Characterization of the Two Small Subunits of Saccharomyces cerevisiae DNA Polymerase δ*

Yeast DNA polymerase δ (Polδ) has three subunits of 125, 58, and 55 kDa. The gene for the 125-kDa catalytic subunit (POL3) has been known for several years. Here we describe the cloning of the genes for the 58- and 55-kDa subunits using peptide sequence analysis and searching of the yeast genome data base. The 58-kDa subunit, encoded by the POL31 gene, shows 23–28% sequence similarity to the 48-kDa subunit of human Polδ and to S. pombe Cdc1. POL31 is allelic toHYS2 and SDP5. The 55-kDa subunit is encoded by the POL32 gene (ORF YJR043c in the yeast data base). Very limited sequence similarity was observed between Pol32p andSchizosaccharomyces pombe Cdc27, the functionally analogous subunit in S. pombe Polδ. The POL32 gene is not essential, but a deletion mutant shows cold sensitivity for growth and is sensitive to hydroxyurea and DNA damaging agents. In addition, lethality was observed when the POL32 deletion mutation was combined with conditional mutations in either the POL3 orPOL31 gene. Pol32Δ strains are weak antimutators and are defective for damage-induced mutagenesis. ThePOL32 gene product binds proliferating cell nuclear antigen. A gel filtration analysis showed that Pol32p is a dimer in solution. When POL31 and POL32 were co-expressed in Escherichia coli, a tetrameric (Pol31p·Pol32p)2 species was detected by gel filtration, indicating that the two subunits form a complex.

[1]  P. Burgers,et al.  Structure and Processivity of Two Forms of Saccharomyces cerevisiae DNA Polymerase δ* , 1998, The Journal of Biological Chemistry.

[2]  A. Hinnebusch,et al.  Identification of GCD14 and GCD15, novel genes required for translational repression of GCN4 mRNA in Saccharomyces cerevisiae. , 1998, Genetics.

[3]  J. C. Eissenberg,et al.  Mutations in yeast proliferating cell nuclear antigen define distinct sites for interaction with DNA polymerase delta and DNA polymerase epsilon , 1997, Molecular and cellular biology.

[4]  Z. Kelman,et al.  DNA polymerase delta isolated from Schizosaccharomyces pombe contains five subunits. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[5]  R. Chanet,et al.  Involvement of the yeast DNA polymerase delta in DNA repair in vivo. , 1997, Genetics.

[6]  Marietta Y. W. T. Lee,et al.  Expression and Characterization of the Small Subunit of Human DNA Polymerase δ* , 1997, The Journal of Biological Chemistry.

[7]  D. Lane,et al.  Homologous regions of Fen1 and p21Cip1 compete for binding to the same site on PCNA: a potential mechanism to co-ordinate DNA replication and repair , 1997, Oncogene.

[8]  R. Hindges,et al.  DNA polymerase delta, an essential enzyme for DNA transactions. , 1997, Biological chemistry.

[9]  A. Halaś,et al.  Involvement of the RE V3 gene in the methylated base-excision repair system. Co-operation of two DNA polymerases, δ and Rev3p, in the repair of MMS-induced lesions in the DNA of Saccharomyces cerevisiae , 1997, Current Genetics.

[10]  C. Tan,et al.  The small subunit is required for functional interaction of DNA polymerase delta with the proliferating cell nuclear antigen. , 1997, Nucleic acids research.

[11]  J. Gulbis,et al.  The Influence of the Proliferating Cell Nuclear Antigen-interacting Domain of p21CIP1 on DNA Synthesis Catalyzed by the Human and Saccharomyces cerevisiae Polymerase δ Holoenzymes* , 1997, The Journal of Biological Chemistry.

[12]  John Kuriyan,et al.  Structure of the C-Terminal Region of p21WAF1/CIP1 Complexed with Human PCNA , 1996, Cell.

[13]  Asad Umar,et al.  Requirement for PCNA in DNA Mismatch Repair at a Step Preceding DNA Resynthesis , 1996, Cell.

[14]  S. Moreno,et al.  The fission yeast Cdc1 protein, a homologue of the small subunit of DNA polymerase delta, binds to Pol3 and Cdc27. , 1996, The EMBO journal.

[15]  E. Fanning,et al.  DNA polymerase epsilon may be dispensable for SV40‐ but not cellular‐DNA replication. , 1996, The EMBO journal.

[16]  M. Lieber,et al.  Lagging Strand DNA Synthesis at the Eukaryotic Replication Fork Involves Binding and Stimulation of FEN-1 by Proliferating Cell Nuclear Antigen (*) , 1995, The Journal of Biological Chemistry.

[17]  K. Matsumoto,et al.  HYS2, an essential gene required for DNA replication in Saccharomyces cerevisiae. , 1995, Nucleic acids research.

[18]  A. Sugino,et al.  Yeast DNA polymerases and their role at the replication fork. , 1995, Trends in biochemical sciences.

