Skip to main content
. 2014 Mar 26;1:14016. doi: 10.1038/hortres.2014.16

Figure 6.

Figure 6

Expression profiles of VvWRKY genes in response to abiotic stresses. Expression of VvWRKY genes in the V. vinifera cv ‘Cabernet Sauvignon’ (microarray) or 4-week-old in vitro explants of V. vinifera PN40024 genotype (qRT-PCR) in response to cold (cold), drought (WS) and salt stress (SS). Microarray analysis presented in a and b. qRT-PCR data presented in c. Microarray data were downloaded from the NCBI GEO datasets (GSE31594 and GSE31677), processed as log2 of the ratio between treated and untreated samples and graphically represented with MeV software. (a) V. vinifera cv ‘Cabernet Sauvignon’ plants grown in a hydroponic drip system were treated with 120 mM salt (SS), polyethylene glycol (PEG), cold (5 °C) or left untreated. Shoots with leaves were collected at 0, 1, 4 and 8 h for all treatments, and at 24 h for all treatments except cold (GEO series GSE31594). (b) Potted V. vinifera cv ‘Cabernet Sauvignon’ vines in the greenhouse were exposed to a water-deficit stress (WC) by withholding water or a salt stress (SS) by watering plants with a saline solution for 16 days. Non-stressed, normally watered plants served as the control for both treatments. Shoot tips were harvested every 4 days (0, 4, 8, 12 and 16 days) (GEO series GSE31677). (c) qRT-PCR expression analysis of VvWRKYs in V. vinifera PN40024 genotype subjected to a drought treatment. Transcripts were normalized to the actin gene expression. The mean±s.d. of three biological replicates are presented. Asterisks indicate that the corresponding gene was significantly up- or downregulated in a given organ (*p≤0.05, **p≤0.01). MeV, Multi Experiment Viewer.