Evaluation of a whole-genome amplification method based on adaptor-ligation PCR of randomly sheared genomic DNA
Article first published online: 11 AUG 2003
Copyright © 2003 Wiley-Liss, Inc.
Genes, Chromosomes and Cancer
Volume 38, Issue 2, pages 168–176, October 2003
How to Cite
Tanabe, C., Aoyagi, K., Sakiyama, T., Kohno, T., Yanagitani, N., Akimoto, S., Sakamoto, M., Sakamoto, H., Yokota, J., Ohki, M., Terada, M., Yoshida, T. and Sasaki, H. (2003), Evaluation of a whole-genome amplification method based on adaptor-ligation PCR of randomly sheared genomic DNA. Genes Chromosom. Cancer, 38: 168–176. doi: 10.1002/gcc.10269
- Issue published online: 20 AUG 2003
- Article first published online: 11 AUG 2003
- Manuscript Accepted: 17 JUN 2003
- Manuscript Received: 25 FEB 2003
- Ministry of Health, Labor and Welfare of Japan
- Organization for Pharmaceutical Safety and Research of Japan
High-throughput genetic studies often require large quantities of DNA for a variety of analyses. Developing and assessing a whole-genome amplification method is thus important, especially with the current desire for large-scale genotyping in previously collected samples for which limited DNA is available. The method we have developed, called PRSG, is based on an adaptor-ligation–mediated PCR of randomly sheared genomic DNA. An unbiased representation was evaluated by performing PCR on 2,607 exons of 367 genes, which are randomly distributed throughout the genome, on PRSG products of hundreds of individuals. An infrequent loss (<1%) of the exon sequence on the PRSG products was found. Out of 307 microsatellites on various chromosomes, 258 (84%) were amplified in both the PRSG product and an original DNA, whereas 49 (16%) microsatellites were lost only in the PRSG product. Array CGH analysis of 287 loci for measuring the relative gene copy number demonstrated that a low bias was detected. Moreover, this method was validated on 100–1,000 laser-captured cells from paraffin-embedded tissues. These data show that PRSG can provide a sufficient amount of genomic sequence for a variety of genetic analyses as well as for long-term storage for future work. © 2003 Wiley-Liss, Inc.