Adjustment of the PIF7‐HFR1 transcriptional module activity controls plant shade adaptation
Abstract Shade caused by the proximity of neighboring vegetation triggers a set of acclimation responses to either avoid or tolerate shade. Comparative analyses between the shade‐avoider Arabidopsis thaliana and the shade‐tolerant Cardamine hirsuta revealed a role for the atypical basic‐helix‐loop‐h...
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| Autor*in: |
Paulišić, Sandi [verfasserIn] Qin, Wenting [verfasserIn] Arora Verasztó, Harshul [verfasserIn] Then, Christiane [verfasserIn] Alary, Benjamin [verfasserIn] Nogue, Fabien [verfasserIn] Tsiantis, Miltos [verfasserIn] Hothorn, Michael [verfasserIn] Martínez‐García, Jaime F [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2020 |
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| Schlagwörter: |
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| Anmerkung: |
© The Author(s) 2020 |
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| Übergeordnetes Werk: |
Enthalten in: The EMBO Journal - Nature Publishing Group UK, 2023, 40(2020), 1 vom: 02. Dez. |
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| Übergeordnetes Werk: |
volume:40 ; year:2020 ; number:1 ; day:02 ; month:12 |
| Links: |
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| DOI / URN: |
10.15252/embj.2019104273 |
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| Katalog-ID: |
SPR058066292 |
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| 520 | |a Abstract Shade caused by the proximity of neighboring vegetation triggers a set of acclimation responses to either avoid or tolerate shade. Comparative analyses between the shade‐avoider Arabidopsis thaliana and the shade‐tolerant Cardamine hirsuta revealed a role for the atypical basic‐helix‐loop‐helix LONG HYPOCOTYL IN FR 1 (HFR1) in maintaining the shade tolerance in C. hirsuta, inhibiting hypocotyl elongation in shade and constraining expression profile of shade‐induced genes. We showed that C. hirsuta HFR1 protein is more stable than its A. thaliana counterpart, likely due to its lower binding affinity to CONSTITUTIVE PHOTOMORPHOGENIC 1 (COP1), contributing to enhance its biological activity. The enhanced HFR1 total activity is accompanied by an attenuated PHYTOCHROME INTERACTING FACTOR (PIF) activity in C. hirsuta. As a result, the PIF‐HFR1 module is differently balanced, causing a reduced PIF activity and attenuating other PIF‐mediated responses such as warm temperature‐induced hypocotyl elongation (thermomorphogenesis) and dark‐induced senescence. By this mechanism and that of the already‐known of phytochrome A photoreceptor, plants might ensure to properly adapt and thrive in habitats with disparate light amounts. | ||
| 520 | |a Synopsis Plant shade triggers distinct acclimation responses in neighboring vegetation. Here, comparison of shade‐avoiding Arabidopsis thaliana and shade‐tolerant Cardamine hirsuta reveals that enhanced repressor activity of the photomorphogenesis regulator HFR1 promotes shade tolerance in C. hirsuta via regulation of the transcription factor PIF7. HFR1 activity is enhanced and PIF7 activity attenuated in C. hirsuta compared to A. thaliana.Cardamine hirsuta HFR1 protein is more stable than its A. thaliana counterpart.Cardamine hirsuta HFR1 has lower binding affinity to COP1, which contributes to enhance its biological activity.Other PIF‐mediated growth responses, such as temperature‐induced hypocotyl elongation and dark‐induced senescence, are attenuated in C. hirsuta. | ||
| 520 | |a Graphical Abstract Modulation of the stability and COP1 interaction of the photomorphogenesis regulator HFR1 regulates shade tolerance differences in Arabidopsis and C. hirsuta seedlings. | ||
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| 700 | 1 | |a Then, Christiane |e verfasserin |0 (orcid)0000-0001-8867-7080 |4 aut | |
| 700 | 1 | |a Alary, Benjamin |e verfasserin |0 (orcid)0000-0002-7845-0058 |4 aut | |
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| 700 | 1 | |a Martínez‐García, Jaime F |e verfasserin |0 (orcid)0000-0003-1516-0341 |4 aut | |
