About: MRE11 complex links RECQ5 helicase to sites of DNA damage     Goto   Sponge   NotDistinct   Permalink

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  • RECQ5 DNA helicase suppresses homologous recombination (HR) possibly through disruption of RAD51 filaments. We show that RECQ5 is constitutively associated with the MRE11-RAD50-NBS1 (MRN) complex, a primary sensor of DNA double-strand breaks (DSBs) that promotes DSB repair and regulates DNA damage signaling via activation of ATM kinase. Experiments indicated that RECQ5 interacts with the MRN complex through both MRE11 and NBS1, and that RECQ5 specifically inhibited the 3´-5´ exonuclease activity of MRE11, while MRN had no effect on the helicase activity of RECQ5. At the cellular level, we observed that the MRN complex was required for recruitment of RECQ5 to sites of DNA damage. Accumulation of RECQ5 at DSBs was neither dependent on MDC1 that mediates binding of MRN to DSB-flanking chromatin nor on CtIP that acts in conjunction with MRN to promote resection of DSBs for repair by HR. These data suggest that the MRN complex recruits RECQ5 to sites of DNA damage to regulate DNA repair.
  • RECQ5 DNA helicase suppresses homologous recombination (HR) possibly through disruption of RAD51 filaments. We show that RECQ5 is constitutively associated with the MRE11-RAD50-NBS1 (MRN) complex, a primary sensor of DNA double-strand breaks (DSBs) that promotes DSB repair and regulates DNA damage signaling via activation of ATM kinase. Experiments indicated that RECQ5 interacts with the MRN complex through both MRE11 and NBS1, and that RECQ5 specifically inhibited the 3´-5´ exonuclease activity of MRE11, while MRN had no effect on the helicase activity of RECQ5. At the cellular level, we observed that the MRN complex was required for recruitment of RECQ5 to sites of DNA damage. Accumulation of RECQ5 at DSBs was neither dependent on MDC1 that mediates binding of MRN to DSB-flanking chromatin nor on CtIP that acts in conjunction with MRN to promote resection of DSBs for repair by HR. These data suggest that the MRN complex recruits RECQ5 to sites of DNA damage to regulate DNA repair. (en)
Title
  • MRE11 complex links RECQ5 helicase to sites of DNA damage
  • MRE11 complex links RECQ5 helicase to sites of DNA damage (en)
skos:prefLabel
  • MRE11 complex links RECQ5 helicase to sites of DNA damage
  • MRE11 complex links RECQ5 helicase to sites of DNA damage (en)
skos:notation
  • RIV/68378050:_____/09:00333644!RIV10-AV0-68378050
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • P(GA204/09/0565), Z(AV0Z50520514)
http://linked.open...iv/cisloPeriodika
  • 8
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
  • 327876
http://linked.open...ai/riv/idVysledku
  • RIV/68378050:_____/09:00333644
http://linked.open...riv/jazykVysledku
http://linked.open.../riv/klicovaSlova
  • homologous recombination,; RECQ5 helicase; MRE11; DNA repair (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • GB - Spojené království Velké Británie a Severního Irska
http://linked.open...ontrolniKodProRIV
  • [52BCEA56B476]
http://linked.open...i/riv/nazevZdroje
  • Nucleic Acids Research
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
  • 37
http://linked.open...iv/tvurceVysledku
  • Shevelev, Igor
  • Janščák, Pavel
  • Kanagaraj, R.
  • Mihaljevic, B.
  • Zheng, L.
  • Schwendener, S.
  • Gerrits, B.
  • Sartori, A. A.
http://linked.open...ain/vavai/riv/wos
  • 000265953000029
http://linked.open...n/vavai/riv/zamer
issn
  • 0305-1048
number of pages
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