NASCArrays Information at The BAR
NASCArrays Information at The BAR
Welcome to NASCArrays information at the BAR. This page hosts meta-information from the NASCArrays service (2002-2013). This information was parsed
from text files available on the NASCArrays site. NASCArrays data is on iPlant server. To download experiment data from iPlant, please click on the
experiment number. To download the CEL files, please click on the ftp link.
| Experiment: | 28 |
| Title: | The role of the OX1 protein kinase in H2O2 signal transduction |
| Date: | 2002-10-16 |
| Description: | Expression of the OX1 gene coding for a putative protein kinase was shown to be induced in Col-0 WS and RLD seedlings by treatment with H2O2 superoxidecolddroughtsalt and cellulase (elicitor). All of these treatments will ultimately lead to production of H2O2 either as a secondary effect of the applied stress through disturbance of electron transport processes or as a direct product of the plant NADPH oxidases (oxidative burst). However the sets of protective genes switched on (end-responses) will differ depending on the original stress. The induction characteristics of OX1 point to a role of this kinase in signal transduction downstream of H2O2; however it is not clear which primary signal is relayed. OX1 may function in the perception of oxidative stress caused by all/any one of the environmental stresses and/or it may be important in signalling downstream of the oxidative burst triggered by pathogen infection and wounding. An OX1 knock-out was isolated from the Wisconsin T-DNA lines with an insertion between the first and second conserved kinase domains rendering the protein product non-functional. Aim of the microarray experiment is to compare gene induction in the homozygous knock-out line to that in the wild-type (ecotype WS) following H2O2 treatment. To this end 7 day-old seedlings will be immersed in 10 mM solution for 1 h. Analysis of differences in expression of genes belonging to a certain end-response will disclose the signalling pathway which OX1 functions in. This is necessary for further planned experiments e.g. analysis of inducible OX1 antisense and constitutive lines as well as kinase activity assays. |
| ftp Link: | ftp Link |
| Slide ID | Slide Name | Genetic Background | Tissue | Stock Code | Cel File |
|---|---|---|---|---|---|
| Rente_1-1_WS2-HO_Rep1_ATH1 | 256 | Whole seedlings | N1601 | Rente_1-1_WS2-HO_Rep1_ATH1.cel | |
| Treatment: At 7 days, seedlings immersed in H2O2 for 1 hour | |||||
| Rente_1-2_KKO-HO_Rep1_ATH1 | 202 | ws-2 N1601 | Whole seedlings | Rente_1-2_KKO-HO_Rep1_ATH1.cel | |
| Treatment: At 7 days, seedlings immersed in H2O2 for 1 hour | |||||
| Rente_1-3_WS2-Control_Rep1_ATH1 | 204 | Whole seedlings | N1601 | Rente_1-3_WS2-Control_Rep1_ATH1.cel | |
| Rente_1-4_KKO-Control_Rep1_ATH1 | 257 | ws-2 N1601 | Whole seedlings | Rente_1-4_KKO-Control_Rep1_ATH1.cel | |