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10.15252/embj.2019104273 doi (DE-627)SPR058066292 (SPR)embj.2019104273-e DE-627 ger DE-627 rakwb eng Paulišić, Sandi verfasserin (orcid)0000-0003-4696-5134 aut Adjustment of the PIF7‐HFR1 transcriptional module activity controls plant shade adaptation 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s) 2020 Abstract Shade caused by the proximity of neighboring vegetation triggers a set of acclimation responses to either avoid or tolerate shade. Comparative analyses between the shade‐avoider Arabidopsis thaliana and the shade‐tolerant Cardamine hirsuta revealed a role for the atypical basic‐helix‐loop‐helix LONG HYPOCOTYL IN FR 1 (HFR1) in maintaining the shade tolerance in C. hirsuta, inhibiting hypocotyl elongation in shade and constraining expression profile of shade‐induced genes. We showed that C. hirsuta HFR1 protein is more stable than its A. thaliana counterpart, likely due to its lower binding affinity to CONSTITUTIVE PHOTOMORPHOGENIC 1 (COP1), contributing to enhance its biological activity. The enhanced HFR1 total activity is accompanied by an attenuated PHYTOCHROME INTERACTING FACTOR (PIF) activity in C. hirsuta. As a result, the PIF‐HFR1 module is differently balanced, causing a reduced PIF activity and attenuating other PIF‐mediated responses such as warm temperature‐induced hypocotyl elongation (thermomorphogenesis) and dark‐induced senescence. By this mechanism and that of the already‐known of phytochrome A photoreceptor, plants might ensure to properly adapt and thrive in habitats with disparate light amounts. Synopsis Plant shade triggers distinct acclimation responses in neighboring vegetation. Here, comparison of shade‐avoiding Arabidopsis thaliana and shade‐tolerant Cardamine hirsuta reveals that enhanced repressor activity of the photomorphogenesis regulator HFR1 promotes shade tolerance in C. hirsuta via regulation of the transcription factor PIF7. HFR1 activity is enhanced and PIF7 activity attenuated in C. hirsuta compared to A. thaliana.Cardamine hirsuta HFR1 protein is more stable than its A. thaliana counterpart.Cardamine hirsuta HFR1 has lower binding affinity to COP1, which contributes to enhance its biological activity.Other PIF‐mediated growth responses, such as temperature‐induced hypocotyl elongation and dark‐induced senescence, are attenuated in C. hirsuta. Graphical Abstract Modulation of the stability and COP1 interaction of the photomorphogenesis regulator HFR1 regulates shade tolerance differences in Arabidopsis and C. hirsuta seedlings. HFR1 (dpeaa)DE-He213 PIFs (dpeaa)DE-He213 shade avoidance (dpeaa)DE-He213 shade tolerance (dpeaa)DE-He213 Qin, Wenting verfasserin (orcid)0000-0002-7221-2067 aut Arora Verasztó, Harshul verfasserin (orcid)0000-0002-0702-6022 aut Then, Christiane verfasserin (orcid)0000-0001-8867-7080 aut Alary, Benjamin verfasserin (orcid)0000-0002-7845-0058 aut Nogue, Fabien verfasserin (orcid)0000-0003-0619-4638 aut Tsiantis, Miltos verfasserin (orcid)0000-0001-7150-1855 aut Hothorn, Michael verfasserin (orcid)0000-0002-3597-5698 aut Martínez‐García, Jaime F verfasserin (orcid)0000-0003-1516-0341 aut Enthalten in The EMBO Journal Nature Publishing Group UK, 2023 40(2020), 1 vom: 02. Dez. (DE-627)266022529 (DE-600)1467419-1 1460-2075 nnns volume:40 year:2020 number:1 day:02 month:12 https://dx.doi.org/10.15252/embj.2019104273 X:SPRINGER Resolving-System lizenzpflichtig Volltext SYSFLAG_0 GBV_SPRINGER GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_72 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_168 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_211 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_252 GBV_ILN_266 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4029 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4116 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4155 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4311 GBV_ILN_4313 GBV_ILN_4314 GBV_ILN_4318 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4598 GBV_ILN_4700 AR 40 2020 1 02 12 |
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10.15252/embj.2019104273 doi (DE-627)SPR058066292 (SPR)embj.2019104273-e DE-627 ger DE-627 rakwb eng Paulišić, Sandi verfasserin (orcid)0000-0003-4696-5134 aut Adjustment of the PIF7‐HFR1 transcriptional module activity controls plant shade adaptation 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s) 2020 Abstract Shade caused by the proximity of neighboring vegetation triggers a set of acclimation responses to either avoid or tolerate shade. Comparative analyses between the shade‐avoider Arabidopsis thaliana and the shade‐tolerant Cardamine hirsuta revealed a role for the atypical basic‐helix‐loop‐helix LONG HYPOCOTYL IN FR 1 (HFR1) in maintaining the shade tolerance in C. hirsuta, inhibiting hypocotyl elongation in shade and constraining expression profile of shade‐induced genes. We showed that C. hirsuta HFR1 protein is more stable than its A. thaliana counterpart, likely due to its lower binding affinity to CONSTITUTIVE PHOTOMORPHOGENIC 1 (COP1), contributing to enhance its biological activity. The enhanced HFR1 total activity is accompanied by an attenuated PHYTOCHROME INTERACTING FACTOR (PIF) activity in C. hirsuta. As a result, the PIF‐HFR1 module is differently balanced, causing a reduced PIF activity and attenuating other PIF‐mediated responses such as warm temperature‐induced hypocotyl elongation (thermomorphogenesis) and