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Sic1-induced Dna Rereplication During Meiosis

机译:减数分裂过程中Sic1诱导的Dna复制

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摘要

Orderly progression through meiosis requires strict regulation of DNA metabolic events, so that a single round of DNA replication is systematically followed by a recombination phase and 2 rounds of chromosome segregation. We report here the disruption of this sequence of events in Saccharomyces cerevisiae through meiosis specific induction of the cyclin-dependent kinase (CDK) inhibitor Sic1 mutated at multiple phosphorylation sites. Accumulation of this stabilized version of Sic1 led to significant DNA rereplication in the absence of normal chromosome segregation. Deletion of DMC1 abolished DNA rereplication, but additional deletion of RAD17 restored the original phenotype. Therefore, activation of the meiotic recombination checkpoint, which arrests meiotic progression at pachytene, suppressed DNA rereplication resulting from Sic1 stabilization. In contrast to deletion of DMC1, deletion of NDT8Q, which encodes a transcription factor required for pachytene exit, did not inhibit DNA rereplication. Our results provide strong evidence that CDK activity is required to prevent inappropriate initiation of DNA synthesis before the meiotic divisions.
机译:通过减数分裂的有序进展需要严格调节DNA代谢事件,因此系统地进行单轮DNA复制,之后是重组阶段和2轮染色体分离。我们在这里报告通过酿酒酵母的减数分裂特异性诱导的在多个磷酸化位点突变的细胞周期蛋白依赖性激酶(CDK)抑制剂Sic1的减数分裂特异性诱导这一事件序列在酿酒酵母中的破坏。在没有正常染色体分离的情况下,这种稳定版本的Sic1的积累导致大量的DNA复制。 DMC1的删除取消了DNA复制,但RAD17的其他删除恢复了原始表型。因此,减数分裂重组检查点的激活阻止了粗线粒体的减数分裂进程,从而抑制了由Sic1稳定产生的DNA复制。与DMC1的删除相反,NDT8Q的删除不编码DNA复制,而NDT8Q的删除编码长晶烯出口所需的转录因子。我们的结果提供了有力的证据,证明CDK活性对于防止减数分裂分裂之前DNA合成的不适当启动是必需的。

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