Mcm2 and Mcm3, two proteins important for ARS activity, are related in structure and function.

MCM2 and MCM3 are essential genes believed to play important roles in the initiation of DNA replication in Saccharomyces cerevisiae. Mutants defective in Mcm2 or Mcm3 are remarkably similar in phenotype. They both show an autonomously replicating sequence (ARS)-specific minichromosome maintenance defect, although their ARS specificities are not identical. In addition, these mutants exhibit a premitotic cell cycle arrest and an increase in chromosome loss and recombination. Genetic studies suggest that the two MCM gene products play interacting or complementary roles in DNA replication. Double mutants of mcm2-1 and mcm3-1 are inviable at the permissive growth temperature (23 degrees C) for each of the single mutants. Furthermore, overproduction of Mcm3 accentuates the deleterious effect of the mcm2-1 mutation, whereas overproduction of Mcm2 partially complements the mcm3-1 mutation. MCM2 encodes a protein of 890 amino acids containing a putative zinc-finger domain that is essential for Mcm2 function. Mcm2 shows striking homology to Mcm3 and three other proteins, Cdc46 of S. cerevisiae, and Nda4 and Cdc21 of Schizosaccharomyces pombe. The phenotypes of mutants defective in these proteins suggest that they belong to a protein family involved in the early steps of DNA replication.

[1]  B. Tye,et al.  Autonomously replicating sequences in Saccharomyces cerevisiae. , 1980, Proceedings of the National Academy of Sciences of the United States of America.

[2]  D. Botstein,et al.  Subcellular localization of yeast CDC46 varies with the cell cycle. , 1990, Genes & development.

[3]  S. Biswas,et al.  ARS binding factor I of the yeast Saccharomyces cerevisiae binds to sequences in telomeric and nontelomeric autonomously replicating sequences , 1990, Molecular and cellular biology.

[4]  R. Smith,et al.  Expression of calf prochymosin in Saccharomyces cerevisiae. , 1984, Gene.

[5]  S. Kearsey Structural requirements for the function of a yeast chromosomal replicator , 1984, Cell.

[6]  J. Broach,et al.  Localization and sequence analysis of yeast origins of DNA replication. , 1983, Cold Spring Harbor symposia on quantitative biology.

[7]  F. Sanger,et al.  DNA sequencing with chain-terminating inhibitors. , 1977, Proceedings of the National Academy of Sciences of the United States of America.

[8]  Arthur Kornberg,et al.  A model for initiation at origins of DNA replication , 1988, Cell.

[9]  A. Cigan,et al.  Mutations at a Zn(II) finger motif in the yeast elF-2β gene alter ribosomal start-site selection during the scanning process , 1988, Cell.

[10]  L. Guarente,et al.  Functional dissection and sequence of yeast HAP1 activator , 1989, Cell.

[11]  R. Rothstein 18 – One-Step Gene Disruption in Yeast , 1989 .

[12]  J. Messing [2] New M13 vectors for cloning , 1983 .

[13]  S. J. Flint,et al.  DNA‐binding properties of an adenovirus 289R E1A protein. , 1988, The EMBO journal.

[14]  S. Francesconi,et al.  A DNA replication enhancer in Saccharomyces cerevisiae. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[15]  J. Diffley,et al.  Purification of a yeast protein that binds to origins of DNA replication and a transcriptional silencer. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[16]  Thomas A. Kunkel,et al.  Rapid and efficient site-specific mutagenesis without phenotypic selection. , 1985, Proceedings of the National Academy of Sciences of the United States of America.

[17]  B. Stillman,et al.  Initiation of eukaryotic DNA replication in vitro. , 1988, BioEssays : news and reviews in molecular, cellular and developmental biology.

[18]  J. Culp,et al.  The 289-amino acid E1A protein of adenovirus binds zinc in a region that is important for trans-activation. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[19]  G. Fink,et al.  Methods in yeast genetics , 1979 .

[20]  C. Newlon,et al.  Close association of a DNA replication origin and an ARS element on chromosome III of the yeast, Saccharomyces cerevisiae. , 1988, Nucleic acids research.

[21]  N. M. Hollingsworth,et al.  The HOP1 gene encodes a meiosis-specific component of yeast chromosomes , 1990, Cell.

[22]  R. Elble,et al.  A protein involved in minichromosome maintenance in yeast binds a transcriptional enhancer conserved in eukaryotes. , 1989, Genes & development.

[23]  S. Eisenberg,et al.  Specific interaction between a Saccharomyces cerevisiae protein and a DNA element associated with certain autonomously replicating sequences. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[24]  D. Botstein,et al.  A Saccharomyces cerevisiae genomic plasmid bank based on a centromere-containing shuttle vector. , 1987, Gene.

[25]  K. Murata,et al.  Transformation of intact yeast cells treated with alkali cations , 1983 .

[26]  R. W. Davis,et al.  High-frequency transformation of yeast: autonomous replication of hybrid DNA molecules. , 1979, Proceedings of the National Academy of Sciences of the United States of America.

[27]  B. Tye,et al.  The phenotype of the minichromosome maintenance mutant mcm3 is characteristic of mutants defective in DNA replication , 1990, Molecular and cellular biology.

[28]  B. Tye,et al.  Mutants of S. cerevisiae defective in the maintenance of minichromosomes. , 1984, Genetics.

[29]  B. Tye,et al.  A mutant that affects the function of autonomously replicating sequences in yeast. , 1986, Journal of molecular biology.

[30]  R. Elble,et al.  Saccharomyces cerevisiae protein involved in plasmid maintenance is necessary for mating of MAT alpha cells. , 1988, Journal of molecular biology.

[31]  R. Umek,et al.  The ease of DNA unwinding as a determinant of initiation at yeast replication origins , 1988, Cell.

[32]  R. Dale,et al.  A rapid single-stranded cloning strategy for producing a sequential series of overlapping clones for use in DNA sequencing: application to sequencing the corn mitochondrial 18 S rDNA. , 1985, Plasmid.

[33]  R. Evans,et al.  Zinc fingers: Gilt by association , 1988, Cell.

[34]  D. Botstein,et al.  Construction and genetic characterization of temperature-sensitive mutant alleles of the yeast actin gene. , 1984, Proceedings of the National Academy of Sciences of the United States of America.

[35]  D. Williamson,et al.  The use of fluorescent DNA-binding agent for detecting and separating yeast mitochondrial DNA. , 1975, Methods in cell biology.

[36]  R. Rothstein One-step gene disruption in yeast. , 1983, Methods in enzymology.

[37]  Clarence S. M. Chan,et al.  Organization of DNA sequences and replication origins at yeast telomeres , 1983, Cell.

[38]  M. Osley,et al.  Identification of a sequence responsible for periodic synthesis of yeast histone 2A mRNA. , 1982, Proceedings of the National Academy of Sciences of the United States of America.

[39]  J. Broach,et al.  Identification of sites required for repression of a silent mating type locus in yeast. , 1984, Journal of molecular biology.

[40]  J. Devereux,et al.  A comprehensive set of sequence analysis programs for the VAX , 1984, Nucleic Acids Res..

[41]  J. Berg Zinc finger domains: hypotheses and current knowledge. , 1990, Annual review of biophysics and biophysical chemistry.