Benink Hélène A, Bement William M
Department of Zoology, University of Wisconsin-Madison, Madison, WI 53706, USA.
J Cell Biol. 2005 Jan 31;168(3):429-39. doi: 10.1083/jcb.200411109.
Rho GTPases control many cytoskeleton-dependent processes, but how they regulate spatially distinct features of cytoskeletal function within a single cell is poorly understood. Here, we studied active RhoA and Cdc42 in wounded Xenopus oocytes, which assemble and close a dynamic ring of actin filaments (F-actin) and myosin-2 around wound sites. RhoA and Cdc42 are rapidly activated around wound sites in a calcium-dependent manner and segregate into distinct, concentric zones around the wound, with active Cdc42 in the approximate middle of the F-actin array and active RhoA on the interior of the array. These zones form before F-actin accumulation, and then move in concert with the closing array. Microtubules and F-actin are required for normal zone organization and dynamics, as is crosstalk between RhoA and Cdc42. Each of the zones makes distinct contributions to the organization and function of the actomyosin wound array. We propose that similar rho activity zones control related processes such as cytokinesis.
Rho GTP酶控制着许多依赖细胞骨架的过程,但它们如何在单个细胞内调节细胞骨架功能的空间不同特征却知之甚少。在这里,我们研究了爪蟾卵母细胞伤口处的活性RhoA和Cdc42,它们在伤口部位组装并封闭一个由肌动蛋白丝(F-肌动蛋白)和肌球蛋白-2组成的动态环。RhoA和Cdc42在伤口部位以钙依赖的方式迅速被激活,并在伤口周围分离成不同的同心区域,活性Cdc42位于F-肌动蛋白阵列的大致中间位置,活性RhoA位于阵列内部。这些区域在F-肌动蛋白积累之前形成,然后与闭合的阵列协同移动。微管和F-肌动蛋白对于正常的区域组织和动态变化是必需的,RhoA和Cdc42之间的相互作用也是如此。每个区域对肌动球蛋白伤口阵列的组织和功能都有不同的贡献。我们提出,类似的rho活性区域控制着诸如胞质分裂等相关过程。