Fulka J, Moor R M, Fulka J
Babraham Institute, Department of Development and Signalling, Cambridge, United Kingdom.
Exp Cell Res. 1995 Aug;219(2):414-9. doi: 10.1006/excr.1995.1247.
Mouse oocytes at different stages of maturation were fused together and the ensuing cell cycle events were analyzed with the objective of identifying checkpoints in meiosis. Fusion of maturing oocytes just undergoing germinal vesicle breakdown (GVBD) induces PCC (premature chromosome condensation) but no spindle formation in immature (GV) partner oocytes. On the other hand, fusion of metaphase I (MI) oocytes containing spindles to GV oocytes induces both PCC and spindle formation in the immature partner. Thus, while molecules required for condensation are present throughout metaphase, those involved in spindle formation are absent in early M-phase. Oocytes cultured for 6 h--early metaphase I (i.e., approximately 2 h before the onset of anaphase I)--and then fused to anaphase-telophase I (A-TI) fusion partners block meiotic progression in the more advanced oocytes and induce chromatin dispersal on the spindle. By contrast, oocytes cultured for 8 h (late MI) before fusion to A-TI partners are driven into anaphase by signals from the more advanced oocytes and thereafter advance in synchrony to telophase I. When early (10 h) or late (12 h) metaphase II oocytes were fused to A-TI partners the signals generated from early MII oocytes block the anaphase to telophase I transition and induce a dispersal of A-TI chromosomes along the spindle. On the other hand, late MII oocytes respond to A-TI signals by exiting from the MII block and undergoing the A-TII transition. Moreover, the oocytes in late MI are not arrested in this stage and progress without any delay through A-TI to MII when fused to metaphase II partners. The signals from the less-developed partner force the MII oocyte through A-TII to MIII. In total, these studies demonstrate that the metaphase period is divided into at least three distinct phases and that a checkpoint in late metaphase controls the progress of meiosis in mammalian oocytes.
将处于不同成熟阶段的小鼠卵母细胞融合在一起,并分析随后的细胞周期事件,目的是确定减数分裂中的检查点。刚经历生发泡破裂(GVBD)的成熟卵母细胞与未成熟(GV)的卵母细胞融合,会诱导早熟染色体凝聚(PCC),但在未成熟的伙伴卵母细胞中不会形成纺锤体。另一方面,含有纺锤体的中期I(MI)卵母细胞与GV卵母细胞融合,会在未成熟的伙伴细胞中诱导PCC和纺锤体形成。因此,虽然在整个中期都存在凝聚所需的分子,但参与纺锤体形成的分子在M期早期并不存在。培养6小时的卵母细胞——中期I早期(即大约在后期I开始前2小时)——然后与后期-末期I(A-TI)融合伙伴融合,会阻止更成熟卵母细胞中的减数分裂进程,并诱导染色质在纺锤体上分散。相比之下,在与A-TI伙伴融合前培养8小时(MI后期)的卵母细胞,会被来自更成熟卵母细胞的信号驱动进入后期,然后同步进入末期I。当早期(10小时)或晚期(12小时)的中期II卵母细胞与A-TI伙伴融合时,早期MII卵母细胞产生的信号会阻止后期向末期I的转变,并诱导A-TI染色体沿纺锤体分散。另一方面,晚期MII卵母细胞通过退出MII阻滞并经历A-TII转变来响应A-TI信号。此外,MI后期的卵母细胞不会停滞在这个阶段,当与中期II伙伴融合时,会毫无延迟地通过A-TI进入MII。来自发育程度较低伙伴的信号迫使MII卵母细胞通过A-TII进入MIII。总的来说,这些研究表明中期被分为至少三个不同的阶段,并且中期后期的一个检查点控制着哺乳动物卵母细胞减数分裂的进程。