Literature DB >> 8134343

The kinetics of spontaneous DNA branch migration.

I G Panyutin1, P Hsieh.   

Abstract

An important step in genetic recombination is DNA branch migration, the movement of the Holliday junction or exchange point between two homologous duplex DNAs. We have determined kinetic parameters of spontaneous branch migration as a function of temperature and ionic conditions. The branch migration substrates consist of two homologous duplex DNAs each having two single-strand tails at one end that are complementary to the corresponding single-strand tails of the other duplex. Upon rapid annealing of the two duplex DNAs, a four-stranded intermediate is formed that has a Holliday junction at one end of the duplexes. Branch migration to the opposite end of the duplexes results in complete strand exchange and formation of two duplex products. The rate of branch migration is exceedingly sensitive to the type of metal ions present. In magnesium, branch migration is quite slow with a step time, tau, equal to 300 msec at 37 degrees C. Surprisingly, branch migration in the absence of magnesium was 1000 times faster. Despite this difference in rates, apparent activation energies for the branch migration step in the presence and absence of magnesium are similar. Since metal ions have a profound effect on the structure of the Holliday junction, it appears that the structure of the branch point plays a key role in determining the rate of spontaneous DNA branch migration. We discuss the role of proteins in promoting the branch migration step during homologous recombination.

Entities:  

Mesh:

Substances:

Year:  1994        PMID: 8134343      PMCID: PMC43301          DOI: 10.1073/pnas.91.6.2021

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  19 in total

1.  Kinetics of branch migration in double-stranded DNA.

Authors:  B J Thompson; M N Camien; R C Warner
Journal:  Proc Natl Acad Sci U S A       Date:  1976-07       Impact factor: 11.205

2.  ATP-dependent branch migration of Holliday junctions promoted by the RuvA and RuvB proteins of E. coli.

Authors:  I R Tsaneva; B Müller; S C West
Journal:  Cell       Date:  1992-06-26       Impact factor: 41.582

3.  Behavior of a cross-linked attachment site: testing the role of branch migration in site-specific recombination.

Authors:  M Cowart; S J Benkovic; H A Nash
Journal:  J Mol Biol       Date:  1991-08-05       Impact factor: 5.469

4.  Cruciform transitions in DNA.

Authors:  R R Sinden; D E Pettijohn
Journal:  J Biol Chem       Date:  1984-05-25       Impact factor: 5.157

5.  Construction of improved M13 vectors using oligodeoxynucleotide-directed mutagenesis.

Authors:  J Norrander; T Kempe; J Messing
Journal:  Gene       Date:  1983-12       Impact factor: 3.688

6.  Cruciform formation in a negatively supercoiled DNA may be kinetically forbidden under physiological conditions.

Authors:  A J Courey; J C Wang
Journal:  Cell       Date:  1983-07       Impact factor: 41.582

7.  Uptake of homologous single-stranded fragments by superhelical DNA. IV. Branch migration.

Authors:  C M Radding; K L Beattie; W K Holloman; R C Wiegand
Journal:  J Mol Biol       Date:  1977-11       Impact factor: 5.469

8.  Slow cruciform transitions in palindromic DNA.

Authors:  M Gellert; M H O'Dea; K Mizuuchi
Journal:  Proc Natl Acad Sci U S A       Date:  1983-09       Impact factor: 11.205

9.  Stimulation of protein-directed strand exchange by a DNA helicase.

Authors:  T Kodadek; B M Alberts
Journal:  Nature       Date:  1987 Mar 19-25       Impact factor: 49.962

10.  The role of metal ions in the conformation of the four-way DNA junction.

Authors:  D R Duckett; A I Murchie; D M Lilley
Journal:  EMBO J       Date:  1990-02       Impact factor: 11.598

View more
  85 in total

1.  A method for preparing genomic DNA that restrains branch migration of Holliday junctions.

Authors:  T Allers; M Lichten
Journal:  Nucleic Acids Res       Date:  2000-01-15       Impact factor: 16.971

2.  Branch migration inhibition in PCR-amplified DNA: homogeneous mutation detection.

Authors:  A Lishanski; N Kurn; E F Ullman
Journal:  Nucleic Acids Res       Date:  2000-05-01       Impact factor: 16.971

3.  Recombinogenic flap ligation pathway for intrinsic repair of topoisomerase IB-induced double-strand breaks.

Authors:  C Cheng; S Shuman
Journal:  Mol Cell Biol       Date:  2000-11       Impact factor: 4.272

4.  Brownian-dynamics simulations of metal-ion binding to four-way junctions.

Authors:  Bernd N M van Buuren; Thomas Hermann; Sybren S Wijmenga; Eric Westhof
Journal:  Nucleic Acids Res       Date:  2002-01-15       Impact factor: 16.971

5.  Direct evidence for spontaneous branch migration in antiparallel DNA Holliday junctions.

Authors:  R Sha; F Liu; N C Seeman
Journal:  Biochemistry       Date:  2000-09-19       Impact factor: 3.162

6.  RuvAB-directed branch migration of individual Holliday junctions is impeded by sequence heterology.

Authors:  Cynthia Dennis; Andrei Fedorov; Emmanuel Käs; Laurence Salomé; Mikhail Grigoriev
Journal:  EMBO J       Date:  2004-05-27       Impact factor: 11.598

7.  Single-molecule study of RuvAB-mediated Holliday-junction migration.

Authors:  A Dawid; V Croquette; M Grigoriev; F Heslot
Journal:  Proc Natl Acad Sci U S A       Date:  2004-08-03       Impact factor: 11.205

8.  Direct observation of RuvAB-catalyzed branch migration of single Holliday junctions.

Authors:  Roee Amit; Opher Gileadi; Joel Stavans
Journal:  Proc Natl Acad Sci U S A       Date:  2004-08-03       Impact factor: 11.205

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

Authors:  Dmytro Palets; Alexander Y Lushnikov; Mikhail A Karymov; Yuri L Lyubchenko
Journal:  Biophys J       Date:  2010-09-22       Impact factor: 4.033

10.  RNase-dependent discontinuities associated with the crossovers of spontaneously formed joint DNA molecules in Physarum polycephalum.

Authors:  Chrystelle Maric; Marianne Bénard; Gérard Pierron
Journal:  Chromosoma       Date:  2010-07-07       Impact factor: 4.316

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.