Literature DB >> 20858437

Effect of single-strand break on branch migration and folding dynamics of Holliday junctions.

Dmytro Palets1, Alexander Y Lushnikov, Mikhail A Karymov, Yuri L Lyubchenko.   

Abstract

The Holliday junction (HJ), or four-way junction, is a central intermediate state of DNA for homologous genetic recombination and other genetic processes such as replication and repair. Branch migration is the process by which the exchange of homologous DNA regions occurs, and it can be spontaneous or driven by proteins. Unfolding of the HJ is required for branch migration. Our previous single-molecule fluorescence studies led to a model according to which branch migration is a stepwise process consisting of consecutive migration and folding steps. Folding of the HJ in one of the folded conformations terminates the branch migration phase. At the same time, in the unfolded state HJ rapidly migrates over entire homology region of the HJ in one hop. This process can be affected by irregularities in the DNA double helical structure, so mismatches almost terminate a spontaneous branch migration. Single-stranded breaks or nicks are the most ubiquitous defects in the DNA helix; however, to date, their effect on the HJ branch migration has not been studied. In addition, although nicked HJs are specific substrates for a number of enzymes involved in DNA recombination and repair, the role of this substrate specificity remains unclear. Our main goal in this work was to study the effect of nicks on the efficiency of HJ branch migration and the dynamics of the HJ. To accomplish this goal, we applied two single-molecule methods: atomic force microscopy and fluorescence resonance energy transfer. The atomic force microscopy data show that the nick does not prevent branch migration, but it does decrease the probability that the HJ will pass the DNA lesion. The single-molecule fluorescence resonance energy transfer approaches were instrumental in detailing the effects of nicks. These studies reveal a dramatic change of the HJ dynamics. The nick changes the structure and conformational dynamics of the junctions, leading to conformations with geometries that are different from those for the intact HJ. On the basis of these data, we propose a model of branch migration in which the propensity of the junction to unfold decreases the lifetimes of folded states, thereby increasing the frequency of junction fluctuations between the folded states.
Copyright © 2010 Biophysical Society. Published by Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 20858437      PMCID: PMC2941029          DOI: 10.1016/j.bpj.2010.07.011

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  30 in total

1.  The importance of repairing stalled replication forks.

Authors:  M M Cox; M F Goodman; K N Kreuzer; D J Sherratt; S J Sandler; K J Marians
Journal:  Nature       Date:  2000-03-02       Impact factor: 49.962

2.  Positive torsional strain causes the formation of a four-way junction at replication forks.

Authors:  L Postow; C Ullsperger; R W Keller; C Bustamante; A V Vologodskii; N R Cozzarelli
Journal:  J Biol Chem       Date:  2000-10-30       Impact factor: 5.157

Review 3.  Recombination at double-strand breaks and DNA ends: conserved mechanisms from phage to humans.

Authors:  G A Cromie; J C Connelly; D R Leach
Journal:  Mol Cell       Date:  2001-12       Impact factor: 17.970

4.  Rescue of stalled replication forks by RecG: simultaneous translocation on the leading and lagging strand templates supports an active DNA unwinding model of fork reversal and Holliday junction formation.

Authors:  P McGlynn; R G Lloyd
Journal:  Proc Natl Acad Sci U S A       Date:  2001-07-17       Impact factor: 11.205

5.  Action of RuvAB at replication fork structures.

Authors:  P McGlynn; R G Lloyd
Journal:  J Biol Chem       Date:  2001-09-10       Impact factor: 5.157

Review 6.  Single-molecule fluorescence resonance energy transfer.

Authors:  T Ha
Journal:  Methods       Date:  2001-09       Impact factor: 3.608

7.  Replication fork reversal in DNA polymerase III mutants of Escherichia coli: a role for the beta clamp.

Authors:  Gianfranco Grompone; Marie Seigneur; S Dusko Ehrlich; Bénédicte Michel
Journal:  Mol Microbiol       Date:  2002-06       Impact factor: 3.501

8.  Molecular dynamics simulation of a DNA containing a single strand break.

Authors:  H Yamaguchi; J G Siebers; A Furukawa; N Otagiri; R Osman
Journal:  Radiat Prot Dosimetry       Date:  2002       Impact factor: 0.972

9.  Structural dynamics of individual Holliday junctions.

Authors:  Sean A McKinney; Anne-Cécile Déclais; David M J Lilley; Taekjip Ha
Journal:  Nat Struct Biol       Date:  2003-02

10.  Efficient second strand cleavage during Holliday junction resolution by RuvC requires both increased junction flexibility and an exposed 5' phosphate.

Authors:  Fekret Osman; Louise Gaskell; Matthew C Whitby
Journal:  PLoS One       Date:  2009-04-28       Impact factor: 3.240

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  3 in total

1.  Active Control of Repetitive Structural Transitions between Replication Forks and Holliday Junctions by Werner Syndrome Helicase.

Authors:  Soochul Shin; Jinwoo Lee; Sangwoon Yoo; Tomasz Kulikowicz; Vilhelm A Bohr; Byungchan Ahn; Sungchul Hohng
Journal:  Structure       Date:  2016-07-14       Impact factor: 5.006

2.  Implications of Metastable Nicks and Nicked Holliday Junctions in Processing Joint Molecules in Mitosis and Meiosis.

Authors:  Félix Machín
Journal:  Genes (Basel)       Date:  2020-12-12       Impact factor: 4.096

3.  Junction resolving enzymes use multivalency to keep the Holliday junction dynamic.

Authors:  Ruobo Zhou; Olivia Yang; Anne-Cécile Déclais; Hyeonseok Jin; Gwang Hyeon Gwon; Alasdair D J Freeman; Yunje Cho; David M J Lilley; Taekjip Ha
Journal:  Nat Chem Biol       Date:  2019-01-21       Impact factor: 15.040

  3 in total

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