Abstract
Penetration of wild-type T7 DNA into the host cell occurs in two steps. The phage particle ejects a few hundred base pairs of the left end of the genome into the host. Translocation of the remainder of the DNA is then coupled to transcription. In a normal infection, transcription-coupled translocation of wild-type T7 DNA is initiated at the major A1, A2, and A3 promoters for Escherichia coli RNA polymerase. At 37 degrees C, various deletion mutants lacking these three promoters grow at the same efficiency as wild-type T7 because the minor B promoter is efficiently transferred from the phage head into the cell. As the temperature of the phage infection decreases, the latent periods of (A1, A2, A3)- phages increase relative to that of wild-type T7; nevertheless, (A1, A2, A3)- phages have normal plating efficiencies at reduced temperatures. Lengthening of the latent period at low temperatures is due to a delay in transferring the complete (A1, A2, A3)- genome into the host cell. The (A1, A2, A3)- phages eject the leading end of their genome into the host, but at low temperature, insufficient DNA is transferred into the cell to allow RNA polymerase immediate access the B promoter. However, by an inefficient transcription-independent process, the B promoter eventually translocates into the cell. Mutant derivatives of (A1, A2, A3)- phages that have growth profiles at low temperatures similar to that of wild-type T7 have been isolated. The mutations allow both (A1, A2, A3)- and (A1, A2, A3)+ phages to translocate their entire genomes into the cell by a transcription-independent mechanism. The mutations are located in gene 16, a gene that encodes a component of the internal virion core. We postulate that gp16 is directly involved with the process of DNA translocation from the virion into the cell.
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Selected References
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- Campbell J. L., Richardson C. C., Studier F. W. Genetic recombination and complementation between bacteriophage T7 and cloned fragments of T7 DNA. Proc Natl Acad Sci U S A. 1978 May;75(5):2276–2280. doi: 10.1073/pnas.75.5.2276. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chung Y. B., Hinkle D. C. Bacteriophage T7 DNA packaging. I. Plasmids containing a T7 replication origin and the T7 concatemer junction are packaged into transducing particles during phage infection. J Mol Biol. 1990 Dec 20;216(4):911–926. doi: 10.1016/S0022-2836(99)80010-2. [DOI] [PubMed] [Google Scholar]
- Davanloo P., Rosenberg A. H., Dunn J. J., Studier F. W. Cloning and expression of the gene for bacteriophage T7 RNA polymerase. Proc Natl Acad Sci U S A. 1984 Apr;81(7):2035–2039. doi: 10.1073/pnas.81.7.2035. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dunn J. J., Studier F. W. Complete nucleotide sequence of bacteriophage T7 DNA and the locations of T7 genetic elements. J Mol Biol. 1983 Jun 5;166(4):477–535. doi: 10.1016/s0022-2836(83)80282-4. [DOI] [PubMed] [Google Scholar]
- Dunn J. J., Studier F. W. T7 early RNAs and Escherichia coli ribosomal RNAs are cut from large precursor RNAs in vivo by ribonuclease 3. Proc Natl Acad Sci U S A. 1973 Dec;70(12):3296–3300. doi: 10.1073/pnas.70.12.3296. [DOI] [PMC free article] [PubMed] [Google Scholar]
- García L. R., Molineux I. J. Rate of translocation of bacteriophage T7 DNA across the membranes of Escherichia coli. J Bacteriol. 1995 Jul;177(14):4066–4076. doi: 10.1128/jb.177.14.4066-4076.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Marinus M. G., Poteete A., Arraj J. A. Correlation of DNA adenine methylase activity with spontaneous mutability in Escherichia coli K-12. Gene. 1984 Apr;28(1):123–125. doi: 10.1016/0378-1119(84)90095-7. [DOI] [PubMed] [Google Scholar]
- McAllister W. T., Morris C., Rosenberg A. H., Studier F. W. Utilization of bacteriophage T7 late promoters in recombinant plasmids during infection. J Mol Biol. 1981 Dec 15;153(3):527–544. doi: 10.1016/0022-2836(81)90406-x. [DOI] [PubMed] [Google Scholar]
- Moffatt B. A., Studier F. W. Entry of bacteriophage T7 DNA into the cell and escape from host restriction. J Bacteriol. 1988 May;170(5):2095–2105. doi: 10.1128/jb.170.5.2095-2105.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pao C. C., Speyer J. F. Order of injection of T7 bacteriophage DNA. J Virol. 1973 Jun;11(6):1024–1026. doi: 10.1128/jvi.11.6.1024-1026.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Roeder G. S., Sadowski P. D. Bacteriophage T7 morphogenesis: phage-related particles in cells infected with wild-type and mutant T7 phage. Virology. 1977 Jan;76(1):263–285. doi: 10.1016/0042-6822(77)90302-6. [DOI] [PubMed] [Google Scholar]
- Saigo K. Polar DNA ejection in bacteriophage T7. Virology. 1975 May;65(1):120–127. doi: 10.1016/0042-6822(75)90012-4. [DOI] [PubMed] [Google Scholar]
- Serwer P. Internal proteins of bacteriophage T7. J Mol Biol. 1976 Nov 5;107(3):271–291. doi: 10.1016/s0022-2836(76)80005-8. [DOI] [PubMed] [Google Scholar]
- Studier F. W. Bacteriophage T7. Science. 1972 Apr 28;176(4033):367–376. doi: 10.1126/science.176.4033.367. [DOI] [PubMed] [Google Scholar]
- Studier F. W. Gene 0.3 of bacteriophage T7 acts to overcome the DNA restriction system of the host. J Mol Biol. 1975 May 15;94(2):283–295. doi: 10.1016/0022-2836(75)90083-2. [DOI] [PubMed] [Google Scholar]
- Tabor S., Richardson C. C. Selective inactivation of the exonuclease activity of bacteriophage T7 DNA polymerase by in vitro mutagenesis. J Biol Chem. 1989 Apr 15;264(11):6447–6458. [PubMed] [Google Scholar]
- Zavriev S. K., Shemyakin M. F. Influence of the deletions of A2-A3 promoters or a terminator of early genes upon the rate of T7 DNA entrance into Escherichia coli cell. FEBS Lett. 1981 Aug 17;131(1):99–102. doi: 10.1016/0014-5793(81)80896-4. [DOI] [PubMed] [Google Scholar]
- Zavriev S. K., Shemyakin M. F. RNA polymerase-dependent mechanism for the stepwise T7 phage DNA transport from the virion into E. coli. Nucleic Acids Res. 1982 Mar 11;10(5):1635–1652. doi: 10.1093/nar/10.5.1635. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Zavriev S. K., Vorob'ev S. M. Evidence for the coupling of T7 DNA injection with its transcription during infection. FEBS Lett. 1984 Jan 2;165(1):31–34. doi: 10.1016/0014-5793(84)80008-3. [DOI] [PubMed] [Google Scholar]