Acute hydroxyurea-induced replication blockade results in replisome components disengagement from nascent DNA without causing fork collapse
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Acute hydroxyurea-induced replication blockade results in replisome components disengagement from nascent DNA without causing fork collapse. / Ercilla, Amaia; Feu, Sonia; Aranda, Sergi; Llopis, Alba; Brynjólfsdóttir, Sólveig Hlín; Sørensen, Claus Storgaard; Toledo, Luis Ignacio; Agell, Neus.
I: Cellular and molecular life sciences : CMLS, Bind 77, 2020, s. 735–749.Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
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T1 - Acute hydroxyurea-induced replication blockade results in replisome components disengagement from nascent DNA without causing fork collapse
AU - Ercilla, Amaia
AU - Feu, Sonia
AU - Aranda, Sergi
AU - Llopis, Alba
AU - Brynjólfsdóttir, Sólveig Hlín
AU - Sørensen, Claus Storgaard
AU - Toledo, Luis Ignacio
AU - Agell, Neus
PY - 2020
Y1 - 2020
N2 - During S phase, replication forks can encounter several obstacles that lead to fork stalling, which if persistent might result in fork collapse. To avoid this collapse and to preserve the competence to restart, cells have developed mechanisms that maintain fork stability upon replication stress. In this study, we aimed to understand the mechanisms involved in fork stability maintenance in non-transformed human cells by performing an isolation of proteins on nascent DNA-mass spectrometry analysis in hTERT-RPE cells under different replication stress conditions. Our results show that acute hydroxyurea-induced replication blockade causes the accumulation of large amounts of single-stranded DNA at the fork. Remarkably, this results in the disengagement of replisome components from nascent DNA without compromising fork restart. Notably, Cdc45-MCM-GINS helicase maintains its integrity and replisome components remain associated with chromatin upon acute hydroxyurea treatment, whereas replisome stability is lost upon a sustained replication stress that compromises the competence to restart.
AB - During S phase, replication forks can encounter several obstacles that lead to fork stalling, which if persistent might result in fork collapse. To avoid this collapse and to preserve the competence to restart, cells have developed mechanisms that maintain fork stability upon replication stress. In this study, we aimed to understand the mechanisms involved in fork stability maintenance in non-transformed human cells by performing an isolation of proteins on nascent DNA-mass spectrometry analysis in hTERT-RPE cells under different replication stress conditions. Our results show that acute hydroxyurea-induced replication blockade causes the accumulation of large amounts of single-stranded DNA at the fork. Remarkably, this results in the disengagement of replisome components from nascent DNA without compromising fork restart. Notably, Cdc45-MCM-GINS helicase maintains its integrity and replisome components remain associated with chromatin upon acute hydroxyurea treatment, whereas replisome stability is lost upon a sustained replication stress that compromises the competence to restart.
U2 - 10.1007/s00018-019-03206-1
DO - 10.1007/s00018-019-03206-1
M3 - Journal article
C2 - 31297568
VL - 77
SP - 735
EP - 749
JO - EXS
JF - EXS
SN - 1023-294X
ER -
ID: 225384632