is a pleiotropic evolutionary conserved DNA exonuclease involved in various DNA repair pathways, replication, antibody diversification, and meiosis. But, whether EXO1 facilitates these DNA metabolic processes through its enzymatic or scaffolding functions remains unclear. Here we dissect the contribution of EXO1 enzymatic versus scaffolding activity by comparing Exo1DA/DA mice expressing a proven nuclease-dead mutant form of EXO1 to entirely EXO1-deficient Exo1−/− and EXO1 wild type Exo1+/+ mice. We show that Exo1DA/DA and Exo1−/− mice are compromised in canonical DNA repair processing, suggesting that the EXO1 enzymatic role is important for error-free DNA mismatch and double-strand break repair pathways. However, in non-canonical repair pathways, EXO1 appears to have a more nuanced function. Next-generation sequencing of heavy chain V region in B cells showed the mutation spectra of Exo1DA/DA mice to be intermediate between Exo1+/+ and Exo1−/− mice, suggesting that both catalytic and scaffolding roles of EXO1 are important for somatic hypermutation. Similarly, while overall class switch recombination in Exo1DA/DA and Exo1−/− mice was comparably defective, switch-switch junction analysis suggests that EXO1 might fulfill an additional scaffolding function downstream of class switching. In contrast to Exo1−/− mice that are infertile, meiosis progressed normally in Exo1DA/DA and Exo1+/+ cohorts, indicating that a structural but not the nuclease function of EXO1 is critical for meiosis. However, both Exo1DA/DA and Exo1−/− mice displayed similar mortality and cancer predisposition profiles. Taken together, these data demonstrate that EXO1 has both scaffolding and enzymatic functions in distinct DNA repair processes and suggest a more composite and intricate role for EXO1 in DNA metabolic processes and disease.

Competing Interest Statement

SR receives research support from Roche/Genentech (imCORE) and Gilead. The rest of the authors declare no conflict of interest.

Footnotes

  • ↵* Contact Information: richard.chahwan{at}uzh.ch (Tel: +41 446353710) winfried.edelmann{at}einsteinmed.org (Tel: +1 7186781086) matthew.scharff{at}einsteinmed.org (Tel: +1 7184303527) sroa{at}unav.es (Tel: +34 948425600)

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
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Posted October 05, 2021.
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Role of EXO1 nuclease activity in genome maintenance, the immune response and tumor suppression in Exo1D173A mice
Shanzhi Wang, Kyeryoung Lee, Stephen Gray, Yongwei Zhang, Catherine Tang, Rikke B. Morrish, Elena Tosti, Johanna van Oers, Paula E. Cohen, Thomas MacCarthy, Sergio Roa, Matthew Scharff, Winfried Edelmann, Richard Chahwan
bioRxiv 2021.10.05.463200; doi: https://doi.org/10.1101/2021.10.05.463200
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Role of EXO1 nuclease activity in genome maintenance, the immune response and tumor suppression in Exo1D173A mice
Shanzhi Wang, Kyeryoung Lee, Stephen Gray, Yongwei Zhang, Catherine Tang, Rikke B. Morrish, Elena Tosti, Johanna van Oers, Paula E. Cohen, Thomas MacCarthy, Sergio Roa, Matthew Scharff, Winfried Edelmann, Richard Chahwan
bioRxiv 2021.10.05.463200; doi: https://doi.org/10.1101/2021.10.05.463200

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