Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
Add more filters











Database
Language
Publication year range
1.
Plant Physiol ; 144(2): 1039-51, 2007 Jun.
Article in English | MEDLINE | ID: mdl-17416636

ABSTRACT

In the tetrapyrrole biosynthetic pathway, isoforms of glutamyl-tRNA reductase (HEMA2) and ferrochelatase1 (FC1) are mainly expressed in nonphotosynthetic tissues. Here, using promoter-beta-glucuronidase constructs, we showed that the expressions of Arabidopsis (Arabidopsis thaliana) HEMA2 (AtHEMA2) and FC1 (AtFC1) were induced in photosynthetic tissues by oxidative stresses such as wounding. Transcript levels and beta-glucronidase activity were rapidly induced within 30 min, specifically in the wound area in a jasmonate-independent manner. Transcriptome analysis of wound-specific early inducible genes showed that AtHEMA2 and AtFC1 were coinduced with hemoproteins outside plastids, which are related to defense responses. Ozone fumigation or reagents generating reactive oxygen species induced the expression of both genes in photosynthetic tissues, suggesting that reactive oxygen species is involved in the induction. Since cycloheximide or puromycin induced the expression of both genes, inhibition of cytosolic protein synthesis is involved in the induction of these genes in photosynthetic tissues. The physiological functions of AtHEMA2 and AtFC1 were investigated using insertional knockout mutants of each gene. Heme contents of the roots of both mutants were about half of that of the respective wild types. In wild-type plants, heme contents were increased by ozone exposure. In both mutants, reduction of the ozone-induced increase in heme content was observed. These results suggest the existence of the tetrapyrrole biosynthetic pathway controlled by AtHEMA2 and AtFC1, which normally functions for heme biosynthesis in nonphotosynthetic tissues, but is induced in photosynthetic tissues under oxidative conditions to supply heme for defensive hemoproteins outside plastids.


Subject(s)
Adaptation, Physiological , Aldehyde Oxidoreductases/metabolism , Arabidopsis/enzymology , Ferrochelatase/metabolism , Tetrapyrroles/biosynthesis , Aldehyde Oxidoreductases/genetics , Arabidopsis/genetics , Arabidopsis/physiology , Ferrochelatase/genetics , Gene Expression Regulation, Plant , Heme/metabolism , Hemeproteins/metabolism , Isoenzymes/metabolism , Mutagenesis, Insertional , Oxidative Stress/physiology , Ozone/metabolism , Reactive Oxygen Species/metabolism
2.
Plant Physiol ; 139(3): 1268-83, 2005 Nov.
Article in English | MEDLINE | ID: mdl-16258017

ABSTRACT

Jasmonic acid (JA) and methyl jasmonate (MeJA), collectively known as JAs, regulate diverse physiological processes in plants, including the response to wounding. Recent reports suggest that a cyclopentenone precursor of JA, 12-oxo-phytodienoic acid (OPDA), can also induce gene expression. However, little is known about the physiological significance of OPDA-dependent gene expression. We used microarray analysis of approximately 21,500 Arabidopsis (Arabidopsis thaliana) genes to compare responses to JA, MeJA, and OPDA treatment. Although many genes responded identically to both OPDA and JAs, we identified a set of genes (OPDA-specific response genes [ORGs]) that specifically responded to OPDA but not to JAs. ORGs primarily encoded signaling components, transcription factors, and stress response-related genes. One-half of the ORGs were induced by wounding. Analysis using mutants deficient in the biosynthesis of JAs revealed that OPDA functions as a signaling molecule in the wounding response. Unlike signaling via JAs, OPDA signaling was CORONATINE INSENSITIVE 1 independent. These results indicate that an OPDA signaling pathway functions independently of JA/MeJA signaling and is required for the wounding response in Arabidopsis.


Subject(s)
Arabidopsis/genetics , Arabidopsis/physiology , Fatty Acids, Unsaturated/pharmacology , Gene Expression Regulation, Plant/drug effects , Plant Diseases/genetics , Acrolein/pharmacology , Arabidopsis/drug effects , Blotting, Northern , Cyclopentanes/pharmacology , Gene Expression Profiling , Genes, Plant/genetics , Mutation/genetics , Oligonucleotide Array Sequence Analysis , Oxylipins , Plant Leaves , RNA, Messenger/genetics , RNA, Messenger/metabolism , Reproducibility of Results , Signal Transduction/drug effects , Time Factors
SELECTION OF CITATIONS
SEARCH DETAIL