Summary
The ocr + gene function (gp 0.3) of bacteriophages T3 and T7 not only counteracts type I (EcoB, EcoK) but also type III restriction endonucleases (EcoP1). Despite the presence of recognition sites, phage DNA as well as simultaneously introduced plasmid DNA are protected by ocr + expression against both the endonucleolytic and the methylating activities of the EcoP1 enzyme. Nevertheless, the EcoP1 protein causes the exclusion of T3 and T7 in P1-lysogenic cells, apparently by exerting a repressor-like effect on phage gene expression. T3 which induces an S-adenosylmethionine hydrolase is less susceptible to the repressor effect of the SAM-stimulated EcoP1 enzyme. The abundance of EcoP1 recognition sites in the T7 genome is explained by their near identity with the T7 DNA primase recognition site.
Similar content being viewed by others
Abbreviations
- d.p.m.:
-
decompositions per min
- EcoB, EcoK, EcoP1, EcoP15, EcoRII, EcoR124, HinfIII:
-
restriction endonucleases coded by Escherichia coli strains B or K, E. coli plasmids P1, P15, RII or R124, and Haemophilus influenzae Rf 232, resp.
- e.o.p.:
-
efficiency of plating
- gp:
-
gene product (in the sense of protein)
- m.o.i.:
-
multiplicity of infection (phage/cell)
- ocr + :
-
gene function which overcomes classical restriction
- p.f.u.:
-
plaque-forming units
- SAM:
-
S-adenosylmethionine
- sam + :
-
gene function with S-adenosylmethionine-cleaving enzyme (SAMase) activity
- UV:
-
ultraviolet light
References
Arber W (1974) DNA modification and restriction. Progr Nucl Acid Res Mol Biol 14:1–37
Arber W, Wauters-Willems D (1970) Host specificity of DNA produced by E. coli. XII. The two restriction and modification systems of strain 15T-. Mol Gen Genet 108:203–217
Arber W, Iida S, Jütte H, Caspers P, Meyer J, Hänni C (1979) Rearrangements of genetic material in E. coli as observed on the bacteriophage P1 plasmid. Cold Spring Harbor Symp Quant Biol 43:1197–1208
Bächi B, Reiser J, Pirrotta V (1979) Methylation and cleavage sequences of the EcoP1 restriction-modification enzyme. J Mol Biol 128:143–163
Boyer HW (1971) DNA restriction and modification mechanisms in bacteria. Annu Rev Microbiol 25:153–176
Clewell DB (1972) Nature of ColE1 plasmid replication in E. coli in the presence of chloramphenicol. J Bacteriol 110:667–676
Cohen SN, Chang ACY, Hsu L (1972) Nonchromosomal antibiotic resistance in bacteria: Genetic transformation of E. coli by R-factor-DNA. Proc Natl Acad Sci USA 69:2110–2114
Dunn JJ, Studier FW (1981) Nucleotide sequence from the genetic left end of bacteriophage T7 DNA to the beginning of gene 4. J Mol Biol 148:303–330
Haberman A (1974) The bacteriophage P1 restriction endonuclease. J Mol Biol 89:545–563
Hadi SM, Bächi B, Shepherd JCW, Yuan R, Ineichen K, Bickle TA (1979) DNA recognition and cleavage by the EcoP15 restriction endonuclease. J Mol Biol 134:655–666
Hausmann R (1967) Synthesis of an S-adenosylmethionine-cleaving enzyme in T3-infected E. coli and its disturbance by co-infection with enzymatically incompetent bacteriophage. J Virol 1:57–63
Hausmann R (1973) Host-dependent gene expression of bacteriophages T3 and T7. In: Hamkalo BA, Papaconstantinon J (eds) Molecular cytogenetics. Plenum Publ, New York, p 263–276
Hershfield V, Boyer HW, Yanofsky C, Lovett M, Helinski DR (1974) Plasmid ColE1 as a molecular vehicle for cloning and amplification of DNA. Proc Natl Acad Sci USA 71:3455–3459
Kauc L, Piekarowicz A (1978) Purification and properties of a new restriction endonuclease from Haemophilus influenzae Rf. Eur J Biochem 92:417–426
Krüger DH, Chernin LS, Hansen S, Rosenthal HA, Goldfarb DM (1978a) Protection of foreign DNA against host-controlled restriction in bacterial cells. I. Protection of F' plasmid DNA by preinfecting with bacteriophages T3 or T7. Mol Gen Genet 159:107–110
