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首页> 外文期刊>FEBS Letters >Getting out of mitosis: spatial and temporal control of mitotic exit and cytokinesis by PP1 and PP2A
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Getting out of mitosis: spatial and temporal control of mitotic exit and cytokinesis by PP1 and PP2A

机译:脱丝症:PP1和PP2A的有丝分裂出口和细胞因子的空间和时间控制

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Here, we will review the evidence showing that mitotic exit is initiated by regulated proteolysis and then driven by the PPP family of phosphoserine/threonine phosphatases. Rapid APC/CCDC20 and ubiquitin‐dependent proteolysis of cyclin B and securin initiates sister chromatid separation, the first step of mitotic exit. Because proteolysis of Aurora and Polo family kinases dependent on APC/CCDH1 is relatively slow, this creates a new regulatory state, anaphase, different to G2 and M‐phase. We will discuss how the CDK1‐counteracting phosphatases PP1 and PP2A‐B55, together with Aurora and Polo kinases, contribute to the temporal regulation and order of events in the different stages of mitotic exit from anaphase to cytokinesis. For PP2A‐B55, these timing properties are created by the ENSA‐dependent inhibitory pathway and differential recognition of phosphoserine and phosphothreonine. Finally, we will discuss how Aurora B and PP2A‐B56 are needed for the spatial regulation of anaphase spindle formation and how APC/C‐dependent destruction of PLK1 acts as a timer for abscission, the final event of cytokinesis.
机译:在这里,我们将审查显示有丝分裂引发的有丝分裂的证据,然后由PPP磷素/苏氨酸磷酸酶驱动。 Cyclin B和Securin的Rapid APC / CCDC20和泛素依赖性蛋白水解引发姐妹染色体分离,丝分裂出口的第一步。因为Aurora和Polo系列激酶依赖于APC / CCDH1的蛋白水解相对较慢,这产生了一种新的调节状态,外延,不同于G2和M阶段。我们将讨论CDK1抵抗磷酸酶PP1和PP2A-B55与极光和酚激酶一起有助于临时调节,其中不同阶段的不同阶段从中源于细胞因子。对于PP2A-B55,这些定时性质由Ensa依赖性抑制途径和磷素和磷酸磷酸胆碱的差异识别产生。最后,我们将讨论Aurora B和PP2A-B56如何进行术语主轴形成的空间调节以及PLK1的APC / C依赖性破坏如何充当脱落的计时器,是细胞因子的最终事件。

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