High-throughput screening for plant defense activators using a β-glucuronidase-reporter gene assay in Arabidopsis thaliana
スポンサーリンク
概要
- 論文の詳細を見る
To develop a screening system for plant defense activators, which are novel substances that protect plants by enhancing their inherent disease-resistance mechanisms, we utilized a GUS histochemical staining assay using promoters of the defense-related genes, PR-1 and PDF1.2. We can perform about 1,000 screenings per week per person by this high-throughput screening method. This GUS assay for plant defense activator candidates was evaluated by QRT-PCR analysis to elucidate the functions of the plant defense activators in detail. In the present preliminary screening, we evaluated two hundred chemicals chosen at random. Some chemicals induced GUS activity in a PR-1 promoter::GUS transformant, i.e., abietic acid, allose, glycine, and thymol. The induction of PR-1 expression by the treatments with these chemicals was confirmed using QRT-PCR. The foliar treatment with abietic acid 1 d prior to inoculation with the fungal pathogen Colletotrichum higginsianum led to a significant reduction of necrotic surface area compared with distilled water treated controls, as observed 6 d after inoculation. These results suggest that this GUS histochemical staining assay is an effective and available screening system for plant defense activators.
- 日本植物細胞分子生物学会の論文
- 2009-06-01
著者
-
Narusaka M
Kobe Univ. Graduate School Of Sci. And Technol. Kobe Jpn
-
SHIRAISHI Tomonori
Laboratory of Plant Pathology and Genetic Engineering, College of Agriculture, Okayama University
-
KOBAYASHI Masatomo
Experimental Plant Division, RIKEN Bio Resource Center
-
Iwabuchi Masaki
Research Institute For Biological Sciences (ribs)
-
NARUSAKA Yoshihiro
Research Institute for Biological Sciences (RIBS) Okayama
-
NARUSAKA Mari
Research Institute for Biological Sciences (RIBS) Okayama
-
ABE Hiroshi
Experimental Plant Division, RIKEN Bio Resource Center
-
HOSAKA Nami
Research Institute for Biological Sciences (RIBS) Okayama
-
Shiraishi Tomonori
Laboratory Of Plant Pathology And Genetic Engineering Faculty Of Agriculture Okayama University
-
Kobayashi Masatomo
Experimental Plant Division Riken Bio Resource Center
-
Kobayashi Masatomo
Experimental Plant Division Bioresource Center Riken Tsukuba Institute
-
Iwabuchi Masaki
Research Institute For Biological Sciences (ribs) Okayama
-
Kobayashi Mari
Institute Of Molecular And Cellular Biosciences The University Of Tokyo
-
Narusaka Y
Research Institute For Biological Sciences (ribs) Okayama
-
Kawashima Makiko
Riken Bioresource Center
-
Abe Hiroshi
Experimental Plant Division Riken Bio Resource Center
-
Narusaka Mari
Research Institute For Biological Sciences
-
SHIRAISHI Tomonori
Laboratory of Plant Pathology & Genetic Engineering, Faculty of Agriculture, Okayama University
-
Narusaka Yoshihiro
Research Institute for Biological Sciences
-
Iwabuchi Masaki
Research Institute for Biological Sciences (RIBS Okayama)
関連論文
- The floral inoculating protocol: a simplified Arabidopsis thaliana transformation method modified from floral dipping
- The floral inoculating protocol : a simplified Arabidopsis thaliana transformation method modified from floral dipping
- A pea NTPase, PsAPY1, recognizes signal molecules from microorganisms
- Identification of genes expressed during spore germination of Mycosphaerella pinodes
- Agrobacterium tumefaciens-mediated transformation as a tool for random mutagenesis of Colletotrichum trifolii
- Gramine Increase Associated with Rapid and Transient Systemic Resistance in Barley Seedlings Induced by Mechanical and Biological Stresses
- Functional Analysis of the Promoters of Phenylalanine Ammonia-Lyase Gene in Pea : ENVIRONMENTAL AND STRESS RESPONSES : GENES STRUCTURE AND EXPRESSION
- Phenylalanine Ammonia-Lyase Genes from Pisum sativum : Structure, Organ-Specific Expression and Regulation by Fungal Elicitor and Suppressor : GENE STRUCTURE AND EXPRESSION
- Expression Profiles of Arabidopsis Phospholipase A IIA Gene in Response to Biotic and Abiotic Stresses
- Profiling gene expression patterns under drought, cold and salt stress using Arabidopsis full-length cDNA microarray