Literature DB >> 14731643

The MCM2-3-5 proteins: are they replication licensing factors?

B K Tye1.   

Abstract

DNA replication occurs only once in each normal mitotic cell cycle. To explain this strict control, a 'licensing factor' was proposed to enter the nucleus periodically as the nuclear envelope disintegrates and reassembles at the end of mitosis. Inactivation of licensing factor immediately following initiation of DNA synthesis would prevent reinitiation until after the next mitosis. The MCM2-3-5 proteins of Saccharomyces cerevisiae may be yeast's equivalent of licensing factor: they are present in the nucleus only between M and S phase, bind to chromatin and are important for the initiation of DNA replication.

Entities:  

Year:  1994        PMID: 14731643     DOI: 10.1016/0962-8924(94)90200-3

Source DB:  PubMed          Journal:  Trends Cell Biol        ISSN: 0962-8924            Impact factor:   20.808


  39 in total

1.  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

2.  Coordinating DNA replication to produce one copy of the genome requires genes that act in ubiquitin metabolism.

Authors:  J D Singer; B M Manning; T Formosa
Journal:  Mol Cell Biol       Date:  1996-04       Impact factor: 4.272

3.  Fission yeast cdc24 is a replication factor C- and proliferating cell nuclear antigen-interacting factor essential for S-phase completion.

Authors:  H Tanaka; K Tanaka; H Murakami; H Okayama
Journal:  Mol Cell Biol       Date:  1999-02       Impact factor: 4.272

4.  Multiple domains of fission yeast Cdc19p (MCM2) are required for its association with the core MCM complex.

Authors:  D A Sherman; S G Pasion; S L Forsburg
Journal:  Mol Biol Cell       Date:  1998-07       Impact factor: 4.138

5.  Establishing genetic interactions by a synthetic dosage lethality phenotype.

Authors:  E S Kroll; K M Hyland; P Hieter; J J Li
Journal:  Genetics       Date:  1996-05       Impact factor: 4.562

6.  Mutational analysis of Cdc19p, a Schizosaccharomyces pombe MCM protein.

Authors:  S L Forsburg; D A Sherman; S Ottilie; J R Yasuda; J A Hodson
Journal:  Genetics       Date:  1997-11       Impact factor: 4.562

7.  Phosphorylation of MCM4 by cdc2 protein kinase inhibits the activity of the minichromosome maintenance complex.

Authors:  M Hendrickson; M Madine; S Dalton; J Gautier
Journal:  Proc Natl Acad Sci U S A       Date:  1996-10-29       Impact factor: 11.205

8.  cDNA cloning and characterisation of a maize homologue of the MCM proteins required for the initiation of DNA replication.

Authors:  P A Sabelli; S R Burgess; A K Kush; M R Young; P R Shewry
Journal:  Mol Gen Genet       Date:  1996-08-27

9.  Cell cycle-regulated nuclear import and export of Cdc47, a protein essential for initiation of DNA replication in budding yeast.

Authors:  S Dalton; L Whitbread
Journal:  Proc Natl Acad Sci U S A       Date:  1995-03-28       Impact factor: 11.205

10.  Schizosaccharomyces pombe Mcm3p, an essential nuclear protein, associates tightly with Nda4p (Mcm5p).

Authors:  D A Sherman; S L Forsburg
Journal:  Nucleic Acids Res       Date:  1998-09-01       Impact factor: 16.971

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