Table of Contents * Complex Genetics * Developmental Genetics * Gene Annotation * Gene Discovery * Genome Sequencing * Functional Genomics * Mutagenesis * Presentations * Verne Chapman Memorial Lecture
Dr. Stephen Kingsmore
Molecular Staging Inc.
300 George Street, Suite 701
New Haven
CT 06443
USA
Co-Authors: Dean FB, Hosono S, Fang L, Wu
X, Faruqi AF, Bray-Ward P, Sun Z, Zong Q, Du Y, Du J, Egholm M, & Lasken RS
Institutions: Molecular Staging
Fundamental to most genetic analysis is availability of genomic DNA of adequate quality & quantity. Since DNA yield from mammalian samples is frequently limiting, much effort has been invested in methods for propagating & archiving genomic DNA. Methods include the creation of EBV-transformed cell lines or whole genome amplification (WGA) by degenerate oligonucleotide-primed PCR. However, WGA methods suffer from high cost or insufficient coverage & inadequate average DNA size. We describe a novel method for WGA using an isothermal, strand-displacing amplification process termed multiple displacement amplification (MDA). Like the rolling circle amplification method recently described for circular DNA propagation(Gen Res 11:1095, 2001), MDA uses phi29 DNA polymerase and random primers. Within 4 hours, 30pg (~9 genomic copies) of genomic DNA was amplified to ~0.04mg. The average fragment length was >10kb. The amplified DNA exhibited normal representation for 10 single nucleotide polymorphisms (SNPs). Representation bias among 8 chromosomal loci was <3-fold in contrast to 4-6 orders of magnitude for PCR-based WGA methods. MDA-amplified DNA is useful for several common methods of genetic analysis, including SNP genotyping, chromosome painting, Southern blotting & RFLP analysis, subcloning, DNA sequencing. MDA-based WGA is a simple & reliable method that could have significant implications for genetic studies & long-term sample storage.
Abstracts * Officers * Bylaws * Application Form * Meeting Calendar * Contact Information * Home * Resources * News and Views * Membership
Base
url http://imgs.org
Last
modified: Wednesday, July 28, 2004