Literature DB >> 9214647

Licensing of DNA replication by a multi-protein complex of MCM/P1 proteins in Xenopus eggs.

Y Kubota1, S Mimura, S Nishimoto, T Masuda, H Nojima, H Takisawa.   

Abstract

In eukaryotes, chromosomal DNA is licensed for a single round of replication in each cell cycle. Xenopus MCM3 protein has been implicated in the licensing of replication in egg extract. We have cloned cDNAs encoding five immunologically distinct proteins associated with Xenopus MCM3 as members of the MCM/P1 family. Six Xenopus MCM proteins formed a physical complex in the egg extract, bound to unreplicated chromatin before the formation of nuclei, and apparently displaced from replicated chromatin. The requirement of six XMCM proteins for the replication activity of the egg extract before nuclear formation suggests that their re-association with replicated chromatin at the end of the mitotic cell cycle is a key step for the licensing of replication.

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Year:  1997        PMID: 9214647      PMCID: PMC1169948          DOI: 10.1093/emboj/16.11.3320

Source DB:  PubMed          Journal:  EMBO J        ISSN: 0261-4189            Impact factor:   11.598


  31 in total

Review 1.  The role of MCM/P1 proteins in the licensing of DNA replication.

Authors:  J P Chong; P Thömmes; J J Blow
Journal:  Trends Biochem Sci       Date:  1996-03       Impact factor: 13.807

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.  Mammalian cell fusion: studies on the regulation of DNA synthesis and mitosis.

Authors:  P N Rao; R T Johnson
Journal:  Nature       Date:  1970-01-10       Impact factor: 49.962

4.  The association and involvement of some members of the P1 protein family in a cell-free DNA replication of Xenopus eggs.

Authors:  A Someya; M Shioda; A Okuyama
Journal:  Biochem Biophys Res Commun       Date:  1995-04-26       Impact factor: 3.575

5.  Identification of the yeast MCM3-related protein as a component of Xenopus DNA replication licensing factor.

Authors:  Y Kubota; S Mimura; S Nishimoto; H Takisawa; H Nojima
Journal:  Cell       Date:  1995-05-19       Impact factor: 41.582

6.  Properties of the nuclear P1 protein, a mammalian homologue of the yeast Mcm3 replication protein.

Authors:  P Thömmes; R Fett; B Schray; R Burkhart; M Barnes; C Kennedy; N C Brown; R Knippers
Journal:  Nucleic Acids Res       Date:  1992-03-11       Impact factor: 16.971

7.  The origin recognition complex in silencing, cell cycle progression, and DNA replication.

Authors:  S Loo; C A Fox; J Rine; R Kobayashi; B Stillman; S Bell
Journal:  Mol Biol Cell       Date:  1995-06       Impact factor: 4.138

8.  Chromatin binding, nuclear localization and phosphorylation of Xenopus cdc21 are cell-cycle dependent and associated with the control of initiation of DNA replication.

Authors:  M Coué; S E Kearsey; M Méchali
Journal:  EMBO J       Date:  1996-03-01       Impact factor: 11.598

9.  Fission yeast cdc21, a member of the MCM protein family, is required for onset of S phase and is located in the nucleus throughout the cell cycle.

Authors:  D Maiorano; G B Van Assendelft; S E Kearsey
Journal:  EMBO J       Date:  1996-02-15       Impact factor: 11.598

10.  Human replication proteins hCdc21, hCdc46 and P1Mcm3 bind chromatin uniformly before S-phase and are displaced locally during DNA replication.

Authors:  T Krude; C Musahl; R A Laskey; R Knippers
Journal:  J Cell Sci       Date:  1996-02       Impact factor: 5.285

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  39 in total

1.  A fission yeast gene, him1(+)/dfp1(+), encoding a regulatory subunit for Hsk1 kinase, plays essential roles in S-phase initiation as well as in S-phase checkpoint control and recovery from DNA damage.

Authors:  T Takeda; K Ogino; E Matsui; M K Cho; H Kumagai; T Miyake; K Arai; H Masai
Journal:  Mol Cell Biol       Date:  1999-08       Impact factor: 4.272

2.  Distinct phosphoisoforms of the Xenopus Mcm4 protein regulate the function of the Mcm complex.

Authors:  I Pereverzeva; E Whitmire; B Khan; M Coué
Journal:  Mol Cell Biol       Date:  2000-05       Impact factor: 4.272

3.  Identification of two residues in MCM5 critical for the assembly of MCM complexes and Stat1-mediated transcription activation in response to IFN-gamma.

Authors:  C J DaFonseca; F Shu; J J Zhang
Journal:  Proc Natl Acad Sci U S A       Date:  2001-03-06       Impact factor: 11.205

4.  MCM2-7 proteins are essential components of prereplicative complexes that accumulate cooperatively in the nucleus during G1-phase and are required to establish, but not maintain, the S-phase checkpoint.

Authors:  K Labib; S E Kearsey; J F Diffley
Journal:  Mol Biol Cell       Date:  2001-11       Impact factor: 4.138

5.  Regulation of initiation of S phase, replication checkpoint signaling, and maintenance of mitotic chromosome structures during S phase by Hsk1 kinase in the fission yeast.

Authors:  T Takeda; K Ogino; K Tatebayashi; H Ikeda; H Masai
Journal:  Mol Biol Cell       Date:  2001-05       Impact factor: 4.138

6.  Xenopus Cut5 is essential for a CDK-dependent process in the initiation of DNA replication.

Authors:  Yoshitami Hashimoto; Haruhiko Takisawa
Journal:  EMBO J       Date:  2003-05-15       Impact factor: 11.598

Review 7.  Eukaryotic MCM proteins: beyond replication initiation.

Authors:  Susan L Forsburg
Journal:  Microbiol Mol Biol Rev       Date:  2004-03       Impact factor: 11.056

8.  The ATPase activity of MCM2-7 is dispensable for pre-RC assembly but is required for DNA unwinding.

Authors:  Carol Y Ying; Jean Gautier
Journal:  EMBO J       Date:  2005-11-24       Impact factor: 11.598

9.  Progesterone blocks estrogen-induced DNA synthesis through the inhibition of replication licensing.

Authors:  Haiyan Pan; Yan Deng; Jeffrey W Pollard
Journal:  Proc Natl Acad Sci U S A       Date:  2006-09-11       Impact factor: 11.205

10.  Evolutionary diversification of MCM3 genes in Xenopus laevis and Danio rerio.

Authors:  Minori Shinya; Daiki Machiki; Thorsten Henrich; Yumiko Kubota; Haruhiko Takisawa; Satoru Mimura
Journal:  Cell Cycle       Date:  2014       Impact factor: 4.534

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