PubMed:25995326 JSONTXT

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    21k_plant_trait_mention

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INSENSITIVE3-LIKE1 and ETHYLENE INSENSITIVE3-LIKE2 Regulate Ethylene Response of Roots and Coleoptiles and Negatively Affect Salt Tolerance in Rice.\nEthylene plays important roles in plant growth, development, and stress responses. The ethylene signaling pathway has been studied extensively, mainly in Arabidopsis (Arabidopsis thaliana). However, the molecular mechanism of ethylene signaling is largely unknown in rice (Oryza sativa). Previously, we have isolated a set of rice ethylene-response mutants. Here, we characterized the mutant maohuzi6 (mhz6). Through map-based cloning, we found that MHZ6 encodes ETHYLENE INSENSITIVE3-LIKE1 (OsEIL1), a rice homolog of ETHYLENE INSENSITIVE3 (EIN3), which is the master transcriptional regulator of ethylene signaling in Arabidopsis. Disruption of MHZ6/OsEIL1 caused ethylene insensitivity mainly in roots, whereas silencing of the closely related OsEIL2 led to ethylene insensitivity mainly in coleoptiles of etiolated seedlings. This organ-specific functional divergence is different from the functional features of EIN3 and EIL1, both of which mediate the incomplete ethylene responses of Arabidopsis etiolated seedlings. In Arabidopsis, EIN3 and EIL1 play positive roles in plant salt tolerance. In rice, however, lack of MHZ6/OsEIL1 or OsEIL2 functions improves salt tolerance, whereas the overexpressing lines exhibit salt hypersensitivity at the seedling stage, indicating that MHZ6/OsEIL1 and OsEIL2 negatively regulate salt tolerance in rice. Furthermore, this negative regulation by MHZ6/OsEIL1 and OsEIL2 in salt tolerance is likely attributable in part to the direct regulation of HIGH-AFFINITY K(+) TRANSPORTER2;1 expression and Na(+) uptake in roots. Additionally, MHZ6/OsEIL1 overexpression promotes grain size and thousand-grain weight. Together, our study provides insights for the functional diversification of MHZ6/OsEIL1 and OsEIL2 in ethylene response and finds a novel mode of ethylene-regulated salt stress response that could be helpful for engineering salt-tolerant crops."}

    OryzaGP_2022

    {"project":"OryzaGP_2022","denotations":[{"id":"T1","span":{"begin":9,"end":36},"obj":"http://identifiers.org/oryzabase.gene/21533"},{"id":"T2","span":{"begin":143,"end":157},"obj":"http://identifiers.org/oryzabase.gene/11642"},{"id":"T3","span":{"begin":630,"end":657},"obj":"http://identifiers.org/oryzabase.gene/21533"},{"id":"T4","span":{"begin":1250,"end":1264},"obj":"http://identifiers.org/oryzabase.gene/11642"},{"id":"T5","span":{"begin":1333,"end":1347},"obj":"http://identifiers.org/oryzabase.gene/11642"},{"id":"T6","span":{"begin":1494,"end":1508},"obj":"http://identifiers.org/oryzabase.gene/11642"},{"id":"T7","span":{"begin":1585,"end":1599},"obj":"http://identifiers.org/oryzabase.gene/11642"}],"text":"MAOHUZI6/ETHYLENE INSENSITIVE3-LIKE1 and ETHYLENE INSENSITIVE3-LIKE2 Regulate Ethylene Response of Roots and Coleoptiles and Negatively Affect Salt Tolerance in Rice.\nEthylene plays important roles in plant growth, development, and stress responses. The ethylene signaling pathway has been studied extensively, mainly in Arabidopsis (Arabidopsis thaliana). However, the molecular mechanism of ethylene signaling is largely unknown in rice (Oryza sativa). Previously, we have isolated a set of rice ethylene-response mutants. Here, we characterized the mutant maohuzi6 (mhz6). Through map-based cloning, we found that MHZ6 encodes ETHYLENE INSENSITIVE3-LIKE1 (OsEIL1), a rice homolog of ETHYLENE INSENSITIVE3 (EIN3), which is the master transcriptional regulator of ethylene signaling in Arabidopsis. Disruption of MHZ6/OsEIL1 caused ethylene insensitivity mainly in roots, whereas silencing of the closely related OsEIL2 led to ethylene insensitivity mainly in coleoptiles of etiolated seedlings. This organ-specific functional divergence is different from the functional features of EIN3 and EIL1, both of which mediate the incomplete ethylene responses of Arabidopsis etiolated seedlings. In Arabidopsis, EIN3 and EIL1 play positive roles in plant salt tolerance. In rice, however, lack of MHZ6/OsEIL1 or OsEIL2 functions improves salt tolerance, whereas the overexpressing lines exhibit salt hypersensitivity at the seedling stage, indicating that MHZ6/OsEIL1 and OsEIL2 negatively regulate salt tolerance in rice. Furthermore, this negative regulation by MHZ6/OsEIL1 and OsEIL2 in salt tolerance is likely attributable in part to the direct regulation of HIGH-AFFINITY K(+) TRANSPORTER2;1 expression and Na(+) uptake in roots. Additionally, MHZ6/OsEIL1 overexpression promotes grain size and thousand-grain weight. Together, our study provides insights for the functional diversification of MHZ6/OsEIL1 and OsEIL2 in ethylene response and finds a novel mode of ethylene-regulated salt stress response that could be helpful for engineering salt-tolerant crops."}

