Sluder G, Miller F J, Rieder C L
J Cell Biol. 1986 Nov;103(5):1873-81. doi: 10.1083/jcb.103.5.1873.
The tight coordination normally found between nuclear events and the doubling of centrosomes at each cell cycle suggests that nuclear activities may be part of the mechanism that controls the reproduction of centrosomes. To determine if this is the case, we used a micropipette to completely remove the nucleus from eggs of the sea urchin Lytechinus variegatus at prophase of the first mitosis, leaving only one centrosome in the cell. The subsequent behavior of this centrosome was then followed in vivo with the polarization microscope. In all cases the centrosome reproduced in a precise 1:2:4:8 fashion with a periodicity that was slightly slower than the centrosome cycle of control eggs. The cell cycle-related changes in centrosome morphology were identical to those of control eggs in that: (a) the astral birefringence varied cyclically to a normal extent, (b) the astral focus enlarged and then flattened during the telophase equivalent, (c) cleavage furrows were initiated as the astral birefringence faded, and (d) daughter centrosomes separated before the increase in astral birefringence at the onset of each mitosis. To determine if centrioles also reproduced normally, enucleate eggs were followed in vivo until they contained eight centrosomes. They were then individually removed from the preparations, fixed, and embedded. Each egg was serially 0.25-micron sectioned for observation with the high voltage electron microscope. We completely reconstructed 23 centrosomes in four eggs; all centrosomes contained two centrioles apiece. These results demonstrate that the subunits for complete centrosome assembly can be stockpiled ahead of time and that the properly controlled use of these subunits for centrosome reproduction does not require nuclear transcription or nuclear DNA synthesis at each cell cycle.
通常在每个细胞周期中核事件与中心体加倍之间发现的紧密协调表明,核活动可能是控制中心体复制机制的一部分。为了确定是否如此,我们使用微量移液器在第一次有丝分裂前期从海胆Lytechinus variegatus的卵中完全移除细胞核,使细胞中仅留下一个中心体。然后用偏光显微镜在体内跟踪这个中心体的后续行为。在所有情况下,中心体都以精确的1:2:4:8方式复制,其周期略慢于对照卵的中心体周期。中心体形态与细胞周期相关的变化与对照卵相同,即:(a)星体双折射在正常范围内周期性变化;(b)星体焦点在相当于末期时先扩大然后变平;(c)随着星体双折射消失开始形成分裂沟;(d)在每次有丝分裂开始时星体双折射增加之前子中心体分离。为了确定中心粒是否也能正常复制,在体内跟踪去核卵直到它们含有八个中心体。然后将它们从制备物中单独取出,固定并包埋。每个卵连续切成0.25微米的切片,用高压电子显微镜观察。我们在四个卵中完全重建了23个中心体;所有中心体每个都含有两个中心粒。这些结果表明,完整中心体组装的亚基可以提前储备,并且在每个细胞周期中对这些亚基进行适当控制用于中心体复制并不需要核转录或核DNA合成。