Bischof Johanna, Brand Christoph A, Somogyi Kálmán, Májer Imre, Thome Sarah, Mori Masashi, Schwarz Ulrich S, Lénárt Péter
Cell Biology and Biophysics Unit, European Molecular Biology Laboratory (EMBL), Meyerhofstrasse 1, 69117, Heidelberg, Germany.
Institute for Theoretical Physics and BioQuant, Heidelberg University, Philosophenweg 19, 69120, Heidelberg, Germany.
Nat Commun. 2017 Oct 11;8(1):849. doi: 10.1038/s41467-017-00979-6.
Surface contraction waves (SCWs) in oocytes and embryos lead to large-scale shape changes coupled to cell cycle transitions and are spatially coordinated with the cell axis. Here, we show that SCWs in the starfish oocyte are generated by a traveling band of myosin II-driven cortical contractility. At the front of the band, contractility is activated by removal of cdk1 inhibition of the RhoA/RhoA kinase/myosin II signaling module, while at the rear, contractility is switched off by negative feedback originating downstream of RhoA kinase. The SCW's directionality and speed are controlled by a spatiotemporal gradient of cdk1-cyclinB. This gradient is formed by the release of cdk1-cyclinB from the asymmetrically located nucleus, and progressive degradation of cyclinB. By combining quantitative imaging, biochemical and mechanical perturbations with mathematical modeling, we demonstrate that the SCWs result from the spatiotemporal integration of two conserved regulatory modules, cdk1-cyclinB for cell cycle regulation and RhoA/Rok/NMYII for actomyosin contractility.Surface contraction waves (SCWs) are prominent shape changes coupled to cell cycle transitions in oocytes. Here the authors show that SCWs are patterned by the spatiotemporal integration of two conserved modules, cdk1-cyclinB for cell cycle regulation and RhoA/Rok/NMYII for actomyosin contractility.
卵母细胞和胚胎中的表面收缩波(SCWs)会导致与细胞周期转变相关的大规模形状变化,并在空间上与细胞轴协调。在这里,我们表明海星卵母细胞中的SCWs是由肌球蛋白II驱动的皮质收缩性的移动带产生的。在带的前端,通过去除cdk1对RhoA/RhoA激酶/肌球蛋白II信号模块的抑制来激活收缩性,而在后端,收缩性通过源自RhoA激酶下游的负反馈关闭。SCW的方向性和速度由cdk1 - cyclinB的时空梯度控制。这个梯度是由cdk1 - cyclinB从不对称定位的细胞核中释放以及cyclinB的逐步降解形成的。通过将定量成像、生化和机械扰动与数学建模相结合,我们证明SCWs是由两个保守调节模块的时空整合产生的,即用于细胞周期调节的cdk1 - cyclinB和用于肌动球蛋白收缩性的RhoA/Rok/NMYII。表面收缩波(SCWs)是卵母细胞中与细胞周期转变相关的显著形状变化。在这里,作者表明SCWs是由两个保守模块的时空整合形成的,即用于细胞周期调节的cdk1 - cyclinB和用于肌动球蛋白收缩性的RhoA/Rok/NMYII。