Please use this identifier to cite or link to this item:
|Title:||An oligo-based microarray offers novel transcriptomic approaches for the analysis of pathogen resistance and fruit quality traits in melon (Cucumis melo L.)|
|Authors:||Mascarell-Creus, Albert, Cañizares, Joaquín, Vilarrasa-Blasi, Josep, Mora-García, Santiago, Blanca, José M., González-Ibeas, Daniel, Saladié, Montserrat, Roig, Cristina, Deleu, Wim, Picó-Silvent, Belén, López-Bigas, Nuria, Aranda, Miguel A., García-Mas, Jordi, Nuez, Fernando, Puigdomènech, Pere, Caño-Delgado, Ana|
|Abstract:||Background: Melon (Cucumis melo) is a horticultural specie of significant nutritional value, which belongs to the
Cucurbitaceae family, whose economic importance is second only to the Solanaceae. Its small genome of approx.
450 Mb coupled to the high genetic diversity has prompted the development of genetic tools in the last decade.
However, the unprecedented existence of a transcriptomic approaches in melon, highlight the importance of
designing new tools for high-throughput analysis of gene expression.|
Results: We report the construction of an oligo-based microarray using a total of 17,510 unigenes derived from 33,418 high-quality melon ESTs. This chip is particularly enriched with genes that are expressed in fruit and during interaction with pathogens. Hybridizations for three independent experiments allowed the characterization of global gene expression profiles during fruit ripening, as well as in response to viral and fungal infections in plant cotyledons and roots, respectively. Microarray construction, statistical analyses and validation together with functional-enrichment analysis are presented in this study.
Conclusion: The platform validation and enrichment analyses shown in our study indicate that this oligo-based microarray is amenable for future genetic and functional genomic studies of a wide range of experimental conditions in melon.
|Description:||15 pages, 4 figures, 3 tables, 1 appendix, 3 additional files.|
|Publisher version (URL):||http://dx.doi.org/10.1186/1471-2164-10-467|
|Citation:||BMC Genomics 10(467): (2009)|
|Appears in Collections:||(CEBAS) Artículos|