About: ATR-Chk1-APC/CCdh1-dependent stabilization of Cdc7-ASK (Dbf4) kinase is required for DNA lesion bypass under replication stress     Goto   Sponge   NotDistinct   Permalink

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  • Cdc7 kinase regulates DNA replication. However, its role in DNA repair and recombination is poorly understood. Here we describe a pathway that stabilizes the human Cdc7-ASK (activator of S-phase kinase; also called Dbf4), its regulation, and its function in cellular responses to compromised DNA replication. Stalled DNA replication evoked stabilization of the Cdc7-ASK (Dbf4) complex in a manner dependent on ATR-Chk1-mediated checkpoint signaling and its interplay with the anaphase-promoting complex/cyclosome(Cdh1) (APC/C-Cdh1) ubiquitin ligase. Mechanistically, Chk1 kinase inactivates APC/C-Cdh1 through degradation of Cdh1 upon replication block, thereby stabilizing APC/C-Cdh1 substrates, including Cdc7-ASK (Dbf4). Furthermore, motif C of ASK (Dbf4) interacts with the N-terminal region of RAD18 ubiquitin ligase, and this interaction is required for chromatin binding of RAD18. Impaired interaction of ASK (Dbf4) with RAD18 disables foci formation by RAD18 and hinders chromatin loading of translesion DNA polymerase eta. These findings define a novel mechanism that orchestrates replication checkpoint signaling and ubiquitin-proteasome machinery with the DNA damage bypass pathway to guard against replication collapse under conditions of replication stress.
  • Cdc7 kinase regulates DNA replication. However, its role in DNA repair and recombination is poorly understood. Here we describe a pathway that stabilizes the human Cdc7-ASK (activator of S-phase kinase; also called Dbf4), its regulation, and its function in cellular responses to compromised DNA replication. Stalled DNA replication evoked stabilization of the Cdc7-ASK (Dbf4) complex in a manner dependent on ATR-Chk1-mediated checkpoint signaling and its interplay with the anaphase-promoting complex/cyclosome(Cdh1) (APC/C-Cdh1) ubiquitin ligase. Mechanistically, Chk1 kinase inactivates APC/C-Cdh1 through degradation of Cdh1 upon replication block, thereby stabilizing APC/C-Cdh1 substrates, including Cdc7-ASK (Dbf4). Furthermore, motif C of ASK (Dbf4) interacts with the N-terminal region of RAD18 ubiquitin ligase, and this interaction is required for chromatin binding of RAD18. Impaired interaction of ASK (Dbf4) with RAD18 disables foci formation by RAD18 and hinders chromatin loading of translesion DNA polymerase eta. These findings define a novel mechanism that orchestrates replication checkpoint signaling and ubiquitin-proteasome machinery with the DNA damage bypass pathway to guard against replication collapse under conditions of replication stress. (en)
Title
  • ATR-Chk1-APC/CCdh1-dependent stabilization of Cdc7-ASK (Dbf4) kinase is required for DNA lesion bypass under replication stress
  • ATR-Chk1-APC/CCdh1-dependent stabilization of Cdc7-ASK (Dbf4) kinase is required for DNA lesion bypass under replication stress (en)
skos:prefLabel
  • ATR-Chk1-APC/CCdh1-dependent stabilization of Cdc7-ASK (Dbf4) kinase is required for DNA lesion bypass under replication stress
  • ATR-Chk1-APC/CCdh1-dependent stabilization of Cdc7-ASK (Dbf4) kinase is required for DNA lesion bypass under replication stress (en)
skos:notation
  • RIV/61989592:15110/13:33145215!RIV14-GA0-15110___
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • P(ED0030/01/01), P(GPP301/11/P554)
http://linked.open...iv/cisloPeriodika
  • 22
http://linked.open...vai/riv/dodaniDat
http://linked.open...aciTvurceVysledku
http://linked.open.../riv/druhVysledku
http://linked.open...iv/duvernostUdaju
http://linked.open...titaPredkladatele
http://linked.open...dnocenehoVysledku
  • 62461
http://linked.open...ai/riv/idVysledku
  • RIV/61989592:15110/13:33145215
http://linked.open...riv/jazykVysledku
http://linked.open.../riv/klicovaSlova
  • ALKYLATION DAMAGE; INDUCED MUTAGENESIS; BUDDING YEAST; POLYMERASE-ETA; SACCHAROMYCES-CEREVISIAE; HOMOLOGOUS RECOMBINATION; CELL-CYCLE; S-PHASE CHECKPOINT; HUMAN CDC7-RELATED KINASE; ANAPHASE-PROMOTING COMPLEX (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • US - Spojené státy americké
http://linked.open...ontrolniKodProRIV
  • [814B243F610D]
http://linked.open...i/riv/nazevZdroje
  • Genes & Development
http://linked.open...in/vavai/riv/obor
http://linked.open...ichTvurcuVysledku
http://linked.open...cetTvurcuVysledku
http://linked.open...vavai/riv/projekt
http://linked.open...UplatneniVysledku
http://linked.open...v/svazekPeriodika
  • 27
http://linked.open...iv/tvurceVysledku
  • Bártek, Jiří
  • Mistrík, Martin
  • Watanabe, K.
  • Lukas, J.
  • Veselá, Eva
  • Mailand, N.
  • Lee, Mh
  • Masai, H.
  • Protivánková, Iva
  • Yamada, Masayuki
http://linked.open...ain/vavai/riv/wos
  • 000327321300007
issn
  • 0890-9369
number of pages
http://bibframe.org/vocab/doi
  • 10.1101/gad.224568.113
http://localhost/t...ganizacniJednotka
  • 15110
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