...
首页> 外文期刊>Molecular and Cellular Biology >Cyclin B-Cdk1 Kinase Stimulates ORC- and Cdc6-Independent Steps of Semiconservative Plasmid Replication in Yeast Nuclear Extracts
【24h】

Cyclin B-Cdk1 Kinase Stimulates ORC- and Cdc6-Independent Steps of Semiconservative Plasmid Replication in Yeast Nuclear Extracts

机译:细胞周期蛋白B Cdk1激酶刺激酵母核提取物中半保守质粒复制的ORC和Cdc6独立步骤。

获取原文
   

获取外文期刊封面封底 >>

       

摘要

Nuclear extracts from Saccharomyces cerevisiae cells synchronized in S phase support the semiconservative replication of supercoiled plasmids in vitro. We examined the dependence of this reaction on the prereplicative complex that assembles at yeast origins and on S-phase kinases that trigger initiation in vivo. We found that replication in nuclear extracts initiates independently of the origin recognition complex (ORC), Cdc6p, and an autonomously replicating sequence (ARS) consensus. Nonetheless, quantitative density gradient analysis showed that S- and M-phase nuclear extracts consistently promote semiconservative DNA replication more efficiently than G1-phase extracts. The observed semiconservative replication is compromised in S-phase nuclear extracts deficient for the Cdk1 kinase (Cdc28p) but not in extracts deficient for the Cdc7p kinase. In a cdc4-1 G1-phase extract, which accumulates high levels of the specific Clb-Cdk1 inhibitor p40SIC1, very low levels of semiconservative DNA replication were detected. Recombinant Clb5-Cdc28 restores replication in a cdc28-4 S-phase extract yet fails to do so in the cdc4-1 G1-phase extract. In contrast, the addition of recombinant Xenopus CycB-Cdc2, which is not sensitive to inhibition by p40SIC1, restores efficient replication to both extracts. Our results suggest that in addition to its well-characterized role in regulating the origin-specific prereplication complex, the Clb-Cdk1 complex modulates the efficiency of the replication machinery itself.
机译:在S期同步化的酿酒酵母细胞的核提取物支持超螺旋质粒在体外的半保守复制。我们检查了该反应对在酵母起源处组装的复制前复合物和在体内触发起始的S期激酶的依赖性。我们发现核提取物中的复制独立于起源识别复合物(ORC),Cdc6p和自主复制序列(ARS)共识而启动。但是,定量密度梯度分析表明,S和M相核提取物比G 1 相提取物更有效地促进半保守DNA复制。观察到的半保守复制在缺乏Cdk1激酶(Cdc28p)的S期核提取物中受损,但在缺乏Cdc7p激酶的提取物中没有受损。在 cdc4-1 G 1 相提取物中,该提取物积累了高水平的特定Clb-Cdk1抑制剂p40 SIC1 ,检测到非常低水平的半保守DNA复制。重组Clb5-Cdc28恢复 cdc28-4 S期提取物中的复制,但未能在 cdc4-1 G 1 期中恢复复制提取。相比之下,添加重组非洲爪蟾 CycB-Cdc2对p40 SIC1 的抑制不敏感,因此可以有效地复制到两种提取物中。我们的结果表明,除了在调节起源特异的预复制复合体中发挥很好的作用外,Clb-Cdk1复合体还调节复制机制本身的效率。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号