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Reproduction, Fertility and Development
  An international journal at the forefront of reproduction and developmental science
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Potential and limitations of bovine-specific arrays for the analysis of mRNA levels in early development: preliminary analysis using a bovine embryonic array

Marc-André Sirard A D, Isabelle Dufort A, Maud Vallée A, Lyne Massicotte A, Catherine Gravel A, Hélène Reghenas A, Andrew J. Watson B, W. Allan King C and Claude Robert A

A Centre de Recherche en Biologie de la Reproduction, Département des Sciences Animales, Université Laval, Sainte-Foy, QC G1K 7P4, Canada.
B Departments of Obstetrics and Gynaecology and Physiology and Pharmacology, University of Western Ontario, London, ON N6A 5C1, Canada.
C Department of Biomedical Sciences, University of Guelph, Guelph, ON N1G 2W1, Canada.
D Corresponding author. Email: marc-andre.sirard@crbr.ulaval.ca


Abstract

New insights into the early development of large mammals are becoming available through the measurement of differential mRNA levels in oocytes and preimplantation embryos. These advances in knowledge are rapidly picking up in pace, mainly owing to the advantages brought by new molecular biology approaches being developed. The possibility of amplifying the starting material and therefore making measurements in single embryo units is now feasible. With these tools, the evaluation of variations in gene expression patterns during the preimplantation period or the impact of culture on mRNA levels is now possible. However, it is important to keep in mind that these methods still have limitations associated with sample preparation or the use of the appropriate controls. Even proper methods of analysis are very important to achieve the full benefit of the application of these tools. The present paper describes some of the potential, as well as limitations, of mRNA level analysis in early embryos, especially for microarray analysis. We have generated a bovine cDNA array (>2000 clones) that contains expressed sequence tags (ESTs) collected from various preimplantation development stages. Using this chip, we have initiated the characterisation of global mRNA level patterns of several key developmental stages from the immature oocyte to the blastocyst stage. As expected, the hybridisation results indicate very different expression profiles involving hundreds of genes when comparing oocyte and blastocyst samples to a reference mRNA sample made from a pool of ESTs from pooled somatic tissues. Although this array is still in its preliminary stage and the EST bank has not been processed to contain only unigenes, it is already a very useful tool for discovering candidate genes that may play important roles during early embryonic life.

Reproduction, Fertility and Development 17(2) 47–57    doi:10.1071/RD04113
Submitted: 1 August 2004    Accepted: 1 October 2004    Published: 1 January 2005





   
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