    pqqtest_sentence

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INSENSITIVE3-LIKE1 and ETHYLENE INSENSITIVE3-LIKE2 Regulate Ethylene Response of Roots and Coleoptiles and Negatively Affect Salt Tolerance in Rice.\nEthylene plays important roles in plant growth, development, and stress responses. The ethylene signaling pathway has been studied extensively, mainly in Arabidopsis (Arabidopsis thaliana). However, the molecular mechanism of ethylene signaling is largely unknown in rice (Oryza sativa). Previously, we have isolated a set of rice ethylene-response mutants. Here, we characterized the mutant maohuzi6 (mhz6). Through map-based cloning, we found that MHZ6 encodes ETHYLENE INSENSITIVE3-LIKE1 (OsEIL1), a rice homolog of ETHYLENE INSENSITIVE3 (EIN3), which is the master transcriptional regulator of ethylene signaling in Arabidopsis. Disruption of MHZ6/OsEIL1 caused ethylene insensitivity mainly in roots, whereas silencing of the closely related OsEIL2 led to ethylene insensitivity mainly in coleoptiles of etiolated seedlings. This organ-specific functional divergence is different from the functional features of EIN3 and EIL1, both of which mediate the incomplete ethylene responses of Arabidopsis etiolated seedlings. In Arabidopsis, EIN3 and EIL1 play positive roles in plant salt tolerance. In rice, however, lack of MHZ6/OsEIL1 or OsEIL2 functions improves salt tolerance, whereas the overexpressing lines exhibit salt hypersensitivity at the seedling stage, indicating that MHZ6/OsEIL1 and OsEIL2 negatively regulate salt tolerance in rice. Furthermore, this negative regulation by MHZ6/OsEIL1 and OsEIL2 in salt tolerance is likely attributable in part to the direct regulation of HIGH-AFFINITY K(+) TRANSPORTER2;1 expression and Na(+) uptake in roots. Additionally, MHZ6/OsEIL1 overexpression promotes grain size and thousand-grain weight. Together, our study provides insights for the functional diversification of MHZ6/OsEIL1 and OsEIL2 in ethylene response and finds a novel mode of ethylene-regulated salt stress response that could be helpful for engineering salt-tolerant crops."}

