Center for Nonlinear Dynamics and Department of Physics, The University of Texas at Austin, Austin, Texas, United States of America.
PLoS One. 2013 Jul 1;8(7):e67710. doi: 10.1371/journal.pone.0067710. Print 2013.
To complete meiosis II in animal cells, the male DNA material needs to meet the female DNA material contained in the female pronucleus at the egg center, but it is not known how the male pronucleus, deposited by the sperm at the periphery of the cell, finds the cell center in large eggs. Pronucleus centering is an active process that appears to involve microtubules and molecular motors. For small and medium-sized cells, the force required to move the centrosome can arise from either microtubule pushing on the cortex, or cortically-attached dynein pulling on microtubules. However, in large cells, such as the fertilized Xenopus laevis embryo, where microtubules are too long to support pushing forces or they do not reach all boundaries before centrosome centering begins, a different force generating mechanism must exist. Here, we present a centrosome positioning model in which the cytosolic drag experienced by cargoes hauled by cytoplasmic dynein on the sperm aster microtubules can move the centrosome towards the cell's center. We find that small, fast cargoes (diameter ∼100 nm, cargo velocity ∼2 µm/s) are sufficient to move the centrosome in the geometry of the Xenopus laevis embryo within the experimentally observed length and time scales.
为了完成动物细胞的减数分裂 II,雄性 DNA 物质需要与卵子中心处雌性原核内包含的雌性 DNA 物质相遇,但目前尚不清楚精子在细胞外周沉积的雄性原核如何在大卵子中找到细胞中心。原核定位是一个主动过程,似乎涉及微管和分子马达。对于小细胞和中等大小的细胞,移动中心体所需的力可以来自微管对皮质的推动,或者皮质附着的动力蛋白拉动微管。然而,在大细胞中,例如受精的非洲爪蟾胚胎,微管太长以至于无法支撑推动力,或者在中心体定位开始之前,它们无法到达所有边界,因此必须存在不同的力产生机制。在这里,我们提出了一种中心体定位模型,其中由细胞质动力蛋白在精子星状微管上拖动的货物所经历的细胞溶质阻力可以将中心体移动到细胞的中心。我们发现,在实验观察到的长度和时间尺度内,小而快速的货物(直径约为 100nm,货物速度约为 2μm/s)足以在非洲爪蟾胚胎的几何形状中移动中心体。