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GCNA Interacts with Spartan and Topoisomerase II to Regulate Genome Stability

  • Gregoriy A. Dokshin
  • , Gregory M. Davis
  • , Ashley D. Sawle
  • , Matthew D. Eldridge
  • , Peter K. Nicholls
  • , Taylin E. Gourley
  • , Katherine A. Romer
  • , Luke W. Molesworth
  • , Hannah R. Tatnell
  • , Ahmet R. Ozturk
  • , Dirk G. De Rooij
  • , Gregory J. Hannon
  • , David C. Page
  • , Craig C. Mello
  • , Michelle A. Carmell

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

GCNA proteins are expressed across eukarya in pluripotent cells and have conserved functions in fertility. GCNA homologs Spartan (DVC-1) and Wss1 resolve DNA-protein crosslinks (DPCs), including Topoisomerase-DNA adducts, during DNA replication. Here, we show that GCNA mutants in mouse and C. elegans display defects in genome maintenance including DNA damage, aberrant chromosome condensation, and crossover defects in mouse spermatocytes and spontaneous genomic rearrangements in C. elegans. We show that GCNA and topoisomerase II (TOP2) physically interact in both mice and worms and colocalize on condensed chromosomes during mitosis in C. elegans embryos. Moreover, C. elegans gcna-1 mutants are hypersensitive to TOP2 poison. Together, our findings support a model in which GCNA provides genome maintenance functions in the germline and may do so, in part, by promoting the resolution of TOP2 DPCs.
Original languageEnglish
Pages (from-to)53-68.e6
JournalDevelopmental Cell
Volume52
Issue number1
DOIs
Publication statusPublished - 6 Jan 2020

Keywords

  • GCNA
  • DVC-1
  • Spartan
  • SprT
  • topoisomerase
  • Top2
  • Top1
  • DNA-protein crosslink (DPC) repair
  • Germ cells

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