Repression of shade - avoidance reactions by sunfleck induction of HY5 expression in Arabidopsis
The light environment provides signals that play a critical role in the control of stem growth in plants. The reduced irradiance and altered spectral composition of shade light promote stem growth compared with unfiltered sunlight. However, whereas most studies have used seedlings exposed to contras...
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| Lenguaje: | Inglés |
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| Acceso en línea: | http://ri.agro.uba.ar/files/intranet/articulo/2011Sellaro.pdf LINK AL EDITOR |
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| 100 | 1 | |9 67310 |a Sellaro, Romina | |
| 245 | 0 | 0 | |a Repression of shade - avoidance reactions by sunfleck induction of HY5 expression in Arabidopsis |
| 520 | |a The light environment provides signals that play a critical role in the control of stem growth in plants. The reduced irradiance and altered spectral composition of shade light promote stem growth compared with unfiltered sunlight. However, whereas most studies have used seedlings exposed to contrasting but constant light treatments, the natural light environment may exhibit strong fluctuations. As a result of gaps in the canopy, plants shaded by neighbours may experience sunflecks, i.e. brief periods of exposure to unfiltered sunlight. Here, we show that sunflecks are perceived by phytochromes A and B, and inhibit hypocotyl growth in Arabidopsis thaliana mainly if they occur during the final portion of the photoperiod. By using forward and reverse genetic approaches we found that ELONGATED HYPOCOTYL 5, LATE ELONGATED HYPOCOTYL, PHYTOCHROME KINASE SUBSTRATE 4 and auxin signalling are key players in this response. | ||
| 653 | 0 | |a ARABIDOPSIS | |
| 653 | 0 | |a AUXIN | |
| 653 | 0 | |a HY5 | |
| 653 | 0 | |a HYPOCOTYL | |
| 653 | 0 | |a PHYTOCHROME | |
| 653 | 0 | |a SHADE AVOIDANCE | |
| 653 | 0 | |a BIOLOGY | |
| 653 | 0 | |a PLANTS [BOTANY] | |
| 653 | 0 | |a ARABIDOPSIS PROTEIN | |
| 653 | 0 | |a BASIC LEUCINE ZIPPER TRANSCRIPTION FACTOR | |
| 653 | 0 | |a NUCLEAR PROTEIN | |
| 653 | 0 | |a PHYA PROTEIN, ARABIDOPSIS | |
| 653 | 0 | |a PHYB PROTEIN, ARABIDOPSIS | |
| 653 | 0 | |a PHYTOCHROME A | |
| 653 | 0 | |a PHYTOCHROME B | |
| 653 | 0 | |a PKS4 PROTEIN, ARABIDOPSIS | |
| 653 | 0 | |a PROTEIN SERINE THREONINE KINASE | |
| 653 | 0 | |a REPRESSOR PROTEIN | |
| 653 | 0 | |a CIRCADIAN RHYTHM | |
| 653 | 0 | |a GENE EXPRESSION PROFILING | |
| 653 | 0 | |a GENE EXPRESSION REGULATION | |
| 653 | 0 | |a GENETICS | |
| 653 | 0 | |a GROWTH, DEVELOPMENT AND AGING | |
| 653 | 0 | |a METABOLISM | |
| 653 | 0 | |a MOLECULAR CLONING | |
| 653 | 0 | |a PHOTOPERIODICITY | |
| 653 | 0 | |a PLANT GENE | |
| 653 | 0 | |a PLANT GROWTH | |
| 653 | 0 | |a PLANT STEM | |
| 653 | 0 | |a RADIATION EXPOSURE | |
| 653 | 0 | |a SUNLIGHT | |
| 653 | 0 | |a BASIC-LEUCINE ZIPPER TRANSCRIPTION FACTORS | |
| 653 | 0 | |a CIRCADIAN CLOCKS | |
| 653 | 0 | |a CLONING, MOLECULAR | |
| 653 | 0 | |a GENE EXPRESSION PROFILING | |
| 653 | 0 | |a GENE EXPRESSION REGULATION, PLANT | |
| 653 | 0 | |a GENES, PLANT | |
| 653 | 0 | |a NUCLEAR PROTEINS | |
| 653 | 0 | |a PHOTOPERIOD | |
| 653 | 0 | |a PLANT STEMS | |
| 653 | 0 | |a PROTEIN-SERINE-THREONINE KINASES | |
| 653 | 0 | |a REPRESSOR PROTEINS | |
| 653 | 0 | |a TIME FACTORS | |
| 653 | 0 | |a ARABIDOPSIS THALIANA | |
