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We are analyzing https://www.nature.com/articles/s41467-017-00979-6.

Title:
A cdk1 gradient guides surface contraction waves in oocytes | Nature Communications
Description:
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.
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Keywords {🔍}

cell, scw, oocytes, article, pubmed, cdkcyclinb, google, scholar, fig, rhoa, oocyte, supplementary, gradient, cas, surface, cdk, contraction, nature, shape, scws, curvature, biol, starfish, band, data, cycle, cortical, time, movie, axis, activity, central, change, contractility, animal, waves, cortex, radii, scale, wave, model, spatial, fluorescence, tension, pole, show, module, molecular, meiosis, shown,

Topics {✒️}

nature portfolio privacy policy advertising 20 mg/ml 500 kda dextran-cy5 open side 25–30 min social media cdna library rhoa/rok/myosin ii module {{k_0} + {k_1}\frac{{apc}}{{{ tools reprints rhotekin gtp-binding domain conserved rhoa/rok/nmyii module nature nature 349 nature 457 middle plot overlaid fast z-focusing device chan–vese energy function49 cortical er-mrna domain }}{a_0}} + \frac{{{k_v}}}{2}{\left marinus scientific south coast bio-marine scientific computing cdk1-cyclinb reaction-diffusion system oocyte expressing rgbd-egfp oocyte expressing egfp-rgbd $${t_c} = \frac{{\delta utrophin-ch domain-megfp46 cdk1-cyclinb gradient guides ap-vp axis perpendicular transmitted light movie microtubule label eb3-3megfp cdk1-cyclinb diffuses slowly ect2-centralspindlin complex regulates oocyte expressing cyclinb-egfp microtubule-mediated waves prior cdk1-cyclinb gradient drives metachronous cell-cycle state rhoa/rok/nmyii module cdk1-cyclinb gradient originating active cdk1-cyclinb protein author information authors permissions high cdk1-cyclinb concentration millimeter-sized amphibian oocytes central spindle accounts simulated cdk1-cyclinb intensity pseudo-color scale shown cortical fluorescence intensities

Schema {🗺️}

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         headline:A cdk1 gradient guides surface contraction waves in oocytes
         description: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.
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      headline:A cdk1 gradient guides surface contraction waves in oocytes
      description: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.
      datePublished:2017-10-11T00:00:00Z
      dateModified:2018-01-10T00:00:00Z
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