Shimizu T
Eur J Cell Biol. 1983 Mar;30(1):74-82.
Microfilaments in the Tubifex egg undergoing polar body formation can be decorated with heavy meromyosin (HMM). Since the HMM-arrowheads on filaments are dissociated by rinsing with ATP, they are identified as actin filaments. From metaphase through telophase of the second meiotic division, actin filaments are present in the cortex and in the meiotic apparatus. Consistent with the previous observations [26, 27], cortical filaments show stage-specific localization patterns. At metaphase the thick filamentous layer is localized at the animal pole, that means the region overlying the peripheral aster of the meiotic apparatus; filaments are organized in a meshwork. Upon the onset of anaphase chromosome movement, the filament meshwork mostly disappears and the remaining filaments are found to be solitary. Surrounding the animal pole region, but not extending over the animal pole, more and more filaments reappear during anaphase. As the polar body forms at the animal pole, filaments surrounding its base are organized into small bundles which are oriented randomly. By early telophase these filaments come to run circumferentially in the cortical layer (i.e. they form the contractile ring) engirding the cleavage furrow which develops at the base of the polar body. In the remaining cortex, filaments run along the surface and are oriented randomly. At all stages, adjacent filaments are often found to have opposite polarities; in favorable sections, HMM-decorated filaments appear to attach to the oolemma. The mechanism underlying the filament alignment of the contractile ring is discussed in relation to formation of the polar body.
正经历极体形成过程的颤蚓卵中的微丝可用重酶解肌球蛋白(HMM)进行标记。由于用ATP冲洗后,微丝上的HMM箭头会解离,所以它们被鉴定为肌动蛋白丝。从第二次减数分裂的中期到末期,肌动蛋白丝存在于皮质和减数分裂装置中。与先前的观察结果[26, 27]一致,皮质丝呈现出阶段特异性的定位模式。在中期,粗丝状层位于动物极,即位于减数分裂装置外周星体上方的区域;微丝排列成网状。在后期染色体移动开始时,丝状网大多消失,剩余的微丝呈孤立状态。在动物极区域周围,但不延伸到动物极,在后期越来越多的微丝重新出现。当极体在动物极形成时,围绕其基部的微丝被组织成随机定向的小束。到末期早期,这些微丝在皮质层中沿圆周方向排列(即它们形成收缩环),围绕在极体基部形成的卵裂沟。在其余的皮质中,微丝沿表面排列且随机定向。在所有阶段,常常发现相邻的微丝具有相反的极性;在合适的切片中,用HMM标记的微丝似乎附着在卵膜上。结合极体的形成讨论了收缩环微丝排列的潜在机制。