Heitz M J, Petersen J, Valovin S, Hagan I M
School of Biological Sciences, 2.205 Stopford Building, University of Manchester, Stopford Building, Oxford Road, Manchester M13 9PT, UK.
J Cell Sci. 2001 Dec;114(Pt 24):4521-32. doi: 10.1242/jcs.114.24.4521.
Microtubules polymerise from nucleation templates containing gamma tubulin. These templates are generally concentrated in discrete structures called microtubule organising centres (MTOCs). In Schizosaccharomyces pombe, an equatorial MTOC (EMTOC) forms mid-way through anaphase B and then disassembles during the final stages of cell separation. We show that the EMTOC was generated by recruiting gamma tubulin to the equatorial F-actin ring before it constricted to cleave the cell in two during cytokinesis. The EMTOC was not a continuous ring. It had a variable structure ranging from a horseshoe to a number of short bars. EMTOC integrity depended upon the integrity of the F-actin but not the microtubule cytoskeleton. EMTOC assembly required the activity of both the septation-inducing network (SIN) that regulates the onset of cytokinesis and the anaphase-promoting complex. Activation of the SIN in interphase cells induced F-actin ring formation and contraction and the synthesis of the primary septum but did not promote EMTOC assembly. In contrast, overproduction of the polo-like kinase, Plo1, which also induced multiple rounds of septation in interphase cells, induced EMTOC formation. Thus, the network governing EMTOC formation shared many of the regulatory elements that control cytokinesis but was more complex and revealed an additional function for Plo1 during mitotic exit.
微管从含有γ微管蛋白的成核模板聚合而来。这些模板通常集中在称为微管组织中心(MTOCs)的离散结构中。在粟酒裂殖酵母中,一个赤道微管组织中心(EMTOC)在后期B的中途形成,然后在细胞分离的最后阶段解体。我们发现,EMTOC是通过在赤道F-肌动蛋白环收缩以在胞质分裂期间将细胞一分为二之前,将γ微管蛋白招募到该环上而产生的。EMTOC不是一个连续的环。它具有从马蹄形到许多短棒的可变结构。EMTOC的完整性取决于F-肌动蛋白的完整性,而不是微管细胞骨架的完整性。EMTOC的组装需要调节胞质分裂起始的隔膜诱导网络(SIN)和后期促进复合物的活性。在间期细胞中激活SIN会诱导F-肌动蛋白环的形成和收缩以及初级隔膜的合成,但不会促进EMTOC的组装。相反,在间期细胞中也诱导多轮隔膜形成的类polo激酶Plo1的过量表达会诱导EMTOC的形成。因此,控制EMTOC形成的网络共享了许多控制胞质分裂的调节元件,但更为复杂,并揭示了Plo1在有丝分裂退出期间的额外功能。