Literature DB >> 21660704

Assays for structure-selective DNA endonucleases.

William D Wright1, Kirk T Ehmsen, Wolf-Dietrich Heyer.   

Abstract

Structure-selective nucleases perform DNA strand incisions crucial to the repair/resolution of branched DNA molecules arising during DNA replication, recombination, and repair. From a combination of genetics and in vitro nuclease assay studies, we are just beginning to understand how these enzymes recognize their substrates and to identify their in vivo DNA structure targets. By performing nuclease assays on a variety of substrates meant to mimic cellular intermediates, structural features of branched DNA molecules that are important for robust catalysis can be defined. However, since these enzymes often are capable of cleaving a range of DNA structures, caution must be taken not to overemphasize the significance of incision of a certain structure before a careful and detailed kinetic analysis of a variety of DNA substrates with different polarities and structural features has been completed. Here, we provide protocols for the production of a variety of oligo-based DNA joint molecules and their use in endonuclease assays, which can be used to derive the kinetic parameters KM and kcat. Determination of these values for a variety of substrates provides meaningful comparisons that allow inferences to be made regarding in vivo DNA structure target(s).

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 21660704      PMCID: PMC4096161          DOI: 10.1007/978-1-61779-129-1_20

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  7 in total

Review 1.  The Mus81 solution to resolution: generating meiotic crossovers without Holliday junctions.

Authors:  Nancy M Hollingsworth; Steven J Brill
Journal:  Genes Dev       Date:  2004-01-15       Impact factor: 11.361

Review 2.  Holliday junctions in the eukaryotic nucleus: resolution in sight?

Authors:  Wolf Dietrich Heyer; Kirk T Ehmsen; Jachen A Solinger
Journal:  Trends Biochem Sci       Date:  2003-10       Impact factor: 13.807

Review 3.  Nucleases and helicases take center stage in homologous recombination.

Authors:  Eleni P Mimitou; Lorraine S Symington
Journal:  Trends Biochem Sci       Date:  2009-04-15       Impact factor: 13.807

Review 4.  GEN1/Yen1 and the SLX4 complex: Solutions to the problem of Holliday junction resolution.

Authors:  Jennifer M Svendsen; J Wade Harper
Journal:  Genes Dev       Date:  2010-03-04       Impact factor: 11.361

5.  A junction branch point adjacent to a DNA backbone nick directs substrate cleavage by Saccharomyces cerevisiae Mus81-Mms4.

Authors:  Kirk Tevebaugh Ehmsen; Wolf-Dietrich Heyer
Journal:  Nucleic Acids Res       Date:  2009-02-11       Impact factor: 16.971

Review 6.  Structural and functional relationships of the XPF/MUS81 family of proteins.

Authors:  Alberto Ciccia; Neil McDonald; Stephen C West
Journal:  Annu Rev Biochem       Date:  2008       Impact factor: 23.643

7.  Saccharomyces cerevisiae Mus81-Mms4 is a catalytic, DNA structure-selective endonuclease.

Authors:  Kirk Tevebaugh Ehmsen; Wolf-Dietrich Heyer
Journal:  Nucleic Acids Res       Date:  2008-02-16       Impact factor: 16.971

  7 in total
  4 in total

Review 1.  Guidelines for DNA recombination and repair studies: Mechanistic assays of DNA repair processes.

Authors:  Hannah L Klein; Kenny K H Ang; Michelle R Arkin; Emily C Beckwitt; Yi-Hsuan Chang; Jun Fan; Youngho Kwon; Michael J Morten; Sucheta Mukherjee; Oliver J Pambos; Hafez El Sayyed; Elizabeth S Thrall; João P Vieira-da-Rocha; Quan Wang; Shuang Wang; Hsin-Yi Yeh; Julie S Biteen; Peter Chi; Wolf-Dietrich Heyer; Achillefs N Kapanidis; Joseph J Loparo; Terence R Strick; Patrick Sung; Bennett Van Houten; Hengyao Niu; Eli Rothenberg
Journal:  Microb Cell       Date:  2019-01-07

2.  Substrate preference of Gen endonucleases highlights the importance of branched structures as DNA damage repair intermediates.

Authors:  Stephanie P Bellendir; Danielle J Rognstad; Lydia P Morris; Grzegorz Zapotoczny; William G Walton; Matthew R Redinbo; Dale A Ramsden; Jeff Sekelsky; Dorothy A Erie
Journal:  Nucleic Acids Res       Date:  2017-05-19       Impact factor: 16.971

3.  Rad54 functions as a heteroduplex DNA pump modulated by its DNA substrates and Rad51 during D loop formation.

Authors:  William Douglass Wright; Wolf-Dietrich Heyer
Journal:  Mol Cell       Date:  2014-01-30       Impact factor: 17.970

4.  The Mus81-Mms4 structure-selective endonuclease requires nicked DNA junctions to undergo conformational changes and bend its DNA substrates for cleavage.

Authors:  Sucheta Mukherjee; William Douglass Wright; Kirk Tevebaugh Ehmsen; Wolf-Dietrich Heyer
Journal:  Nucleic Acids Res       Date:  2014-04-17       Impact factor: 16.971

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.