Literature DB >> 16793406

Methods for studying the cellular response to DNA damage: influence of the Mre11 complex on chromosome metabolism.

Jan-Willem F Theunissen1, John H J Petrini.   

Abstract

Dramatic progress in understanding the mediators and mechanisms of chromosome break metabolism has been made in recent years. As a result, the links between disease and defects in chromosome dynamics have become clearer. In this chapter, we discuss techniques employed in our laboratory to study chromosome break metabolism, which include assessments at the molecular and cellular level. In our laboratory, we use the Mre11 complex as a tool to study this process, but the techniques discussed are of general relevance.

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Year:  2006        PMID: 16793406     DOI: 10.1016/S0076-6879(05)09015-4

Source DB:  PubMed          Journal:  Methods Enzymol        ISSN: 0076-6879            Impact factor:   1.600


  24 in total

1.  The mef/elf4 transcription factor fine tunes the DNA damage response.

Authors:  Goro Sashida; Narae Bae; Silvana Di Giandomenico; Takashi Asai; Nadia Gurvich; Elena Bazzoli; Yan Liu; Gang Huang; Xinyang Zhao; Silvia Menendez; Stephen D Nimer
Journal:  Cancer Res       Date:  2011-05-26       Impact factor: 12.701

2.  The mre11 complex and the response to dysfunctional telomeres.

Authors:  Claire L Attwooll; Müge Akpinar; John H J Petrini
Journal:  Mol Cell Biol       Date:  2009-08-10       Impact factor: 4.272

3.  Loss of ATM/Chk2/p53 pathway components accelerates tumor development and contributes to radiation resistance in gliomas.

Authors:  Massimo Squatrito; Cameron W Brennan; Karim Helmy; Jason T Huse; John H Petrini; Eric C Holland
Journal:  Cancer Cell       Date:  2010-12-14       Impact factor: 31.743

4.  A hypomorphic Artemis human disease allele causes aberrant chromosomal rearrangements and tumorigenesis.

Authors:  Cheryl Jacobs; Ying Huang; Tehmina Masud; William Lu; Gerwin Westfield; William Giblin; JoAnn M Sekiguchi
Journal:  Hum Mol Genet       Date:  2010-12-08       Impact factor: 6.150

5.  Phosphorylation of MLL by ATR is required for execution of mammalian S-phase checkpoint.

Authors:  Han Liu; Shugaku Takeda; Rakesh Kumar; Todd D Westergard; Eric J Brown; Tej K Pandita; Emily H-Y Cheng; James J-D Hsieh
Journal:  Nature       Date:  2010-09-05       Impact factor: 49.962

6.  A mouse PRMT1 null allele defines an essential role for arginine methylation in genome maintenance and cell proliferation.

Authors:  Zhenbao Yu; Taiping Chen; Josée Hébert; En Li; Stéphane Richard
Journal:  Mol Cell Biol       Date:  2009-03-16       Impact factor: 4.272

7.  The E3 ligase PIRH2 polyubiquitylates CHK2 and regulates its turnover.

Authors:  M Bohgaki; A Hakem; M J Halaby; T Bohgaki; Q Li; P A Bissey; J Shloush; T Kislinger; O Sanchez; Y Sheng; R Hakem
Journal:  Cell Death Differ       Date:  2013-03-01       Impact factor: 15.828

8.  Defective p53 engagement after the induction of DNA damage in cells deficient in topoisomerase 3beta.

Authors:  Subhasis Mohanty; Terrence Town; Tomohito Yagi; Christina Scheidig; Kelvin Y Kwan; Heather G Allore; Richard A Flavell; Albert C Shaw
Journal:  Proc Natl Acad Sci U S A       Date:  2008-03-26       Impact factor: 11.205

9.  Chk2 suppresses the oncogenic potential of DNA replication-associated DNA damage.

Authors:  Travis H Stracker; Suzana S Couto; Carlos Cordon-Cardo; Tulio Matos; John H J Petrini
Journal:  Mol Cell       Date:  2008-07-11       Impact factor: 17.970

10.  Disease-associated MRE11 mutants impact ATM/ATR DNA damage signaling by distinct mechanisms.

Authors:  Joshua A Regal; Todd A Festerling; Jeffrey M Buis; David O Ferguson
Journal:  Hum Mol Genet       Date:  2013-08-02       Impact factor: 6.150

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