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The promoter activity of Hd3a was detected in transgenic plants expressing β-glucuronidase (GUS) under the control of the Hd3a promoter in the vascular cells of leaf blades.
The cells of leaf pieces treated with 3 mM HCl solution died 4.02 ± 1.02 h following treatment.
GL2 is normally expressed in developing trichomes and surrounding epidermal cells of leaf primordia, but is also detected in the petiole and mid-vein of developing leaves.
The localization of TaSUT2 transcripts in the mesophyll cells of leaf blade might imply their significance in regulating intracellular sucrose partitioning within these cells of a leaf tissue.
Recently it has been shown that simultaneous depletion of myosins XI-1, XI-2 and XI-K caused defects in organization of actin filaments in root hairs and in the cells of leaf midvein epidermis [ 22].
We investigated patterns of expression of cDNA for green fluorescent protein (GFP) under the control of the FIL promoter (the cDNA was designated FILp GFP), which is expressed in abaxial cells of leaf primordia (Watanabe and Okada, 2003).
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Increasing in the presence of large clusters of cells on leaf surfaces was demonstrated after 4 and 24 h.
The relative size of the terminal cell of leaf petioles glandular hairs, in particular, is the best criterion to differentiate the populations of the three provenances.
The closer analysis of the narrow leaf phenotypes suggested a role in cell polarity of leaf cells, such that the length of individual cells was increased and the width reduced [ 15, 20].
Mature adaxial leaf epidermal cells of crinkly leaf and Hedou 12 were analyzed by scanning electron microscopy.
On the other hand, another study demonstrated that at least one Class II gene (i.e., AtTPS6) involved in the regulation of cell shape and plant architecture was able to rescue the yeast Tsp1 mutant phenotype, suggesting that "AtTPS6 gene may be unique among class II AtTPS genes in affecting the cell shape of leaf pavement cells" [37].
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