Protein-nucleic acid interactions in bacteriophage phi 29 DNA replication. 1995

M Salas, and R Freire, and M S Soengas, and J A Esteban, and J Méndez, and A Bravo, and M Serrano, and M A Blasco, and J M Lázaro, and L Blanco
Centro de Biología Molecular Severo Ochoa (CSIC-UAM), Universidad Autónoma, Madrid, Spain.

phi 29 DNA replication starts at both DNA ends by a protein priming mechanism. The formation of the terminal protein-dAMP initiation complex is directed by the second nucleotide from the 3' end of the template. The transition from protein-primed initiation to normal DNA elongation has been proposed to occur by a sliding-back mechanism that is necessary for maintaining the sequences at the phi 29 DNA ends. Structure-function studies have been carried out in the phi 29 DNA polymerase. By site-directed mutagenesis of amino acids conserved among distantly related DNA polymerases we have shown that the N-terminal domain of phi 29 DNA polymerase contains the 3'-5' exonuclease activity and the strand-displacement capacity, whereas the C-terminal domain contains the synthetic activities (protein-primed initiation and DNA polymerization). Viral protein p6 stimulates the initiation of phi 29 DNA replication. The structure of the protein p6-DNA complex has been determined, as well as the main signals at the phi 29 DNA ends recognized by protein p6. The DNA binding domain of protein p6 has been studied. The results indicate that an alpha-helical structure located in the N-terminal region of protein p6 is involved in DNA binding through the minor groove. The phi 29 protein p5 is the single-stranded DNA binding (SSB) protein involved in phi 29 DNA replication, by binding to the displaced single-stranded DNA (ssDNA) in the replication intermediates. In addition, protein p5 is able to unwind duplex DNA. The properties of the phi 29 SSB-ssDNA complex are described. Using the four viral proteins, terminal protein, DNA polymerase, protein p6 and the SSB protein, it was possible to amplify the 19,285-bp phi 29 DNA molecule by a factor of 4000 after 1 h of incubation at 30 degrees C. The infectivity of the in vitro amplified DNA was identical to that of phi 29 DNA obtained from virions.

UI MeSH Term Description Entries
D004247 DNA A deoxyribonucleotide polymer that is the primary genetic material of all cells. Eukaryotic and prokaryotic organisms normally contain DNA in a double-stranded state, yet several important biological processes transiently involve single-stranded regions. DNA, which consists of a polysugar-phosphate backbone possessing projections of purines (adenine and guanine) and pyrimidines (thymine and cytosine), forms a double helix that is held together by hydrogen bonds between these purines and pyrimidines (adenine to thymine and guanine to cytosine). DNA, Double-Stranded,Deoxyribonucleic Acid,ds-DNA,DNA, Double Stranded,Double-Stranded DNA,ds DNA
D004259 DNA-Directed DNA Polymerase DNA-dependent DNA polymerases found in bacteria, animal and plant cells. During the replication process, these enzymes catalyze the addition of deoxyribonucleotide residues to the end of a DNA strand in the presence of DNA as template-primer. They also possess exonuclease activity and therefore function in DNA repair. DNA Polymerase,DNA Polymerases,DNA-Dependent DNA Polymerases,DNA Polymerase N3,DNA Dependent DNA Polymerases,DNA Directed DNA Polymerase,DNA Polymerase, DNA-Directed,DNA Polymerases, DNA-Dependent,Polymerase N3, DNA,Polymerase, DNA,Polymerase, DNA-Directed DNA,Polymerases, DNA,Polymerases, DNA-Dependent DNA
D004261 DNA Replication The process by which a DNA molecule is duplicated. Autonomous Replication,Replication, Autonomous,Autonomous Replications,DNA Replications,Replication, DNA,Replications, Autonomous,Replications, DNA
D004268 DNA-Binding Proteins Proteins which bind to DNA. The family includes proteins which bind to both double- and single-stranded DNA and also includes specific DNA binding proteins in serum which can be used as markers for malignant diseases. DNA Helix Destabilizing Proteins,DNA-Binding Protein,Single-Stranded DNA Binding Proteins,DNA Binding Protein,DNA Single-Stranded Binding Protein,SS DNA BP,Single-Stranded DNA-Binding Protein,Binding Protein, DNA,DNA Binding Proteins,DNA Single Stranded Binding Protein,DNA-Binding Protein, Single-Stranded,Protein, DNA-Binding,Single Stranded DNA Binding Protein,Single Stranded DNA Binding Proteins
D004277 DNA, Single-Stranded A single chain of deoxyribonucleotides that occurs in some bacteria and viruses. It usually exists as a covalently closed circle. Single-Stranded DNA,DNA, Single Stranded,Single Stranded DNA
D005784 Gene Amplification A selective increase in the number of copies of a gene coding for a specific protein without a proportional increase in other genes. It occurs naturally via the excision of a copy of the repeating sequence from the chromosome and its extrachromosomal replication in a plasmid, or via the production of an RNA transcript of the entire repeating sequence of ribosomal RNA followed by the reverse transcription of the molecule to produce an additional copy of the original DNA sequence. Laboratory techniques have been introduced for inducing disproportional replication by unequal crossing over, uptake of DNA from lysed cells, or generation of extrachromosomal sequences from rolling circle replication. Amplification, Gene
D013329 Structure-Activity Relationship The relationship between the chemical structure of a compound and its biological or pharmacological activity. Compounds are often classed together because they have structural characteristics in common including shape, size, stereochemical arrangement, and distribution of functional groups. Relationship, Structure-Activity,Relationships, Structure-Activity,Structure Activity Relationship,Structure-Activity Relationships
D014764 Viral Proteins Proteins found in any species of virus. Gene Products, Viral,Viral Gene Products,Viral Gene Proteins,Viral Protein,Protein, Viral,Proteins, Viral
D014779 Virus Replication The process of intracellular viral multiplication, consisting of the synthesis of PROTEINS; NUCLEIC ACIDS; and sometimes LIPIDS, and their assembly into a new infectious particle. Viral Replication,Replication, Viral,Replication, Virus,Replications, Viral,Replications, Virus,Viral Replications,Virus Replications
D017103 Bacillus Phages Viruses whose host is Bacillus. Frequently encountered Bacillus phages include bacteriophage phi 29 and bacteriophage phi 105. Bacteriophage phi 105,Bacteriophage phi 29,Phage phi 105,Phage phi 29,Bacillus Bacteriophages,Bacillus Bacteriophage,Bacillus Phage,Bacteriophage, Bacillus,Bacteriophages, Bacillus