[19]  P. Burgers,et al.  A mutational analysis of the yeast proliferating cell nuclear antigen indicates distinct roles in DNA replication and DNA repair , 1995, Molecular and cellular biology.

[20]  M. Nakanishi,et al.  The C-terminal Region of p21 Is Involved in Proliferating Cell Nuclear Antigen Binding but Does Not Appear to Be Required for Growth Inhibition (*) , 1995, The Journal of Biological Chemistry.

[21]  M. Budd,et al.  DNA polymerases required for repair of UV-induced damage in Saccharomyces cerevisiae , 1995, Molecular and cellular biology.

[22]  P. Burgers DNA polymerase from Saccharomyces cerevisiae. , 1995, Methods in enzymology.

[23]  L. Loeb,et al.  DNA polymerase delta is required for base excision repair of DNA methylation damage in Saccharomyces cerevisiae. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[24]  B. Stillman,et al.  Anatomy of a DNA replication fork revealed by reconstitution of SV40 DNA replication in vitro , 1994, Nature.

[25]  R. G. Ritzel,et al.  The mutator mut7-1 of Saccharomyces cerevisiae. , 1993, Mutation research.

[26]  Jonathan A. Cooper,et al.  Mammalian Ras interacts directly with the serine/threonine kinase raf , 1993, Cell.

[27]  O. Ozier-Kalogeropoulos,et al.  A simple and efficient method for direct gene deletion in Saccharomyces cerevisiae. , 1993, Nucleic acids research.

[28]  L. Johnston,et al.  Pathway correcting DNA replication errors in Saccharomyces cerevisiae. , 1993, The EMBO journal.

[29]  Smith Rf,et al.  Pattern-induced multi-sequence alignment (PIMA) algorithm employing secondary structure-dependent gap penalties for use in comparative protein modelling. , 1992 .

[30]  G. Faye,et al.  The 3′ to 5′ exonuclease activity located in the DNA polymerase delta subunit of Saccharomyces cerevisiae is required for accurate replication. , 1991, The EMBO journal.

[31]  H. Kawasaki,et al.  Production and separation of peptides from proteins stained with Coomassie brilliant blue R-250 after separation by sodium dodecyl sulfate-polyacrylamide gel electrophoresis. , 1990, Analytical biochemistry.

[32]  J. Lemontt,et al.  REV3, a Saccharomyces cerevisiae gene whose function is required for induced mutagenesis, is predicted to encode a nonessential DNA polymerase , 1989, Journal of bacteriology.

[33]  S. Fields,et al.  A novel genetic system to detect protein–protein interactions , 1989, Nature.

[34]  G. Faye,et al.  Structure and function of the Saccharomyces cerevisiae CDC2 gene encoding the large subunit of DNA polymerase III. , 1989, The EMBO journal.

[35]  R. Sikorski,et al.  A system of shuttle vectors and yeast host strains designed for efficient manipulation of DNA in Saccharomyces cerevisiae. , 1989, Genetics.

[36]  K. Sitney,et al.  DNA polymerase III, a second essential DNA polymerase, is encoded by the S. cerevisiae CDC2 gene , 1989, Cell.

[37]  P. Burgers,et al.  Molecular cloning and primary structure of the uracil-DNA-glycosylase gene from Saccharomyces cerevisiae. , 1989, The Journal of biological chemistry.

[38]  P. Burgers,et al.  The yeast analog of mammalian cyclin/proliferating-cell nuclear antigen interacts with mammalian DNA polymerase delta. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[39]  H. Klein,et al.  Genetic control of intrachromosomal recombination in Saccharomyces cerevisiae. I. Isolation and genetic characterization of hyper-recombination mutations. , 1988, Genetics.

[40]  P. Burgers,et al.  DNA polymerase III from Saccharomyces cerevisiae. II. Inhibitor studies and comparison with DNA polymerases I and II. , 1988, The Journal of biological chemistry.

[41]  P. Burgers,et al.  DNA polymerase III from Saccharomyces cerevisiae. I. Purification and characterization. , 1988, The Journal of biological chemistry.

[42]  H. Schägger,et al.  Tricine-sodium dodecyl sulfate-polyacrylamide gel electrophoresis for the separation of proteins in the range from 1 to 100 kDa. , 1987, Analytical biochemistry.

[43]  M. Kobayashi,et al.  Isolation of enzymes from polyacrylamide disk gels by a centrifugal homogenization method. , 1985, Analytical biochemistry.

[44]  C. Tan,et al.  Further studies on calf thymus DNA polymerase delta purified to homogeneity by a new procedure. , 1984, Biochemistry.

[45]  J. Morrissey,et al.  Silver stain for proteins in polyacrylamide gels: a modified procedure with enhanced uniform sensitivity. , 1981, Analytical biochemistry.

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

[47]  L. Hartwell Sequential function of gene products relative to DNA synthesis in the yeast cell cycle. , 1976, Journal of molecular biology.

[48]  M. M. Bradford A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. , 1976, Analytical biochemistry.