| Literature DB >> 31839537 |
Varsha Bhargava1, Courtney D Goldstein1, Logan Russell2, Lin Xu3, Murtaza Ahmed4, Wei Li5, Amanda Casey1, Kelly Servage6, Rahul Kollipara7, Zachary Picciarelli2, Ralf Kittler8, Alexander Yatsenko2, Michelle Carmell9, Kim Orth6, James F Amatruda10, Judith L Yanowitz11, Michael Buszczak12.
Abstract
The propagation of species depends on the ability of germ cells to protect their genome from numerous exogenous and endogenous threats. While these cells employ ubiquitous repair pathways, specialized mechanisms that ensure high-fidelity replication, chromosome segregation, and repair of germ cell genomes remain incompletely understood. We identified Germ Cell Nuclear Acidic Peptidase (GCNA) as a conserved regulator of genome stability in flies, worms, zebrafish, and human germ cell tumors. GCNA contains an acidic intrinsically disordered region (IDR) and a protease-like SprT domain. In addition to chromosomal instability and replication stress, Gcna mutants accumulate DNA-protein crosslinks (DPCs). GCNA acts in parallel with the SprT domain protein Spartan. Structural analysis reveals that while the SprT domain is needed to limit DNA damage, the IDR imparts significant function. This work shows that GCNA protects germ cells from various sources of damage, providing insights into conserved mechanisms that promote genome integrity across generations.Entities:
Keywords: ACRC; DNA repair; DNA-protein crosslink; SprT domain; acidic repeat containing; chromosome instability; chromosome segregation; germ cell; intrinsically disordered region; transgenerational inheritance
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Year: 2019 PMID: 31839537 PMCID: PMC6946843 DOI: 10.1016/j.devcel.2019.11.007
Source DB: PubMed Journal: Dev Cell ISSN: 1534-5807 Impact factor: 12.270