Skip to main content
. 2022 Jul 21;221(9):e202205058. doi: 10.1083/jcb.202205058

Figure 4.

Figure 4.

Ana2’s change in diffusion rate does not appear to depend on the CC or STAN domain, but this change is perturbed if Ana2 cannot be phosphorylated by Cdk/Cyclins. (A) Schematic illustration of the Ana2 protein and the deletion/mutant forms analyzed in this study: central coiled-coil (CC) domain (aa195-229); STil/ANa2 (STAN) domain (aa316-383); the 12 S/T residues in S/T-P motifs that were mutated to Alanine. (B and C) Graphs show cytoplasmic FCS diffusion measurements (mean ± SEM) in embryos laid by females of the following genotypes: B (i) eAna2-mNG/+; B (ii) eAna2(∆CC)-mNG/+; B (iii) eAna2(∆STAN)-mNG; C (i) eAna2-mNG; C (ii) eAna2(12A)-mNG. Measurements were taken every 2 min from the start of nuclear cycle 12. The timing window of NEB is depicted in red and mitosis in blue. Each data point represents the average of 4–6× 10-s recordings from an individual embryo (N ≥ 13). Statistical significance was assessed using a paired one-way ANOVA test (for Gaussian-distributed data) or a Friedman test (****, P < 0.0001; **, P < 0.01).