    OryzaGP_2021_v2

    {"project":"OryzaGP_2021_v2","denotations":[{"id":"T1","span":{"begin":143,"end":147},"obj":"http://identifiers.org/oryzabase.gene/451"},{"id":"T2","span":{"begin":617,"end":621},"obj":"http://identifiers.org/oryzabase.gene/6125"},{"id":"T3","span":{"begin":617,"end":621},"obj":"http://identifiers.org/oryzabase.gene/21533"},{"id":"T4","span":{"begin":658,"end":669},"obj":"http://identifiers.org/oryzabase.gene/6881"},{"id":"T5","span":{"begin":659,"end":665},"obj":"http://identifiers.org/oryzabase.gene/6125"},{"id":"T6","span":{"begin":659,"end":665},"obj":"http://identifiers.org/oryzabase.gene/21533"},{"id":"T7","span":{"begin":709,"end":713},"obj":"http://identifiers.org/oryzabase.gene/6125"},{"id":"T8","span":{"begin":814,"end":825},"obj":"http://identifiers.org/oryzabase.gene/21533"},{"id":"T9","span":{"begin":914,"end":920},"obj":"http://identifiers.org/oryzabase.gene/6126"},{"id":"T10","span":{"begin":1084,"end":1088},"obj":"http://identifiers.org/oryzabase.gene/6125"},{"id":"T11","span":{"begin":1093,"end":1097},"obj":"http://identifiers.org/oryzabase.gene/6125"},{"id":"T12","span":{"begin":1093,"end":1097},"obj":"http://identifiers.org/oryzabase.gene/21533"},{"id":"T13","span":{"begin":1207,"end":1211},"obj":"http://identifiers.org/oryzabase.gene/6125"},{"id":"T14","span":{"begin":1216,"end":1220},"obj":"http://identifiers.org/oryzabase.gene/6125"},{"id":"T15","span":{"begin":1216,"end":1220},"obj":"http://identifiers.org/oryzabase.gene/21533"},{"id":"T16","span":{"begin":1292,"end":1303},"obj":"http://identifiers.org/oryzabase.gene/21533"},{"id":"T17","span":{"begin":1307,"end":1313},"obj":"http://identifiers.org/oryzabase.gene/6126"},{"id":"T18","span":{"begin":1451,"end":1462},"obj":"http://identifiers.org/oryzabase.gene/21533"},{"id":"T19","span":{"begin":1467,"end":1473},"obj":"http://identifiers.org/oryzabase.gene/6126"},{"id":"T20","span":{"begin":1559,"end":1570},"obj":"http://identifiers.org/oryzabase.gene/21533"},{"id":"T21","span":{"begin":1575,"end":1581},"obj":"http://identifiers.org/oryzabase.gene/6126"},{"id":"T22","span":{"begin":1745,"end":1756},"obj":"http://identifiers.org/oryzabase.gene/21533"},{"id":"T23","span":{"begin":1895,"end":1906},"obj":"http://identifiers.org/oryzabase.gene/21533"},{"id":"T24","span":{"begin":1911,"end":1917},"obj":"http://identifiers.org/oryzabase.gene/6126"},{"id":"T12716","span":{"begin":143,"end":147},"obj":"http://identifiers.org/rapdb.locus/Os01g0348900"},{"id":"T96804","span":{"begin":617,"end":621},"obj":"http://identifiers.org/rapdb.locus/Os03g0324300"},{"id":"T10830","span":{"begin":617,"end":621},"obj":"http://identifiers.org/rapdb.locus/Os03g0324200"},{"id":"T95434","span":{"begin":659,"end":665},"obj":"http://identifiers.org/rapdb.locus/Os03g0324300"},{"id":"T89029","span":{"begin":659,"end":665},"obj":"http://identifiers.org/rapdb.locus/Os03g0324200"},{"id":"T77628","span":{"begin":709,"end":713},"obj":"http://identifiers.org/rapdb.locus/Os03g0324200"},{"id":"T59016","span":{"begin":814,"end":825},"obj":"http://identifiers.org/rapdb.locus/Os03g0324300"},{"id":"T82845","span":{"begin":914,"end":920},"obj":"http://identifiers.org/rapdb.locus/Os07g0685700"},{"id":"T48479","span":{"begin":1084,"end":1088},"obj":"http://identifiers.org/rapdb.locus/Os03g0324200"},{"id":"T83786","span":{"begin":1093,"end":1097},"obj":"http://identifiers.org/rapdb.locus/Os03g0324300"},{"id":"T37762","span":{"begin":1093,"end":1097},"obj":"http://identifiers.org/rapdb.locus/Os03g0324200"},{"id":"T80591","span":{"begin":1207,"end":1211},"obj":"http://identifiers.org/rapdb.locus/Os03g0324200"},{"id":"T27278","span":{"begin":1216,"end":1220},"obj":"http://identifiers.org/rapdb.locus/Os03g0324300"},{"id":"T39157","span":{"begin":1216,"end":1220},"obj":"http://identifiers.org/rapdb.locus/Os03g0324200"},{"id":"T37267","span":{"begin":1292,"end":1303},"obj":"http://identifiers.org/rapdb.locus/Os03g0324300"},{"id":"T21845","span":{"begin":1307,"end":1313},"obj":"http://identifiers.org/rapdb.locus/Os07g0685700"},{"id":"T94638","span":{"begin":1451,"end":1462},"obj":"http://identifiers.org/rapdb.locus/Os03g0324300"},{"id":"T83158","span":{"begin":1467,"end":1473},"obj":"http://identifiers.org/rapdb.locus/Os07g0685700"},{"id":"T60971","span":{"begin":1559,"end":1570},"obj":"http://identifiers.org/rapdb.locus/Os03g0324300"},{"id":"T136","span":{"begin":1575,"end":1581},"obj":"http://identifiers.org/rapdb.locus/Os07g0685700"},{"id":"T61907","span":{"begin":1745,"end":1756},"obj":"http://identifiers.org/rapdb.locus/Os03g0324300"},{"id":"T97340","span":{"begin":1895,"end":1906},"obj":"http://identifiers.org/rapdb.locus/Os03g0324300"},{"id":"T23405","span":{"begin":1911,"end":1917},"obj":"http://identifiers.org/rapdb.locus/Os07g0685700"}],"text":"MAOHUZI6/ETHYLENE INSENSITIVE3-LIKE1 and ETHYLENE INSENSITIVE3-LIKE2 Regulate Ethylene Response of Roots and Coleoptiles and Negatively Affect Salt Tolerance in Rice.\nEthylene plays important roles in plant growth, development, and stress responses. The ethylene signaling pathway has been studied extensively, mainly in Arabidopsis (Arabidopsis thaliana). However, the molecular mechanism of ethylene signaling is largely unknown in rice (Oryza sativa). Previously, we have isolated a set of rice ethylene-response mutants. Here, we characterized the mutant maohuzi6 (mhz6). Through map-based cloning, we found that MHZ6 encodes ETHYLENE INSENSITIVE3-LIKE1 (OsEIL1), a rice homolog of ETHYLENE INSENSITIVE3 (EIN3), which is the master transcriptional regulator of ethylene signaling in Arabidopsis. Disruption of MHZ6/OsEIL1 caused ethylene insensitivity mainly in roots, whereas silencing of the closely related OsEIL2 led to ethylene insensitivity mainly in coleoptiles of etiolated seedlings. This organ-specific functional divergence is different from the functional features of EIN3 and EIL1, both of which mediate the incomplete ethylene responses of Arabidopsis etiolated seedlings. In Arabidopsis, EIN3 and EIL1 play positive roles in plant salt tolerance. In rice, however, lack of MHZ6/OsEIL1 or OsEIL2 functions improves salt tolerance, whereas the overexpressing lines exhibit salt hypersensitivity at the seedling stage, indicating that MHZ6/OsEIL1 and OsEIL2 negatively regulate salt tolerance in rice. Furthermore, this negative regulation by MHZ6/OsEIL1 and OsEIL2 in salt tolerance is likely attributable in part to the direct regulation of HIGH-AFFINITY K(+) TRANSPORTER2;1 expression and Na(+) uptake in roots. Additionally, MHZ6/OsEIL1 overexpression promotes grain size and thousand-grain weight. Together, our study provides insights for the functional diversification of MHZ6/OsEIL1 and OsEIL2 in ethylene response and finds a novel mode of ethylene-regulated salt stress response that could be helpful for engineering salt-tolerant crops."}

