9 results on '"Shinya, Tomonori"'
Search Results
2. Chitin‐signaling‐dependent responses to insect oral secretions in rice cells propose the involvement of chitooligosaccharides in plant defense against herbivores.
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Kanda, Yasukazu, Shinya, Tomonori, Wari, David, Hojo, Yuko, Fujiwara, Yuka, Tsuchiya, Wataru, Fujimoto, Zui, Thomma, Bart P. H. J., Nishizawa, Yoko, Kamakura, Takashi, Galis, Ivan, and Mori, Masaki
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PATTERN perception receptors , *CATERPILLARS , *FUNGAL proteins , *RICE , *JASMONIC acid , *CHITIN - Abstract
SUMMARY Plants recognize molecules related to a variety of biotic stresses through pattern recognition receptors to activate plant immunity. In the interactions between plants and chewing herbivores, such as lepidopteran larvae, oral secretions (OS) are deposited on wounded sites, which results in the elicitation of plant immune responses. The widely conserved receptor‐like kinase CHITIN ELICITOR RECEPTOR KINASE 1 (CERK1) has been broadly associated with the recognition of microbial components, such as fungal chitin, but its relevance to herbivory remained unclear. In this study, we used receptor‐knockout rice (Oryza sativa) and larvae of the lepidopteran pest Mythimna loreyi to demonstrate that the induction of immune responses triggered by larval OS in rice cells largely depends on CERK1 (OsCERK1). CHITIN ELICITOR‐BINDING PROTEIN (CEBiP), an OsCERK1‐interacting receptor‐like protein that was proposed as the main chitin receptor, also contributed to the responses of rice cells to OS collected from three different lepidopteran species. Furthermore, CEBiP knockout rice seedlings showed lower OS‐triggered accumulation of jasmonic acid. These results strongly suggest that the OsCERK1 and CEBiP recognize a particular OS component in chewing lepidopteran herbivores, and point toward the presence of chitooligosaccharides in the OS. Targeted perturbation to chitin recognition, through the use of fungal effector proteins, confirmed the presence of chitooligosaccharides in the OS. Treatments of wounds on rice plants with chitooligosaccharides enhanced a set of immune responses, leading to resistance against an herbivorous insect. Our data show that rice recognizes chitooligosaccharides during larval herbivory to activate resistance, and identifies chitin as a novel herbivore‐associated molecular pattern. [ABSTRACT FROM AUTHOR]
- Published
- 2024
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3. Oral Secretions Affect HIPVs Induced by Generalist (Mythimna loreyi) and Specialist (Parnara guttata) Herbivores in Rice
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Sobhy, Islam S., Miyake, Atsushi, Shinya, Tomonori, and Galis, Ivan
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- 2017
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4. BSR1, a Rice Receptor-like Cytoplasmic Kinase, Positively Regulates Defense Responses to Herbivory.
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Kanda, Yasukazu, Shinya, Tomonori, Maeda, Satoru, Mujiono, Kadis, Hojo, Yuko, Tomita, Keisuke, Okada, Kazunori, Kamakura, Takashi, Galis, Ivan, and Mori, Masaki
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PLANT defenses , *GENETIC regulation , *NOCTUIDAE , *PHYTOALEXINS , *LEPIDOPTERA - Abstract
Crops experience herbivory by arthropods and microbial infections. In the interaction between plants and chewing herbivores, lepidopteran larval oral secretions (OS) and plant-derived damage-associated molecular patterns (DAMPs) trigger plant defense responses. However, the mechanisms underlying anti-herbivore defense, especially in monocots, have not been elucidated. The receptor-like cytoplasmic kinase Broad-Spectrum Resistance 1 (BSR1) of Oryza sativa L. (rice) mediates cytoplasmic defense signaling in response to microbial pathogens and enhances disease resistance when overexpressed. Here, we investigated whether BSR1 contributes to anti-herbivore defense responses. BSR1 knockout suppressed rice responses triggered by OS from the chewing herbivore Mythimna loreyi Duponchel (Lepidoptera: Noctuidae) and peptidic DAMPs OsPeps, including the activation of genes required for biosynthesis of diterpenoid phytoalexins (DPs). BSR1-overexpressing rice plants exhibited hyperactivation of DP accumulation and ethylene signaling after treatment with simulated herbivory and acquired enhanced resistance to larval feeding. As the biological significance of herbivory-induced accumulation of rice DPs remains unexplained, their physiological activities in M. loreyi were analyzed. The addition of momilactone B, a rice DP, to the artificial diet suppressed the growth of M. loreyi larvae. Altogether, this study revealed that BSR1 and herbivory-induced rice DPs are involved in the defense against chewing insects, in addition to pathogens. [ABSTRACT FROM AUTHOR]
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- 2023
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5. Ethylene functions as a suppressor of volatile production in rice.
