Molecular stretching of long DNA in agarose gel using alternating current electric fields.

We demonstrate a novel method for stretching a long DNA molecule in agarose gel with alternating current (AC) electric fields. The molecular motion of a long DNA (T4 DNA; 165.6 kb) in agarose gel was studied using fluorescence microscopy. The effects of a wide range of field frequencies, field strengths, and gel concentrations were investigated. Stretching was only observed in the AC field when a frequency of approximately 10 Hz was used. The maximal length of the stretched DNA had the longest value when a field strength of 200 to 400 V/cm was used. Stretching was not sensitive to a range of agarose gel concentrations from 0.5 to 3%. Together, these experiments indicate that the optimal conditions for stretching long DNA in an AC electric field are a frequency of 10 Hz with a field strength of 200 V/cm and a gel concentration of 1% agarose. Using these conditions, we were able to successfully stretch Saccharomyces cerevisiae chromosomal DNA molecules (225-2,200 kb). These results may aid in the development of a novel method to stretch much longer DNA, such as human chromosomal DNA, and may contribute to the analysis of a single chromosomal DNA from a single cell.

[1]  M. Quesada,et al.  Polyacrylamide solutions for DNA sequencing by capillary electrophoresis: Mesh sizes, separation and dispersion , 1996, Electrophoresis.

[2]  K. Yoshikawa,et al.  Molecular Motion of Long Deoxyribonucleic Acid Chains in a Concentrated Polymer Solution Depending on the Frequency of Alternating Electric Field , 1999 .

[3]  J. Wiegant,et al.  High-resolution in situ hybridization using DNA halo preparations. , 1992, Human molecular genetics.

[4]  D. Schwartz,et al.  Ordered restriction maps of Saccharomyces cerevisiae chromosomes constructed by optical mapping. , 1993, Science.

[5]  P. Sanseau,et al.  Two simple procedures for releasing chromatin from routinely fixed cells for fluorescence in situ hybridization. , 1994, Cytogenetics and cell genetics.

[6]  M. Maaloum,et al.  Agarose gel structure using atomic force microscopy: Gel concentration and ionic strength effects , 1998, Electrophoresis.

[7]  S Povey,et al.  Dynamic molecular combing: stretching the whole human genome for high-resolution studies. , 1997, Science.

[8]  F. Sor,et al.  Irreversible trapping of DNA during crossed‐field gel electrophoresis , 1992, Electrophoresis.

[9]  N. Dovichi,et al.  Correlating cell cycle with metabolism in single cells: combination of image and metabolic cytometry. , 1999, Cytometry.

[10]  Stretching of Long DNA under Alternating Current Electric Fields in a Concentrated Polymer Solution , 1997 .

[11]  N. Dovichi,et al.  Single‐cell analysis using capillary electrophoresis: Influence of surface support properties on cell injection into the capillary , 2000, Electrophoresis.

[12]  S. Nie,et al.  Probing single molecules in single living cells. , 2000, Analytical chemistry.

[13]  M. Ueda,et al.  Dynamics of long DNA confined by linear polymers. , 1999, Journal of biochemical and biophysical methods.

[14]  S. Edwards,et al.  The Theory of Polymer Dynamics , 1986 .

[15]  B. Zimm Lakes-straits model of field-inversion gel electrophoresis of DNA , 1991 .

[16]  H Oana,et al.  Visualization of a specific sequence on a single large DNA molecule using fluorescence microscopy based on a new DNA-stretching method. , 1999, Biochemical and biophysical research communications.