    OryzaGP_2021_FLAIR

    {"project":"OryzaGP_2021_FLAIR","denotations":[{"id":"M_0","span":{"begin":709,"end":713},"obj":"hunflair:NA:Gene"},{"id":"M_1","span":{"begin":1084,"end":1088},"obj":"hunflair:NA:Gene"},{"id":"M_2","span":{"begin":1207,"end":1211},"obj":"hunflair:NA:Gene"},{"id":"M_3","span":{"begin":440,"end":452},"obj":"hunflair:NA:Species"},{"id":"M_4","span":{"begin":569,"end":573},"obj":"hunflair:NA:Gene"},{"id":"M_5","span":{"begin":659,"end":665},"obj":"hunflair:NA:Gene"},{"id":"M_6","span":{"begin":819,"end":825},"obj":"hunflair:NA:Gene"},{"id":"M_7","span":{"begin":1297,"end":1303},"obj":"hunflair:NA:Gene"},{"id":"M_8","span":{"begin":1456,"end":1462},"obj":"hunflair:NA:Gene"},{"id":"M_9","span":{"begin":1564,"end":1570},"obj":"hunflair:NA:Gene"},{"id":"M_10","span":{"begin":1750,"end":1756},"obj":"hunflair:NA:Gene"},{"id":"M_11","span":{"begin":1900,"end":1906},"obj":"hunflair:NA:Gene"},{"id":"M_12","span":{"begin":617,"end":621},"obj":"hunflair:NA:Gene"},{"id":"M_13","span":{"begin":814,"end":818},"obj":"hunflair:NA:Gene"},{"id":"M_14","span":{"begin":1292,"end":1296},"obj":"hunflair:NA:Gene"},{"id":"M_15","span":{"begin":1451,"end":1455},"obj":"hunflair:NA:Gene"},{"id":"M_16","span":{"begin":1559,"end":1563},"obj":"hunflair:NA:Gene"},{"id":"M_17","span":{"begin":1745,"end":1749},"obj":"hunflair:NA:Gene"},{"id":"M_18","span":{"begin":1895,"end":1899},"obj":"hunflair:NA:Gene"},{"id":"M_19","span":{"begin":1390,"end":1411},"obj":"hunflair:NA:Disease"},{"id":"M_20","span":{"begin":78,"end":86},"obj":"hunflair:NA:Chemical"},{"id":"M_21","span":{"begin":167,"end":175},"obj":"hunflair:NA:Chemical"},{"id":"M_22","span":{"begin":914,"end":920},"obj":"hunflair:NA:Gene"},{"id":"M_23","span":{"begin":1307,"end":1313},"obj":"hunflair:NA:Gene"},{"id":"M_24","span":{"begin":1467,"end":1473},"obj":"hunflair:NA:Gene"},{"id":"M_25","span":{"begin":1575,"end":1581},"obj":"hunflair:NA:Gene"},{"id":"M_26","span":{"begin":1911,"end":1917},"obj":"hunflair:NA:Gene"},{"id":"M_27","span":{"begin":334,"end":354},"obj":"hunflair:NA:Species"},{"id":"M_28","span":{"begin":0,"end":8},"obj":"hunflair:NA:Gene"},{"id":"M_29","span":{"begin":161,"end":165},"obj":"hunflair:NA:Species"},{"id":"M_30","span":{"begin":254,"end":262},"obj":"hunflair:NA:Chemical"},{"id":"M_31","span":{"begin":393,"end":401},"obj":"hunflair:NA:Chemical"},{"id":"M_32","span":{"begin":498,"end":506},"obj":"hunflair:NA:Chemical"},{"id":"M_33","span":{"begin":765,"end":773},"obj":"hunflair:NA:Chemical"},{"id":"M_34","span":{"begin":833,"end":841},"obj":"hunflair:NA:Chemical"},{"id":"M_35","span":{"begin":928,"end":936},"obj":"hunflair:NA:Chemical"},{"id":"M_36","span":{"begin":1136,"end":1144},"obj":"hunflair:NA:Chemical"},{"id":"M_37","span":{"begin":1921,"end":1929},"obj":"hunflair:NA:Chemical"},{"id":"M_38","span":{"begin":1965,"end":1973},"obj":"hunflair:NA:Chemical"},{"id":"M_39","span":{"begin":434,"end":438},"obj":"hunflair:NA:Species"},{"id":"M_40","span":{"begin":493,"end":497},"obj":"hunflair:NA:Species"},{"id":"M_41","span":{"begin":670,"end":674},"obj":"hunflair:NA:Species"},{"id":"M_42","span":{"begin":1269,"end":1273},"obj":"hunflair:NA:Species"},{"id":"M_43","span":{"begin":1512,"end":1516},"obj":"hunflair:NA:Species"},{"id":"M_44","span":{"begin":1093,"end":1097},"obj":"hunflair:NA:Gene"},{"id":"M_45","span