Abstract

BackgroundGene expression profiles of non-model mammals may provide valuable data for biomedical and evolutionary studies. However, due to lack of sequence information of other species, DNA microarrays are currently restricted to humans and a few model species. This limitation may be overcome by using arrays developed for a given species to analyse gene expression in a related one, an approach known as "cross-species analysis". In spite of its potential usefulness, the accuracy and reproducibility of the gene expression measures obtained in this way are still open to doubt. The present study examines whether or not hybridization values from cross-species analyses are as reproducible as those from same-species analyses when using Affymetrix oligonucleotide microarrays.ResultsThe reproducibility of the probe data obtained hybridizing deer, Old-World primates, and human RNA samples to Affymetrix human GeneChip® U133 Plus 2.0 was compared. The results show that cross-species hybridization affected neither the distribution of the hybridization reproducibility among different categories, nor the reproducibility values of the individual probes. Our analyses also show that a 0.5% of the probes analysed in the U133 plus 2.0 GeneChip are significantly associated to un-reproducible hybridizations. Such probes-called in the text un-reproducible probe sequences- do not increase in number in cross-species analyses.ConclusionOur study demonstrates that cross-species analyses do not significantly affect hybridization reproducibility of GeneChips, at least within the range of the mammal species analysed here. The differences in reproducibility between same-species and cross-species analyses observed in previous studies were probably caused by the analytical methods used to calculate the gene expression measures. Together with previous observations on the accuracy of GeneChips for cross-species analysis, our analyses demonstrate that cross-species hybridizations may provide useful gene expression data. However, the reproducibility and accuracy of these measures largely depends on the use of appropriated algorithms to derive the gene expression data from the probe data. Also, the identification of probes associated to un-reproducible hybridizations-useless for gene expression analyses- in the studied GeneChip, stress the need of a re-evaluation of the probes' performance.

Highlights

  • Gene expression profiles of non-model mammals may provide valuable data for biomedical and evolutionary studies

  • Twenty six of the repeated sequences (13 perfect match (PM) and 13 MM), corresponding to 52 probes (26 PM and 26 MM), hybridize to non-human RNA transcripts included in the array as spikes to test the array performance

  • We showed here that over 95% of the 7736 PM sequences repeated in different probe sets of the human U133 plus 2.0 GeneChip, yielded reproducible hybridizations in all the mammalian species analysed

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Summary

Introduction

Gene expression profiles of non-model mammals may provide valuable data for biomedical and evolutionary studies. Due to lack of sequence information of other species, DNA microarrays are currently restricted to humans and a few model species This limitation may be overcome by using arrays developed for a given species to analyse gene expression in a related one, an approach known as "cross-species analysis". DNA microarrays are currently restricted to humans and a few model species, due to lack of sequence information for other species This limitation could be overcome by using arrays developed for a given species to analyse gene expression in a related one [4,8,9,10,11,12]. These studies assume that the short time of divergence between mammals (less that 100 million years) and the preservation of their protein function assures enough nucleotide-sequence conservation among species [9]

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