Dynactin-dependent cortical dynein and spherical spindle shape correlate temporally with meiotic spindle rotation in Caenorhabditis elegans.
Dynactin-dependent cortical dynein and spherical spindle shape correlate temporally with meiotic spindle rotation in Caenorhabditis elegans.
复制标题
DOI:
10.1091/mbc.e15-05-0290
复制
发表时间:
2015-09-01
影响因子:
3.3
通讯作者:
McNally FJ
中科院分区:
文献类型:
--
作者:
Crowder ME;Flynn JR;McNally KP;Cortes DB;Price KL;Kuehnert PA;Panzica MT;Andaya A;Leary JA;McNally FJ
Cytoplasmic dynein accumulates on the cortex of Caenorhabditis elegans female meiotic spindles just before they rotate in a dynein-dependent manner. These spindles also shorten to a spherical shape that might reduce the drag that opposes cortical pulling by dynein. Oocyte meiotic spindles orient with one pole juxtaposed to the cortex to facilitate extrusion of chromosomes into polar bodies. In Caenorhabditis elegans, these acentriolar spindles initially orient parallel to the cortex and then rotate to the perpendicular orientation. To understand the mechanism of spindle rotation, we characterized events that correlated temporally with rotation, including shortening of the spindle in the pole-to pole axis, which resulted in a nearly spherical spindle at rotation. By analyzing large spindles of polyploid C. elegans and a related nematode species, we found that spindle rotation initiated at a defined spherical shape rather than at a defined spindle length. In addition, dynein accumulated on the cortex just before rotation, and microtubules grew from the spindle with plus ends outward during rotation. Dynactin depletion prevented accumulation of dynein on the cortex and prevented spindle rotation independently of effects on spindle shape. These results support a cortical pulling model in which spindle shape might facilitate rotation because a sphere can rotate without deforming the adjacent elastic cytoplasm. We also present evidence that activation of spindle rotation is promoted by dephosphorylation of the basic domain of p150 dynactin.