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. 2017 Nov 14;114(48):E10389–E10398. doi: 10.1073/pnas.1711408114

Fig. 1.

Fig. 1.

Effect of loss of Tango1 on cell, ER, and Golgi morphology. (AC) Bright field (BF) images of homozygous tango12L3443 mutant tracheal cells expressing GFP (btlFRT > GFP) allow the visualization of number of branches and the presence of air in terminal cells. Unlike control cells (A and A′), homozygous tango12L3443 cells are not air-filled (area surrounded by dotted line in B and B′). (C and C′) Expression of Tango1-GFP in mutant cells suppresses the air-filling defects and reestablishes near-normal number of branches (D). Control, n = 11; tango12L3443, n = 14; tango12L3443+Tango1-GFP, n = 11. Bars represent mean ± SEM. Significance was determined using two-tailed t test. (EH) Airyscan microscopy images of control (E and G) and tango1 knockdown cells (F and H), stained for Tango1 (EF) and Sec16 (E′F′) and for ERGIC53-GFP (GH; fTRG library, expressed at endogenous levels) and Sec16 (G′H′). Insets in EH are magnifications of representative regions, indicated by the white squares. (Scale bars: AC, 40 μm; EH, 5 μm; Insets, 1 μm.)