» Articles » PMID: 8130350

The Solution Structure of the Four-way DNA Junction at Low-salt Conditions: a Fluorescence Resonance Energy Transfer Analysis

Overview
Journal Biophys J
Publisher Cell Press
Specialty Biophysics
Date 1994 Jan 1
PMID 8130350
Citations 47
Authors
Affiliations
Soon will be listed here.
Abstract

The four-way DNA (Holliday) junction is an important postulated intermediate in the process of genetic recombination. Earlier studies have suggested that the junction exists in two alternative conformations, depending upon the salt concentration present. At high salt concentrations the junction folds into a stacked X structure, while at low salt concentrations the data indicate an extended unstacked conformation. The stereochemical conformation of the four-way DNA junction at low salt (low alkali ion concentration and no alkaline earth ions) was established by comparing the efficiency of fluorescence resonance energy transfer (FRET) between donor and acceptor molecules attached pairwise in three permutations to the 5' termini of the duplex arms. A new variation of FRET was implemented based upon a systematic variation of the fraction of donor labeled single strands. The FRET results indicate that the structure of the four-way DNA junction at low salt exists as an unstacked, extended, square arrangement of the four duplex arms. The donor titration measurements made in the presence of magnesium ions clearly show the folding of the junction into the X stacked structure. In addition, the FRET efficiency can be measured. The fluorescence anisotropy of the acceptor in the presence of Mg2+ during donor titrations was also measured; the FRET efficiency can be calculated from the anisotropy data and the results are consistent with the folded, stacked X structure.

Citing Articles

Site-specific investigation of DNA Holliday Junction dynamics and structure with 6-Methylisoxanthopterin, a fluorescent guanine analog.

Lombardo Z, Mukerji I Trends Photochem Photobiol. 2024; 22:85-102.

PMID: 39371247 PMC: 11450702.


Minimizing Structural Heterogeneity in DNA Self-Assembled Dye Templating via DNA Origami-Tuned Conformations.

Cervantes-Salguero K, Kadrmas M, Ward B, Lysne D, Wolf A, Piantanida L Langmuir. 2024; 40(19):10195-10207.

PMID: 38690801 PMC: 11100016. DOI: 10.1021/acs.langmuir.4c00470.


Site-Specific Investigation of DNA Holliday Junction Dynamics and Structure with 6-Methylisoxanthopterin, a Fluorescent Guanine Analog.

Lombardo Z, Mukerji I bioRxiv. 2024; .

PMID: 38659790 PMC: 11042373. DOI: 10.1101/2024.04.19.590264.


An optofluidic antenna for enhancing the sensitivity of single-emitter measurements.

Morales-Inostroza L, Folz J, Kuhnemuth R, Felekyan S, Wieser F, Seidel C Nat Commun. 2024; 15(1):2545.

PMID: 38514627 PMC: 10957926. DOI: 10.1038/s41467-024-46730-w.


Computational investigation of the impact of core sequence on immobile DNA four-way junction structure and dynamics.

Adendorff M, Tang G, Millar D, Bathe M, Bricker W Nucleic Acids Res. 2021; 50(2):717-730.

PMID: 34935970 PMC: 8789063. DOI: 10.1093/nar/gkab1246.


References
1.
Clegg R, Murchie A, Zechel A, Carlberg C, Diekmann S, Lilley D . Fluorescence resonance energy transfer analysis of the structure of the four-way DNA junction. Biochemistry. 1992; 31(20):4846-56. DOI: 10.1021/bi00135a016. View

2.
Duckett D, Lilley D . Effects of base mismatches on the structure of the four-way DNA junction. J Mol Biol. 1991; 221(1):147-61. DOI: 10.1016/0022-2836(91)80211-c. View

3.
Kubitscheck U, KIRCHEIS M, Schweitzer-Stenner R, Dreybrodt W, Jovin T, Pecht I . Fluorescence resonance energy transfer on single living cells. Application to binding of monovalent haptens to cell-bound immunoglobulin E. Biophys J. 1991; 60(2):307-18. PMC: 1260066. DOI: 10.1016/S0006-3495(91)82055-0. View

4.
Haas E, Steinberg I . Intramolecular dynamics of chain molecules monitored by fluctuations in efficiency of excitation energy transfer. A theoretical study. Biophys J. 1984; 46(4):429-37. PMC: 1435022. DOI: 10.1016/S0006-3495(84)84040-0. View

5.
Kitts P, NASH H . Homology-dependent interactions in phage lambda site-specific recombination. Nature. 1987; 329(6137):346-8. DOI: 10.1038/329346a0. View