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Cyclin K regulates prereplicative complex assembly to promote mammalian cell proliferation.

Tingjun LeiPeixuan ZhangXudong ZhangXue XiaoJingli ZhangTong QiuQian DaiYujun ZhangLing MinQian LiRutie YinPing DingNi LiYi QuDezhi MuJun QinXiaofeng ZhuZhi-Xiong XiaoQintong Li
Published in: Nature communications (2018)
The assembly of prereplicative complex (pre-RC) during G1 phase must be tightly controlled to sustain cell proliferation and maintain genomic stability. Mechanisms to prevent pre-RC formation in G2/M and S phases are well appreciated, whereas how cells ensure efficient pre-RC assembly during G1 is less clear. Here we report that cyclin K regulates pre-RC formation. We find that cyclin K expression positively correlates with cell proliferation, and knockdown of cyclin K or its cognate kinase CDK12 prevents the assembly of pre-RC in G1 phase. Mechanistically we uncover that cyclin K promotes pre-RC assembly by restricting cyclin E1 activity in G1. We identify a cyclin K-dependent, novel phosphorylation site in cyclin E1 that disrupts its interaction with CDK2. Importantly, this antagonistic relationship is largely recapitulated in cyclin E1-overexpressing tumors. We discuss the implications of our findings in light of recent reports linking cyclin K and CDK12 to human tumorigenesis.
Keyphrases
  • cell cycle
  • cell proliferation
  • cell cycle arrest
  • pi k akt
  • cell death
  • endothelial cells
  • emergency department
  • signaling pathway
  • dna methylation
  • genome wide
  • binding protein