Literature DB >> 12546694

Role of the Saccharomyces cerevisiae Rad9 protein in sensing and responding to DNA damage.

G W-L Toh1, N F Lowndes.   

Abstract

Eukaryotic cells have evolved surveillance mechanisms, known as DNA-damage checkpoints, that sense and respond to genome damage. DNA-damage checkpoint pathways ensure co-ordinated cellular responses to DNA damage, including cell cycle delays and activation of repair mechanisms. RAD9, from Saccharomyces cerevisiae, was the first damage checkpoint gene to be identified, although its biochemical function remained unknown until recently. This review examines briefly work that provides significant insight into how Rad9 activates the checkpoint signalling kinase Rad53.

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Year:  2003        PMID: 12546694     DOI: 10.1042/bst0310242

Source DB:  PubMed          Journal:  Biochem Soc Trans        ISSN: 0300-5127            Impact factor:   5.407


  33 in total

1.  RAD51-dependent break-induced replication differs in kinetics and checkpoint responses from RAD51-mediated gene conversion.

Authors:  Anna Malkova; Maria L Naylor; Miyuki Yamaguchi; Grzegorz Ira; James E Haber
Journal:  Mol Cell Biol       Date:  2005-02       Impact factor: 4.272

2.  UV sensitive mutations in histone H3 in Saccharomyces cerevisiae that alter specific K79 methylation states genetically act through distinct DNA repair pathways.

Authors:  Margery L Evans; Lindsey J Bostelman; Ashley M Albrecht; Andrew M Keller; Natasha T Strande; Jeffrey S Thompson
Journal:  Curr Genet       Date:  2008-03-08       Impact factor: 3.886

3.  Dissection of Rad9 BRCT domain function in the mitotic checkpoint response to telomere uncapping.

Authors:  Chinonye C Nnakwe; Mohammed Altaf; Jacques Côté; Stephen J Kron
Journal:  DNA Repair (Amst)       Date:  2009-10-31

4.  Blunt-ended DNA double-strand breaks induced by endonucleases PvuII and EcoRV are poor substrates for repair in Saccharomyces cerevisiae.

Authors:  James W Westmoreland; Jennifer A Summers; Cory L Holland; Michael A Resnick; L Kevin Lewis
Journal:  DNA Repair (Amst)       Date:  2010-03-30

5.  DNA damage checkpoints are involved in postreplication repair.

Authors:  Leslie Barbour; Lindsay G Ball; Ke Zhang; Wei Xiao
Journal:  Genetics       Date:  2006-10-22       Impact factor: 4.562

6.  FACT prevents the accumulation of free histones evicted from transcribed chromatin and a subsequent cell cycle delay in G1.

Authors:  Macarena Morillo-Huesca; Douglas Maya; Mari Cruz Muñoz-Centeno; Rakesh Kumar Singh; Vincent Oreal; Gajjalaiahvari Ugander Reddy; Dun Liang; Vincent Géli; Akash Gunjan; Sebastián Chávez
Journal:  PLoS Genet       Date:  2010-05-20       Impact factor: 5.917

7.  Silenced yeast chromatin is maintained by Sir2 in preference to permitting histone acetylations for efficient NER.

Authors:  Agurtzane Irizar; Yachuan Yu; Simon H Reed; Edward J Louis; Raymond Waters
Journal:  Nucleic Acids Res       Date:  2010-04-12       Impact factor: 16.971

8.  Dynamics of Rad9 chromatin binding and checkpoint function are mediated by its dimerization and are cell cycle-regulated by CDK1 activity.

Authors:  Magda Granata; Federico Lazzaro; Daniele Novarina; Davide Panigada; Fabio Puddu; Carla Manuela Abreu; Ramesh Kumar; Muriel Grenon; Noel F Lowndes; Paolo Plevani; Marco Muzi-Falconi
Journal:  PLoS Genet       Date:  2010-08-05       Impact factor: 5.917

9.  S-phase checkpoint pathways stimulate the mobility of the retrovirus-like transposon Ty1.

Authors:  M Joan Curcio; Alison E Kenny; Sharon Moore; David J Garfinkel; Matthew Weintraub; Eric R Gamache; Derek T Scholes
Journal:  Mol Cell Biol       Date:  2007-10-08       Impact factor: 4.272

10.  Elevated levels of the polo kinase Cdc5 override the Mec1/ATR checkpoint in budding yeast by acting at different steps of the signaling pathway.

Authors:  Roberto Antonio Donnianni; Matteo Ferrari; Federico Lazzaro; Michela Clerici; Benjamin Tamilselvan Nachimuthu; Paolo Plevani; Marco Muzi-Falconi; Achille Pellicioli
Journal:  PLoS Genet       Date:  2010-01-22       Impact factor: 5.917

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