PubMed:28559550 JSONTXT

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    21k_plant_trait_mention

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The calli with OsCHD mutation showed markedly decreased SA accumulation. These results indicate that OsWRKY62 and OsWRKY76 function as negative regulators of biosynthetic defense-related metabolites and provide evidence for an important role of phenylpropanoid pathway in SA production in rice."}

    OryzaGP_2021

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and transcriptional alternations for defense by interfering OsWRKY62 and OsWRKY76 transcriptions in rice.\nMetabolomic and transcriptomic approaches were used to dissect the enhanced disease resistance in the plants harbouring a RNA interfering construct of OsWRKY62 and OsWRKY76 (dsOW62/76) genes. The primary metabolic pathways were activated in dsOW62/76 compared with wild-type (ZH17) plants, revealed by increased accumulation of amino acids and constituents of citric acid cycle etc. Contents of phenolic acids derived from phenylpropanoid pathway were elevated in dsOW62/76 plants. Importantly, phenolamides, conjugates of the phenolic acids with amines, were detected in large number and mostly at higher levels in dsOW62/76 compared with ZH17 plants; however, the free pools of flavonoids were mostly decreased in dsOW62/76. Salicylic acid (SA) and jasmonic acid (JA)/JA-Ile contents were increased in dsOW62/76 and knockout lines of individual OsWRKY62 and OsWRKY76 genes. Transcription of isochorismate synthase (OsICS1) gene was suppressed in dsOW62/76 and in MeJA-treated rice plants, whereas the transcription level of cinnamoyl-CoA hydratase-dehydrogenase (OsCHD) gene for β-oxidation in peroxisome was increased. The calli with OsCHD mutation showed markedly decreased SA accumulation. These results indicate that OsWRKY62 and OsWRKY76 function as negative regulators of biosynthetic defense-related metabolites and provide evidence for an important role of phenylpropanoid pathway in SA production in rice."}

    OryzaGP_2022

    {"project":"OryzaGP_2022","denotations":[{"id":"T1","span":{"begin":1142,"end":1155},"obj":"http://identifiers.org/oryzabase.gene/23751"}],"text":"Metabolic and transcriptional alternations for defense by interfering OsWRKY62 and OsWRKY76 transcriptions in rice.\nMetabolomic and transcriptomic approaches were used to dissect the enhanced disease resistance in the plants harbouring a RNA interfering construct of OsWRKY62 and OsWRKY76 (dsOW62/76) genes. The primary metabolic pathways were activated in dsOW62/76 compared with wild-type (ZH17) plants, revealed by increased accumulation of amino acids and constituents of citric acid cycle etc. Contents of phenolic acids derived from phenylpropanoid pathway were elevated in dsOW62/76 plants. Importantly, phenolamides, conjugates of the phenolic acids with amines, were detected in large number and mostly at higher levels in dsOW62/76 compared with ZH17 plants; however, the free pools of flavonoids were mostly decreased in dsOW62/76. Salicylic acid (SA) and jasmonic acid (JA)/JA-Ile contents were increased in dsOW62/76 and knockout lines of individual OsWRKY62 and OsWRKY76 genes. Transcription of isochorismate synthase (OsICS1) gene was suppressed in dsOW62/76 and in MeJA-treated rice plants, whereas the transcription level of cinnamoyl-CoA hydratase-dehydrogenase (OsCHD) gene for β-oxidation in peroxisome was increased. The calli with OsCHD mutation showed markedly decreased SA accumulation. These results indicate that OsWRKY62 and OsWRKY76 function as negative regulators of biosynthetic defense-related metabolites and provide evidence for an important role of phenylpropanoid pathway in SA production in rice."}

