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Leaf Oil Body Functions as a Subcellular Factory for the Production of a Phytoalexin in Arabidopsis
Oil bodies are intracellular structures present in the seed and leaf cells of many land plants. Seed oil bodies are known to function as storage compartments for lipids. However, the physiological function of leaf oil bodies is unknown. Here, we show that leaf oil bodies function as subcellular fact...
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Published in: | Plant physiology (Bethesda) 2014-01, Vol.164 (1), p.105-118 |
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creator | Shimada, Takashi L. Takano, Yoshitaka Shimada, Tomoo Fujiwara, Masayuki Fukao, Yoichiro Mori, Masashi Okazaki, Yozo Saito, Kazuki Sasaki, Ryosuke Aoki, Koh Hara-Nishimura, Ikuko |
description | Oil bodies are intracellular structures present in the seed and leaf cells of many land plants. Seed oil bodies are known to function as storage compartments for lipids. However, the physiological function of leaf oil bodies is unknown. Here, we show that leaf oil bodies function as subcellular factories for the production of a stable phytoalexin in response to fungal infection and senescence. Proteomic analysis of oil bodies prepared from Arabidopsis (Ambidopsis thaliana) leaves identified caleosin (CLO3) and a-dioxygenase (α-DOX1). Both CLO3 and α-DOX1 were localized on the surface of oil bodies. Infection with the pathogenic fungus Colletotrichum higginsianum promoted the formation of CLO3-and α-DOX1-positive oil bodies in perilesional areas surrounding the site of infection. α-DOX1 catalyzes the reaction from α-linolenic acid (a major fatty acid component of oil bodies) to an unstable compound, 2-hydroperoxyoctadecatrienoic acid (2-HPOT). Intriguingly, a combination of α-DOX1 and CLO3 produced a stable compound, 2-hydroxyoctadecatrienoic acid (2-HOT), from α-linolenic acid. This suggests that the colocalization of α-DOX1 and CLO3 on oil bodies might prevent the degradation of unstable 2-HPOT by efficiently converting 2-HPOT into the stable compound 2-HOT. We found that 2-HOT had antifungal activity against members of the genus Colletotrichum and that infection with C. higginsianum induced 2-HOT production. These results defined 2-HOT as an Arabidopsis phytoalexin. This study provides, to our knowledge, the first evidence that leaf oil bodies produce a phytoalexin under a pathological condition, which suggests a new mechanism of plant defense. |
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Seed oil bodies are known to function as storage compartments for lipids. However, the physiological function of leaf oil bodies is unknown. Here, we show that leaf oil bodies function as subcellular factories for the production of a stable phytoalexin in response to fungal infection and senescence. Proteomic analysis of oil bodies prepared from Arabidopsis (Ambidopsis thaliana) leaves identified caleosin (CLO3) and a-dioxygenase (α-DOX1). Both CLO3 and α-DOX1 were localized on the surface of oil bodies. Infection with the pathogenic fungus Colletotrichum higginsianum promoted the formation of CLO3-and α-DOX1-positive oil bodies in perilesional areas surrounding the site of infection. α-DOX1 catalyzes the reaction from α-linolenic acid (a major fatty acid component of oil bodies) to an unstable compound, 2-hydroperoxyoctadecatrienoic acid (2-HPOT). Intriguingly, a combination of α-DOX1 and CLO3 produced a stable compound, 2-hydroxyoctadecatrienoic acid (2-HOT), from α-linolenic acid. This suggests that the colocalization of α-DOX1 and CLO3 on oil bodies might prevent the degradation of unstable 2-HPOT by efficiently converting 2-HPOT into the stable compound 2-HOT. We found that 2-HOT had antifungal activity against members of the genus Colletotrichum and that infection with C. higginsianum induced 2-HOT production. These results defined 2-HOT as an Arabidopsis phytoalexin. This study provides, to our knowledge, the first evidence that leaf oil bodies produce a phytoalexin under a pathological condition, which suggests a new mechanism of plant defense.