Rrm3 and Pif1 division of labor during replication through leading and lagging strand G-quadruplex

被引:5
|
作者
Varon, Mor [1 ,2 ]
Dovrat, Daniel [1 ,2 ]
Heuze, Jonathan [3 ]
Tsirkas, Ioannis [1 ,2 ]
Singh, Saurabh P. [4 ]
Pasero, Philippe [3 ]
Galletto, Roberto [4 ]
Aharoni, Amir [1 ,2 ]
机构
[1] Ben Gurion Univ Negev, Dept Life Sci, IL-84105 Beer Sheva, Israel
[2] Ben Gurion Univ Negev, Natl Inst Biotechnol Negev, IL-84105 Beer Sheva, Israel
[3] Univ Montpellier, CNRS, Inst Genet Humaine, Equipe Labellisee Ligue Canc, F-34396 Montpellier, France
[4] Washington Univ, Sch Med, Dept Biochem & Mol Biophys, St Louis, MO 63110 USA
基金
美国国家卫生研究院;
关键词
FORK PROGRESSION; DNA-REPLICATION; HELICASE; YEAST; PCNA; INSTABILITY; SEQUENCES; COMPLEX; MOTIFS;
D O I
10.1093/nar/gkad1205
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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. Graphical Abstract
引用
收藏
页码:1753 / 1762
页数:10
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