    pqqtest_sentence

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xzyao:38628"},{"id":"M_26","span":{"begin":867,"end":875},"obj":"funRiceGene:9"},{"id":"M_27","span":{"begin":511,"end":525},"obj":"xzyao:4520"},{"id":"M_28","span":{"begin":643,"end":657},"obj":"xzyao:4520"},{"id":"M_29","span":{"begin":1081,"end":1085},"obj":"hunflair:NA:Chemical"},{"id":"M_30","span":{"begin":290,"end":299},"obj":"hunflair:NA:CellLine"},{"id":"M_31","span":{"begin":357,"end":366},"obj":"hunflair:NA:CellLine"},{"id":"M_32","span":{"begin":580,"end":589},"obj":"hunflair:NA:CellLine"},{"id":"M_33","span":{"begin":732,"end":741},"obj":"hunflair:NA:CellLine"},{"id":"M_34","span":{"begin":832,"end":841},"obj":"hunflair:NA:CellLine"},{"id":"M_35","span":{"begin":920,"end":929},"obj":"hunflair:NA:CellLine"},{"id":"M_36","span":{"begin":1064,"end":1073},"obj":"hunflair:NA:CellLine"},{"id":"M_37","span":{"begin":1009,"end":1031},"obj":"hunflair:NA:Gene"},{"id":"M_38","span":{"begin":796,"end":806},"obj":"hunflair:NA:Chemical"},{"id":"M_39","span":{"begin":539,"end":554},"obj":"hunflair:NA:Chemical"},{"id":"M_40","span":{"begin":1483,"end":1498},"obj":"hunflair:NA:Chemical"},{"id":"M_41","span":{"begin":1142,"end":1179},"obj":"hunflair:NA:Gene"},{"id":"M_42","span":{"begin":580,"end":596},"obj":"hunflair:NA:Species"},{"id":"M_43","span":{"begin":1033,"end":1039},"obj":"hunflair:NA:Gene"},{"id":"M_44","span":{"begin":511,"end":525},"obj":"hunflair:NA:Chemical"},{"id":"M_45","span":{"begin":643,"end":657},"obj":"hunflair:NA:Chemical"},{"id":"M_46","span":{"begin":83,"end":91},"obj":"hunflair:NA:Gene"},{"id":"M_47","span":{"begin":280,"end":288},"obj":"hunflair:NA:Gene"},{"id":"M_48","span":{"begin":976,"end":984},"obj":"hunflair:NA:Gene"},{"id":"M_49","span":{"begin":1352,"end":1360},"obj":"hunflair:NA:Gene"},{"id":"M_50","span":{"begin":1181,"end":1186},"obj":"hunflair:NA:Gene"},{"id":"M_51","span":{"begin":1253,"end":1258},"obj":"hunflair:NA:Gene"},{"id":"M_52","span":{"begin":1142,"end":1155},"obj":"hunflair:NA:Chemical"},{"id":"M_53","span":{"begin":444,"end":455},"obj":"hunflair:NA:Chemical"},{"id":"M_54","span":{"begin":70,"end":78},"obj":"hunflair:NA:Gene"},{"id":"M_55","span":{"begin":267,"end":275},"obj":"hunflair:NA:Gene"},{"id":"M_56","span":{"begin":963,"end":971},"obj":"hunflair:NA:Gene"},{"id":"M_57","span":{"begin":1339,"end":1347},"obj":"hunflair:NA:Gene"},{"id":"M_58","span":{"begin":290,"end":299},"obj":"hunflair:NA:Gene"},{"id":"M_59","span":{"begin":357,"end":366},"obj":"hunflair:NA:Gene"},{"id":"M_60","span":{"begin":580,"end":589},"obj":"hunflair:NA:Gene"},{"id":"M_61","span":{"begin":732,"end":741},"obj":"hunflair:NA:Gene"},{"id":"M_62","span":{"begin":832,"end":841},"obj":"hunflair:NA:Gene"},{"id":"M_63","span":{"begin":920,"end":929},"obj":"hunflair:NA:Gene"},{"id":"M_64","span":{"begin":1064,"end":1073},"obj":"hunflair:NA:Gene"},{"id":"M_65","span":{"begin":663,"end":669},"obj":"hunflair:NA:Chemical"},{"id":"M_66","span":{"begin":886,"end":892},"obj":"hunflair:NA:Chemical"},{"id":"M_67","span":{"begin":476,"end":487},"obj":"hunflair:NA:Chemical"},{"id":"M_68","span":{"begin":843,"end":857},"obj":"hunflair:NA:Chemical"},{"id":"M_69","span":{"begin":867,"end":880},"obj":"hunflair:NA:Chemical"},{"id":"M_70","span":{"begin":110,"end":114},"obj":"hunflair:NA:Species"},{"id":"M_71","span":{"begin":1094,"end":1098},"obj":"hunflair:NA:Species"},{"id":"M_72","span":{"begin":1527,"end":1531},"obj":"hunflair:NA:Species"},{"id":"M_73","span":{"begin":611,"end":623},"obj":"hunflair:NA:Chemical"},{"id":"M_74","span":{"begin":843,"end":857},"obj":"pubtator:MESH:D020156:Chemical"},{"id":"M_75","span":{"begin":1142,"end":1155},"obj":"pubtator:MESH:C022903:Chemical"},{"id":"M_76","span":{"begin":476,"end":487},"obj":"pubtator:MESH:D019343:Chemical"},{"id":"M_77","span":{"begin":539,"end":554},"obj":"pubtator:MESH:C520402:Chemical"},{"id":"M_78","span":{"begin":1483,"end":1498},"obj":"pubtator:MESH:C520402:Chemical"},{"id":"M_79","span":{"begin":1081,"end":1085},"obj":"pubtator:MESH:C404562:Chemical"},{"id":"M_80","span":{"begin":867,"end":880},"obj":"pubtator:MESH:C011006:Chemical"},{"id":"M_81","span":{"begin":1181,"end":1186},"obj":"pubtator::Disease"},{"id":"M_82","span":{"begin":1253,"end":1258},"obj":"pubtator::Disease"},{"id":"M_83","span":{"begin":611,"end":623},"obj":"pubtator::Chemical"},{"id":"M_84","span":{"begin":110,"end":114},"obj":"pubtator:4530:Species"},{"id":"M_85","span":{"begin":1094,"end":1098},"obj":"pubtator:4530:Species"},{"id":"M_86","span":{"begin":1527,"end":1531},"obj":"pubtator:4530:Species"},{"id":"M_87","span":{"begin":511,"end":525},"obj":"pubtator:MESH:C017616:Chemical"},{"id":"M_88","span":{"begin":643,"end":657},"obj":"pubtator:MESH:C017616:Chemical"},{"id":"M_89","span":{"begin":796,"end":806},"obj":"pubtator:MESH:D005419:Chemical"},{"id":"M_90","span":{"begin":663,"end":669},"obj":"pubtator:MESH:D000588:Chemical"}],"text":"Metabolic and transcriptional alternations for defense by interfering OsWRKY62 and OsWRKY76 transcriptions in rice.\nMetabolomic and transcriptomic approaches were used to dissect the enhanced disease resistance in the plants harbouring a RNA interfering construct of OsWRKY62 and OsWRKY76 (dsOW62/76) genes. The primary metabolic pathways were activated in dsOW62/76 compared with wild-type (ZH17) plants, revealed by increased accumulation of amino acids and constituents of citric acid cycle etc. Contents of phenolic acids derived from phenylpropanoid pathway were elevated in dsOW62/76 plants. Importantly, phenolamides, conjugates of the phenolic acids with amines, were detected in large number and mostly at higher levels in dsOW62/76 compared with ZH17 plants; however, the free pools of flavonoids were mostly decreased in dsOW62/76. Salicylic acid (SA) and jasmonic acid (JA)/JA-Ile contents were increased in dsOW62/76 and knockout lines of individual OsWRKY62 and OsWRKY76 genes. Transcription of isochorismate synthase (OsICS1) gene was suppressed in dsOW62/76 and in MeJA-treated rice plants, whereas the transcription level of cinnamoyl-CoA hydratase-dehydrogenase (OsCHD) gene for β-oxidation in peroxisome was increased. The calli with OsCHD mutation showed markedly decreased SA accumulation. These results indicate that OsWRKY62 and OsWRKY76 function as negative regulators of biosynthetic defense-related metabolites and provide evidence for an important role of phenylpropanoid pathway in SA production in rice."}

