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. 2009 Feb;21(2):494–506. doi: 10.1105/tpc.108.061259

Figure 3.

Figure 3.

Role of phyA in the Phosphorylation of GFP-FHY1 and Endogenous FHY1.

(A) to (D) Immunoblot analysis of proteins extracted from seedlings grown for 3 d in darkness and then transferred to red light for the time periods indicated in minutes (m). Seedlings tested were as follows: 35S:GFP-FHY1 and 35S:GFP-FHY1/phyA-1 (A), wild type and phyA-1 (B), 35S:GFP-FHY1/phyB-1 and 35S:GFP-FHY1/cry1 (C), and phyB-1, phyBDE, and cry1 cry2 (D).

(E) Three-day-old dark-grown wild type, phyA-1, and cry1cry2 seedlings were transferred to blue light (B) for the time periods indicated.

In (A) to (E), immunoblots were probed with anti-FHY1 antibody. Asterisks indicate slower migrating phosphorylated forms of GFP-FHY1 and FHY1.