TY - JOUR
T1 - Rrm3 and Pif1 division of labor during replication through leading and lagging strand G-quadruplex
AU - Varon, Mor
AU - Dovrat, Daniel
AU - Heuzé, Jonathan
AU - Tsirkas, Ioannis
AU - Singh, Saurabh P.
AU - Pasero, Philippe
AU - Galletto, Roberto
AU - Aharoni, Amir
N1 - Publisher Copyright: © The Author(s) 2023.
PY - 2024/2/28
Y1 - 2024/2/28
N2 - Members of the conserved Pif1 family of 5'-3' DNA helicases can unwind G4s and mitigate their negative impact on genome stability. In Saccharomyces cerevisiae, two Pif1 family members, Pif1 and Rrm3, contribute to the suppression of genomic instability at diverse regions including telomeres, centromeres and tRNA genes. While Pif1 can resolve lagging strand G4s in vivo, little is known regarding Rrm3 function at G4s and its cooperation with Pif1 for G4 replication. Here, we monitored replication through G4 sequences in real time to show that Rrm3 is essential for efficient replisome progression through G4s located on the leading strand template, but not on the lagging strand. We found that Rrm3 importance for replication through G4s is dependent on its catalytic activity and its N-terminal unstructured region. Overall, we show that Rrm3 and Pif1 exhibit a division of labor that enables robust replication fork progression through leading and lagging strand G4s, respectively.
AB - Members of the conserved Pif1 family of 5'-3' DNA helicases can unwind G4s and mitigate their negative impact on genome stability. In Saccharomyces cerevisiae, two Pif1 family members, Pif1 and Rrm3, contribute to the suppression of genomic instability at diverse regions including telomeres, centromeres and tRNA genes. While Pif1 can resolve lagging strand G4s in vivo, little is known regarding Rrm3 function at G4s and its cooperation with Pif1 for G4 replication. Here, we monitored replication through G4 sequences in real time to show that Rrm3 is essential for efficient replisome progression through G4s located on the leading strand template, but not on the lagging strand. We found that Rrm3 importance for replication through G4s is dependent on its catalytic activity and its N-terminal unstructured region. Overall, we show that Rrm3 and Pif1 exhibit a division of labor that enables robust replication fork progression through leading and lagging strand G4s, respectively.
UR - http://www.scopus.com/inward/record.url?scp=85186749861&partnerID=8YFLogxK
U2 - https://doi.org/10.1093/nar/gkad1205
DO - https://doi.org/10.1093/nar/gkad1205
M3 - Article
C2 - 38117984
SN - 0305-1048
VL - 52
SP - 1753
EP - 1762
JO - Nucleic acids research
JF - Nucleic acids research
IS - 4
ER -