Krüger DH, Gola G, Weisshuhn I, Hansen S (1978b) The ocr gene function of bacterial viruses T3 and T7 prevents host-controlled modification. J Gen Virol 41:189–192
Krüger DH, Presber W, Hansen S, Rosenthal HA (1977a) Different restriction of bacteriophages T3 and T7 by Pl-lysogenic cells and the role of the T3-coded SAMase. Z Allg Mikrobiol 17:581–591
Krüger DH, Reuter M, Chernin LS, Rosenthal HA (1981) Transformation in E. coli: Protection of plasmid DNA by the ocr + gene function of bacteriophages T3 and T7 against restriction. In: Polsinelli M and Mazza G (eds) Transformation '80. Cotswold Press, Oxford, p. 327–337
Krüger DH, Schroeder C (1981) Bacteriophage T3 and bacteriophage T7 virus—host cell interactions. Microbiol Revs 45:9–51
Krüger DH, Schroeder C, Hansen S, Rosenthal HA (1977b) Active protection by bacteriophages T3 and T7 against E. coli B- and K-specific restriction of their DNA. Mol Gen Genet 153:99–106
Mandel M, Higa A (1970) Calcium-dependent bacteriophage DNA infection. J Mol Biol 53:159–162
Mark KK, Studier FW (1981) Purification of the gene 0.3 protein of bacteriophage T7, an inhibitor of the DNA restriction system of E. coli. J. Biol Chem. 256:2573–2578
McAllister WT, Carter AD (1980) Regulation of promoter selection by the bacteriophage T7 RNA polymerase in vitro. Nucl Acids Res 8:4821–4837
Reiser J, Yuan R (1977) Purification and properties of the P15-specific restriction endonuclease from E. coli. J Biol Chem 252:451–456
Reuter M, Krüger DH, Scholz D, Rosenthal HA (1980) Schutz zellfremder DNA vor wirtskontrollierter Restriktion in Bakterienzellen. II. Schutz des Plasmids pSF2124 durch die ocr + Genfunktion der Bakteriophagen T3 and T7. Z Allg Mikrobiol 20:345–354
Saito H, Tabor S, Tamonoi F, Richardson CC (1980) Nucleotide sequence of the primary origin of bacteriophage T7 DNA replication: Relationship to adjacent genes and regulatory elements. Proc Natl Acad Sci USA 77:3917–3921
Scott JR (1980) Immunity and repression in bacteriophages Pl and P7. Progr Nucl Acid Res Mol Biol 90:49–65
So M, Gill R, Falkow S (1975) The generation of a ColEl-ApR cloning vehicle which allows detection of inserted DNA. Mol Gen Genet 142:239–249
Spoerel N, Herrlich P, Bickle TA (1979) A novel bacteriophage defence mechanism: the anti-restriction protein. Nature 278:30–34
Stahl SJ, Zinn K (1981) Nucleotide sequence of the cloned gene for bacteriophage T7 RNA polymerase. J Mol Biol 148:481–485
Studier FW (1975) Gene 0.3 of bacteriophage T7 acts to overcome the DNA restriction system of the host. J Mol Biol 94:283–295
Studier FW, Movva NR (1976) SAMase gene of bacteriophage T3 is responsible for overcoming host restriction. J Virol 19:136–145
Tabor S, Richardson CC (1981) Template recognition sequence for RNA primer synthesis by gene 4 protein of bacteriphage T7. Proc Natl Acad Sci USA 78:205–209
Yuan R, Reiser J (1978) Steps in the reaction mechanism of the E. coli plasmid P15-specific restriction endonuclease. J Mol Biol 122:433–445
Zavriev SK, Shemyakin MF (1979) Blockage of phage T7 DNA injection into E. coli cells by bacterial RNA polymerase inhibitors (in Russian). Dokl Akad Nauk SSSR 246:475–478
Zaychikov EF, Pletnyov AG (1980) Nucleotide sequence of the promoter region AO of T7 phage DNA (in Russian). Bioorg Khim 6:1268–1271
Author information
Authors and Affiliations
Additional information
Communicated by W. Arber
Dedicated to Professor Konstantin Spies on the occasion of his sixtieth birthday
Rights and permissions
About this article
Cite this article
Krüger, D.H., Reuter, M., Hansen, S. et al. Influence of phage T3 and T7 gene functions on a type III (EcoP1) DNA restriction-modification system in vivo. Mol Gen Genet 185, 457–461 (1982). https://doi.org/10.1007/BF00334140
Received:
Issue Date:
DOI: https://doi.org/10.1007/BF00334140