":{"begin":1216,"end":1220},"obj":"hunflair:NA:Gene"},{"id":"M_46","span":{"begin":321,"end":332},"obj":"hunflair:NA:Species"},{"id":"M_47","span":{"begin":334,"end":345},"obj":"hunflair:NA:Species"},{"id":"M_48","span":{"begin":787,"end":798},"obj":"hunflair:NA:Species"},{"id":"M_49","span":{"begin":1158,"end":1169},"obj":"hunflair:NA:Species"},{"id":"M_50","span":{"begin":1194,"end":1205},"obj":"hunflair:NA:Species"},{"id":"M_51","span":{"begin":41,"end":68},"obj":"hunflair:NA:Gene"},{"id":"M_52","span":{"begin":559,"end":567},"obj":"hunflair:NA:Gene"},{"id":"M_53","span":{"begin":9,"end":30},"obj":"hunflair:NA:Gene"},{"id":"M_54","span":{"begin":41,"end":62},"obj":"hunflair:NA:Gene"},{"id":"M_55","span":{"begin":630,"end":651},"obj":"hunflair:NA:Gene"},{"id":"M_56","span":{"begin":686,"end":707},"obj":"hunflair:NA:Gene"},{"id":"M_57","span":{"begin":9,"end":36},"obj":"hunflair:NA:Gene"},{"id":"M_58","span":{"begin":630,"end":657},"obj":"hunflair:NA:Gene"},{"id":"M_59","span":{"begin":9,"end":17},"obj":"hunflair:NA:Chemical"},{"id":"M_60","span":{"begin":41,"end":49},"obj":"hunflair:NA:Chemical"},{"id":"M_61","span":{"begin":630,"end":638},"obj":"hunflair:NA:Chemical"},{"id":"M_62","span":{"begin":686,"end":694},"obj":"hunflair:NA:Chemical"}],"text":"MAOHUZI6/ETHYLENE INSENSITIVE3-LIKE1 and ETHYLENE INSENSITIVE3-LIKE2 Regulate Ethylene Response of Roots and Coleoptiles and Negatively Affect Salt Tolerance in Rice.\nEthylene plays important roles in plant growth, development, and stress responses. The ethylene signaling pathway has been studied extensively, mainly in Arabidopsis (Arabidopsis thaliana). However, the molecular mechanism of ethylene signaling is largely unknown in rice (Oryza sativa). Previously, we have isolated a set of rice ethylene-response mutants. Here, we characterized the mutant maohuzi6 (mhz6). Through map-based cloning, we found that MHZ6 encodes ETHYLENE INSENSITIVE3-LIKE1 (OsEIL1), a rice homolog of ETHYLENE INSENSITIVE3 (EIN3), which is the master transcriptional regulator of ethylene signaling in Arabidopsis. Disruption of MHZ6/OsEIL1 caused ethylene insensitivity mainly in roots, whereas silencing of the closely related OsEIL2 led to ethylene insensitivity mainly in coleoptiles of etiolated seedlings. This organ-specific functional divergence is different from the functional features of EIN3 and EIL1, both of which mediate the incomplete ethylene responses of Arabidopsis etiolated seedlings. In Arabidopsis, EIN3 and EIL1 play positive roles in plant salt tolerance. In rice, however, lack of MHZ6/OsEIL1 or OsEIL2 functions improves salt tolerance, whereas the overexpressing lines exhibit salt hypersensitivity at the seedling stage, indicating that MHZ6/OsEIL1 and OsEIL2 negatively regulate salt tolerance in rice. Furthermore, this negative regulation by MHZ6/OsEIL1 and OsEIL2 in salt tolerance is likely attributable in part to the direct regulation of HIGH-AFFINITY K(+) TRANSPORTER2;1 expression and Na(+) uptake in roots. Additionally, MHZ6/OsEIL1 overexpression promotes grain size and thousand-grain weight. Together, our study provides insights for the functional diversification of MHZ6/OsEIL1 and OsEIL2 in ethylene response and finds a novel mode of ethylene-regulated salt stress response that could be helpful for engineering salt-tolerant crops."}

