|
Resolution: standard / high Figure 8.
Role of specific residues in the sea bream Aqp1b C-terminal tail for intracellular
trafficking in oocytes. (A) Water permeability of oocytes expressing wild-type (WT) or mutant Aqp1b. Oocytes
were injected with cRNAs encoding WT Aqp1b (0.25 or 1 ng), Aqp1b-T229A (1 ng), Aqp1b-L234A/L235A
(1 ng), Aqp1b-S254A (0.25 ng) or Aqp1b-S254D (0.25 ng). Permeability is expressed
in % related to oocytes injected with WT Aqp1b. Values are the mean ± SEM of 3–5 experiments
(n = 10–15 oocytes per treatment). The asterisks denote statistically significant
differences (*, p < 0.05; **, p < 0.01). (B-E) Immunoblots of total and plasma membrane equivalents (TM and PM, respectively)
of oocytes expressing WT or mutant Aqp1b. The apparent molecular mass of a 29-kDa
marker is indicated on the left. (F-J) Localization of Aqp1b mutants in oocytes. The
plasma membrane is indicated by arrows, and retention of Aqp1b-L234A/L235A proteins
possibly in the ER is indicated by arrowheads (H). Bars, 100 μm.
Tingaud-Sequeira et al. BMC Evolutionary Biology 2008 8:259 doi:10.1186/1471-2148-8-259 |