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Cell cycle oscillators underlying orderly proteolysis of E2F8

机译:E2F8有序蛋白分解的细胞周期振荡器

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E2F8 is a transcriptional repressor that antagonizes E2F1 at the crossroads of the cell cycle, apoptosis, and cancer. Previously, we discovered that E2F8 is a direct target of the APC/C ubiquitin ligase. Nevertheless, it remains unknown how E2F8 is dynamically controlled throughout the entirety of the cell cycle. Here, using newly developed human cell-free systems that recapitulate distinct inter-mitotic and G1 phases and a continuous transition from prometaphase to G1, we reveal an interlocking dephosphorylation switch coordinating E2F8 degradation with mitotic exit and the activation of APC/CsupCdh1/sup. Further, we uncover differential proteolysis rates for E2F8 at different points within G1 phase, accounting for its accumulation in late G1 while APC/CsupCdh1/sup is still active. Finally, we demonstrate that the F-box protein Cyclin F regulates E2F8 in G2-phase. Altogether, our data define E2F8 regulation throughout the cell cycle, illuminating an extensive coordination between phosphorylation, ubiquitination and transcription in mammalian cell cycle.
机译:E2F8是一种转录抑制因子,其在细胞周期,细胞凋亡和癌症的十字路口中拮抗E2F1。以前,我们发现E2F8是APC / C泛素连接酶的直接靶标。然而,它仍然未知E2F8在整个细胞周期的整个整个整个细胞周期中如何动态控制。这里,使用新开发的人细胞无细胞系统,该系统重新承载不同的多种间接细胞和G1阶段,并且从普丙醇酶到G1的连续转变,我们揭示了互锁定的去磷酸化开关协调与有丝分裂出口和APC / C 。此外,我们在G1相位内的不同点发现E2F8的差分蛋白水解率,占G1晚期的累积,而APC / C CDH1 仍然有效。最后,我们证明F型盒蛋白质Cyclin F调节G2相中的E2F8。完全,我们的数据在整个细胞周期中定义了E2F8规则,在磷酸化,泛磷酸化和转录之间照亮了广泛的协调。

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