Bioinformatics Advance Access originally published online on August 27, 2004
Bioinformatics 2005 21(3):325-332; doi:10.1093/bioinformatics/bti001
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Bioinformatics vol. 21 issue 3 © Oxford University Press 2005; all rights reserved.
Dual-genome primer design for construction of DNA microarrays
1 Department of Biotechnology, KTHRoyal Institute of Technology SE-106 91 Stockholm, Sweden
2 Department of Molecular Evolution, Evolutionary Biology Center, Uppsala University SE-752 36 Uppsala, Sweden
*To whom correspondence should be addressed.
Motivation: Microarray experiments using probes covering a whole transcriptome are expensive to initiate, and a major part of the costs derives from synthesizing gene-specific PCR primers or hybridization probes. The high costs may force researchers to limit their studies to a single organism, although comparing gene expression in different species would yield valuable information.
Results: We have developed a method, implemented in the software DualPrime, that reduces the number of primers required to amplify the genes of two different genomes. The software identifies regions of high sequence similarity, and from these regions selects PCR primers shared between the genomes, such that either one or, preferentially, both primers in a given PCR can be used for amplification from both genomes. To assure high microarray probe specificity, the software selects primer pairs that generate products of low sequence similarity to other genes within the same genome. We used the software to design PCR primers for 2182 and 1960 genes from the hyperthermophilic archaea Sulfolobus solfataricus and Sulfolobus acidocaldarius, respectively. Primer pairs were shared among 705 pairs of genes, and single primers were shared among 1184 pairs of genes, resulting in a saving of 31% compared to using only unique primers. We also present an alternative primer design method, in which each gene shares primers with two different genes of the other genome, enabling further savings.
3. Availability: The software is freely available at http://www.biotech.kth.se/molbio/microarray/
Contact: anders.andersson{at}biotech.kth.se
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
N. Kim and C. Lee QPRIMER: a quick web-based application for designing conserved PCR primers from multigenome alignments Bioinformatics, September 1, 2007; 23(17): 2331 - 2333. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Lundgren and R. Bernander Genome-wide transcription map of an archaeal cell cycle PNAS, February 20, 2007; 104(8): 2939 - 2944. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. J. J. Brouns, J. Walther, A. P. L. Snijders, H. J. G. van de Werken, H. L. D. M. Willemen, P. Worm, M. G. J. de Vos, A. Andersson, M. Lundgren, H. F. M. Mazon, et al. Identification of the Missing Links in Prokaryotic Pentose Oxidation Pathways: EVIDENCE FOR ENZYME RECRUITMENT J. Biol. Chem., September 15, 2006; 281(37): 27378 - 27388. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Mehlmann, E. D. Dawson, M. B. Townsend, J. A. Smagala, C. L. Moore, C. B. Smith, N. J. Cox, R. D. Kuchta, and K. L. Rowlen Robust Sequence Selection Method Used To Develop the FluChip Diagnostic Microarray for Influenza Virus. J. Clin. Microbiol., August 1, 2006; 44(8): 2857 - 2862. [Abstract] [Full Text] [PDF] |
||||



