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. 2011 Jul 15;22(14):2458–2469. doi: 10.1091/mbc.E11-03-0205

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© 2011 Gutiérrez-Escribano et al. This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License (http://creativecommons.org/licenses/by-nc-sa/3.0).

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FIGURE 7: — mob24A hyphae activate cell separation. (A) Flocculation of JC613 and JC785 hyphal cultures after 5 h of serum induction. Cells from these cultures were recovered 3 h after induction and stained with calcofluor white (A, B). Arrowheads, separated hyphal compartments. (B) The graph on the right shows the expression of Ace2-target genes CHT3 and SCW11 measured by quantitative RT-PCR in the wild-type, mob24E, and mob24A strains normalized using ADE2. The data are means of two independent experiments, and the error bars indicate standard deviations. The results of pairwise t tests are shown above the brackets: ***p < 0.0001, **p = 0.0005, *p = 0.0054.