38th Annual Meeting of the Society for Invertebrate Pathology

August 7-11, 2005  Anchorage, Alaska, U.S.A
   

Microarray technology, genomics and proteomics in entomopathogen research

Peter J Krell1, David A Theilmann2,4, Luke Masson3, Manuella van Munster3 Dan-Hui Yang1, Ilse Huijskens2,4 and Martin A Erlandson5

1Dept. of Molecular and Cellular Biology, University of Guelph, Guelph, ON, Canada, 2Agriculture and Agri-Food Canada, Pacific Agri-Food Centre, Summerland, BC, Canada, 3 Biotechnology Research Institute, NRC, Montreal, QC, Canada, 4Faculty of Agricultural Sciences, University of British Columbia, Vancouver, BC, Canada, and 5Agriculture and Agri-Food Canada, Saskatoon Research Centre, Saskatoon, SK, Canada

The exhaustive data base provided by genomics of entomopathogens allows us to address the expression, interactions, and functions of the many ORFs uncovered. However, this multitude of genes exceeds the capacity for traditional molecular tools such as Northern blotting and protein expression. DNA microarrays provide a high throughput alternative for evaluating simultaneously the transcriptional profiles of all genes within a genome. For example, one DNA microarray hybridization is equivalent to up to 3,000 or more identical Northern blots, each probed with a different DNA fragment and allowing for comparison of global gene expression under different conditions (e.g. infected vs. uninfected cells). DNA microarrays have been applied to studies on single nucleotide changes (SNPs), loss or acquisition/amplification of DNA, diagnostics, identifying members of consortia and even DNA replication. This workshop introduces the methodology behind DNA microarray printing, sample preparation, hybridization and data analysis. Using insect viruses as examples, we will explore the application of this technology to viral gene expression and their use in research on other entomopathogens. Proteomics, following on the heels of this technology, allows researchers to track the synthesis of specific proteins under different conditions and to identify protein-protein partners in a complex milieu of many proteins.

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