dark‐induced senescence. By this mechanism and that of the already‐known of phytochrome A photoreceptor, plants might ensure to properly adapt and thrive in habitats with disparate light amounts. Synopsis Plant shade triggers distinct acclimation responses in neighboring vegetation. Here, comparison of shade‐avoiding Arabidopsis thaliana and shade‐tolerant Cardamine hirsuta reveals that enhanced repressor activity of the photomorphogenesis regulator HFR1 promotes shade tolerance in C. hirsuta via regulation of the transcription factor PIF7. HFR1 activity is enhanced and PIF7 activity attenuated in C. hirsuta compared to A. thaliana.Cardamine hirsuta HFR1 protein is more stable than its A. thaliana counterpart.Cardamine hirsuta HFR1 has lower binding affinity to COP1, which contributes to enhance its biological activity.Other PIF‐mediated growth responses, such as temperature‐induced hypocotyl elongation and dark‐induced senescence, are attenuated in C. hirsuta. Graphical Abstract Modulation of the stability and COP1 interaction of the photomorphogenesis regulator HFR1 regulates shade tolerance differences in Arabidopsis and C. hirsuta seedlings. HFR1 (dpeaa)DE-He213 PIFs (dpeaa)DE-He213 shade avoidance (dpeaa)DE-He213 shade tolerance (dpeaa)DE-He213 Qin, Wenting verfasserin (orcid)0000-0002-7221-2067 aut Arora Verasztó, Harshul verfasserin (orcid)0000-0002-0702-6022 aut Then, Christiane verfasserin (orcid)0000-0001-8867-7080 aut Alary, Benjamin verfasserin (orcid)0000-0002-7845-0058 aut Nogue, Fabien verfasserin (orcid)0000-0003-0619-4638 aut Tsiantis, Miltos verfasserin (orcid)0000-0001-7150-1855 aut Hothorn, Michael verfasserin (orcid)0000-0002-3597-5698 aut Martínez‐García, Jaime F verfasserin (orcid)0000-0003-1516-0341 aut Enthalten in The EMBO Journal Nature Publishing Group UK, 2023 40(2020), 1 vom: 02. Dez. (DE-627)266022529 (DE-600)1467419-1 1460-2075 nnns volume:40 year:2020 number:1 day:02 month:12 https://dx.doi.org/10.15252/embj.2019104273 X:SPRINGER Resolving-System lizenzpflichtig Volltext SYSFLAG_0 GBV_SPRINGER GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_72 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_168 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_211 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_252 GBV_ILN_266 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4029 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4116 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4155 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4311 GBV_ILN_4313 GBV_ILN_4314 GBV_ILN_4318 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4598 GBV_ILN_4700 AR 40 2020 1 02 12 |
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10.15252/embj.2019104273 doi (DE-627)SPR058066292 (SPR)embj.2019104273-e DE-627 ger DE-627 rakwb eng Paulišić, Sandi verfasserin (orcid)0000-0003-4696-5134 aut Adjustment of the PIF7‐HFR1 transcriptional module activity controls plant shade adaptation 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s) 2020 Abstract Shade caused by the proximity of neighboring vegetation triggers a set of acclimation responses to either avoid or tolerate shade. Comparative analyses between the shade‐avoider Arabidopsis thaliana and the shade‐tolerant Cardamine hirsuta revealed a role for the atypical basic‐helix‐loop‐helix LONG HYPOCOTYL IN FR 1 (HFR1) in maintaining the shade tolerance in C. hirsuta, inhibiting hypocotyl elongation in shade and constraining expression profile of shade‐induced genes. We showed that C. hirsuta HFR1 protein is more stable than its A. thaliana counterpart, likely due to its lower binding affinity to CONSTITUTIVE PHOTOMORPHOGENIC 1 (COP1), contributing to enhance its biological activity. The enhanced HFR1 total activity is accompanied by an attenuated PHYTOCHROME INTERACTING FACTOR (PIF) activity in C. hirsuta. As a result, the PIF‐HFR1 module is differently balanced, causing a reduced PIF activity and attenuating other PIF‐mediated responses such as warm temperature‐induced hypocotyl elongation (thermomorphogenesis) and dark‐induced senescence. By this mechanism and that of the already‐known of phytochrome A photoreceptor, plants might ensure to properly adapt and thrive in habitats with disparate light amounts. Synopsis Plant shade triggers distinct acclimation responses in neighboring vegetation. Here, comparison of shade‐avoiding Arabidopsis thaliana and shade‐tolerant Cardamine hirsuta reveals that enhanced repressor activity of the photomorphogenesis regulator HFR1 promotes shade tolerance in C. hirsuta via regulation of the transcription factor PIF7. HFR1 activity is enhanced and PIF7 activity attenuated in C. hirsuta compared to A. thaliana.Cardamine hirsuta HFR1 protein is more stable than its A. thaliana counterpart.Cardamine