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. 2012 Jul 31;24(7):3135–3152. doi: 10.1105/tpc.112.101287

Figure 3.

Figure 3.

Expression of MOMT4 in Arabidopsis and Histochemical Analysis of Transgenic Plants.

(A) MOMT4 overexpression cassette driven by a bean Phe ammonia lyase promoter.

(B) RT-PCR analysis on the transgenes of MOMT4 and loss-function variant IEMT (E165R); both transgenes were expressed in the selected transgenic lines.

(C) Morphological phenotype of wild-type, control, and MOMT4 expression plants. WT, the wild type.

(D) UV autofluorescence of a stem section from the first node of a 10-week-old Arabidopsis control plant. if, interfascicular fiber; xy, xylem.

(E) UV autofluorescence of a stem section from the first node of a 10-week-old MOMT4-3 transgenic line.

(F) Phloroglucinol-HCl staining of a stem section from the second basal node of the control line, which indicates the total lignin in violet-red.

(G) Phloroglucinol-HCl staining of a stem section from the second basal node the MOMT4-3 transgenic line.

(H) Mӓule staining of a stem section from the second basal node of a control plant. The staining indicates syringyl lignin subunit in red.

(I) Mӓule staining of a stem section from the second basal node of a MOMT4-3 transgenic plant.

Bars = 50 µm