    OryzaGP_2021_v2

    {"project":"OryzaGP_2021_v2","denotations":[{"id":"T1","span":{"begin":70,"end":78},"obj":"http://identifiers.org/oryzabase.gene/6577"},{"id":"T2","span":{"begin":83,"end":91},"obj":"http://identifiers.org/oryzabase.gene/6591"},{"id":"T3","span":{"begin":267,"end":275},"obj":"http://identifiers.org/oryzabase.gene/6577"},{"id":"T4","span":{"begin":280,"end":288},"obj":"http://identifiers.org/oryzabase.gene/6591"},{"id":"T5","span":{"begin":859,"end":861},"obj":"http://identifiers.org/oryzabase.gene/332"},{"id":"T6","span":{"begin":859,"end":861},"obj":"http://identifiers.org/oryzabase.gene/320"},{"id":"T7","span":{"begin":963,"end":971},"obj":"http://identifiers.org/oryzabase.gene/6577"},{"id":"T8","span":{"begin":976,"end":984},"obj":"http://identifiers.org/oryzabase.gene/6591"},{"id":"T9","span":{"begin":1033,"end":1039},"obj":"http://identifiers.org/oryzabase.gene/10462"},{"id":"T10","span":{"begin":1181,"end":1186},"obj":"http://identifiers.org/oryzabase.gene/13872"},{"id":"T11","span":{"begin":1253,"end":1258},"obj":"http://identifiers.org/oryzabase.gene/13872"},{"id":"T12","span":{"begin":1294,"end":1296},"obj":"http://identifiers.org/oryzabase.gene/332"},{"id":"T13","span":{"begin":1294,"end":1296},"obj":"http://identifiers.org/oryzabase.gene/320"},{"id":"T14","span":{"begin":1339,"end":1347},"obj":"http://identifiers.org/oryzabase.gene/6577"},{"id":"T15","span":{"begin":1352,"end":1360},"obj":"http://identifiers.org/oryzabase.gene/6591"},{"id":"T16","span":{"begin":1510,"end":1512},"obj":"http://identifiers.org/oryzabase.gene/332"},{"id":"T17","span":{"begin":1510,"end":1512},"obj":"http://identifiers.org/oryzabase.gene/320"},{"id":"T87659","span":{"begin":70,"end":78},"obj":"http://identifiers.org/rapdb.locus/Os09g0417800"},{"id":"T81779","span":{"begin":83,"end":91},"obj":"http://identifiers.org/rapdb.locus/Os09g0417600"},{"id":"T86639","span":{"begin":267,"end":275},"obj":"http://identifiers.org/rapdb.locus/Os09g0417800"},{"id":"T8526","span":{"begin":280,"end":288},"obj":"http://identifiers.org/rapdb.locus/Os09g0417600"},{"id":"T18733","span":{"begin":963,"end":971},"obj":"http://identifiers.org/rapdb.locus/Os09g0417800"},{"id":"T77872","span":{"begin":976,"end":984},"obj":"http://identifiers.org/rapdb.locus/Os09g0417600"},{"id":"T74921","span":{"begin":1033,"end":1039},"obj":"http://identifiers.org/rapdb.locus/Os09g0361500"},{"id":"T23796","span":{"begin":1181,"end":1186},"obj":"http://identifiers.org/rapdb.locus/Os02g0274100"},{"id":"T1142","span":{"begin":1253,"end":1258},"obj":"http://identifiers.org/rapdb.locus/Os02g0274100"},{"id":"T59786","span":{"begin":1339,"end":1347},"obj":"http://identifiers.org/rapdb.locus/Os09g0417800"},{"id":"T79854","span":{"begin":1352,"end":1360},"obj":"http://identifiers.org/rapdb.locus/Os09g0417600"}],"text":"Metabolic and transcriptional alternations for defense by interfering OsWRKY62 and OsWRKY76 transcriptions in rice.\nMetabolomic and transcriptomic approaches were used to dissect the enhanced disease resistance in the plants harbouring a RNA interfering construct of OsWRKY62 and OsWRKY76 (dsOW62/76) genes. The primary metabolic pathways were activated in dsOW62/76 compared with wild-type (ZH17) plants, revealed by increased accumulation of amino acids and constituents of citric acid cycle etc. Contents of phenolic acids derived from phenylpropanoid pathway were elevated in dsOW62/76 plants. Importantly, phenolamides, conjugates of the phenolic acids with amines, were detected in large number and mostly at higher levels in dsOW62/76 compared with ZH17 plants; however, the free pools of flavonoids were mostly decreased in dsOW62/76. Salicylic acid (SA) and jasmonic acid (JA)/JA-Ile contents were increased in dsOW62/76 and knockout lines of individual OsWRKY62 and OsWRKY76 genes. Transcription of isochorismate synthase (OsICS1) gene was suppressed in dsOW62/76 and in MeJA-treated rice plants, whereas the transcription level of cinnamoyl-CoA hydratase-dehydrogenase (OsCHD) gene for β-oxidation in peroxisome was increased. The calli with OsCHD mutation showed markedly decreased SA accumulation. These results indicate that OsWRKY62 and OsWRKY76 function as negative regulators of biosynthetic defense-related metabolites and provide evidence for an important role of phenylpropanoid pathway in SA production in rice."}

