Abstract
Microarray data acquired during time-course experiments allow the temporal variations in gene expression to be monitored. An original postprandial fasting experiment was conducted in the mouse and the expression of 200 genes was monitored with a dedicated macroarray at 11 time points between 0 and 72 hours of fasting. The aim of this study was to provide a relevant clustering of gene expression temporal profiles. This was achieved by focusing on the shapes of the curves rather than on the absolute level of expression. Actually, we combined spline smoothing and first derivative computation with hierarchical and partitioning clustering. A heuristic approach was proposed to tune the spline smoothing parameter using both statistical and biological considerations. Clusters are illustrated a posteriori through principal component analysis and heatmap visualization. Most results were found to be in agreement with the literature on the effects of fasting on the mouse liver and provide promising directions for future biological investigations.
[1,2,3,4,5,6,7,8,9,10,11,12,13,14,15,16,17,18,19,20,21,22,23,24]
Contributor Information
S Déjean, Email: sebastien.dejean@math.ups-tlse.fr.
PGP Martin, Email: pascal.martin@toulouse.inra.fr.
A Baccini, Email: alain.baccini@math.ups-tlse.fr.
P Besse, Email: philippe.besse@math.ups-tlse.fr.
References
- Park T, Yi S-G, Lee S. et al. Statistical tests for identifying differentially expressed genes in time-course microarray experiments. Bioinformatics. 2003;19(6):694–703. doi: 10.1093/bioinformatics/btg068. [DOI] [PubMed] [Google Scholar]
- Peddada SD, Lobenhofer EK, Li L, Afshari CA, Weinberg CR, Umbach DM. Gene selection and clustering for time-course and dose-response microarray experiments using order-restricted inference. Bioinformatics. 2003;19(7):834–841. doi: 10.1093/bioinformatics/btg093. [DOI] [PubMed] [Google Scholar]
- Storey JD, Xiao W, Leek JT, Tompkins RG, Davis RW. Significance analysis of time course microarray experiments. Proceedings of the National Academy of Sciences of the United States of America. 2005;102(36):12837–12842. doi: 10.1073/pnas.0504609102. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tai YC, Speed TP. A multivariate empirical Bayes statistic for replicated microarray time course data. The Annals of Statistics. 2006;34(5):2387–2412. doi: 10.1214/009053606000000759. [DOI] [Google Scholar]
- Ramoni MF, Sebastiani P, Kohane IS. Cluster analysis of gene expression dynamics. Proceedings of the National Academy of Sciences of the United States of America. 2002;99(14):9121–9126. doi: 10.1073/pnas.132656399. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ernst J, Nau GJ, Bar-Joseph Z. Clustering short time series gene expression data. Bioinformatics. 2005;21(1):i159–i168. doi: 10.1093/bioinformatics/bti1022. [DOI] [PubMed] [Google Scholar]
- Giurcǎneanu CD, Tǎbuş I, Astola J. Clustering time series gene expression data based on sum-of-exponentials fitting. EURASIP Journal on Applied Signal Processing. 2005;2005(8):1159–1173. doi: 10.1155/ASP.2005.1159. [DOI] [Google Scholar]
- Heard NA, Holmes CC, Stephens DA, Hand DJ, Dimopoulos G. Bayesian coclustering of Anopheles gene expression time series: study of immune defense response to multiple experimental challenges. Proceedings of the National Academy of Sciences of the United States of America. 2005;102(47):16939–16944. doi: 10.1073/pnas.0408393102. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Conesa A, Nueda MJ, Ferrer A, Talón M. maSigPro: a method to identify significantly differential expression profiles in time-course microarray experiments. Bioinformatics. 2006;22(9):1096–1102. doi: 10.1093/bioinformatics/btl056. [DOI] [PubMed] [Google Scholar]
- Letowski J, Brousseau R, Masson L. Designing better probes: effect of probe size, mismatch position and number on hybridization in DNA oligonucleotide microarrays. Journal of Microbiological Methods. 2004;57(2):269–278. doi: 10.1016/j.mimet.2004.02.002. [DOI] [PubMed] [Google Scholar]
- Ramsay J, Silverman B. Functional Data Analysis. 2. Springer, New York, NY, USA; 2005. [Google Scholar]
- Bar-Joseph Z, Gerber GK, Gifford DK, Jaakkola TS, Simon I. Continuous representations of time-series gene expression data. Journal of Computational Biology. 2003;10(3-4):341–356. doi: 10.1089/10665270360688057. [DOI] [PubMed] [Google Scholar]
- Bar-Joseph Z. Analyzing time series gene expression data. Bioinformatics. 2004;20(16):2493–2503. doi: 10.1093/bioinformatics/bth283. [DOI] [PubMed] [Google Scholar]
-
Martin PGP, Lasserre F, Calleja C. et al. Transcriptional modulations by RXR agonists are only partially subordinated to PPAR
signaling and attest additional, organ-specific, molecular cross-talks. Gene Expression. 2005;12(3):177–192. doi: 10.3727/000000005783992098. [DOI] [PMC free article] [PubMed] [Google Scholar] -
Martin PGP, Guillou H, Lasserre F. et al. Novel aspects of PPAR
-mediated regulation of lipid and xenobiotic metabolism revealed through a nutrigenomic study. Hepatology. 2007;45(3):767–777. doi: 10.1002/hep.21510. [DOI] [PubMed] [Google Scholar] - INRArray. Laboratoire de Pharmacologie et Toxicologie, INRA. 2005. http://www.inra.fr/internet/Centres/toulouse/pharmacologie/lpt.htm http://www.inra.fr/internet/Centres/toulouse/pharmacologie/lpt.htm
- Silverman B. Some aspects of the spline smoothing approach to non-parametric regression curve fitting. Journal of the Royal Statistical Society: Series B. 1985;47(1):1–52. [Google Scholar]
- Besse P Cardot H Ferraty F Simultaneous non-parametric regressions of unbalanced longitudinal data Computational Statistics & Data Analysis 1997243255–270. 10.1016/S0167-9473(96)00067-921757463 [DOI] [Google Scholar]
- Seber GAF. Multivariate Observations. John Wiley & Sons, New York, NY, USA; 1984. [Google Scholar]
- Yeung KY, Ruzzo WL. Principal component analysis for clustering gene expression data. Bioinformatics. 2001;17(9):763–774. doi: 10.1093/bioinformatics/17.9.763. [DOI] [PubMed] [Google Scholar]
- Chipman H, Hastie TJ, Tibshirani T. In: Statistical Analysis of Gene Expression Microarray Data. Speed T, editor. Chapmann & Hall/CRC Press, Boca Raton, Fla, USA; 2003. Clustering microarray data; pp. 159–200. [Google Scholar]
-
Kersten S, Seydoux J, Peters JM, Gonzalez FJ, Desvergne B, Wahli W. Peroxisome proliferator-activated receptor
mediates the adaptive response to fasting. Journal of Clinical Investigation. 1999;103(11):1489–1498. doi: 10.1172/JCI6223. [DOI] [PMC free article] [PubMed] [Google Scholar] -
Mandard S, Müller M, Kersten S. Peroxisome proliferator-activated receptor
target genes. Cellular and Molecular Life Sciences. 2004;61(4):393–416. doi: 10.1007/s00018-003-3216-3. [DOI] [PMC free article] [PubMed] [Google Scholar] - Bauer M, Hamm AC, Bonaus M. et al. Starvation response in mouse liver shows strong correlation with life-span-prolonging processes. Physiological Genomics. 2004;17(2):230–244. doi: 10.1152/physiolgenomics.00203.2003. [DOI] [PubMed] [Google Scholar]
