Houliston E, Elinson R P
Department of Zoology, University of Toronto, Ontario, Canada.
Development. 1991 May;112(1):107-17. doi: 10.1242/dev.112.1.107.
Following fertilization, the Xenopus egg cortex rotates relative to the cytoplasm by 30 degrees about a horizontal axis. The direction of rotation, and as a result the orientation of the embryonic body axes, is normally specified by the position of sperm entry. The mechanism of rotation appears to involve an array of aligned microtubules in the vegetal cortex (Elinson and Rowning, 1988, Devl Biol. 128, 185-197). We performed anti-tubulin immunofluorescence on sections to follow the formation of this array. Microtubules disappear rapidly from the egg following fertilization, and reappear first in the sperm aster. Surprisingly, astral microtubules then extend radially through both the animal and vegetal cytoplasm. The cortical array arises as they reach the vegetal cell surface. The eccentric position of the sperm aster gives asymmetry to the formation of the array and may explain its alignment since microtubules reaching the cortex tend to bend away from the sperm entry side. The radial polymerization of cytoplasmic microtubules is not dependent on the sperm aster or on the female pronucleus: similar but more symmetric patterns arise in artificially activated and enucleate eggs, slightly later than in fertilized eggs. These observations suggest that the cortical microtubule array forms as a result of asymmetric microtubule growth outward from cytoplasm to cortex and, since cortical and cytoplasmic microtubules remain connected throughout the period of the rotation, that the microtubules of the array rotate with the cytoplasm.
受精后,非洲爪蟾卵的皮层围绕水平轴相对于细胞质旋转30度。旋转方向以及胚胎体轴的取向通常由精子进入的位置决定。旋转机制似乎涉及植物皮层中排列成行的微管阵列(埃林森和罗宁,1988年,《发育生物学》。128,185 - 197)。我们对切片进行抗微管蛋白免疫荧光检测以追踪该阵列的形成。受精后微管迅速从卵中消失,并首先在精子星体中重新出现。令人惊讶的是,星体微管随后径向延伸穿过动物和植物细胞质。当它们到达植物细胞表面时,皮层阵列形成。精子星体的偏心位置使阵列的形成不对称,这可能解释了其排列方式,因为到达皮层的微管往往会从精子进入的一侧弯曲离开。细胞质微管的径向聚合不依赖于精子星体或雌性原核:在人工激活的去核卵中会出现类似但更对称的模式,只是比受精卵稍晚一些。这些观察结果表明,皮层微管阵列是由于微管从细胞质向外不对称生长到皮层而形成的,并且由于在整个旋转期间皮层和细胞质微管保持连接,所以阵列中的微管会随着细胞质一起旋转。