    OryzaGP_2021_FLAIR

    {"project":"OryzaGP_2021_FLAIR","denotations":[{"id":"M_0","span":{"begin":886,"end":892},"obj":"hunflair:NA:Chemical"},{"id":"M_1","span":{"begin":843,"end":857},"obj":"hunflair:NA:Chemical"},{"id":"M_2","span":{"begin":1033,"end":1039},"obj":"hunflair:NA:Gene"},{"id":"M_3","span":{"begin":290,"end":299},"obj":"hunflair:NA:Gene"},{"id":"M_4","span":{"begin":357,"end":366},"obj":"hunflair:NA:Gene"},{"id":"M_5","span":{"begin":580,"end":589},"obj":"hunflair:NA:Gene"},{"id":"M_6","span":{"begin":732,"end":741},"obj":"hunflair:NA:Gene"},{"id":"M_7","span":{"begin":832,"end":841},"obj":"hunflair:NA:Gene"},{"id":"M_8","span":{"begin":920,"end":929},"obj":"hunflair:NA:Gene"},{"id":"M_9","span":{"begin":1064,"end":1073},"obj":"hunflair:NA:Gene"},{"id":"M_10","span":{"begin":796,"end":806},"obj":"hunflair:NA:Chemical"},{"id":"M_11","span":{"begin":70,"end":78},"obj":"hunflair:NA:Gene"},{"id":"M_12","span":{"begin":267,"end":275},"obj":"hunflair:NA:Gene"},{"id":"M_13","span":{"begin":963,"end":971},"obj":"hunflair:NA:Gene"},{"id":"M_14","span":{"begin":1339,"end":1347},"obj":"hunflair:NA:Gene"},{"id":"M_15","span":{"begin":539,"end":554},"obj":"hunflair:NA:Chemical"},{"id":"M_16","span":{"begin":1483,"end":1498},"obj":"hunflair:NA:Chemical"},{"id":"M_17","span":{"begin":110,"end":114},"obj":"hunflair:NA:Species"},{"id":"M_18","span":{"begin":1094,"end":1098},"obj":"hunflair:NA:Species"},{"id":"M_19","span":{"begin":1527,"end":1531},"obj":"hunflair:NA:Species"},{"id":"M_20","span":{"begin":580,"end":596},"obj":"hunflair:NA:Species"},{"id":"M_21","span":{"begin":1009,"end":1031},"obj":"hunflair:NA:Gene"},{"id":"M_22","span":{"begin":290,"end":299},"obj":"hunflair:NA:CellLine"},{"id":"M_23","span":{"begin":357,"end":366},"obj":"hunflair:NA:CellLine"},{"id":"M_24","span":{"begin":580,"end":589},"obj":"hunflair:NA:CellLine"},{"id":"M_25","span":{"begin":732,"end":741},"obj":"hunflair:NA:CellLine"},{"id":"M_26","span":{"begin":832,"end":841},"obj":"hunflair:NA:CellLine"},{"id":"M_27","span":{"begin":920,"end":929},"obj":"hunflair:NA:CellLine"},{"id":"M_28","span":{"begin":1064,"end":1073},"obj":"hunflair:NA:CellLine"},{"id":"M_29","span":{"begin":867,"end":880},"obj":"hunflair:NA:Chemical"},{"id":"M_30","span":{"begin":1142,"end":1155},"obj":"hunflair:NA:Chemical"},{"id":"M_31","span":{"begin":511,"end":525},"obj":"hunflair:NA:Chemical"},{"id":"M_32","span":{"begin":643,"end":657},"obj":"hunflair:NA:Chemical"},{"id":"M_33","span":{"begin":611,"end":623},"obj":"hunflair:NA:Chemical"},{"id":"M_34","span":{"begin":1081,"end":1085},"obj":"hunflair:NA:Chemical"},{"id":"M_35","span":{"begin":1181,"end":1186},"obj":"hunflair:NA:Gene"},{"id":"M_36","span":{"begin":1253,"end":1258},"obj":"hunflair:NA:Gene"},{"id":"M_37","span":{"begin":444,"end":455},"obj":"hunflair:NA:Chemical"},{"id":"M_38","span":{"begin":476,"end":487},"obj":"hunflair:NA:Chemical"},{"id":"M_39","span":{"begin":663,"end":669},"obj":"hunflair:NA:Chemical"},{"id":"M_40","span":{"begin":83,"end":91},"obj":"hunflair:NA:Gene"},{"id":"M_41","span":{"begin":280,"end":288},"obj":"hunflair:NA:Gene"},{"id":"M_42","span":{"begin":976,"end":984},"obj":"hunflair:NA:Gene"},{"id":"M_43","span":{"begin":1352,"end":1360},"obj":"hunflair:NA:Gene"},{"id":"M_44","span":{"begin":1142,"end":1179},"obj":"hunflair:NA:Gene"}],"text":"Metabolic and transcriptional alternations for defense by interfering OsWRKY62 and OsWRKY76 transcriptions in rice.\nMetabolomic and transcriptomic approaches were used to dissect the enhanced disease resistance in the plants harbouring a RNA interfering construct of OsWRKY62 and OsWRKY76 (dsOW62/76) genes. The primary metabolic pathways were activated in dsOW62/76 compared with wild-type (ZH17) plants, revealed by increased accumulation of amino acids and constituents of citric acid cycle etc. Contents of phenolic acids derived from phenylpropanoid pathway were elevated in dsOW62/76 plants. Importantly, phenolamides, conjugates of the phenolic acids with amines, were detected in large number and mostly at higher levels in dsOW62/76 compared with ZH17 plants; however, the free pools of flavonoids were mostly decreased in dsOW62/76. Salicylic acid (SA) and jasmonic acid (JA)/JA-Ile contents were increased in dsOW62/76 and knockout lines of individual OsWRKY62 and OsWRKY76 genes. Transcription of isochorismate synthase (OsICS1) gene was suppressed in dsOW62/76 and in MeJA-treated rice plants, whereas the transcription level of cinnamoyl-CoA hydratase-dehydrogenase (OsCHD) gene for β-oxidation in peroxisome was increased. The calli with OsCHD mutation showed markedly decreased SA accumulation. These results indicate that OsWRKY62 and OsWRKY76 function as negative regulators of biosynthetic defense-related metabolites and provide evidence for an important role of phenylpropanoid pathway in SA production in rice."}