</description><identifier>ISSN: 0032-0889</identifier><identifier>EISSN: 1532-2548</identifier><identifier>DOI: 10.1104/pp.113.230185</identifier><identifier>PMID: 24214535</identifier><language>eng</language><publisher>United States: American Society of Plant Biologists</publisher><subject>alpha-Linolenic Acid - metabolism ; Antifungal Agents - metabolism ; Arabidopsis ; Arabidopsis - genetics ; Arabidopsis - metabolism ; Arabidopsis - microbiology ; Arabidopsis Proteins - genetics ; Arabidopsis Proteins - metabolism ; Calcium-Binding Proteins - genetics ; Calcium-Binding Proteins - metabolism ; CELL BIOLOGY ; Colletotrichum ; Colletotrichum - drug effects ; Colletotrichum - pathogenicity ; Dioxygenases - metabolism ; Fatty acids ; fungi ; Infections ; Leaf oils ; Leaves ; Lipid bodies ; Lipid Peroxides - metabolism ; Nicotiana - genetics ; Oxylipins - metabolism ; Oxylipins - pharmacology ; Pathogens ; Phytoalexins ; Plant cells ; Plant Leaves - cytology ; Plant Leaves - metabolism ; Plant Leaves - microbiology ; Plant Proteins - genetics ; Plant Proteins - metabolism ; Plants ; Plants, Genetically Modified ; Sesquiterpenes - metabolism ; Sesquiterpenes - pharmacology ; Solvents</subject><ispartof>Plant physiology (Bethesda), 2014-01, Vol.164 (1), p.105-118</ispartof><rights>2014 American Society of Plant Biologists</rights><rights>2014 American Society of Plant Biologists. All Rights Reserved. 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/43191271$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/43191271$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,776,780,881,27901,27902,58213,58446</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24214535$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shimada, Takashi L.</creatorcontrib><creatorcontrib>Takano, Yoshitaka</creatorcontrib><creatorcontrib>Shimada, Tomoo</creatorcontrib><creatorcontrib>Fujiwara, Masayuki</creatorcontrib><creatorcontrib>Fukao, Yoichiro</creatorcontrib><creatorcontrib>Mori, Masashi</creatorcontrib><creatorcontrib>Okazaki, Yozo</creatorcontrib><creatorcontrib>Saito, Kazuki</creatorcontrib><creatorcontrib>Sasaki, Ryosuke</creatorcontrib><creatorcontrib>Aoki, Koh</creatorcontrib><creatorcontrib>Hara-Nishimura, Ikuko</creatorcontrib><title>Leaf Oil Body Functions as a Subcellular Factory for the Production of a Phytoalexin in Arabidopsis</title><title>Plant physiology (Bethesda)</title><addtitle>Plant Physiol</addtitle><description>Oil bodies are intracellular structures present in the seed and leaf cells of many land plants. Seed oil bodies are known to function as storage compartments for lipids. However, the physiological function of leaf oil bodies is unknown. Here, we show that leaf oil bodies function as subcellular factories for the production of a stable phytoalexin in response to fungal infection and senescence. Proteomic analysis of oil bodies prepared from Arabidopsis (Ambidopsis thaliana) leaves identified caleosin (CLO3) and a-dioxygenase (α-DOX1). Both CLO3 and α-DOX1 were localized on the surface of oil bodies. Infection with the pathogenic fungus Colletotrichum higginsianum promoted the formation of CLO3-and α-DOX1-positive oil bodies in perilesional areas surrounding the site of infection. α-DOX1 catalyzes the reaction from α-linolenic acid (a major fatty acid component of oil bodies) to an unstable compound, 2-hydroperoxyoctadecatrienoic acid (2-HPOT). Intriguingly, a combination of α-DOX1 and CLO3 produced a stable compound, 2-hydroxyoctadecatrienoic acid (2-HOT), from α-linolenic acid. This suggests that the colocalization of α-DOX1 and CLO3 on oil bodies might prevent the degradation of unstable 2-HPOT by efficiently converting 2-HPOT into the stable compound 2-HOT. We found that 2-HOT had antifungal activity against members of the genus Colletotrichum and that infection with C. higginsianum induced 2-HOT production. These results defined 2-HOT as an Arabidopsis phytoalexin. This study provides, to our knowledge, the first evidence that leaf oil bodies produce a phytoalexin under a pathological condition, which suggests a new mechanism of plant defense.