Literature DB >> 8175912

A human nuclear protein with sequence homology to a family of early S phase proteins is required for entry into S phase and for cell division.

I T Todorov1, R Pepperkok, R N Philipova, S E Kearsey, W Ansorge, D Werner.   

Abstract

Molecular cloning and characterisation of a human nuclear protein designated BM28 is reported. On the amino acid level this 892 amino acid protein, migrating on SDS-gels as a 125 kDa polypeptide, shares areas of significant similarity with a recently defined family of early S phase proteins. The members of this family, the Saccharomyces cerevisiae Mcm2p, Mcm3p, Cdc46p/Mcm5p, the Schizosaccharomyces pombe Cdc21p and the mouse protein P1 are considered to be involved in the onset of DNA replication. The highest similarity was found with Mcm2p (42% identity over the whole length and higher than 75% over a conservative region of 215 amino acid residues), suggesting that BM28 could represent the human homologue of the S. cerevisiae MCM2. Using antibodies raised against the recombinant BM28 the corresponding antigen was found to be localised in the nuclei of various mammalian cells. Microinjection of anti-BM28 antibody into synchronised mouse NIH3T3 or human HeLa cells presents evidence for the involvement of the protein in cell cycle progression. When injected in G1 phase the anti-BM28 antibody inhibits the onset of subsequent DNA synthesis as tested by the incorporation of bromodeoxyuridine. Microinjection during the S phase had no effect on DNA synthesis, but inhibits cell division. The data suggest that the nuclear protein BM28 is required for two events of the cell cycle, for the onset of DNA replication and for cell division.

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Year:  1994        PMID: 8175912     DOI: 10.1242/jcs.107.1.253

Source DB:  PubMed          Journal:  J Cell Sci        ISSN: 0021-9533            Impact factor:   5.285


  33 in total

1.  Selective instability of Orc1 protein accounts for the absence of functional origin recognition complexes during the M-G(1) transition in mammals.

Authors:  D A Natale; C J Li; W H Sun; M L DePamphilis
Journal:  EMBO J       Date:  2000-06-01       Impact factor: 11.598

2.  A requirement for MCM7 and Cdc45 in chromosome unwinding during eukaryotic DNA replication.

Authors:  Marcin Pacek; Johannes C Walter
Journal:  EMBO J       Date:  2004-08-26       Impact factor: 11.598

Review 3.  Eukaryotic MCM proteins: beyond replication initiation.

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

4.  MCM proteins are associated with RNA polymerase II holoenzyme.

Authors:  K Yankulov; I Todorov; P Romanowski; D Licatalosi; K Cilli; S McCracken; R Laskey; D L Bentley
Journal:  Mol Cell Biol       Date:  1999-09       Impact factor: 4.272

5.  A cell signal pathway involving laminin-5, alpha3beta1 integrin, and mitogen-activated protein kinase can regulate epithelial cell proliferation.

Authors:  M Gonzales; K Haan; S E Baker; M Fitchmun; I Todorov; S Weitzman; J C Jones
Journal:  Mol Biol Cell       Date:  1999-02       Impact factor: 4.138

Review 6.  Coordinating DNA replication with cell division: current status of the licensing concept.

Authors:  M Botchan
Journal:  Proc Natl Acad Sci U S A       Date:  1996-09-17       Impact factor: 11.205

7.  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

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

Authors:  Y Kubota; S Mimura; S Nishimoto; T Masuda; H Nojima; H Takisawa
Journal:  EMBO J       Date:  1997-06-02       Impact factor: 11.598

10.  The RLF-M component of the replication licensing system forms complexes containing all six MCM/P1 polypeptides.

Authors:  P Thömmes; Y Kubota; H Takisawa; J J Blow
Journal:  EMBO J       Date:  1997-06-02       Impact factor: 11.598

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