Donaldson A D
Department of Biochemistry, University of Dundee, Scotland, UK.
EMBO Rep. 2000 Dec;1(6):507-12. doi: 10.1093/embo-reports/kvd108.
Cyclin-dependent kinases (CDKs) drive the cell cycle, central to which is the accurate control of chromosome replication. In Saccharomyces cerevisiae, six closely related B-type cyclins (Clb1-6) drive the events of S phase and mitosis. Either Clb5 or Clb6 can activate early-firing replication origins, whereas only Clb5 can activate late origins. Clb1-4 are expressed later in the cell cycle. Whether Clb cyclins differ only in timing of expression, or else impart different kinase specificities is under ongoing investigation. This study shows that the expression of Clb2 during S phase in cells lacking Clb5 failed to rescue late origin activation. Early expression of Clb2 in cells lacking both Clb5 and Clb6 did not activate early origins on schedule to restore the correct S phase entry time. Therefore, Clb2 cannot drive timely activation of either early or late replication origins, demonstrating that Clb2-directed CDK has a specificity distinct from that driven by Clb5 and Clb6.
细胞周期蛋白依赖性激酶(CDK)驱动细胞周期,其中对染色体复制的精确控制至关重要。在酿酒酵母中,六种密切相关的B型细胞周期蛋白(Clb1 - 6)驱动S期和有丝分裂事件。Clb5或Clb6均可激活早期启动的复制起点,而只有Clb5能激活晚期起点。Clb1 - 4在细胞周期后期表达。Clb细胞周期蛋白是仅在表达时间上有所不同,还是具有不同的激酶特异性,仍在研究中。本研究表明,在缺乏Clb5的细胞中,S期时Clb2的表达未能挽救晚期起点激活。在同时缺乏Clb5和Clb6的细胞中,Clb2的早期表达未能按时激活早期起点以恢复正确的S期进入时间。因此,Clb2不能驱动早期或晚期复制起点的及时激活,这表明Clb2指导的CDK具有与Clb5和Clb6驱动的CDK不同的特异性。