Literature DB >> 9792427

The replication licensing system.

S Tada1, J J Blow.   

Abstract

The replication licensing system acts to ensure that no section of the genome is replicated more than once in a single cell cycle. Experiments using Xenopus egg extracts have revealed that the licensing system consists of two components, named RLF-M and RLF-B. Whereas the function of RLF-B is still unclear, RLF-M has been shown to consist of all six members of the MCM/P1 family proteins, which appear to be the structural component of the licensing system. The origin recognition complex (ORC) and Cdc6/Cdc18 are needed on chromatin before the licensing reaction can take place, although they are not themselves components of the licensing system. Cell cycle events and cyclin-dependent protein kinases (Cdks) also seem to be involved in controlling the licensing system to ensure once per cell cycle DNA replication. The subject of this review is to detail our current understanding of the licensing system and the way that it interacts with other components of the cell cycle machinery.

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Year:  1998        PMID: 9792427      PMCID: PMC3604913     

Source DB:  PubMed          Journal:  Biol Chem        ISSN: 1431-6730            Impact factor:   3.915


  83 in total

1.  Regulation of the replication initiator protein p65cdc18 by CDK phosphorylation.

Authors:  P V Jallepalli; G W Brown; M Muzi-Falconi; D Tien; T J Kelly
Journal:  Genes Dev       Date:  1997-11-01       Impact factor: 11.361

2.  A role for the nuclear envelope in controlling DNA replication within the cell cycle.

Authors:  J J Blow; R A Laskey
Journal:  Nature       Date:  1988-04-07       Impact factor: 49.962

3.  Nuclear reconstitution in vitro: stages of assembly around protein-free DNA.

Authors:  J Newport
Journal:  Cell       Date:  1987-01-30       Impact factor: 41.582

4.  A mutant that affects the function of autonomously replicating sequences in yeast.

Authors:  P Sinha; V Chang; B K Tye
Journal:  J Mol Biol       Date:  1986-12-20       Impact factor: 5.469

5.  Persistent initiation of DNA replication and chromatin-bound MCM proteins during the cell cycle in cdc6 mutants.

Authors:  C Liang; B Stillman
Journal:  Genes Dev       Date:  1997-12-15       Impact factor: 11.361

6.  Mcm2 is a target of regulation by Cdc7-Dbf4 during the initiation of DNA synthesis.

Authors:  M Lei; Y Kawasaki; M R Young; M Kihara; A Sugino; B K Tye
Journal:  Genes Dev       Date:  1997-12-15       Impact factor: 11.361

7.  Mutants of S. cerevisiae defective in the maintenance of minichromosomes.

Authors:  G T Maine; P Sinha; B K Tye
Journal:  Genetics       Date:  1984-03       Impact factor: 4.562

8.  Regulated replication of DNA microinjected into eggs of Xenopus laevis.

Authors:  R M Harland; R A Laskey
Journal:  Cell       Date:  1980-10       Impact factor: 41.582

9.  Initiation of DNA replication in nuclei and purified DNA by a cell-free extract of Xenopus eggs.

Authors:  J J Blow; R A Laskey
Journal:  Cell       Date:  1986-11-21       Impact factor: 41.582

10.  Nuclei act as independent and integrated units of replication in a Xenopus cell-free DNA replication system.

Authors:  J J Blow; J V Watson
Journal:  EMBO J       Date:  1987-07       Impact factor: 11.598

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  12 in total

1.  Expression of FGF2 in the limb blastema of two Salamandridae correlates with their regenerative capability.

Authors:  S Giampaoli; S Bucci; M Ragghianti; G Mancino; F Zhang; P Ferretti
Journal:  Proc Biol Sci       Date:  2003-11-07       Impact factor: 5.349

2.  Suppression of Reserve MCM Complexes Chemosensitizes to Gemcitabine and 5-Fluorouracil.

Authors:  Victoria L Bryant; Roy M Elias; Susan M McCarthy; Timothy J Yeatman; Mark G Alexandrow
Journal:  Mol Cancer Res       Date:  2015-06-10       Impact factor: 5.852

3.  Saccharomyces cerevisiae Mob1p is required for cytokinesis and mitotic exit.

Authors:  F C Luca; M Mody; C Kurischko; D M Roof; T H Giddings; M Winey
Journal:  Mol Cell Biol       Date:  2001-10       Impact factor: 4.272

4.  Nucleoplasmin-mediated chromatin remodelling is required for Xenopus sperm nuclei to become licensed for DNA replication.

Authors:  P J Gillespie; J J Blow
Journal:  Nucleic Acids Res       Date:  2000-01-15       Impact factor: 16.971

Review 5.  The Xenopus cell cycle: an overview.

Authors:  Anna Philpott; P Renee Yew
Journal:  Mol Biotechnol       Date:  2008-02-12       Impact factor: 2.695

6.  The RLF-B component of the replication licensing system is distinct from Cdc6 and functions after Cdc6 binds to chromatin.

Authors:  S Tada; J P Chong; H M Mahbubani; J J Blow
Journal:  Curr Biol       Date:  1999-02-25       Impact factor: 10.834

7.  Changes in association of the Xenopus origin recognition complex with chromatin on licensing of replication origins.

Authors:  A Rowles; S Tada; J J Blow
Journal:  J Cell Sci       Date:  1999-06       Impact factor: 5.285

8.  Repression of origin assembly in metaphase depends on inhibition of RLF-B/Cdt1 by geminin.

Authors:  S Tada; A Li; D Maiorano; M Méchali; J J Blow
Journal:  Nat Cell Biol       Date:  2001-02       Impact factor: 28.824

9.  Sequential MCM/P1 subcomplex assembly is required to form a heterohexamer with replication licensing activity.

Authors:  T A Prokhorova; J J Blow
Journal:  J Biol Chem       Date:  2000-01-28       Impact factor: 5.157

Review 10.  Myc and the Replicative CMG Helicase: The Creation and Destruction of Cancer: Myc Over-Activation of CMG Helicases Drives Tumorigenesis and Creates a Vulnerability in CMGs for Therapeutic Intervention.

Authors:  Damon R Reed; Mark G Alexandrow
Journal:  Bioessays       Date:  2020-02-20       Impact factor: 4.345

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