Abstract
The gene expression profile of bovine bone marrow stromal cells undergoing adipogenesis was established using a custom cDNA microarray. Cells that were treated with adipogenic stimulants and those that were not were collected at each of the six time points, and gene expression differences between the treated and untreated samples within each time point were compared using a microarray. Statistical analyses revealed that 158 genes showed a minimum fold change of 2 in at least one of the five post-differentiation time points. These genes are involved in various cellular pathways and functions, including lipogenesis, glycolysis, cytoskeleton remodelling, extracellular matrix, transcription as well as various signalling pathways such as insulin, calcium and wingless signalling. The experiment also identified 17 differentially expressed (DE) microarray elements with no assigned function. Quantitative real-time PCR was employed to validate eight DE genes, and the PCR data were found to reproduce the microarray data for these eight genes. Subsequent gene ontology annotation was able to provide a global overview of the molecular function of DE genes during adipogenesis. This analysis was able to indicate the importance of different gene categories at various stages of adipogenic conversion, thereby providing further insights into the molecular changes during bovine adipogenesis.
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Acknowledgements
This research was supported by the Cooperative Research Center for Cattle and Beef Quality and its core partners: The University of New England, NSW Agriculture, CSIRO and Queensland Department of Primary Industries, as well as by Meat and Livestock Australia (BSC.010). The authors are grateful to Drs. Ross Tellam and James Kijas for their critical comments and to Dr. Nicholas Hudson for his help with the use of SigmaPlot.
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Tan, S.H., Reverter, A., Wang, Y. et al. Gene expression profiling of bovine in vitro adipogenesis using a cDNA microarray. Funct Integr Genomics 6, 235–249 (2006). https://doi.org/10.1007/s10142-005-0016-x
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DOI: https://doi.org/10.1007/s10142-005-0016-x