    OryzaGP_2021

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INSENSITIVE3-LIKE1 and ETHYLENE INSENSITIVE3-LIKE2 Regulate Ethylene Response of Roots and Coleoptiles and Negatively Affect Salt Tolerance in Rice.\nEthylene plays important roles in plant growth, development, and stress responses. The ethylene signaling pathway has been studied extensively, mainly in Arabidopsis (Arabidopsis thaliana). However, the molecular mechanism of ethylene signaling is largely unknown in rice (Oryza sativa). Previously, we have isolated a set of rice ethylene-response mutants. Here, we characterized the mutant maohuzi6 (mhz6). Through map-based cloning, we found that MHZ6 encodes ETHYLENE INSENSITIVE3-LIKE1 (OsEIL1), a rice homolog of ETHYLENE INSENSITIVE3 (EIN3), which is the master transcriptional regulator of ethylene signaling in Arabidopsis. Disruption of MHZ6/OsEIL1 caused ethylene insensitivity mainly in roots, whereas silencing of the closely related OsEIL2 led to ethylene insensitivity mainly in coleoptiles of etiolated seedlings. This organ-specific functional divergence is different from the functional features of EIN3 and EIL1, both of which mediate the incomplete ethylene responses of Arabidopsis etiolated seedlings. In Arabidopsis, EIN3 and EIL1 play positive roles in plant salt tolerance. In rice, however, lack of MHZ6/OsEIL1 or OsEIL2 functions improves salt tolerance, whereas the overexpressing lines exhibit salt hypersensitivity at the seedling stage, indicating that MHZ6/OsEIL1 and OsEIL2 negatively regulate salt tolerance in rice. Furthermore, this negative regulation by MHZ6/OsEIL1 and OsEIL2 in salt tolerance is likely attributable in part to the direct regulation of HIGH-AFFINITY K(+) TRANSPORTER2;1 expression and Na(+) uptake in roots. Additionally, MHZ6/OsEIL1 overexpression promotes grain size and thousand-grain weight. Together, our study provides insights for the functional diversification of MHZ6/OsEIL1 and OsEIL2 in ethylene response and finds a novel mode of ethylene-regulated salt stress response that could be helpful for engineering salt-tolerant crops."}