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Mujiono, Kadis, Tohi, Tilisa, Sobhy, Islam S, Hojo, Yuko, Ho, Nhan Thanh, Shinya, Tomonori, and Galis, Ivan
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ETHYLENE ,VOLATILE organic compounds ,RICE ,JASMONATE ,PLANT development ,PLANT defenses - Abstract
We examined the role of ethylene in the production of rice (Oryza sativa) volatile organic compounds (VOCs), which act as indirect defense signals against herbivores in tritrophic interactions. Rice plants were exposed to exogenous ethylene (1 ppm) after simulated herbivory, which consisted of mechanical wounding supplemented with oral secretions (WOS) from the generalist herbivore larva Mythimna loreyi. Ethylene treatment highly suppressed VOCs in WOS-treated rice leaves, which was further corroborated by the reduced transcript levels of major VOC biosynthesis genes in ethylene-treated rice. In contrast, the accumulation of jasmonates (JA), known to control VOCs in higher plants, and transcript levels of primary JA response genes, including OsMYC2 , were not largely affected by ethylene application. At the functional level, flooding is known to promote internode elongation in young rice via ethylene signaling. Consistent with the negative role of ethylene on VOC genes, the accumulation of VOCs in water-submerged rice leaves was suppressed. Furthermore, in mature rice plants, which naturally produce less volatiles, VOCs could be rescued by the application of the ethylene perception inhibitor 1-methylcyclopropene. Our data suggest that ethylene acts as an endogenous suppressor of VOCs in rice plants during development and under stress. [ABSTRACT FROM AUTHOR]
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- 2020
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6. Integration of danger peptide signals with herbivore‐associated molecular pattern signaling amplifies anti‐herbivore defense responses in rice.
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Shinya, Tomonori, Yasuda, Shigetaka, Hyodo, Kiwamu, Tani, Rena, Hojo, Yuko, Fujiwara, Yuka, Hiruma, Kei, Ishizaki, Takuma, Fujita, Yasunari, Saijo, Yusuke, and Galis, Ivan
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PEPTIDES , *RICE yields , *PLANT defenses , *CELLULAR signal transduction , *PROTEIN kinases - Abstract
Summary: Plant defense against herbivores is modulated by herbivore‐associated molecular patterns (HAMPs) from oral secretions (OS) and/or saliva of insects. Furthermore, feeding wounds initiate plant self‐damage responses modulated by danger‐associated molecular patterns (DAMPs) such as immune defense‐promoting plant elicitor peptides (Peps). While temporal and spatial co‐existence of both patterns during herbivory implies a possibility of their close interaction, the molecular mechanisms remain undetermined. Here we report that exogenous application of rice (
Oryza sativa ) peptides (OsPeps) can elicit multiple defense responses in rice cell cultures. Specific activation ofOsPROPEP3 gene transcripts in rice leaves by wounding and OS treatments further suggests a possible involvement of the OsPep3 peptide in rice–herbivore interactions. Correspondingly, we found that simultaneous application of OsPep3 andMythimna loreyi OS significantly amplifies an array of defense responses in rice cells, including mitogen‐activated protein kinase activation, and generation of defense‐related hormones and metabolites. The induction ofOsPROPEP3/4 by OsPep3 points to a positive auto‐feedback loop in OsPep signaling which may contribute to additional enhancement of defense signal(s). Finally, the overexpression of the OsPep receptor OsPEPR1 increases the sensitivity of rice plants not only to the cognate OsPeps but also to OS signals. Our findings collectively suggest that HAMP–DAMP signal integration provides a critical step in the amplification of defense signaling in plants. [ABSTRACT FROM AUTHOR]- Published
- 2018
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7. Molecular evidence for biochemical diversification of phenolamide biosynthesis in rice plants.
