首页> 美国卫生研究院文献>The Journal of Biological Chemistry >Small Ubiquitin-related Modifier Ligase Activity of Mms21 Is Required for Maintenance of Chromosome Integrity during the Unperturbed Mitotic Cell Division Cycle in Saccharomyces cerevisiae
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Small Ubiquitin-related Modifier Ligase Activity of Mms21 Is Required for Maintenance of Chromosome Integrity during the Unperturbed Mitotic Cell Division Cycle in Saccharomyces cerevisiae

机译:Mms21的小泛素相关修饰修饰酶连接酶活性是酿酒酵母在无扰动的有丝分裂过程中维持染色体完整性所必需的。

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摘要

The SUMO ligase activity of Mms21/Nse2, a conserved member of the Smc5/6 complex, is required for resisting extrinsically induced genotoxic stress. We report that the Mms21 SUMO ligase activity is also required during the unchallenged mitotic cell cycle in Saccharomyces cerevisiae. SUMO ligase-defective cells were slow growing and spontaneously incurred DNA damage. These cells required caffeine-sensitive Mec1 kinase-dependent checkpoint signaling for survival even in the absence of extrinsically induced genotoxic stress. SUMO ligase-defective cells were sensitive to replication stress and displayed synthetic growth defects with DNA damage checkpoint-defective mutants such as mec1, rad9, and rad24. MMS21 SUMO ligase and mediator of replication checkpoint 1 gene (MRC1) were epistatic with respect to hydroxyurea-induced replication stress or methyl methanesulfonate-induced DNA damage sensitivity. Subjecting Mms21 SUMO ligase-deficient cells to transient replication stress resulted in enhancement of cell cycle progression defects such as mitotic delay and accumulation of hyperploid cells. Consistent with the spontaneous activation of the DNA damage checkpoint pathway observed in the Mms21-mediated sumoylation-deficient cells, enhanced frequency of chromosome breakage and loss was detected in these mutant cells. A mutation in the conserved cysteine 221 that is engaged in coordination of the zinc ion in Loop 2 of the Mms21 SPL-RING E3 ligase catalytic domain resulted in strong replication stress sensitivity and also conferred slow growth and Mec1 dependence to unchallenged mitotically dividing cells. Our findings establish Mms21-mediated sumoylation as a determinant of cell cycle progression and maintenance of chromosome integrity during the unperturbed mitotic cell division cycle in budding yeast.
机译:Mms21 / Nse2(Smc5 / 6复合体的保守成员)的SUMO连接酶活性是抵抗外源性遗传毒性胁迫所必需的。我们报告在酿酒酵母中无挑战的有丝分裂细胞周期中还需要Mms21 SUMO连接酶活性。 SUMO连接酶缺陷细胞生长缓慢,并自发引起DNA损伤。这些细胞需要咖啡因敏感的Mec1激酶依赖性检查点信号才能存活,即使在没有外源性遗传毒性胁迫的情况下也是如此。 SUMO连接酶缺陷细胞对复制压力敏感,并显示出具有DNA损伤检查点缺陷突变体(例如mec1,rad9和rad24)的合成生长缺陷。 MMS21 SUMO连接酶和复制检查点1基因(MRC1)的介导者对羟基脲诱导的复制应激或甲磺酸甲酯诱导的DNA损伤敏感性具有抑制作用。 Mms21 SUMO连接酶缺陷细胞受到短暂的复制压力导致细胞周期进程缺陷的增强,如有丝分裂延迟和超倍体细胞的积累。与Mms21介导的sumoylation缺陷细胞中观察到的DNA损伤检查点途径的自发激活相一致,在这些突变细胞中检测到染色体断裂和丢失的频率增加。 Mms21 SPL-RING E3连接酶催化域的环2中参与锌离子配位的保守半胱氨酸221中的突变导致强烈的复制应激敏感性,并赋予缓慢生长和Mec1依赖于未受挑战的有丝分裂分裂细胞。我们的发现建立了Mms21介导的sumoylation作为细胞周期进程的决定因素,并在发芽酵母中不受干扰的有丝分裂细胞分裂周期中维持了染色体完整性。

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