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. 2012 Oct 9;24(10):3967–3981. doi: 10.1105/tpc.112.103044

Figure 1.

Figure 1.

Distribution of Cytokinin and Cytokinin Response in Roots.

(A) Quantification of cytokinin levels in the zones of LRP initiation zone, formation, and emergence. Error bars denote se (*P < 0.05; Student’s t test; n = 3).

(B) to (F) TCS:GFP expression in 8-d-old untreated roots detected in the root cap, but not in the root meristem, basal meristem, and developmental window (B); in the individual xylem pole pericycle cells between developing young primordia (C); in the provasculature tissue in emerging LRPs (D); in the endodermal cells adjacent to early-stage LRPs (E); and continuously in the endodermis of the emerging primordium zone (F).

(G) to (J) TCS:GFP expression in 8-d-old roots treated for 16 h with 10 μM benzyl adenine induced in the provasculature of the root, but not basal, meristem (G) and in all tissues of the differentiation zone ([G] and [H]), including primordia at all developmental stages ([I] and [J]).

Plasma membranes were visualized by propidium iodide staining. c, cortex; cc, central cylinder; cZ, cis-zeatin; cZ9G, cis-zeatin-9-glucoside; cZR, cis-zeatin riboside; DHZ, dihydrozeatin; DHZ9G, dihydrozeatin-9-glucoside; DHZR, dihydrozeatin riboside; en, endodermis; ep, epidermis; iP, isopentenyladenine; iP9G; isopentenyladenine-9-glucoside; iPR, isopentenyl adenosine; p, pericycle; tZ, trans-zeatin; tZ9G, trans-zeatin-9-glucoside; tZR, trans-zeatin riboside. White asterisks indicate borders of LRPs. Bars = 50 μm.