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Short Communication

Light-dependent destabilization of PHL in Arabidopsis

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Article: e28118 | Received 28 Jan 2014, Accepted 05 Feb 2014, Published online: 10 Mar 2014

Figures & data

Figure 1. Flowering phenotype and protein stabilization of 35S::PHL-YFP. (A, B) Plants were grown under 16h light/8h dark long day and 8h light/16h dark short day conditions at 22 °C. Mean ± SD (n ≥ 12). (C) 35S::PHL-YFP were grown under continuous white light (cW), continuous dark (cD) for 7 d. Seedlings grown under cD were then exposed to white light for 1 to 24 h (cD + cW). YFP fluorescence was observed under a laser scanning confocal microscope. Bar = 50 µm

Figure 1. Flowering phenotype and protein stabilization of 35S::PHL-YFP. (A, B) Plants were grown under 16h light/8h dark long day and 8h light/16h dark short day conditions at 22 °C. Mean ± SD (n ≥ 12). (C) 35S::PHL-YFP were grown under continuous white light (cW), continuous dark (cD) for 7 d. Seedlings grown under cD were then exposed to white light for 1 to 24 h (cD + cW). YFP fluorescence was observed under a laser scanning confocal microscope. Bar = 50 µm

Figure 2. PHL-GUS stabilization under light and dark conditions. Ten-day-old PHLpro::PHL-GUS phl-1 plants grown under continuous white light (cW) and continuous dark (cD) (A) and 1 to 24h exposure of white light to the cD grown seedlings (B). Bar=1 mm

Figure 2. PHL-GUS stabilization under light and dark conditions. Ten-day-old PHLpro::PHL-GUS phl-1 plants grown under continuous white light (cW) and continuous dark (cD) (A) and 1 to 24h exposure of white light to the cD grown seedlings (B). Bar=1 mm

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