    Oryza_sentences

    {"project":"Oryza_sentences","blocks":[{"id":"T1","span":{"begin":0,"end":166},"obj":"Sentence"},{"id":"T2","span":{"begin":167,"end":249},"obj":"Sentence"},{"id":"T3","span":{"begin":250,"end":356},"obj":"Sentence"},{"id":"T4","span":{"begin":357,"end":454},"obj":"Sentence"},{"id":"T5","span":{"begin":455,"end":524},"obj":"Sentence"},{"id":"T6","span":{"begin":525,"end":575},"obj":"Sentence"},{"id":"T7","span":{"begin":576,"end":996},"obj":"Sentence"},{"id":"T8","span":{"begin":997,"end":1190},"obj":"Sentence"},{"id":"T9","span":{"begin":1191,"end":1265},"obj":"Sentence"},{"id":"T10","span":{"begin":1266,"end":1517},"obj":"Sentence"},{"id":"T11","span":{"begin":1518,"end":1730},"obj":"Sentence"},{"id":"T12","span":{"begin":1731,"end":1818},"obj":"Sentence"},{"id":"T13","span":{"begin":1819,"end":2063},"obj":"Sentence"}],"text":"MAOHUZI6/ETHYLENE INSENSITIVE3-LIKE1 and ETHYLENE INSENSITIVE3-LIKE2 Regulate Ethylene Response of Roots and Coleoptiles and Negatively Affect Salt Tolerance in Rice.\nEthylene plays important roles in plant growth, development, and stress responses. The ethylene signaling pathway has been studied extensively, mainly in Arabidopsis (Arabidopsis thaliana). However, the molecular mechanism of ethylene signaling is largely unknown in rice (Oryza sativa). Previously, we have isolated a set of rice ethylene-response mutants. Here, we characterized the mutant maohuzi6 (mhz6). Through map-based cloning, we found that MHZ6 encodes ETHYLENE INSENSITIVE3-LIKE1 (OsEIL1), a rice homolog of ETHYLENE INSENSITIVE3 (EIN3), which is the master transcriptional regulator of ethylene signaling in Arabidopsis. Disruption of MHZ6/OsEIL1 caused ethylene insensitivity mainly in roots, whereas silencing of the closely related OsEIL2 led to ethylene insensitivity mainly in coleoptiles of etiolated seedlings. This organ-specific functional divergence is different from the functional features of EIN3 and EIL1, both of which mediate the incomplete ethylene responses of Arabidopsis etiolated seedlings. In Arabidopsis, EIN3 and EIL1 play positive roles in plant salt tolerance. In rice, however, lack of MHZ6/OsEIL1 or OsEIL2 functions improves salt tolerance, whereas the overexpressing lines exhibit salt hypersensitivity at the seedling stage, indicating that MHZ6/OsEIL1 and OsEIL2 negatively regulate salt tolerance in rice. Furthermore, this negative regulation by MHZ6/OsEIL1 and OsEIL2 in salt tolerance is likely attributable in part to the direct regulation of HIGH-AFFINITY K(+) TRANSPORTER2;1 expression and Na(+) uptake in roots. Additionally, MHZ6/OsEIL1 overexpression promotes grain size and thousand-grain weight. Together, our study provides insights for the functional diversification of MHZ6/OsEIL1 and OsEIL2 in ethylene response and finds a novel mode of ethylene-regulated salt stress response that could be helpful for engineering salt-tolerant crops."}