2025
Dbl2 interacts with helicases and an endonuclease to maintain the integrity of repetitive regions
BAKOSOVA, Anetta; Lubos CIPAK; Nina MAYEROVA; Kamil KROL; Zsigmond BENKO et al.Základní údaje
Originální název
Dbl2 interacts with helicases and an endonuclease to maintain the integrity of repetitive regions
Autoři
BAKOSOVA, Anetta; Lubos CIPAK; Nina MAYEROVA; Kamil KROL; Zsigmond BENKO; Alexandra PITELOVA; Peter KOLESÁR; Dominika PIATROVA; Maria SMONDRKOVA; Anna MARESOVA; Lucia MOLNAROVA; Ingrid CIPAKOVA; Veronika ALTMANNOVÁ; Jana BELLOVA; Peter BARATH; Martin PREVOROVSKY; Jan PALEČEK; Lumír KREJČÍ; Juraj GREGAN; Adrianna SKONECZNA a Silvia BAGELOVA POLAKOVA
Vydání
Scientific Reports, Berlin, NATURE RESEARCH, 2025, 2045-2322
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
10608 Biochemistry and molecular biology
Stát vydavatele
Německo
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 3.900 v roce 2024
Označené pro přenos do RIV
Ano
Organizační jednotka
Lékařská fakulta
UT WoS
EID Scopus
Klíčová slova anglicky
Schizosaccharomyces pombe; DNA repair; Homologous recombination; Dbl2; Helicases
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 24. 2. 2026 07:21, Mgr. Tereza Miškechová
Anotace
V originále
Helicases and endonucleases play crucial roles in genome maintenance by unwinding or cleaving various forms of DNA and RNA structures in order to facilitate essential biological processes, such as DNA replication and recombination. Here, we identified fission yeast Dbl2 as a potential interactor of several complexes that exhibit either helicase or endonuclease activity, namely Fml1-MHF, SCFFbh1, Rqh1-Top3-Rmi1, and Mus81-Eme1. In vitro, Dbl2 binds to DNA, with a preference for branched molecules, such as D-loops, mobile Holliday junctions, and fork structures, making it a good candidate to play a central role in modulating the activity of helicases and endonucleases during replication and recombination repair. Previously, we showed that Dbl2 recruits Fbh1 to the ongoing homologous recombination sites, affecting the Rad51-nucleofilament. In this study, we determined that deleting dbl2 in an fbh1 Delta background did not increase sensitivity to DNA-damaging agents or the frequency of Tf2 ectopic recombination. Therefore, Dbl2 and Fbh1 might be involved in the same molecular pathway, maintaining genome integrity by hindering ectopic recombination at repetitive elements.
Návaznosti
| GA23-05284S, projekt VaV |
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