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Standard Gene Set Name | LALOI_SINGLET-OXYGEN_UP |
Species | Arabidopsis thaliana |
Brief Description | Up-regulated at least 2-fold 30 minutes after the release of singlet oxygen and co-regulated in flu, flu-overexpressing tAPX, wild-type and wild-type- (Table 1 PubmedID:17197417) |
Full Description/Abstract | Upon a dark-to-light shift, the conditional fluorescent (flu) mutant of Arabidopsis releases singlet oxygen (1O2) within the plastid compartment. Distinct sets of nuclear genes are activated that are different from those induced by superoxide (O2 ??) and/or hydrogen peroxide (H2O2), suggesting that different types of reactive oxygen species activate distinct signaling pathways. It is not known whether the pathways operate separately or interact with each other. We have addressed this problem by modulating noninvasively the level of H2O2 in plastids by means of a transgenic line that overexpresses the thylakoid-bound ascorbate peroxidase (tAPX). The overexpression of the H2O2-specific scavenger reduced strongly the activation of nuclear genes in plants treated with the herbicide paraquat that in the light leads to the enhanced generation of O2 ?? and H2O2. In the flu mutant overexpressing tAPX, the intensity of 1O2-mediated cell death and growth inhibition was increased when compared with the flu parental line. Also, the expression of most of the nuclear genes that were rapidly activated after the release of 1O2 was significantly higher in flu plants overexpressing tAPX, whereas in wild-type plants, overexpression of tAPX did not lead to visible stress responses and had only a very minor impact on nuclear gene expression. The results suggest that H2O2 antagonizes the 1O2-mediated signaling of stress responses as seen in the flu mutant. This cross-talk between H2O2- and 1O2-dependent signaling pathways might contribute to the overall stability and robustness of wild-type plants exposed to adverse environmental stress conditions. |
External Pathway ID/Pubmed ID | 17197417 |
Source | Literature |
Contributor/Author | Liming Lai and Xijin Ge |
Organization of contributer | South Dakota State University |
External URL | http://www.pnas.org/content/104/2/672.full.pdf+html |