The Gurdon Institute and the Department of Genetics, University of Cambridge, Cambridge, United Kingdom.
The Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, United Kingdom.
Elife. 2017 Oct 16;6:e27237. doi: 10.7554/eLife.27237.
The localisation of mRNA to the posterior of the oocyte defines where the abdomen and germ cells form in the embryo. Kinesin 1 transports mRNA to the oocyte posterior along a polarised microtubule cytoskeleton that grows from non-centrosomal microtubule organising centres (ncMTOCs) along the anterior/lateral cortex. Here, we show that the formation of this polarised microtubule network also requires the posterior regulation of microtubule growth. A missense mutation in the dynactin Arp1 subunit causes most mRNA to localise in the posterior cytoplasm rather than cortically. mRNA transport and anchoring are normal in this mutant, but the microtubules fail to reach the posterior pole. Thus, dynactin acts as an anti-catastrophe factor that extends microtubule growth posteriorly. Kinesin 1 transports dynactin to the oocyte posterior, creating a positive feedback loop that increases the length and persistence of the posterior microtubules that deliver mRNA to the cortex.
mRNA 在卵母细胞后部的定位决定了胚胎中腹部和生殖细胞的形成位置。驱动蛋白 1 沿着从前到侧皮质生长的从非中心体微管组织中心 (ncMTOCs) 延伸出的极化微管细胞骨架将 mRNA 运送到卵母细胞后部。在这里,我们表明这种极化微管网络的形成也需要微管生长的后部调节。动力蛋白 Arp1 亚基中的错义突变导致大多数 mRNA 定位于后细胞质中,而不是皮质中。在这种突变体中,mRNA 的运输和锚定是正常的,但微管无法到达后极。因此,动力蛋白作为一种抗解聚因子,将微管生长向后延伸。驱动蛋白 1 将动力蛋白运输到卵母细胞后部,形成一个正反馈回路,增加了将 mRNA 运送到皮质的后部微管的长度和持久性。