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Tanabe, Kimiaki, Hojo, Yuko, Shinya, Tomonori, and Galis, Ivan
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PLANTING ,RICE ,BIOSYNTHESIS ,CROP diversification ,PLANT metabolism ,POLYAMINES - Abstract
Two phenolamides (PAs), p-coumaroylputrescine and feruloylputrescine strongly accumulate in rice ( Oryza sativa cv. Nipponbare) leaves subjected to attack of chewing and sucking herbivores. Here we identified and characterized in vitro three novel rice genes that mediated coumaroyl-CoA/feruloyl-CoA conjugation to polyamines, putrescine and agmatine. Interestingly, two genes were highly specific for their polyamine substrates, encoding putrescine N-hydroxycinnamoyltransferase and agmatine N-hydroxycinnamoyltransferase, while the third enzyme could use both polyamines and it was therefore annotated as putrescine/agmatine N-hydroxycinnamoyltransferase. All genes were preferentially expressed in rice roots and developing flowers, and in addition, the putrescine/ agmatine N -hydroxycinnamoyltransferase transcripts were strongly induced by wounding in the young rice leaves. Because the wound response of this gene was only partially suppressed in the jasmonoyl-L-isoleucine deficient plants ( Osjar1), it suggests that its upregulation (as well as inducible PAs in rice) may be largely independent of jasmonoyl-L-isoleucine signaling pathway. The finding of three closely related genes with a similar and/or overlapping activity in PA biosynthesis provides another striking example of rapid diversification of plant metabolism in response to environmental stresses in nature. [ABSTRACT FROM AUTHOR]
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- 2016
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8. Functional Characterization of CEBiP and CERK1 Homologs in Arabidopsis and Rice Reveals the Presence of Different Chitin Receptor Systems in Plants.
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Shinya, Tomonori, Motoyama, Noriko, Ikeda, Asahi, Wada, Miyuki, Kamiya, Kota, Hayafune, Masahiro, Kaku, Hanae, and Shibuya, Naoto
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KINASES , *ARABIDOPSIS , *RICE , *CHITIN , *CELL receptors , *PLANT physiology , *DISEASE resistance of plants - Abstract
Chitin is a representative microbe-associated molecular pattern (MAMP) molecule for various fungi and induces immune responses in many plant species. It has been clarified that the chitin signaling in rice requires a receptor kinase OsCERK1 and a receptor-like protein (Os)CEBiP, which specifically binds chitin oligosaccharides. On the other hand, Arabidopsis requires a receptor kinase (At)CERK1 for chitin signaling but it is not clear whether the plant also requires a CEBiP-like molecule for chitin perception/signaling. To clarify the similarity/difference of the chitin receptor in these two model plants, we first characterized CEBiP homologs in Arabidopsis. Only one of three CEBiP homologs, AtCEBiP (LYM2), showed a high-affinity binding for chitin oligosaccharides similar to rice CEBiP. AtCEBiP also represented the major chitin-binding protein in the Arabidopsis membrane. However, the single/triple knockout (KO) mutants of Arabidopsis CEBiP homologs and the overexpressor of AtCEBiP showed chitin-induced defense responses similar to wild-type Arabidopsis, indicating that AtCEBiP is biochemically functional as a chitin-binding protein but does not contribute to signaling. Studies of the chitin binding properties of the ectodomains of At/OsCERK1 and the chimeric receptors consisting of ecto/cytosolic domains of these molecules indicated that AtCERK1 is sufficient for chitin perception by itself. [ABSTRACT FROM PUBLISHER]
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- 2012
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9. Biochemical and phylogenetic analysis of CEBiP-like LysM domain-containing extracellular proteins in higher plants
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Fliegmann, Judith, Uhlenbroich, Sandra, Shinya, Tomonori, Martinez, Yves, Lefebvre, Benoit, Shibuya, Naoto, and Bono, Jean-Jacques
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PLANT proteins , *PLANT phylogeny , *BOTANICAL chemistry , *GEL electrophoresis , *HORSERADISH , *OLIGOSACCHARIDES , *PHOSPHOLIPASES , *CARRIER proteins , *RICE - Abstract
Abstract: The chitin elicitor-binding protein (CEBiP) from rice was the first plant lysin motif (LysM) protein for which the biological and biochemical function had been established. It belongs to a plant-specific family of extracellular LysM proteins (LYMs) for which we analyzed the phylogeny. LYMs are present in vascular plants only, where an early gene duplication event might have resulted in two types which were retained in present day genomes. LYMs consist of a signal peptide, three consecutive LysMs, separated by cysteine pairs, and a C-terminal region without any known signature, whose length allows the distinction between the two types, and which may be followed by a glycosylphosphatidylinositol (GPI) anchor motif. We analyzed a representative of each type, MtLYM1 and MtLYM2, from Medicago truncatula at the biochemical level and with respect to their expression patterns and observed some similarities but also marked differences. MtLYM1 and MtLYM2 proved to be very different with regard to abundance and apparent molecular mass on SDS-PAGE. Both undergo several post-translational modifications, including N-glycosylation and the addition of a GPI anchor, which would position the proteins at the outer face of the plasma membrane. Only MtLYM2, but not MtLYM1, showed specific binding to biotinylated N-acetylchitooctaose in a manner similar to CEBiP, which belongs to the same type. We postulate that LYM2-type proteins likely function in the perception of chitin-related molecules, whereas possible functions of LYM1-type proteins remain to be elucidated. [Copyright &y& Elsevier]
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- 2011
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