hirsuta HFR1 has lower binding affinity to COP1, which contributes to enhance its biological activity.Other PIF‐mediated growth responses, such as temperature‐induced hypocotyl elongation and dark‐induced senescence, are attenuated in C. hirsuta. Graphical Abstract Modulation of the stability and COP1 interaction of the photomorphogenesis regulator HFR1 regulates shade tolerance differences in Arabidopsis and C. hirsuta seedlings. HFR1 (dpeaa)DE-He213 PIFs (dpeaa)DE-He213 shade avoidance (dpeaa)DE-He213 shade tolerance (dpeaa)DE-He213 Qin, Wenting verfasserin (orcid)0000-0002-7221-2067 aut Arora Verasztó, Harshul verfasserin (orcid)0000-0002-0702-6022 aut Then, Christiane verfasserin (orcid)0000-0001-8867-7080 aut Alary, Benjamin verfasserin (orcid)0000-0002-7845-0058 aut Nogue, Fabien verfasserin (orcid)0000-0003-0619-4638 aut Tsiantis, Miltos verfasserin (orcid)0000-0001-7150-1855 aut Hothorn, Michael verfasserin (orcid)0000-0002-3597-5698 aut Martínez‐García, Jaime F verfasserin (orcid)0000-0003-1516-0341 aut Enthalten in The EMBO Journal Nature Publishing Group UK, 2023 40(2020), 1 vom: 02. Dez. (DE-627)266022529 (DE-600)1467419-1 1460-2075 nnns volume:40 year:2020 number:1 day:02 month:12 https://dx.doi.org/10.15252/embj.2019104273 X:SPRINGER Resolving-System lizenzpflichtig Volltext SYSFLAG_0 GBV_SPRINGER GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_72 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_168 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_211 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_252 GBV_ILN_266 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4029 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4116 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4155 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4311 GBV_ILN_4313 GBV_ILN_4314 GBV_ILN_4318 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4598 GBV_ILN_4700 AR 40 2020 1 02 12 |
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10.15252/embj.2019104273 doi (DE-627)SPR058066292 (SPR)embj.2019104273-e DE-627 ger DE-627 rakwb eng Paulišić, Sandi verfasserin (orcid)0000-0003-4696-5134 aut Adjustment of the PIF7‐HFR1 transcriptional module activity controls plant shade adaptation 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s) 2020 Abstract Shade caused by the proximity of neighboring vegetation triggers a set of acclimation responses to either avoid or tolerate shade. Comparative analyses between the shade‐avoider Arabidopsis thaliana and the shade‐tolerant Cardamine hirsuta revealed a role for the atypical basic‐helix‐loop‐helix LONG HYPOCOTYL IN FR 1 (HFR1) in maintaining the shade tolerance in C. hirsuta, inhibiting hypocotyl elongation in shade and constraining expression profile of shade‐induced genes. We showed that C. hirsuta HFR1 protein is more stable than its A. thaliana counterpart, likely due to its lower binding affinity to CONSTITUTIVE PHOTOMORPHOGENIC 1 (COP1), contributing to enhance its biological activity. The enhanced HFR1 total activity is accompanied by an attenuated PHYTOCHROME INTERACTING FACTOR (PIF) activity in C. hirsuta. As a result, the PIF‐HFR1 module is differently balanced, causing a reduced PIF activity and attenuating other PIF‐mediated responses such as warm temperature‐induced hypocotyl elongation (thermomorphogenesis) and dark‐induced senescence. By this mechanism and that of the already‐known of phytochrome A photoreceptor, plants might ensure to properly adapt and thrive in habitats with disparate light amounts. Synopsis Plant shade triggers distinct acclimation responses in neighboring vegetation. Here, comparison of shade‐avoiding Arabidopsis thaliana and shade‐tolerant Cardamine hirsuta reveals that enhanced repressor activity of the photomorphogenesis regulator HFR1 promotes shade tolerance in C. hirsuta via regulation of the transcription factor PIF7. HFR1 activity is enhanced and PIF7 activity attenuated in C. hirsuta compared to A. thaliana.Cardamine hirsuta HFR1 protein is more stable than its A. thaliana counterpart.Cardamine hirsuta HFR1 has lower binding affinity to COP1, which contributes to enhance its biological activity.Other PIF‐mediated growth responses, such as temperature‐induced hypocotyl elongation and dark‐induced senescence, are attenuated in C. hirsuta. Graphical Abstract Modulation of the stability and COP1 interaction of the photomorphogenesis regulator HFR1 regulates shade tolerance differences in Arabidopsis and C. hirsuta seedlings. HFR1 (dpeaa)DE-He213 PIFs (dpeaa)DE-He213 shade avoidance (dpeaa)DE-He213 shade tolerance (dpeaa)DE-He213 Qin, Wenting verfasserin (orcid)0000-0002-7221-2067 aut Arora Verasztó, Harshul verfasserin (orcid)0000-0002-0702-6022 aut Then, Christiane verfasserin (orcid)0000-0001-8867-7080 