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. 2017 May 30;114(24):E4877–E4883. doi: 10.1073/pnas.1617967114

Fig. 4.

Fig. 4.

Targeting of tonoplast proteins but not FERONIA the key plasma membrane receptor is interfered in synergids by AP1G loss of function. (A and B) CLSM of ProDD39:GFP-NRT2.7 in synergids of WT or ap1g1/+ g2. Pistils from ProDD39:GFP-NRT2.7 or ProDD39:GFP-NRT2.7;ap1g1/+ g2 plants were either emasculated at maturation for visualization (A) or emasculated and pollinated with ProLAT52:DsRed pollen and visualized at 8 HAP (B). Merges of GFP, RFP, and BF channels are shown at the right side in B. Dotted lines illustrate synergid cells. (C–F) CLSM of ProDD39:FER-YFP in synergids of WT (C and D) or ap1g1/+ g2 (E and F). Pistils from ProDD39:FER-YFP or ProDD39:FER-YFP;ap1g1/+ g2 plants were either emasculated at maturation for visualization (C and E) or emasculated and pollinated with ProLAT52:DsRed pollen and visualized at 8 HAP (D and F). Merges of GFP, RFP, and BFA channels are shown at the right side in D and F. Insets in C and E are their corresponding close-ups at the micropylar region. dPt, discharged pollen tube; Pt, pollen tube. (Scale bars: A and B, 10 µm; D and F and C and E, Inset, 25 µm.)