| 700 | 1 | |9 11465 |a Yanovsky, Marcelo J. | |
| 700 | 1 | |9 792 |a Casal, Jorge José | |
| 773 | |t The Plant Journal |g Vol.68, no.5 (2011), p.919-928 | ||
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| 900 | |a ^tRepression of shade-avoidance reactions by sunfleck induction of HY5 expression in Arabidopsis | ||
| 900 | |a ^aSellaro^bR. | ||
| 900 | |a ^aYanovsky^bM.J. | ||
| 900 | |a ^aCasal^bJ.J. | ||
| 900 | |a ^aSellaro^bR. | ||
| 900 | |a ^aYanovsky^bM. J. | ||
| 900 | |a ^aCasal^bJ. J. | ||
| 900 | |a ^aSellaro, R.^tIFEVA, Facultad de Agronomía, Universidad de Buenos Aires, 1417 Buenos Aires, Argentina | ||
| 900 | |a ^aYanovsky, M.J.^tFundacion Instituto Leloir, IIBBA, CONICET, Buenos Aires, Argentina | ||
| 900 | |a ^aCasal, J.J.^t | ||
| 900 | |a ^tThe Plant Journal^cPlant J. | ||
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| 900 | |a Vol. 68, no. 5 | ||
| 900 | |a 928 | ||
| 900 | |a ARABIDOPSIS | ||
| 900 | |a AUXIN | ||
| 900 | |a HY5 | ||
| 900 | |a HYPOCOTYL | ||
| 900 | |a PHYTOCHROME | ||
| 900 | |a SHADE AVOIDANCE | ||
| 900 | |a BIOLOGY | ||
| 900 | |a PLANTS [BOTANY] | ||
| 900 | |a ARABIDOPSIS PROTEIN | ||
| 900 | |a BASIC LEUCINE ZIPPER TRANSCRIPTION FACTOR | ||
| 900 | |a NUCLEAR PROTEIN | ||
| 900 | |a PHYA PROTEIN, ARABIDOPSIS | ||
| 900 | |a PHYB PROTEIN, ARABIDOPSIS | ||
| 900 | |a PHYTOCHROME A | ||
| 900 | |a PHYTOCHROME B | ||
| 900 | |a PKS4 PROTEIN, ARABIDOPSIS | ||
| 900 | |a PROTEIN SERINE THREONINE KINASE | ||
| 900 | |a REPRESSOR PROTEIN | ||
| 900 | |a CIRCADIAN RHYTHM | ||
| 900 | |a GENE EXPRESSION PROFILING | ||
| 900 | |a GENE EXPRESSION REGULATION | ||
| 900 | |a GENETICS | ||
| 900 | |a GROWTH, DEVELOPMENT AND AGING | ||
| 900 | |a METABOLISM | ||
| 900 | |a MOLECULAR CLONING | ||
| 900 | |a PHOTOPERIODICITY | ||
| 900 | |a PLANT GENE | ||
| 900 | |a PLANT GROWTH | ||
| 900 | |a PLANT STEM | ||
| 900 | |a RADIATION EXPOSURE | ||
| 900 | |a SUNLIGHT | ||
| 900 | |a BASIC-LEUCINE ZIPPER TRANSCRIPTION FACTORS | ||
| 900 | |a CIRCADIAN CLOCKS | ||
| 900 | |a CLONING, MOLECULAR | ||
| 900 | |a GENE EXPRESSION PROFILING | ||
| 900 | |a GENE EXPRESSION REGULATION, PLANT | ||
| 900 | |a GENES, PLANT | ||
| 900 | |a NUCLEAR PROTEINS | ||
| 900 | |a PHOTOPERIOD | ||
| 900 | |a PLANT STEMS | ||
| 900 | |a PROTEIN-SERINE-THREONINE KINASES | ||
| 900 | |a REPRESSOR PROTEINS | ||
| 900 | |a TIME FACTORS | ||
| 900 | |a ARABIDOPSIS THALIANA | ||
| 900 | |a The light environment provides signals that play a critical role in the control of stem growth in plants. The reduced irradiance and altered spectral composition of shade light promote stem growth compared with unfiltered sunlight. However, whereas most studies have used seedlings exposed to contrasting but constant light treatments, the natural light environment may exhibit strong fluctuations. As a result of gaps in the canopy, plants shaded by neighbours may experience sunflecks, i.e. brief periods of exposure to unfiltered sunlight. Here, we show that sunflecks are perceived by phytochromes A and B, and inhibit hypocotyl growth in Arabidopsis thaliana mainly if they occur during the final portion of the photoperiod. By using forward and reverse genetic approaches we found that ELONGATED HYPOCOTYL 5, LATE ELONGATED HYPOCOTYL, PHYTOCHROME KINASE SUBSTRATE 4 and auxin signalling are key players in this response. | ||
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