Cdt1 Interactions in the Licensing Process: A Model for Dynamic Spatio-temporal Control of Licensing

Within each cell cycle, a cell must ensure that the processes of selection of replication origins (licensing) and initiation of DNA replication are well coordinated to prevent re-initiation of DNA replication from the same DNA segment during the same cell cycle. This is achieved by restricting the licensing process to G1 phase when the prereplicative complexes (preRCs) are assembled onto the origin DNA, while DNA replication is initiated only during S phase when de novo preRC assembly is blocked. Cdt1 is an important member of the preRC complex and its tight regulation through ubiquitin-dependent proteolysis and binding to its inhibitor Geminin ensure that Cdt1 will only be present in G1 phase, preventing relicensing of replication origins. We have recently reported that Cdt1 associates with chromatin in a dynamic way and recruits its inhibitor Geminin onto chromatin in vivo. Here we discuss how these dynamic Cdt1-chromatin interactions and the local recruitment of Geminin onto origins of replication by Cdt1 may provide a tight control of the licensing process in time and in space.

[1]  Maria Dimaki,et al.  Cdt1 associates dynamically with chromatin throughout G1 and recruits Geminin onto chromatin , 2007, The EMBO journal.

[2]  M. Méchali,et al.  A Cdt1–geminin complex licenses chromatin for DNA replication and prevents rereplication during S phase in Xenopus , 2006, The EMBO journal.

[3]  Anindya Dutta,et al.  PCNA Is a Cofactor for Cdt1 Degradation by CUL4/DDB1-mediated N-terminal Ubiquitination* , 2006, Journal of Biological Chemistry.

[4]  K. Nakayama,et al.  Two E3 ubiquitin ligases, SCF‐Skp2 and DDB1‐Cul4, target human Cdt1 for proteolysis , 2006, The EMBO journal.

[5]  J. Walter,et al.  Getting a grip on licensing: mechanism of stable Mcm2-7 loading onto replication origins. , 2006, Molecular cell.

[6]  T. Misteli,et al.  Chinese hamster ORC subunits dynamically associate with chromatin throughout the cell-cycle. , 2005, Experimental cell research.

[7]  D. Takeda,et al.  Degradation of Cdt1 during S Phase Is Skp2-independent and Is Required for Efficient Progression of Mammalian Cells through S Phase* , 2005, Journal of Biological Chemistry.

[8]  J. Julian Blow,et al.  Preventing re-replication of chromosomal DNA , 2005, Nature Reviews Molecular Cell Biology.

[9]  J. Blow,et al.  Functional domains of the Xenopus replication licensing factor Cdt1 , 2005, Nucleic acids research.

[10]  R. Knippers,et al.  The Replicative Regulator Protein Geminin on Chromatin in the HeLa Cell Cycle* , 2004, Journal of Biological Chemistry.

[11]  C. McCall,et al.  Targeted ubiquitination of CDT1 by the DDB1–CUL4A–ROC1 ligase in response to DNA damage , 2004, Nature Cell Biology.

[12]  J. Diffley,et al.  Regulation of Early Events in Chromosome Replication , 2004, Current Biology.

[13]  Yunje Cho,et al.  Structural basis for inhibition of the replication licensing factor Cdt1 by geminin , 2004, Nature.

[14]  D. Takeda,et al.  A dimerized coiled-coil domain and an adjoining part of geminin interact with two sites on Cdt1 for replication inhibition. , 2004, Molecular cell.

[15]  T. Nishimoto,et al.  Proteolysis of DNA Replication Licensing Factor Cdt1 in S-phase Is Performed Independently of Geminin through Its N-terminal Region* , 2004, Journal of Biological Chemistry.

[16]  Tom Misteli,et al.  Global Nature of Dynamic Protein-Chromatin Interactions In Vivo: Three-Dimensional Genome Scanning and Dynamic Interaction Networks of Chromatin Proteins , 2004, Molecular and Cellular Biology.

[17]  Jianyu Zheng,et al.  Radiation-mediated proteolysis of CDT1 by CUL4–ROC1 and CSN complexes constitutes a new checkpoint , 2003, Nature Cell Biology.

[18]  Xiaohua Wu,et al.  The SCFSkp2 Ubiquitin Ligase Complex Interacts with the Human Replication Licensing Factor Cdt1 and Regulates Cdt1 Degradation* , 2003, Journal of Biological Chemistry.

[19]  Anindya Dutta,et al.  A p53-dependent checkpoint pathway prevents rereplication. , 2003, Molecular cell.

[20]  T. Mizuno,et al.  Mouse Geminin Inhibits Not Only Cdt1-MCM6 Interactions but Also a Novel Intrinsic Cdt1 DNA Binding Activity* , 2002, The Journal of Biological Chemistry.

[21]  H. Nishitani,et al.  Control of DNA replication licensing in a cell cycle , 2002, Genes to cells : devoted to molecular & cellular mechanisms.

[22]  D. Gilbert,et al.  Mammalian nuclei become licensed for DNA replication during late telophase. , 2002, Journal of cell science.

[23]  Anindya Dutta,et al.  DNA replication in eukaryotic cells. , 2002, Annual review of biochemistry.

[24]  J. Blow,et al.  Reconstitution of licensed replication origins on Xenopus sperm nuclei using purified proteins , 2001, BMC Biochemistry.

[25]  Zoi Lygerou,et al.  The Human Licensing Factor for DNA Replication Cdt1 Accumulates in G1 and Is Destabilized after Initiation of S-phase* , 2001, The Journal of Biological Chemistry.

[26]  J. Pines,et al.  Stability, chromatin association and functional activity of mammalian pre‐replication complex proteins during the cell cycle , 2001, The EMBO journal.

[27]  M. Méchali,et al.  Repression of origin assembly in metaphase depends on inhibition of RLF-B/Cdt1 by geminin , 2001, Nature Cell Biology.

[28]  J A Wohlschlegel,et al.  Inhibition of eukaryotic DNA replication by geminin binding to Cdt1. , 2000, Science.

[29]  Zoi Lygerou,et al.  The Cdt1 protein is required to license DNA for replication in fission yeast , 2000, Nature.

[30]  M. Méchali,et al.  Stepwise Regulated Chromatin Assembly of MCM2–7 Proteins* , 2000, The Journal of Biological Chemistry.

[31]  O. Aparicio,et al.  Components and Dynamics of DNA Replication Complexes in S. cerevisiae: Redistribution of MCM Proteins and Cdc45p during S Phase , 1997, Cell.

[32]  Y. Ishimi A DNA Helicase Activity Is Associated with an MCM4, -6, and -7 Protein Complex* , 1997, The Journal of Biological Chemistry.

[33]  Paul Nurse,et al.  Ordering S phase and M phase in the cell cycle , 1994, Cell.

[34]  A. de Recondo [DNA replication in eukaryotic cells]. , 1977, Biochimie.