Abstract
Cross-species gene-expression comparison is a powerful tool for the discovery of evolutionarily conserved mechanisms and pathways of expression control. The usefulness of cDNA microarrays in this context is that broad areas of homology are compared and hybridization probes are sufficiently large that small inter-species differences in nucleotide sequence would not affect the analytical results. This comparative genomics approach would allow a common set of genes within a specific developmental, metabolic, or disease-related gene pathway to be evaluated in experimental models of human diseases. The objective of this study was to investigate the feasibility and reproducibility of cross-species analysis employing a human cDNA microarray as probe. As a proof of principle, total RNA derived from human and bovine fetal brains was used as a source of labelled targets for hybridisation onto a human cDNA microarray composed of 349 characterised genes. Each gene was spotted 20 times representing 6,980 data points thus enabling highly reproducible spot quantification. Employing high stringency hybridisation and washing conditions, followed by data analysis, revealed slight differences in the expression levels and reproducibility of the signals between the two species. We also assigned each of the genes into three expression level categories- i.e. high, medium and low. The correlation co-efficient of cross hybridisation between the orthologous genes was 0.94. Verification of the array data by semi-quantitative RT-PCR using common primer sequences enabled co-amplification of both human and bovine transcripts. Finally, we were able to assign gene names to previously uncharacterised bovine ESTs. Results of our study demonstrate the harnessing and utilisation power of comparative genomics and prove the feasibility of using human microarrays to facilitate the identification of co-expressed orthologous genes in common tissues derived from different species.
MeSH Terms
Animals
Brain/embryology,metabolism
Brain Chemistry/genetics
Cattle
DNA, Complementary/genetics
Evolution, Molecular
Feasibility Studies
Gene Expression Profiling/methods
Gene Expression Regulation/genetics
Gene Expression Regulation, Developmental/genetics
Genes/physiology
Genetic Variation/genetics
Humans
Microarray Analysis/methods
Nucleic Acid Hybridization/methods
Reproducibility of Results
Reverse Transcriptase Polymerase Chain Reaction/methods
Sequence Alignment/methods
Sequence Homology, Nucleic Acid
Species Specificity
Chemicals
DNA, Complementary
Authors & Affiliations
11 authors, click to expand affiliations / ORCID
Adjaye James
Max Planck Institute for Molecular Genetics, Department of Vertebrate Genomics, Ihnestrasse 73, D-14195, Berlin, Germany.
[email protected]
Herwig Ralf
Herrmann Doris
Wruck Wasco
Benkahla Alia
Brink Thore C
Nowak Monika
Carnwath Joseph W
Hultschig Claus
Niemann Heiner
Lehrach Hans
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