aut Alary, Benjamin verfasserin (orcid)0000-0002-7845-0058 aut Nogue, Fabien verfasserin (orcid)0000-0003-0619-4638 aut Tsiantis, Miltos verfasserin (orcid)0000-0001-7150-1855 aut Hothorn, Michael verfasserin (orcid)0000-0002-3597-5698 aut Martínez‐García, Jaime F verfasserin (orcid)0000-0003-1516-0341 aut Enthalten in The EMBO Journal Nature Publishing Group UK, 2023 40(2020), 1 vom: 02. Dez. (DE-627)266022529 (DE-600)1467419-1 1460-2075 nnns volume:40 year:2020 number:1 day:02 month:12 https://dx.doi.org/10.15252/embj.2019104273 X:SPRINGER Resolving-System lizenzpflichtig Volltext SYSFLAG_0 GBV_SPRINGER GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_72 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_168 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_211 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_252 GBV_ILN_266 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4029 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4116 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4155 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4311 GBV_ILN_4313 GBV_ILN_4314 GBV_ILN_4318 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4598 GBV_ILN_4700 AR 40 2020 1 02 12 |
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10.15252/embj.2019104273 doi (DE-627)SPR058066292 (SPR)embj.2019104273-e DE-627 ger DE-627 rakwb eng Paulišić, Sandi verfasserin (orcid)0000-0003-4696-5134 aut Adjustment of the PIF7‐HFR1 transcriptional module activity controls plant shade adaptation 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s) 2020 Abstract Shade caused by the proximity of neighboring vegetation triggers a set of acclimation responses to either avoid or tolerate shade. Comparative analyses between the shade‐avoider Arabidopsis thaliana and the shade‐tolerant Cardamine hirsuta revealed a role for the atypical basic‐helix‐loop‐helix LONG HYPOCOTYL IN FR 1 (HFR1) in maintaining the shade tolerance in C. hirsuta, inhibiting hypocotyl elongation in shade and constraining expression profile of shade‐induced genes. We showed that C. hirsuta HFR1 protein is more stable than its A. thaliana counterpart, likely due to its lower binding affinity to CONSTITUTIVE PHOTOMORPHOGENIC 1 (COP1), contributing to enhance its biological activity. The enhanced HFR1 total activity is accompanied by an attenuated PHYTOCHROME INTERACTING FACTOR (PIF) activity in C. hirsuta. As a result, the PIF‐HFR1 module is differently balanced, causing a reduced PIF activity and attenuating other PIF‐mediated responses such as warm temperature‐induced hypocotyl elongation (thermomorphogenesis) and dark‐induced senescence. By this mechanism and that of the already‐known of phytochrome A photoreceptor, plants might ensure to properly adapt and thrive in habitats with disparate light amounts. Synopsis Plant shade triggers distinct acclimation responses in neighboring vegetation. Here, comparison of shade‐avoiding Arabidopsis thaliana and shade‐tolerant Cardamine hirsuta reveals that enhanced repressor activity of the photomorphogenesis regulator HFR1 promotes shade tolerance in C. hirsuta via regulation of the transcription factor PIF7. HFR1 activity is enhanced and PIF7 activity attenuated in C. hirsuta compared to A. thaliana.Cardamine hirsuta HFR1 protein is more stable than its A. thaliana counterpart.Cardamine hirsuta HFR1 has lower binding affinity to COP1, which contributes to enhance its biological activity.Other PIF‐mediated growth responses, such as temperature‐induced hypocotyl elongation and dark‐induced senescence, are attenuated in C. hirsuta. Graphical Abstract Modulation of the stability and COP1 interaction of the photomorphogenesis regulator HFR1 regulates shade tolerance differences in Arabidopsis and C. hirsuta seedlings. HFR1 (dpeaa)DE-He213 PIFs (dpeaa)DE-He213 shade avoidance (dpeaa)DE-He213 shade tolerance (dpeaa)DE-He213 Qin, Wenting verfasserin (orcid)0000-0002-7221-2067 aut Arora Verasztó, Harshul verfasserin (orcid)0000-0002-0702-6022 aut Then, Christiane verfasserin (orcid)0000-0001-8867-7080 aut Alary, Benjamin verfasserin (orcid)0000-0002-7845-0058 aut Nogue, Fabien verfasserin (orcid)0000-0003-0619-4638 aut Tsiantis, Miltos verfasserin (orcid)0000-0001-7150-1855 aut Hothorn, Michael verfasserin (orcid)0000-0002-3597-5698 aut Martínez‐García, Jaime F verfasserin (orcid)0000-0003-1516-0341 aut Enthalten in The EMBO Journal Nature Publishing Group UK, 2023 40(2020), 1 vom: 02. Dez. (DE-627)266022529 (DE-600)1467419-1 1460-2075 nnns volume:40 year:2020 number:1 day:02 month:12 https://dx.doi.org/10.15252/embj.2019104273 X:SPRINGER Resolving-System lizenzpflichtig Volltext SYSFLAG_0 GBV_SPRINGER GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_72 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_168 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_211 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_252 GBV_ILN_266 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4029 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4116 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4155 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4311 GBV_ILN_4313 GBV_ILN_4314 GBV_ILN_4318 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4598 GBV_ILN_4700 AR 40 2020 1 02 12 |
