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. 2023 Jan 12;13:1085918. doi: 10.3389/fmicb.2022.1085918

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Copyright © 2023 Habibi Arejan, Ensinck, Diacovich, Patel, Quintanilla, Emami Saleh, Gramajo and Boutte.

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

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Wag31 mutant proteins localize normally in merodiploid strains. (A) Micrographs of WT Msmeg expressing Wag31-GFPmut3 constructs with the indicated mutations. Top: HADA; second: GFP; third: merged; bottom: phase. The scale bar is 5 microns, and it applies to all images. (B) Relative polar intensity of GFPmut3 signal from cells in A. (C) Ratio of normalized signal at the old pole over normalized signal at the new pole, from B. (D) Relative septal intensity of GFPmut3 signal from cells in A. ns, p > 0.05, *p = <0.05, **p = <0.005, ***p = <0.0005, ****p = <0.0001. All p-values (B), (C) were calculated by one-way ANOVA, Dunnett’s multiple comparisons test and the p-values (D) were calculated by the Welch’s t-test.