    funRiceGenes-all

    {"project":"funRiceGenes-all","denotations":[{"id":"PTO-all_T1","span":{"begin":192,"end":210},"obj":"http://purl.obolibrary.org/obo/TO_0000112"}],"text":"Metabolic and transcriptional alternations for defense by interfering OsWRKY62 and OsWRKY76 transcriptions in rice.\nMetabolomic and transcriptomic approaches were used to dissect the enhanced disease resistance in the plants harbouring a RNA interfering construct of OsWRKY62 and OsWRKY76 (dsOW62/76) genes. The primary metabolic pathways were activated in dsOW62/76 compared with wild-type (ZH17) plants, revealed by increased accumulation of amino acids and constituents of citric acid cycle etc. Contents of phenolic acids derived from phenylpropanoid pathway were elevated in dsOW62/76 plants. Importantly, phenolamides, conjugates of the phenolic acids with amines, were detected in large number and mostly at higher levels in dsOW62/76 compared with ZH17 plants; however, the free pools of flavonoids were mostly decreased in dsOW62/76. Salicylic acid (SA) and jasmonic acid (JA)/JA-Ile contents were increased in dsOW62/76 and knockout lines of individual OsWRKY62 and OsWRKY76 genes. Transcription of isochorismate synthase (OsICS1) gene was suppressed in dsOW62/76 and in MeJA-treated rice plants, whereas the transcription level of cinnamoyl-CoA hydratase-dehydrogenase (OsCHD) gene for β-oxidation in peroxisome was increased. The calli with OsCHD mutation showed markedly decreased SA accumulation. These results indicate that OsWRKY62 and OsWRKY76 function as negative regulators of biosynthetic defense-related metabolites and provide evidence for an important role of phenylpropanoid pathway in SA production in rice."}

    funRiceGenes-exact

    {"project":"funRiceGenes-exact","denotations":[{"id":"PTO-exact_T1","span":{"begin":192,"end":210},"obj":"http://purl.obolibrary.org/obo/TO_0000112"}],"text":"Metabolic and transcriptional alternations for defense by interfering OsWRKY62 and OsWRKY76 transcriptions in rice.\nMetabolomic and transcriptomic approaches were used to dissect the enhanced disease resistance in the plants harbouring a RNA interfering construct of OsWRKY62 and OsWRKY76 (dsOW62/76) genes. The primary metabolic pathways were activated in dsOW62/76 compared with wild-type (ZH17) plants, revealed by increased accumulation of amino acids and constituents of citric acid cycle etc. Contents of phenolic acids derived from phenylpropanoid pathway were elevated in dsOW62/76 plants. Importantly, phenolamides, conjugates of the phenolic acids with amines, were detected in large number and mostly at higher levels in dsOW62/76 compared with ZH17 plants; however, the free pools of flavonoids were mostly decreased in dsOW62/76. Salicylic acid (SA) and jasmonic acid (JA)/JA-Ile contents were increased in dsOW62/76 and knockout lines of individual OsWRKY62 and OsWRKY76 genes. Transcription of isochorismate synthase (OsICS1) gene was suppressed in dsOW62/76 and in MeJA-treated rice plants, whereas the transcription level of cinnamoyl-CoA hydratase-dehydrogenase (OsCHD) gene for β-oxidation in peroxisome was increased. The calli with OsCHD mutation showed markedly decreased SA accumulation. These results indicate that OsWRKY62 and OsWRKY76 function as negative regulators of biosynthetic defense-related metabolites and provide evidence for an important role of phenylpropanoid pathway in SA production in rice."}

