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. 2009 Mar;21(3):701–718. doi: 10.1105/tpc.108.061960

Figure 7.

Figure 7.

Defects in Cell Division and Expansion in the Vegetative Actin Double Mutants.

(A) to (H) Scanning electron micrographs of leaf epidermis (adaxial) of the wild type ([A] and [B]) and act2-1 act8-2 ([C] and [D]), act2-1 act7-4 ([E] and [F]), and act8-2 act7-4 ([G] and [H]) double mutants. Pavement cells indicated with dotted lines in the top row ([A], [C], [E], and [G]) are marked along their edges and shown in the second row ([B], [D], [F], and [H]). The numbers on the top of images in the second row indicate the average number of lobes ± sd, calculated from 30 representative cells for each sample.

(I) Cell surface area. Vertical bars represent sd (n = 30).

(J) Rosette leaves.

(K) to (N) Leaf trichomes.

(O) to (R) Organization of cells in 4',6-diamidino-2-phenylindole–stained root apices of 10-d-old seedlings. The brackets indicate the zone of elongation.

(S) and (T) Light micrographs of longitudinal sections of wild-type (S) and act2-1 act7-4 double mutant (T) hypocotyls.

(U) to (W) Inflorescences. Single flower insets are shown at the top of each panel.

(X) Mature siliques of the wild type (top) and the act2-1 act7-4 double mutant (bottom).

Bars = 50 μm in (A), (C), (E), (G), and (O) to (R) and 100 μm in (K) to (N), (S), and (T).