Isolation of the Gene for EILP, an Elicitor-Inducible LRR Receptor-Like Protein, from Tobacco by Differential Display
Identifieur interne : 001D31 ( Istex/Curation ); précédent : 001D30; suivant : 001D32Isolation of the Gene for EILP, an Elicitor-Inducible LRR Receptor-Like Protein, from Tobacco by Differential Display
Auteurs : Daigo Takemoto [Japon] ; Makoto Hayashi [Japon] ; Noriyuki Doke [Japon] ; Mikio Nishimura [Japon] ; Kazuhito Kawakita [Japon]Source :
- Plant and Cell Physiology [ 0032-0781 ] ; 2000.
Abstract
We screened tobacco genes, which are differentially expressed in response to a fungal elicitor, and have isolated a gene which codes for a leucine-rich repeat (LRR) protein closely related to Cf genes in tomato. The EILP (elicitor inducible LRR protein) gene encodes 95 kDa protein, which consists of a putative membrane spanning region, 28 leucine-rich repeats and some N-linked glycosylation sites, and shows high homology to Cf-2/Cf-5 family genes. Southern blot analysis revealed the presence of some genes homologous to EILP in tobacco, like Cf genes in tomato. The expression of EILP was low at the basal level and increased by treatment with elicitor, implying that EILP is involved in both preexisting and inducible surveillance systems. The expression of EILP was activated by a nonpathogen, Pseudomonas syringae pv. glycinea, and in a delayed fashion by the tobacco pathogen P. syringae pv. tabaci, suggesting that the product of EILP may be involved in non-host disease resistance in tobacco.
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DOI: 10.1093/pcp/41.4.458
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University Chikusa, Nagoya</wicri:regionArea></affiliation></author><author><name sortKey="Hayashi, Makoto" sort="Hayashi, Makoto" uniqKey="Hayashi M" first="Makoto" last="Hayashi">Makoto Hayashi</name><affiliation wicri:level="1"><mods:affiliation>Department of Applied Plant Science, Graduate School of Agricultural Science, Tohoku University Aoba-ku, Sendai, 981-8555 Japan</mods:affiliation><country xml:lang="fr">Japon</country><wicri:regionArea>Department of Applied Plant Science, Graduate School of Agricultural Science, Tohoku University Aoba-ku, Sendai</wicri:regionArea></affiliation></author><author><name sortKey="Doke, Noriyuki" sort="Doke, Noriyuki" uniqKey="Doke N" first="Noriyuki" last="Doke">Noriyuki Doke</name><affiliation wicri:level="1"><mods:affiliation>Plant Pathology Laboratory, Graduate School of Bioagricultural Sciences, Nagoya University Chikusa, Nagoya, 464-8601 Japan</mods:affiliation><country xml:lang="fr">Japon</country><wicri:regionArea>Plant Pathology Laboratory, Graduate School of Bioagricultural Sciences, Nagoya University Chikusa, Nagoya</wicri:regionArea></affiliation></author><author><name sortKey="Nishimura, Mikio" sort="Nishimura, Mikio" uniqKey="Nishimura M" first="Mikio" last="Nishimura">Mikio Nishimura</name><affiliation wicri:level="1"><mods:affiliation>Department of Cell Biology, National Institute for Basic Biology Okazaki, 444-0867 Japan</mods:affiliation><country xml:lang="fr">Japon</country><wicri:regionArea>Department of Cell Biology, National Institute for Basic Biology Okazaki</wicri:regionArea></affiliation></author><author><name sortKey="Kawakita, Kazuhito" sort="Kawakita, Kazuhito" uniqKey="Kawakita K" first="Kazuhito" last="Kawakita">Kazuhito Kawakita</name><affiliation wicri:level="1"><mods:affiliation>Plant Pathology Laboratory, Graduate School of Bioagricultural Sciences, Nagoya University Chikusa, Nagoya, 464-8601 Japan</mods:affiliation><country xml:lang="fr">Japon</country><wicri:regionArea>Plant Pathology Laboratory, Graduate School of Bioagricultural Sciences, Nagoya University Chikusa, Nagoya</wicri:regionArea></affiliation></author></analytic><monogr></monogr><series><title level="j" type="main">Plant and Cell Physiology</title><idno type="ISSN">0032-0781</idno><idno type="eISSN">1471-9053</idno><imprint><publisher>Plant and Cell Physiology</publisher><date type="published">2000</date><biblScope unit="vol">41</biblScope><biblScope unit="issue">4</biblScope><biblScope unit="page" from="458">458</biblScope><biblScope unit="page" to="464">464</biblScope></imprint><idno type="ISSN">0032-0781</idno></series></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0032-0781</idno></seriesStmt></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract">We screened tobacco genes, which are differentially expressed in response to a fungal elicitor, and have isolated a gene which codes for a leucine-rich repeat (LRR) protein closely related to Cf genes in tomato. The EILP (elicitor inducible LRR protein) gene encodes 95 kDa protein, which consists of a putative membrane spanning region, 28 leucine-rich repeats and some N-linked glycosylation sites, and shows high homology to Cf-2/Cf-5 family genes. Southern blot analysis revealed the presence of some genes homologous to EILP in tobacco, like Cf genes in tomato. The expression of EILP was low at the basal level and increased by treatment with elicitor, implying that EILP is involved in both preexisting and inducible surveillance systems. The expression of EILP was activated by a nonpathogen, Pseudomonas syringae pv. glycinea, and in a delayed fashion by the tobacco pathogen P. syringae pv. tabaci, suggesting that the product of EILP may be involved in non-host disease resistance in tobacco.</div></front></TEI></record>Pour manipuler ce document sous Unix (Dilib)
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