Figure 2.
Dynein is required for movement of ER membranes toward the minus end of MTs. (A) Demembranated sperm was added after 10 min to a crude interphase X. laevis egg extract containing Alexa fluor 488–labeled tubulin and the hydrophobic dye DiIC18. The extension of membrane tubules was followed over time. Arrowheads indicate the tip of extending ER membrane tubule. The kymograph shows the movement of the same tubule. Bars, 2 µm. (B) As in A, but the extract was incubated for 30 min with and without 6 µM of the CC1 of p150 glued to inhibit dynein function. Network formation was visualized by confocal fluorescence microscopy. Bars, 10 µm.