Wapl依赖性地从原期染色质中移除粘合素需要Nek2a和细胞周期蛋白A2。

IF 9.4 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY EMBO Journal Pub Date : 2024-11-01 Epub Date: 2024-09-13 DOI:10.1038/s44318-024-00228-9
Susanne Hellmuth, Olaf Stemmann
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引用次数: 0

摘要

姐妹染色单体的内聚是由凝聚素复合体介导的。在有丝分裂前期,凝聚素以依赖 Wapl 和磷酸化的方式从染色体臂上移除。Sgo1-PP2A 通过使凝聚素及其相关的 Wapl 拮抗剂 sororin 去磷酸化来保护染色体周边的内聚力。然而,在姐妹染色单体被分离酶分离之前,Sgo1-PP2A 就已经转移到了内侧动点,从而使周中心染色体区域得不到保护。为什么去保护的凝聚素不会被Wapl移除,这仍然是个谜。通过在体外重建依赖 Wapl 从染色质中移除的连接蛋白,我们发现需要 Nek2a 和 Cdk1/2-cyclin A2。这些激酶使与粘合素结合的 Pds5b 磷酸化,从而将其从吸附素--转化为 Wapl--互作因子。用磷酸化模拟变体取代内源性 Pds5b 会导致姐妹染色单体过早分离(PCS)。相反,抗磷酸化的 Pds5b 会损害原染色体停滞细胞中染色体臂的分离,并在 Sgo1 缺失的情况下抑制 PCS。因此,Nek2a和细胞周期蛋白A2的有丝分裂早期降解可能解释了为什么只有分离酶而不是Wapl能触发无丝分裂。
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Requirement of Nek2a and cyclin A2 for Wapl-dependent removal of cohesin from prophase chromatin.

Sister chromatid cohesion is mediated by the cohesin complex. In mitotic prophase cohesin is removed from chromosome arms in a Wapl- and phosphorylation-dependent manner. Sgo1-PP2A protects pericentromeric cohesion by dephosphorylation of cohesin and its associated Wapl antagonist sororin. However, Sgo1-PP2A relocates to inner kinetochores well before sister chromatids are separated by separase, leaving pericentromeric regions unprotected. Why deprotected cohesin is not removed by Wapl remains enigmatic. By reconstituting Wapl-dependent cohesin removal from chromatin in vitro, we discovered a requirement for Nek2a and Cdk1/2-cyclin A2. These kinases phosphorylate cohesin-bound Pds5b, thereby converting it from a sororin- to a Wapl-interactor. Replacement of endogenous Pds5b by a phosphorylation mimetic variant causes premature sister chromatid separation (PCS). Conversely, phosphorylation-resistant Pds5b impairs chromosome arm separation in prometaphase-arrested cells and suppresses PCS in the absence of Sgo1. Early mitotic degradation of Nek2a and cyclin A2 may therefore explain why only separase, but not Wapl, can trigger anaphase.

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来源期刊
EMBO Journal
EMBO Journal 生物-生化与分子生物学
CiteScore
18.90
自引率
0.90%
发文量
246
审稿时长
1.5 months
期刊介绍: The EMBO Journal has stood as EMBO's flagship publication since its inception in 1982. Renowned for its international reputation in quality and originality, the journal spans all facets of molecular biology. It serves as a platform for papers elucidating original research of broad general interest in molecular and cell biology, with a distinct focus on molecular mechanisms and physiological relevance. With a commitment to promoting articles reporting novel findings of broad biological significance, The EMBO Journal stands as a key contributor to advancing the field of molecular biology.
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