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JXB Advance Access originally published online on August 9, 2006
Journal of Experimental Botany 2006 57(12):3109-3122; doi:10.1093/jxb/erl080
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© The Author [2006]. Published by Oxford University Press [on behalf of the Society for Experimental Biology]. All rights reserved. For Permissions, please e-mail: journals.permissions@oxfordjournals.org

RESEARCH PAPER

Transcriptional profiling of sunflower plants growing under low temperatures reveals an extensive down-regulation of gene expression associated with chilling sensitivity

Tarek Hewezi1,2, Mathieu Léger1, Walid El Kayal3 and Laurent Gentzbittel1,*

1Laboratoire de Biotechnologies et Amélioration des Plantes, Ecole Nationale Supérieure Agronomique de Toulouse, Avenue de l'Agrobiopôle, BP 107, Auzeville Tolosane, F-31326 Castanet Tolosan, France
2National Research Center, Genetics and Cytology Department, Dokki, Cairo, Egypt
3Université Paul Sabatier: UMR 5546, ‘Surfaces Cellulaires et Signalisation chez les Végétaux’ Pôle de Biotechnologie Végétale, 24 Chemin de Borde Rouge, BP 42617 Auzeville, F-31326 Castanet-Tolosan, France

*To whom correspondence should be addressed. E-mail: gentz{at}ensat.fr

Being able to sow early to maximize the growing season and to escape drought stress has increased the importance of low-temperature tolerance in sunflower. Yet knowledge about the molecular basis of sunflower response to low temperature is still lacking. To address this issue, nylon microarrays containing >8000 putative unigenes were developed and used. Early- and late-flowering genotypes were sown at 15 °C and grown until the two-leaf stage when they were subjected to 7 °C until the four-leaf stage. The transcriptional profiles of low temperature-grown plants (15 °C and 7 °C) were compared with those grown under standard conditions (25 °C). Two-step ANOVA normalization and analysis models were used to identify the differentially expressed genes. A total of 108 cDNA clones having a P-value <10–3 were found to be differentially expressed between the low temperature-grown plants (15 °C and 7 °C) and their corresponding two-leaf- and four-leaf-stage controls across the two genotypes. About 90% of these genes were down-regulated. This includes genes potentially involved in the metabolism of carbohydrate and energy, protein synthesis, signal transduction, and transport function. Comparing gene expression profiles at 15 °C and 7 °C revealed that only four genes can be considered as differentially expressed, in both genotypes, suggesting that similar genetic programmes underlie the response of sunflower plants to these temperature regimes. The analysis also revealed that early- and late-flowering genotypes respond similarly to low-temperature tolerance as justified by the low number of genes showing a significant genotypextreatment interaction effect. It seems likely that the down-regulation and/or non-induction of genes having a critical role in low-temperature tolerance may be responsible for the sensitivity of sunflower plants to low-temperature tolerance. The results reported provide an initial characterization of the transcriptome activity of sunflower, as a chilling-sensitive plant under suboptimal temperatures, and could be of importance to reveal the potential differences between chilling-sensitive and chilling-tolerant species.

Key words: cDNA microarrays, chilling, global gene expression, Helianthus annuus L., low temperature


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