</description><subject>alpha-Linolenic Acid - metabolism</subject><subject>Antifungal Agents - metabolism</subject><subject>Arabidopsis</subject><subject>Arabidopsis - genetics</subject><subject>Arabidopsis - metabolism</subject><subject>Arabidopsis - microbiology</subject><subject>Arabidopsis Proteins - genetics</subject><subject>Arabidopsis Proteins - metabolism</subject><subject>Calcium-Binding Proteins - genetics</subject><subject>Calcium-Binding Proteins - metabolism</subject><subject>CELL BIOLOGY</subject><subject>Colletotrichum</subject><subject>Colletotrichum - drug effects</subject><subject>Colletotrichum - pathogenicity</subject><subject>Dioxygenases - metabolism</subject><subject>Fatty acids</subject><subject>fungi</subject><subject>Infections</subject><subject>Leaf oils</subject><subject>Leaves</subject><subject>Lipid bodies</subject><subject>Lipid Peroxides - metabolism</subject><subject>Nicotiana - genetics</subject><subject>Oxylipins - metabolism</subject><subject>Oxylipins - pharmacology</subject><subject>Pathogens</subject><subject>Phytoalexins</subject><subject>Plant cells</subject><subject>Plant Leaves - cytology</subject><subject>Plant Leaves - metabolism</subject><subject>Plant Leaves - microbiology</subject><subject>Plant Proteins - genetics</subject><subject>Plant Proteins - metabolism</subject><subject>Plants</subject><subject>Plants, Genetically Modified</subject><subject>Sesquiterpenes - metabolism</subject><subject>Sesquiterpenes - pharmacology</subject><subject>Solvents</subject><issn>0032-0889</issn><issn>1532-2548</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNqFkUtLLDEQhYNc0fGxdKlk6WY0lUd3Z3PBOzgqDCjovqlOp50MPZ026b44_974RFdCQRWcj8OpKkKOgJ0BMHne96mLMy4YFGqLTEAJPuVKFn_IhLE0s6LQu2QvxhVjDATIHbLLJQephJoQs7DY0FvX0n--3tD52JnB-S5STEXvx8rYth1bDHSOZvBhQxsf6LC09C74enyDqW8Se7fcDB5b--w6muoiYOVq30cXD8h2g220hx99nzzMLx9m19PF7dXN7GIxXQkOQwqdKVPUmdGFqVBrzTPLIONoKm4QLVqGwLLcZghNrnTFs5zlkkngVula7JO_77b9WK1tbWw3BGzLPrg1hk3p0ZU_lc4ty0f_vxRFrnLNk8Hph0HwT6ONQ7l28XV_7KwfY8lfD8iBS_gVBalZrlT2hp58j_WV5_MHCTh-B1YxHfhLlwI08BzEC5NrknU</recordid><startdate>20140101</startdate><enddate>20140101</enddate><creator>Shimada, Takashi L.</creator><creator>Takano, Yoshitaka</creator><creator>Shimada, Tomoo</creator><creator>Fujiwara, Masayuki</creator><creator>Fukao, Yoichiro</creator><creator>Mori, Masashi</creator><creator>Okazaki, Yozo</creator><creator>Saito, Kazuki</creator><creator>Sasaki, Ryosuke</creator><creator>Aoki, Koh</creator><creator>Hara-Nishimura, Ikuko</creator><general>American Society of Plant Biologists</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope><scope>5PM</scope></search><sort><creationdate>20140101</creationdate><title>Leaf Oil Body Functions as a Subcellular Factory for the Production of a Phytoalexin in Arabidopsis</title><author>Shimada, Takashi L. ; Takano, Yoshitaka ; Shimada, Tomoo ; Fujiwara, Masayuki ; Fukao, Yoichiro ; Mori, Masashi ; Okazaki, Yozo ; Saito, Kazuki ; Sasaki, Ryosuke ; Aoki, Koh ; Hara-Nishimura, Ikuko</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-j321t-2565c8d6c98cba99926e0162acb2caaeae0a1067e6a1f759b2670740412e59d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>alpha-Linolenic Acid - metabolism</topic><topic>Antifungal Agents - metabolism</topic><topic>Arabidopsis</topic><topic>Arabidopsis - genetics</topic><topic>Arabidopsis - metabolism</topic><topic>Arabidopsis - microbiology</topic><topic>Arabidopsis Proteins - genetics</topic><topic>Arabidopsis Proteins - metabolism</topic><topic>Calcium-Binding Proteins - genetics</topic><topic>Calcium-Binding Proteins - metabolism</topic><topic>CELL BIOLOGY</topic><topic>Colletotrichum</topic><topic>Colletotrichum - drug effects</topic><topic>Colletotrichum - pathogenicity</topic><topic>Dioxygenases - metabolism</topic><topic>Fatty acids</topic><topic>fungi</topic><topic>Infections</topic><topic>Leaf oils</topic><topic>Leaves</topic><topic>Lipid bodies</topic><topic>Lipid Peroxides - metabolism</topic><topic>Nicotiana - genetics</topic><topic>Oxylipins - metabolism</topic><topic>Oxylipins - pharmacology</topic><topic>Pathogens</topic><topic>Phytoalexins</topic><topic>Plant cells</topic><topic>Plant Leaves - cytology</topic><topic>Plant Leaves - metabolism</topic><topic>Plant Leaves - microbiology</topic><topic>Plant Proteins - genetics</topic><topic>Plant Proteins - metabolism</topic><topic>Plants</topic><topic>Plants, Genetically Modified</topic><topic>Sesquiterpenes - metabolism</topic><topic>Sesquiterpenes - pharmacology</topic><topic>Solvents</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shimada, Takashi L.