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Paulišić, Sandi @@aut@@ Qin, Wenting @@aut@@ Arora Verasztó, Harshul @@aut@@ Then, Christiane @@aut@@ Alary, Benjamin @@aut@@ Nogue, Fabien @@aut@@ Tsiantis, Miltos @@aut@@ Hothorn, Michael @@aut@@ Martínez‐García, Jaime F @@aut@@ |
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<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000naa a22002652 4500</leader><controlfield tag="001">SPR058066292</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20241025065102.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">241025s2020 xx |||||o 00| ||eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.15252/embj.2019104273</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)SPR058066292</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(SPR)embj.2019104273-e</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Paulišić, Sandi</subfield><subfield code="e">verfasserin</subfield><subfield code="0">(orcid)0000-0003-4696-5134</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Adjustment of the PIF7‐HFR1 transcriptional module activity controls plant shade adaptation</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2020</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">Text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">Computermedien</subfield><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">Online-Ressource</subfield><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="500" ind1=" " ind2=" "><subfield code="a">© The Author(s) 2020</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Abstract Shade caused by the proximity of neighboring vegetation triggers a set of acclimation responses to either avoid or tolerate shade. Comparative analyses between the shade‐avoider Arabidopsis thaliana and the shade‐tolerant Cardamine hirsuta revealed a role for the atypical basic‐helix‐loop‐helix LONG HYPOCOTYL IN FR 1 (HFR1) in maintaining the shade tolerance in C. hirsuta, inhibiting hypocotyl elongation in shade and constraining expression profile of shade‐induced genes. We showed that C. hirsuta HFR1 protein is more stable than its A. thaliana counterpart, likely due to its lower binding affinity to CONSTITUTIVE PHOTOMORPHOGENIC 1 (COP1), contributing to enhance its biological activity. The enhanced HFR1 total activity is accompanied by an attenuated PHYTOCHROME INTERACTING FACTOR (PIF) activity in C. hirsuta. As a result, the PIF‐HFR1 module is differently balanced, causing a reduced PIF activity and attenuating other PIF‐mediated responses such as warm temperature‐induced hypocotyl elongation (thermomorphogenesis) and dark‐induced senescence. By this mechanism and that of the already‐known of phytochrome A photoreceptor, plants might ensure to properly adapt and thrive in habitats with disparate light amounts.</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Synopsis Plant shade triggers distinct acclimation responses in neighboring vegetation. Here, comparison of shade‐avoiding Arabidopsis thaliana and shade‐tolerant Cardamine hirsuta reveals that enhanced repressor activity of the photomorphogenesis regulator HFR1 promotes shade tolerance in C. hirsuta via regulation of the transcription factor PIF7. HFR1 activity is enhanced and PIF7 activity attenuated in C. hirsuta compared to A. thaliana.Cardamine hirsuta HFR1 protein is more stable than its A. thaliana counterpart.Cardamine hirsuta HFR1 has lower binding affinity to COP1, which contributes to enhance its biological activity.Other PIF‐mediated growth responses, such as temperature‐induced hypocotyl elongation and dark‐induced senescence, are attenuated in C. hirsuta.</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Graphical Abstract Modulation of the stability and COP1 interaction of the photomorphogenesis regulator HFR1 regulates shade tolerance differences in Arabidopsis and C. hirsuta seedlings.