Correction to: Scientific Reports https://doi.org/10.1038/s41598-018-23187-8, published online 27 March 2018

This Article contains an error in the X axis of Figure 6g. The correct Figure 6 appears below as Figure 1.

Figure 1
figure 1

Increased actin polymerization in Cagpi19 null causes slower Ras1 dynamics. (a) Immunostaining of polymerized actin filaments using rhodamine-phalloidin in the wild type (WT) and the Cagpi19 null mutant. Scale bar corresponds to a distance of 5 μm. (b) Quantification of the F-actin levels in the Cagpi19 null relative to the wild type estimated through rhodamine-phalloidin staining. In each case 40 cells were taken for quantification. Students’ t-test was used to calculate the p value (***p value = 1.27 × 10−9). (c,d) Average fluorescence autocorrelation curves G(τ) and plot of amplitude versus diffusion times in individual cells after treating the Cagpi19 null with Cyto D. The data was collected for more than 25 cells in each case. (e) Colocalization of Ras1 with the polymerized F-actin in the Cagpi19 null and the wild type using anti-Ras1 and rhodamine-phalloidin. (f) Colocalization of Ras1 with the total β-actin in the Cagpi19 null and the wild type using anti-Ras1 and anti β-actin antibody. Scale bar corresponds to a distance of 5 μm. (g) Quantification of the extent of colocalization of Ras1 with F-actin/total actin using the Pearson’s correlation coefficient. A minimum of 40 cells were taken for quantification in each case. PM indicates plasma membrane. Scale bar corresponds to a distance of 5 μm. Students’ t-test was used to calculate the p value(***p value = 2.25 × 10−7 for PM; ***p value 3.98 × 10−7 for whole cell). (h) Figure showing a representation of the selection of ROI (region of interest) for calculating the Pearson’s correlation coefficient. The left panel shows the selection for calculating the correlation for the plasma membrane. Points all over the plasma membrane were selected for analysis. The right panel shows the selection of the area for calculating the correlation for the whole cell. ROI was selected such that the whole cell was considered for the analysis. Pearson’s correlation coefficient was then calculated using Fluo View software.