</creatorcontrib><creatorcontrib>Takano, Yoshitaka</creatorcontrib><creatorcontrib>Shimada, Tomoo</creatorcontrib><creatorcontrib>Fujiwara, Masayuki</creatorcontrib><creatorcontrib>Fukao, Yoichiro</creatorcontrib><creatorcontrib>Mori, Masashi</creatorcontrib><creatorcontrib>Okazaki, Yozo</creatorcontrib><creatorcontrib>Saito, Kazuki</creatorcontrib><creatorcontrib>Sasaki, Ryosuke</creatorcontrib><creatorcontrib>Aoki, Koh</creatorcontrib><creatorcontrib>Hara-Nishimura, Ikuko</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Plant physiology (Bethesda)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shimada, Takashi L.</au><au>Takano, Yoshitaka</au><au>Shimada, Tomoo</au><au>Fujiwara, Masayuki</au><au>Fukao, Yoichiro</au><au>Mori, Masashi</au><au>Okazaki, Yozo</au><au>Saito, Kazuki</au><au>Sasaki, Ryosuke</au><au>Aoki, Koh</au><au>Hara-Nishimura, Ikuko</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Leaf Oil Body Functions as a Subcellular Factory for the Production of a Phytoalexin in Arabidopsis</atitle><jtitle>Plant physiology (Bethesda)</jtitle><addtitle>Plant Physiol</addtitle><date>2014-01-01</date><risdate>2014</risdate><volume>164</volume><issue>1</issue><spage>105</spage><epage>118</epage><pages>105-118</pages><issn>0032-0889</issn><eissn>1532-2548</eissn><abstract>Oil bodies are intracellular structures present in the seed and leaf cells of many land plants. Seed oil bodies are known to function as storage compartments for lipids. However, the physiological function of leaf oil bodies is unknown. Here, we show that leaf oil bodies function as subcellular factories for the production of a stable phytoalexin in response to fungal infection and senescence. Proteomic analysis of oil bodies prepared from Arabidopsis (Ambidopsis thaliana) leaves identified caleosin (CLO3) and a-dioxygenase (α-DOX1). Both CLO3 and α-DOX1 were localized on the surface of oil bodies. Infection with the pathogenic fungus Colletotrichum higginsianum promoted the formation of CLO3-and α-DOX1-positive oil bodies in perilesional areas surrounding the site of infection. α-DOX1 catalyzes the reaction from α-linolenic acid (a major fatty acid component of oil bodies) to an unstable compound, 2-hydroperoxyoctadecatrienoic acid (2-HPOT). Intriguingly, a combination of α-DOX1 and CLO3 produced a stable compound, 2-hydroxyoctadecatrienoic acid (2-HOT), from α-linolenic acid. This suggests that the colocalization of α-DOX1 and CLO3 on oil bodies might prevent the degradation of unstable 2-HPOT by efficiently converting 2-HPOT into the stable compound 2-HOT. We found that 2-HOT had antifungal activity against members of the genus Colletotrichum and that infection with C. higginsianum induced 2-HOT production. These results defined 2-HOT as an Arabidopsis phytoalexin. This study provides, to our knowledge, the first evidence that leaf oil bodies produce a phytoalexin under a pathological condition, which suggests a new mechanism of plant defense.</abstract><cop>United States</cop><pub>American Society of Plant Biologists</pub><pmid>24214535</pmid><doi>10.1104/pp.113.230185</doi><tpages>14</tpages><oa>free_for_read</oa></addata></record> |
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subjects | alpha-Linolenic Acid - metabolism Antifungal Agents - metabolism Arabidopsis Arabidopsis - genetics Arabidopsis - metabolism Arabidopsis - microbiology Arabidopsis Proteins - genetics Arabidopsis Proteins - metabolism Calcium-Binding Proteins - genetics Calcium-Binding Proteins - metabolism CELL BIOLOGY Colletotrichum Colletotrichum - drug effects Colletotrichum - pathogenicity Dioxygenases - metabolism Fatty acids fungi Infections Leaf oils Leaves Lipid bodies Lipid Peroxides - metabolism Nicotiana - genetics Oxylipins - metabolism Oxylipins - pharmacology Pathogens Phytoalexins Plant cells Plant Leaves - cytology Plant Leaves - metabolism Plant Leaves - microbiology Plant Proteins - genetics Plant Proteins - metabolism Plants Plants, Genetically Modified Sesquiterpenes - metabolism Sesquiterpenes - pharmacology Solvents |
title | Leaf Oil Body Functions as a Subcellular Factory for the Production of a Phytoalexin in Arabidopsis |
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