A DNA Helicase Activity Is Associated with an MCM4, -6, and -7 Protein Complex*

All six minichromosome maintenance (MCM) proteins have DNA-dependent ATPase motifs in the central domain which is conserved from yeast to mammals. Our group purified MCM protein complexes consisting of MCM2, -4 (Cdc21), -6 (Mis5), and -7 (CDC47) proteins from HeLa cells by using histone-Sepharose column chromatography (Ishimi, Y., Ichinose, S., Omori, A., Sato K., and Kimura, H. (1996) J. Biol. Chem. 271, 24115–24122). The present study revealed that both ATPase activity and DNA helicase activity that displaces oligonucleotides annealed to single-stranded circular DNA are associated with an MCM protein complex. Both ATPase and DNA helicase activities were co-purified with a 600-kDa protein complex that is consisted of equal amounts of MCM4, -6, and -7 proteins. An immunodepletion of the MCM protein complex from the purified fraction using anti-MCM4 antibody resulted in the severe reduction of the DNA helicase activity. Displacement of DNA fragments by the DNA helicase suggested that it migrated along single-stranded DNA in the 3′ to 5′ direction, and the DNA helicase activity was detected only in the presence of hydrolyzable ATP or dATP. These results suggest that this helicase may be involved in the initiation of DNA replication as a DNA unwinding enzyme.

[1]  M. Fujita,et al.  In Vivo Interaction of Human MCM Heterohexameric Complexes with Chromatin , 1997, The Journal of Biological Chemistry.

[2]  K. Sugimoto,et al.  Mouse MCM proteins: complex formation and transportation to the nucleus , 1996, Genes to cells : devoted to molecular & cellular mechanisms.

[3]  J. Gautier,et al.  Phosphorylation of MCM4 by cdc2 protein kinase inhibits the activity of the minichromosome maintenance complex. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[4]  G. Evan,et al.  Interaction between the Origin Recognition Complex and the Replication Licensing Systemin Xenopus , 1996, Cell.

[5]  T. Coleman,et al.  The Xenopus Cdc6 Protein Is Essential for the Initiation of a Single Round of DNA Replication in Cell-Free Extracts , 1996, Cell.

[6]  H. Hameister,et al.  A novel human Mcm protein: homology to the yeast replication protein Mis5 and chromosomal location. , 1996, Genomics.

[7]  H Kimura,et al.  Binding of Human Minichromosome Maintenance Proteins with Histone H3* , 1996, The Journal of Biological Chemistry.

[8]  S. C. West,et al.  DNA Helicases: New Breeds of Translocating Motors and Molecular Pumps , 1996, Cell.

[9]  I. Todorov,et al.  The role of MCM proteins in the cell cycle control of genome duplication , 1996, BioEssays : news and reviews in molecular, cellular and developmental biology.

[10]  P. O’Farrell,et al.  Drosophila MCM protein complexes. , 1996, Molecular biology of the cell.

[11]  Greet Blom van Assendelft,et al.  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. , 1996, The EMBO journal.

[12]  R. Laskey,et al.  Human replication proteins hCdc21, hCdc46 and P1Mcm3 bind chromatin uniformly before S-phase and are displaced locally during DNA replication. , 1996, Journal of cell science.

[13]  W. Dunphy,et al.  Role for a Xenopus Orc2-related protein in controlling DNA replication , 1996, Nature.

[14]  Andreas Richter,et al.  Properties of the human nuclear protein p85Mcm. Expression, nuclear localization and interaction with other Mcm proteins. , 1996, European journal of biochemistry.

[15]  K. Bjornson,et al.  Mechanisms of helicase-catalyzed DNA unwinding. , 1996, Annual review of biochemistry.

[16]  R. Laskey,et al.  The nuclear envelope prevents reinitiation of replication by regulating the binding of MCM3 to chromatin in Xenopus egg extracts , 1995, Current Biology.

[17]  Judith L Campbell,et al.  A yeast gene required for DNA replication encodes a protein with homology to DNA helicases. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[18]  K. Sugimoto,et al.  Molecular cloning of cDNA encoding mouse Cdc21 and CDC46 homologs and characterization of the products: physical interaction between P1(MCM3) and CDC46 proteins. , 1995, Nucleic acids research.

[19]  K. Matsumoto,et al.  Stimulation of DNA synthesis by mouse DNA helicase B in a DNA replication system containing eukaryotic replication origins. , 1995, Biochemistry.

[20]  A. Attaran,et al.  BM28, a human member of the MCM2-3-5 family, is displaced from chromatin during DNA replication , 1995, The Journal of cell biology.

