Microfluidic-assisted analysis of replicating DNA molecules

Single molecule-based protocols have been gaining popularity as a way to visualize DNA replication at the global genomic- and locus-specific levels. These protocols take advantage of the ability of many organisms to incorporate nucleoside analogs during DNA replication, together with a method to display stretched DNA on glass for immunostaining and microscopy. We describe here a microfluidic platform that can be used to stretch and to capture labeled DNA molecules for replication analyses. This platform consists of parallel arrays of three-sided, 3- or 4-μm high, variable-width capillary channels fabricated from polydimethylsiloxane by conventional soft lithography, and of silane-modified glass coverslips to reversibly seal the open side of the channels. Capillary tension in these microchannels facilitates DNA loading, stretching and glass coverslip deposition from microliter-scale DNA samples. The simplicity and extensibility of this platform should facilitate DNA replication analyses using small samples from a variety of biological and clinical sources.

[1]  T. Kunkel,et al.  The fidelity of DNA synthesis by eukaryotic replicative and translesion synthesis polymerases , 2008, Cell Research.

[2]  D. Shore,et al.  How telomerase reaches its end: mechanism of telomerase regulation by the telomeric complex. , 2008, Molecular cell.

[3]  G. Whitesides,et al.  Fabrication of microfluidic systems in poly(dimethylsiloxane) , 2000, Electrophoresis.

[4]  Ana Pombo,et al.  Replicon Clusters Are Stable Units of Chromosome Structure: Evidence That Nuclear Organization Contributes to the Efficient Activation and Propagation of S Phase in Human Cells , 1998, The Journal of cell biology.

[5]  E. Gilson,et al.  How telomeres are replicated , 2007, Nature Reviews Molecular Cell Biology.

[6]  J. Cairns The Chromosome of Escherichia coli , 1963 .

[7]  A. Riggs,et al.  Autoradiography of chromosomal DNA fibers from Chinese hamster cells. , 1966, Proceedings of the National Academy of Sciences of the United States of America.

[8]  Juan J de Pablo,et al.  A microfluidic system for large DNA molecule arrays. , 2004, Analytical chemistry.

[9]  David C. Schwartz,et al.  Chapter 9 A Single Molecule System for Whole Genome Analysis , 2007 .

[10]  T. Helleday,et al.  Methyl methanesulfonate (MMS) produces heat-labile DNA damage but no detectable in vivo DNA double-strand breaks , 2005, Nucleic acids research.

[11]  G J Brakenhoff,et al.  Dynamics of three-dimensional replication patterns during the S-phase, analysed by double labelling of DNA and confocal microscopy. , 1992, Journal of cell science.

[12]  Melvin L. DePamphilis,et al.  DNA replication and human disease , 2006 .

[13]  C. Schildkraut,et al.  Visualization of DNA Replication on Individual Epstein-Barr Virus Episomes , 2001, Science.

[14]  L. Loeb,et al.  DNA polymerases and human disease , 2008, Nature Reviews Genetics.

[15]  B. Birren,et al.  Pulsed-field gel electrophoresis. , 1996, Methods in enzymology.

[16]  B. Alberts DNA replication and recombination , 2003, Nature.

[17]  Gene E Ananiev,et al.  Optical mapping discerns genome wide DNA methylation profiles , 2008, BMC Molecular Biology.

[18]  B. Trask,et al.  A new method for straightening DNA molecules for optical restriction mapping. , 1997, Nucleic acids research.

[19]  A. Berdis DNA polymerases as therapeutic targets. , 2008, Biochemistry.

[20]  R. Woodgate,et al.  What a difference a decade makes: Insights into translesion DNA synthesis , 2007, Proceedings of the National Academy of Sciences.

[21]  G. Whitesides The origins and the future of microfluidics , 2006, Nature.

[22]  Joshua M. Korn,et al.  Mapping and sequencing of structural variation from eight human genomes , 2008, Nature.

[23]  Miron Livny,et al.  Validation of rice genome sequence by optical mapping , 2007, BMC Genomics.

[24]  D. Beebe,et al.  Physics and applications of microfluidics in biology. , 2002, Annual review of biomedical engineering.

[25]  A Bensimon,et al.  Single molecule analysis of DNA replication. , 1999, Biochimie.

[26]  B. Stillman,et al.  Duplication of DNA in eukaryotic cells , 2006 .

[27]  D. Beebe,et al.  Controlled microfluidic interfaces , 2005, Nature.

[28]  A. Folch,et al.  The RecQ helicase WRN is required for normal replication fork progression after DNA damage or replication fork arrest , 2008, Cell cycle.

[29]  A Bensimon,et al.  Alignment and sensitive detection of DNA by a moving interface. , 1994, Science.

[30]  H. Berg Cold Spring Harbor Symposia on Quantitative Biology.: Vol. LII. Evolution of Catalytic Functions. Cold Spring Harbor Laboratory, Cold Spring Harbor, NY, 1987, ISBN 0-87969-054-2, xix + 955 pp., US $150.00. , 1989 .

[31]  David C. Schwartz,et al.  An algorithm for assembly of ordered restriction maps from single DNA molecules , 2006, Proceedings of the National Academy of Sciences.