</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">HFR1</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">PIFs</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">shade avoidance</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">shade tolerance</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Qin, Wenting</subfield><subfield code="e">verfasserin</subfield><subfield code="0">(orcid)0000-0002-7221-2067</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Arora Verasztó, Harshul</subfield><subfield code="e">verfasserin</subfield><subfield code="0">(orcid)0000-0002-0702-6022</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Then, Christiane</subfield><subfield code="e">verfasserin</subfield><subfield code="0">(orcid)0000-0001-8867-7080</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Alary, Benjamin</subfield><subfield code="e">verfasserin</subfield><subfield code="0">(orcid)0000-0002-7845-0058</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Nogue, Fabien</subfield><subfield code="e">verfasserin</subfield><subfield code="0">(orcid)0000-0003-0619-4638</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Tsiantis, Miltos</subfield><subfield code="e">verfasserin</subfield><subfield code="0">(orcid)0000-0001-7150-1855</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Hothorn, Michael</subfield><subfield code="e">verfasserin</subfield><subfield code="0">(orcid)0000-0002-3597-5698</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Martínez‐García, Jaime F</subfield><subfield code="e">verfasserin</subfield><subfield code="0">(orcid)0000-0003-1516-0341</subfield><subfield code="4">aut</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">Enthalten in</subfield><subfield code="t">The EMBO Journal</subfield><subfield code="d">Nature Publishing Group UK, 2023</subfield><subfield code="g">40(2020), 1 vom: 02. 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Paulišić, Sandi |
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Paulišić, Sandi misc HFR1 misc PIFs misc shade avoidance misc shade tolerance Adjustment of the PIF7‐HFR1 transcriptional module activity controls plant shade adaptation |
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Adjustment of the PIF7‐HFR1 transcriptional module activity controls plant shade adaptation HFR1 (dpeaa)DE-He213 PIFs (dpeaa)DE-He213 shade avoidance (dpeaa)DE-He213 shade tolerance (dpeaa)DE-He213 |
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Paulišić, Sandi Qin, Wenting Arora Verasztó, Harshul Then, Christiane Alary, Benjamin Nogue, Fabien Tsiantis, Miltos Hothorn, Michael Martínez‐García, Jaime F |
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Elektronische Aufsätze |
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Paulišić, Sandi |
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10.15252/embj.2019104273 |
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adjustment of the pif7‐hfr1 transcriptional module activity controls plant shade adaptation |
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Adjustment of the PIF7‐HFR1 transcriptional module activity controls plant shade adaptation |
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Abstract Shade caused by the proximity of neighboring vegetation triggers a set of acclimation responses to either avoid or tolerate shade. Comparative analyses between the shade‐avoider Arabidopsis thaliana and the shade‐tolerant Cardamine hirsuta revealed a role for the atypical basic‐helix‐loop‐helix LONG HYPOCOTYL IN FR 1 (HFR1) in maintaining the shade tolerance in C. hirsuta, inhibiting hypocotyl elongation in shade and constraining expression profile of shade‐induced genes. We showed that C. hirsuta HFR1 protein is more stable than its A. thaliana counterpart, likely due to its lower binding affinity to CONSTITUTIVE PHOTOMORPHOGENIC 1 (COP1), contributing to enhance its biological activity. The enhanced HFR1 total activity is accompanied by an attenuated PHYTOCHROME INTERACTING FACTOR (PIF) activity in C. hirsuta. As a result, the PIF‐HFR1 module is differently balanced, causing a reduced PIF activity and attenuating other PIF‐mediated responses such as warm temperature‐induced hypocotyl elongation (thermomorphogenesis) and dark‐induced senescence. By this mechanism and that of the already‐known of phytochrome A photoreceptor, plants might ensure to properly adapt and thrive in habitats with disparate light amounts. Synopsis Plant shade triggers distinct acclimation responses in neighboring vegetation. Here, comparison of shade‐avoiding Arabidopsis thaliana and shade‐tolerant Cardamine hirsuta reveals that enhanced repressor activity of the photomorphogenesis regulator HFR1 promotes shade tolerance in C. hirsuta via regulation of the transcription factor PIF7. HFR1 activity is enhanced and PIF7 activity attenuated in C. hirsuta compared to A. thaliana.Cardamine hirsuta HFR1 protein is more stable than its A. thaliana counterpart.Cardamine hirsuta HFR1 has lower binding affinity to COP1, which contributes to enhance its biological activity.Other PIF‐mediated growth responses, such as temperature‐induced hypocotyl elongation and dark‐induced senescence, are attenuated in C. hirsuta. Graphical Abstract Modulation of the stability and COP1 interaction of the photomorphogenesis regulator HFR1 regulates shade tolerance differences in Arabidopsis and C. hirsuta seedlings. © The Author(s) 2020 |