    OryzaGP

    {"project":"OryzaGP","denotations":[{"id":"T1","span":{"begin":70,"end":78},"obj":"gene"},{"id":"T2","span":{"begin":83,"end":91},"obj":"gene"},{"id":"T3","span":{"begin":267,"end":275},"obj":"gene"},{"id":"T4","span":{"begin":280,"end":288},"obj":"gene"},{"id":"T5","span":{"begin":1033,"end":1039},"obj":"gene"},{"id":"T6","span":{"begin":1181,"end":1186},"obj":"gene"},{"id":"T7","span":{"begin":1253,"end":1258},"obj":"gene"}],"text":"Metabolic and transcriptional alternations for defense by interfering OsWRKY62 and OsWRKY76 transcriptions in rice.\nMetabolomic and transcriptomic approaches were used to dissect the enhanced disease resistance in the plants harbouring a RNA interfering construct of OsWRKY62 and OsWRKY76 (dsOW62/76) genes. The primary metabolic pathways were activated in dsOW62/76 compared with wild-type (ZH17) plants, revealed by increased accumulation of amino acids and constituents of citric acid cycle etc. Contents of phenolic acids derived from phenylpropanoid pathway were elevated in dsOW62/76 plants. Importantly, phenolamides, conjugates of the phenolic acids with amines, were detected in large number and mostly at higher levels in dsOW62/76 compared with ZH17 plants; however, the free pools of flavonoids were mostly decreased in dsOW62/76. Salicylic acid (SA) and jasmonic acid (JA)/JA-Ile contents were increased in dsOW62/76 and knockout lines of individual OsWRKY62 and OsWRKY76 genes. Transcription of isochorismate synthase (OsICS1) gene was suppressed in dsOW62/76 and in MeJA-treated rice plants, whereas the transcription level of cinnamoyl-CoA hydratase-dehydrogenase (OsCHD) gene for β-oxidation in peroxisome was increased. The calli with OsCHD mutation showed markedly decreased SA accumulation. These results indicate that OsWRKY62 and OsWRKY76 function as negative regulators of biosynthetic defense-related metabolites and provide evidence for an important role of phenylpropanoid pathway in SA production in rice."}

    NCBITAXON

    {"project":"NCBITAXON","denotations":[{"id":"T1","span":{"begin":110,"end":114},"obj":"OrganismTaxon"},{"id":"T2","span":{"begin":1094,"end":1098},"obj":"OrganismTaxon"},{"id":"T3","span":{"begin":1527,"end":1531},"obj":"OrganismTaxon"}],"attributes":[{"id":"A1","pred":"db_id","subj":"T1","obj":"4530"},{"id":"A2","pred":"db_id","subj":"T2","obj":"4530"},{"id":"A3","pred":"db_id","subj":"T3","obj":"4530"}],"text":"Metabolic and transcriptional alternations for defense by interfering OsWRKY62 and OsWRKY76 transcriptions in rice.\nMetabolomic and transcriptomic approaches were used to dissect the enhanced disease resistance in the plants harbouring a RNA interfering construct of OsWRKY62 and OsWRKY76 (dsOW62/76) genes. The primary metabolic pathways were activated in dsOW62/76 compared with wild-type (ZH17) plants, revealed by increased accumulation of amino acids and constituents of citric acid cycle etc. Contents of phenolic acids derived from phenylpropanoid pathway were elevated in dsOW62/76 plants. Importantly, phenolamides, conjugates of the phenolic acids with amines, were detected in large number and mostly at higher levels in dsOW62/76 compared with ZH17 plants; however, the free pools of flavonoids were mostly decreased in dsOW62/76. Salicylic acid (SA) and jasmonic acid (JA)/JA-Ile contents were increased in dsOW62/76 and knockout lines of individual OsWRKY62 and OsWRKY76 genes. Transcription of isochorismate synthase (OsICS1) gene was suppressed in dsOW62/76 and in MeJA-treated rice plants, whereas the transcription level of cinnamoyl-CoA hydratase-dehydrogenase (OsCHD) gene for β-oxidation in peroxisome was increased. The calli with OsCHD mutation showed markedly decreased SA accumulation. These results indicate that OsWRKY62 and OsWRKY76 function as negative regulators of biosynthetic defense-related metabolites and provide evidence for an important role of phenylpropanoid pathway in SA production in rice."}