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Activation of ADF/cofilin by phosphorylation-regulated Slingshot phosphatase is required for the meiotic spindle assembly in Xenopus laevis oocytes

机译:非洲爪蟾卵母细胞减数分裂纺锤体组装需要通过磷酸化调节的弹弓磷酸酶激活ADF / cofilin。

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摘要

We identify Xenopus ADF/cofilin (XAC) and its activator, Slingshot phosphatase (XSSH), as key regulators of actin dynamics essential for spindle microtubule assembly during Xenopus oocyte maturation. Phosphorylation of XSSH at multiple sites within the tail domain occurs just after germinal vesicle breakdown (GVBD) and is accompanied by dephosphorylation of XAC, which was mostly phosphorylated in immature oocytes. This XAC dephosphorylation after GVBD is completely suppressed by latrunculin B, an actin monomer–sequestering drug. On the other hand, jasplakinolide, an F-actin–stabilizing drug, induces dephosphorylation of XAC. Effects of latrunculin B and jasplakinolide are reconstituted in cytostatic factor–arrested extracts (CSF extracts), and XAC dephosphorylation is abolished by depletion of XSSH from CSF extracts, suggesting that XSSH functions as an actin filament sensor to facilitate actin filament dynamics via XAC activation. Injection of anti-XSSH antibody, which blocks full phosphorylation of XSSH after GVBD, inhibits both meiotic spindle formation and XAC dephosphorylation. Coinjection of constitutively active XAC with the antibody suppresses this phenotype. Treatment of oocytes with jasplakinolide also impairs spindle formation. These results strongly suggest that elevation of actin dynamics by XAC activation through XSSH phosphorylation is required for meiotic spindle assembly in Xenopus laevis.
机译:我们确定非洲爪蟾ADF / cofilin(XAC)及其激活剂,弹弓磷酸酶(XSSH),是非洲爪蟾卵母细胞成熟过程中纺锤体微管组装所必需的肌动蛋白动力学的关键调节剂。 XSSH的磷酸化在发芽囊泡破裂(GVBD)后立即在尾部域的多个位点发生,并伴有XAC的去磷酸化,XAC的磷酸化大部分在未成熟的卵母细胞中被磷酸化。 latrunculin B(肌动蛋白单体隔离药物)完全抑制了GVBD后XAC的这种去磷酸化作用。另一方面,稳定肌动蛋白的药物jasplakinolide可诱导XAC的去磷酸化。在抑制细胞生长因子的提取物(CSF提取物)中重构了latrunculin B和jasplakinolide的作用,并且通过从CSF提取物中消耗XSSH消除了XAC的去磷酸化作用,这表明XSSH充当肌动蛋白丝传感器,通过XAC激活促进肌动蛋白丝动力学。注射抗XSSH抗体可阻止GVBD后XSSH的完全磷酸化,从而抑制减数分裂纺锤体形成和XAC脱磷酸作用。组成性活性XAC与抗体的共同注射抑制了该表型。用jasplakinolide处理卵母细胞也会损害纺锤体的形成。这些结果强烈表明,非洲爪蟾减数分裂纺锤体组装需要通过XSSH磷酸化通过XAC活化来提高肌动蛋白动力学。

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