| abstractGer |
Abstract Shade caused by the proximity of neighboring vegetation triggers a set of acclimation responses to either avoid or tolerate shade. Comparative analyses between the shade‐avoider Arabidopsis thaliana and the shade‐tolerant Cardamine hirsuta revealed a role for the atypical basic‐helix‐loop‐helix LONG HYPOCOTYL IN FR 1 (HFR1) in maintaining the shade tolerance in C. hirsuta, inhibiting hypocotyl elongation in shade and constraining expression profile of shade‐induced genes. We showed that C. hirsuta HFR1 protein is more stable than its A. thaliana counterpart, likely due to its lower binding affinity to CONSTITUTIVE PHOTOMORPHOGENIC 1 (COP1), contributing to enhance its biological activity. The enhanced HFR1 total activity is accompanied by an attenuated PHYTOCHROME INTERACTING FACTOR (PIF) activity in C. hirsuta. As a result, the PIF‐HFR1 module is differently balanced, causing a reduced PIF activity and attenuating other PIF‐mediated responses such as warm temperature‐induced hypocotyl elongation (thermomorphogenesis) and dark‐induced senescence. By this mechanism and that of the already‐known of phytochrome A photoreceptor, plants might ensure to properly adapt and thrive in habitats with disparate light amounts. Synopsis Plant shade triggers distinct acclimation responses in neighboring vegetation. Here, comparison of shade‐avoiding Arabidopsis thaliana and shade‐tolerant Cardamine hirsuta reveals that enhanced repressor activity of the photomorphogenesis regulator HFR1 promotes shade tolerance in C. hirsuta via regulation of the transcription factor PIF7. HFR1 activity is enhanced and PIF7 activity attenuated in C. hirsuta compared to A. thaliana.Cardamine hirsuta HFR1 protein is more stable than its A. thaliana counterpart.Cardamine hirsuta HFR1 has lower binding affinity to COP1, which contributes to enhance its biological activity.Other PIF‐mediated growth responses, such as temperature‐induced hypocotyl elongation and dark‐induced senescence, are attenuated in C. hirsuta. Graphical Abstract Modulation of the stability and COP1 interaction of the photomorphogenesis regulator HFR1 regulates shade tolerance differences in Arabidopsis and C. hirsuta seedlings. © The Author(s) 2020 |
| abstract_unstemmed |
Abstract Shade caused by the proximity of neighboring vegetation triggers a set of acclimation responses to either avoid or tolerate shade. Comparative analyses between the shade‐avoider Arabidopsis thaliana and the shade‐tolerant Cardamine hirsuta revealed a role for the atypical basic‐helix‐loop‐helix LONG HYPOCOTYL IN FR 1 (HFR1) in maintaining the shade tolerance in C. hirsuta, inhibiting hypocotyl elongation in shade and constraining expression profile of shade‐induced genes. We showed that C. hirsuta HFR1 protein is more stable than its A. thaliana counterpart, likely due to its lower binding affinity to CONSTITUTIVE PHOTOMORPHOGENIC 1 (COP1), contributing to enhance its biological activity. The enhanced HFR1 total activity is accompanied by an attenuated PHYTOCHROME INTERACTING FACTOR (PIF) activity in C. hirsuta. As a result, the PIF‐HFR1 module is differently balanced, causing a reduced PIF activity and attenuating other PIF‐mediated responses such as warm temperature‐induced hypocotyl elongation (thermomorphogenesis) and dark‐induced senescence. By this mechanism and that of the already‐known of phytochrome A photoreceptor, plants might ensure to properly adapt and thrive in habitats with disparate light amounts. Synopsis Plant shade triggers distinct acclimation responses in neighboring vegetation. Here, comparison of shade‐avoiding Arabidopsis thaliana and shade‐tolerant Cardamine hirsuta reveals that enhanced repressor activity of the photomorphogenesis regulator HFR1 promotes shade tolerance in C. hirsuta via regulation of the transcription factor PIF7. HFR1 activity is enhanced and PIF7 activity attenuated in C. hirsuta compared to A. thaliana.Cardamine hirsuta HFR1 protein is more stable than its A. thaliana counterpart.Cardamine hirsuta HFR1 has lower binding affinity to COP1, which contributes to enhance its biological activity.Other PIF‐mediated growth responses, such as temperature‐induced hypocotyl elongation and dark‐induced senescence, are attenuated in C. hirsuta. Graphical Abstract Modulation of the stability and COP1 interaction of the photomorphogenesis regulator HFR1 regulates shade tolerance differences in Arabidopsis and C. hirsuta seedlings. © The Author(s) 2020 |
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| score |
7.4006968 |