[21]  R. Knippers,et al.  A human homologue of the yeast replication protein Cdc21. Interactions with other Mcm proteins. , 1995, European journal of biochemistry.

[22]  R. Laskey,et al.  MCM3 complex required for cell cycle regulation of DNA replication in vertebrate cells , 1995, Nature.

[23]  James P. J. Chong,et al.  Purification of an MCM-containing complex as a component of the DNA replication licensing system , 1995, Nature.

[24]  J. Rine,et al.  The origin recognition complex in silencing, cell cycle progression, and DNA replication. , 1995, Molecular biology of the cell.

[25]  H. Nojima,et al.  Identification of the yeast MCM3-related protein as a component of xenopus DNA replication licensing factor , 1995, Cell.

[26]  M. Starborg,et al.  A murine replication protein accumulates temporarily in the heterochromatic regions of nuclei prior to initiation of DNA replication. , 1995, Journal of cell science.

[27]  T. Eki,et al.  Characterization of DNA synthesis and DNA-dependent ATPase activity at a restrictive temperature in temperature-sensitive tsFT848 cells with thermolabile DNA helicase B , 1995, Molecular and cellular biology.

[28]  S. W. Matson,et al.  Purification and biochemical characterization of enzymes with DNA helicase activity. , 1995, Methods in enzymology.

[29]  K. Sugimoto,et al.  DNA polymerase alpha associated protein P1, a murine homolog of yeast MCM3, changes its intranuclear distribution during the DNA synthetic period. , 1994, The EMBO journal.

[30]  B. Tye The MCM2-3-5 proteins: are they replication licensing factors? , 1994, Trends in cell biology.

[31]  S. W. Matson,et al.  DNA helicases: Enzymes with essential roles in all aspects of DNA metabolism , 1994, BioEssays : news and reviews in molecular, cellular and developmental biology.

[32]  R. Pepperkok,et al.  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. , 1994, Journal of cell science.

[33]  S. Bell,et al.  Yeast origin recognition complex functions in transcription silencing and DNA replication. , 1993, Science.

[34]  J. Rine,et al.  Origin recognition complex (ORC) in transcriptional silencing and DNA replication in S. cerevisiae. , 1993, Science.

[35]  I. Herskowitz,et al.  Isolation of ORC6, a component of the yeast origin recognition complex by a one-hybrid system. , 1993, Science.

[36]  K. Nasmyth,et al.  Yeast origin recognition complex is involved in DNA replication and transcriptional silencing , 1993, Nature.

[37]  B. Tye,et al.  Cell cycle-regulated nuclear localization of MCM2 and MCM3, which are required for the initiation of DNA synthesis at chromosomal replication origins in yeast. , 1993, Genes & development.

[38]  E V Koonin,et al.  A common set of conserved motifs in a vast variety of putative nucleic acid-dependent ATPases including MCM proteins involved in the initiation of eukaryotic DNA replication. , 1993, Nucleic acids research.

[39]  F. Dean,et al.  The simian virus 40 T antigen double hexamer assembles around the DNA at the replication origin. , 1992, The Journal of biological chemistry.

[40]  Bruce Stillman,et al.  ATP-dependent recognition of eukaryotic origins of DNA replication by a multiprotein complex , 1992, Nature.

[41]  B. Tye,et al.  Mcm2 and Mcm3, two proteins important for ARS activity, are related in structure and function. , 1991, Genes & development.

[42]  D. Botstein,et al.  A group of interacting yeast DNA replication genes. , 1991, Genes & development.

[43]  F. Hanaoka,et al.  Further characterization of DNA helicase activity of mouse DNA-dependent adenosinetriphosphatase B (DNA helicase B). , 1988, Biochemistry.

[44]  F. Dean,et al.  The unwinding of duplex regions in DNA by the simian virus 40 large tumor antigen-associated DNA helicase activity. , 1988, The Journal of biological chemistry.

[45]  F. Dean,et al.  In vitro replication of duplex circular DNA containing the simian virus 40 DNA origin site. , 1985, Proceedings of the National Academy of Sciences of the United States of America.

[46]  M. Modak,et al.  Affinity Labeling of Escherichia coli DNA Polymerase I with Thymidine 5′-Triphosphate and 8-Azidoadenosine 5′-Triphosphate: Conditions for Optimum Labeling, Specificity, and Identification of the Labeling Site , 1984 .

[47]  L. Finger,et al.  Stabilization of the hexameric form of Escherichia coli protein rho under ATP hydrolysis conditions. , 1982, Journal of molecular biology.

[48]  U. K. Laemmli,et al.  Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4 , 1970, Nature.