Related Publications

M Salas, and R Freire, and M S Soengas, and J A Esteban, and J Méndez, and A Bravo, and M Serrano, and M A Blasco, and J M Lázaro, and L Blanco
December 1988, Biochimica et biophysica acta,
M Salas, and R Freire, and M S Soengas, and J A Esteban, and J Méndez, and A Bravo, and M Serrano, and M A Blasco, and J M Lázaro, and L Blanco
September 1982, Proceedings of the National Academy of Sciences of the United States of America,
M Salas, and R Freire, and M S Soengas, and J A Esteban, and J Méndez, and A Bravo, and M Serrano, and M A Blasco, and J M Lázaro, and L Blanco
October 1990, Gene,
M Salas, and R Freire, and M S Soengas, and J A Esteban, and J Méndez, and A Bravo, and M Serrano, and M A Blasco, and J M Lázaro, and L Blanco
June 1989, Nucleic acids research,
M Salas, and R Freire, and M S Soengas, and J A Esteban, and J Méndez, and A Bravo, and M Serrano, and M A Blasco, and J M Lázaro, and L Blanco
January 1984, Advances in experimental medicine and biology,
M Salas, and R Freire, and M S Soengas, and J A Esteban, and J Méndez, and A Bravo, and M Serrano, and M A Blasco, and J M Lázaro, and L Blanco
January 2002, Advances in virus research,
M Salas, and R Freire, and M S Soengas, and J A Esteban, and J Méndez, and A Bravo, and M Serrano, and M A Blasco, and J M Lázaro, and L Blanco
September 1984, Proceedings of the National Academy of Sciences of the United States of America,
M Salas, and R Freire, and M S Soengas, and J A Esteban, and J Méndez, and A Bravo, and M Serrano, and M A Blasco, and J M Lázaro, and L Blanco
July 1988, Nucleic acids research,
M Salas, and R Freire, and M S Soengas, and J A Esteban, and J Méndez, and A Bravo, and M Serrano, and M A Blasco, and J M Lázaro, and L Blanco
February 1991, The Journal of biological chemistry,
M Salas, and R Freire, and M S Soengas, and J A Esteban, and J Méndez, and A Bravo, and M Serrano, and M A Blasco, and J M Lázaro, and L Blanco
January 1984, Folia biologica,
Copied contents to your clipboard!