Gene Expression Analyses of Arabidopsis Chromosome 2 Using a Genomic DNA Amplicon Microarray

  1. Heenam Kim1,
  2. Erik C. Snesrud1,
  3. Brian Haas,
  4. Foo Cheung,
  5. Christopher D. Town, and
  6. John Quackenbush2
  1. The Institute for Genomic Research, Rockville, MD 20850, USA.

Abstract

The gene predictions and accompanying functional assignments resulting from the sequencing and annotation of a genome represent hypotheses that can be tested and used to develop a more complete understanding of the organism and its biology. In the model plantArabidopsis thaliana, we developed a novel approach to constructing whole-genome microarrays based on PCR amplification of the 3′ ends of each predicted gene from genomic DNA, and constructed an array representing more than 94% of the predicted genes and pseudogenes on chromosome 2. With this array, we examined various tissues and physiological conditions, providing expression-based validation for 84% of the gene predictions and providing clues as to the functions of many predicted genes. Further, by examining the distribution of expression along the physical chromosome, we were able to identify a region of repressed transcription that may represent a previously undescribed heterochromatic region.

[The sequence data from this study have been submitted to ArrayExpress under accession nos.: For the Array Design, A-TIGR-2. For the three subgroups of experiments: AbioticStress, E-TIGR-2; BioticStress, E-TIGR-3; Tissues, E-TIGR-4.]

Footnotes

  • 1 These authors contributed equally to this work.

  • 2 Corresponding author.

  • E-MAIL johnq{at}tigr.org; FAX (301) 838-0208.

  • Article and publication are at http://www.genome.org/cgi/doi/10.1101/gr.552003.

    • Received July 3, 2002.
    • Accepted December 20, 2002.
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