Structure, Dynamics, and Branch Migration of a DNA Holliday Junction: A Single-Molecule Fluorescence and Modeling Study

被引:19
作者
Karymov, Mikhail A. [1 ]
Chinnaraj, Mathivanan [2 ]
Bogdanov, Aleksey [1 ,3 ]
Srinivasan, Annankoil R. [4 ]
Zheng, Guohui [4 ]
Olson, Wilma K. [4 ]
Lyubchenko, Yuri L. [1 ]
机构
[1] Univ Nebraska, Med Ctr, Dept Pharmaceut Sci, Omaha, NE 68198 USA
[2] Univ Alabama, Birmingham, AL USA
[3] St Petersburg State Univ, Inst Phys Res, Dept Mol Biophys, St Petersburg 198504, Russia
[4] Rutgers State Univ, Dept Chem & Chem Biol, BioMaPS Inst Quantitat Biol, Wright Rieman Labs, Piscataway, NJ USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
D O I
10.1529/biophysj.108.135103
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The Holliday junction (HJ) is a central intermediate of various genetic processes, including homologous and site-specific DNA recombination and DNA replication. Elucidating the structure and dynamics of HJs provides the basis for understanding the molecular mechanisms of these genetic processes. 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. These data led us to the conclusion that one hop can be more than 1 basepair (bp); moreover, we hypothesized that continuous runs over the entire sequence homology (5 bp) can occur. Direct measurements of the dependence of the fluorescence resonance energy transfer (FRET) value on the donor-acceptor (D-A) distance are required to justify this model and are the major goal of this article. To accomplish this goal, we performed single-molecule FRET experiments with a set of six immobile HJ molecules with varying numbers of bps between fluorescent dyes placed on opposite arms. The designs were made in such a way that the distances between the donor and acceptor were equal to the distances between the dyes formed upon 1-bp migration hops of a HJ having 10-bp homology. Using these designs, we confirmed our previous hypothesis that the migration of the junction can be measured with bp accuracy. Moreover, the FRET values determined for each acceptor-donor separation corresponded very well to the values for the steps on the FRET time trajectories, suggesting that each step corresponds to the migration of the branch at a defined depth. We used the dependence of the FRET value on the D-A distance to measure directly the size for each step on the FRET time trajectories. These data showed that one hop is not necessarily 1 bp. The junction is able to migrate over several bps, detected as one hop and confirming our model. The D-A distances extracted from the FRET properties of the immobile junctions formed the basis for modeling the HJ structures. The composite data fit a partially opened, side-by-side model with adjacent double-helical arms slightly kinked at the four-way junction and the junction as a whole adopting a global X-shaped form that mimics the coaxially stacked-X structure implicated in previous solution studies.
引用
收藏
页码:4372 / 4383
页数:12
相关论文
共 59 条
  • [1] Crystal structure of the Holliday junction DNA in complex with a single RuvA tetramer
    Ariyoshi, M
    Nishino, T
    Iwasaki, H
    Shinagawa, H
    Morikawa, K
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (15) : 8257 - 8262
  • [2] Crystal structure of T4 endonuclease VII resolving a Holliday junction
    Biertuempfel, Christian
    Yang, Wei
    Suck, Dietrich
    [J]. NATURE, 2007, 449 (7162) : 616 - U14
  • [3] Branch migration through DNA sequence heterology
    Biswas, I
    Yamamoto, A
    Hsieh, P
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1998, 279 (04) : 795 - 806
  • [4] Discrete and continuous mathematical models of DNA branch migration
    Bruist, MF
    Myers, E
    [J]. JOURNAL OF THEORETICAL BIOLOGY, 2003, 220 (02) : 139 - 156
  • [5] Facilitated target location on DNA by individual Escherichia coli RNA polymerase molecules observed with the scanning force microscope operating in liquid
    Bustamante, C
    Guthold, M
    Zhu, XS
    Yang, GL
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (24) : 16665 - 16668
  • [6] Crystal structure of a Flp recombinase-Holliday junction complex: Assembly of an active oligomer by helix swapping
    Chen, Y
    Narendra, U
    Iype, LE
    Cox, MM
    Rice, PA
    [J]. MOLECULAR CELL, 2000, 6 (04) : 885 - 897
  • [7] CLEGG RM, 1992, METHOD ENZYMOL, V211, P353
  • [8] Recombination at double-strand breaks and DNA ends: Conserved mechanisms from phage to humans
    Cromie, GA
    Connelly, JC
    Leach, DRF
    [J]. MOLECULAR CELL, 2001, 8 (06) : 1163 - 1174
  • [9] Single-molecule protein folding: Diffusion fluorescence resonance energy transfer studies of the denaturation of chymotrypsin inhibitor 2
    Deniz, AA
    Laurence, TA
    Beligere, GS
    Dahan, M
    Martin, AB
    Chemla, DS
    Dawson, PE
    Schultz, PG
    Weiss, S
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (10) : 5179 - 5184
  • [10] Single-pair fluorescence resonance energy transfer on freely diffusing molecules: Observation of Forster distance dependence and subpopulations
    Deniz, AA
    Dahan, M
    Grunwell, JR
    Ha, TJ
    Faulhaber, AE
    Chemla, DS
    Weiss, S
    Schultz, PG
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (07) : 3670 - 3675