Skip to main content
Log in

Establishment of a physical and genetic map for bacteriophage PRD1

  • Published:
Molecular and General Genetics MGG Aims and scope Submit manuscript

Summary

DNA was isolated from the lipid-containing bacteriophage PRD1 and subjected to restriction endonuclease analysis. The total genome size is 14.7 kb. PRD1 DNA was resistant to cutting by fifteen restriction endonucleases with six base specificity. HaeII made thirty-seven cuts in the DNA, MboI made one cut, and MnlI made six cuts. DNA that was not treated with protease yielded two fewer fragments when treated with HaeII. Evidence is presented to indicate that the PRD1 DNA has protein at the ends of the DNA.

The thirty-eight HaeII fragments were ordered using the ladder technique of Smith and Birnstiel (1976) on MboI and MnlI fragments of the genome. Clones of HaeII partial digests of PRD1 DNA in pBR322 were analyzed by HaeII digestion and were then assigned to specific regions of the genome by their HaeII fragment composition. A comparison of marker rescue characteristics of the cloned DNA with the overall restriction fragment map generated a physical map of the genome. Some genes that have not been mapped because of a lack of mutants or leakiness at restrictive conditions were mapped by studying the in vitro protein synthesis of restriction endonuclease fragments.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Bamford DH, Rouhiainen L, Takkinen K, Söderlund H (1981) Comparison of the lipid-containing bacteriophages PRD1, PR3, PR4, PR5, and L17. J Gen Virol 57:365–373

    Google Scholar 

  • Bolivar F, Rodriguez RL, Greene PJ, Betlach MC Heynecker HL, Boyer HW, Crosa JH, Falkow S (1977) Construction and characterization of new cloning vehicles. II. A multipurpose cloning system. Gene 2:95–113

    Google Scholar 

  • Boyer HW, Roulland-Dussoix D (1969) A complementation analysis of the restriction and modification of DNA in Escherichia coli. J Mol Biol 41:459–472

    Google Scholar 

  • Bradley DE, Rutherford EL (1975) Basic characterization of a lipid-containing bacteriophage specific for plasmids of the P, N and W compatibility groups. Canad J Microbiol 21:152–163

    Google Scholar 

  • Clewell DB (1972) Nature of Col E1 plasmid replication in Escherichia coli in the presence of chloramphenicol. J Bacteriol 110:667–672

    Google Scholar 

  • Day LA, Mindich L (1980) The molecular weight of bacteriophage ϕ6 and its nucleocapsid. Virology 103:376–385

    Google Scholar 

  • Kuhn S, Fritz H-J, Starlinger P (1979) Close vicinity of IS1 integration sites in the leader sequence of the gal operon of E. coli. Mol Gen Genet 167:235–241

    Google Scholar 

  • Maxam AM, Gilbert W (1980) Sequencing end-labeled DNA with base-specific chemical cleavages. Methods Enzymol 65:499–560

    Google Scholar 

  • Mindich L, Bamford D, Goldthwaite C, Laverty M, Mackenzie G (1982a) Isolation of nonsense mutants of lipid-containing bacteriophage PRD1. J Virol 44:1013–1020

    Google Scholar 

  • Mindich L, Bamford D, McGraw T, Mackenzie G (1982b) Assembly of bacteriophage PRD1: Particle formation with wild-type and mutant viruses. J Virol 44:1021–1030

    Google Scholar 

  • Mindich L, Cohen J, Weisburd M (1976) Isolation of nonsense suppressor mutants in Pseudomonas. J Bacteriol 126:177–182

    Google Scholar 

  • Mindich L, McGraw T (1983) Molecular cloning of bacteriophage PRD1 genomic fragments. Mol Gen Genet 190:233–236

    Google Scholar 

  • Olsen RH, Siak JS, Gray RH (1974) Characteristics of PRD1, a plasmid-dependent broad host range DNA bacteriophage. J Virol 14:689–699

    Google Scholar 

  • Rigby PWJ, Dieckmann M, Rhodes C, Berg P (1977) Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I. J Mol Biol 113:237–251

    Google Scholar 

  • Smith HO, Bernstiel ML (1976) A simple method for DNA restriction site mapping. Nucl Acids Res 3:2387–2398

    Google Scholar 

  • Smith GE, Summers MD (1980) The bidirectional transfer of DNA and RNA to nitrocellulose or diazobenzyloxymethyl paper. Anal Biochem 109:123–129

    Google Scholar 

  • Sogo JM, Inciarte MR, Corral J, Viñuela E, Salas M (1979) RNA polymerase binding sites and transcription map of the DNA of Bacillus subtilis phage ϕ29. J Mol Biol 127:411–436

    Google Scholar 

  • Sutcliffe JG (1978) pBR322 restriction map marked from the DNA sequence: Accurate DNA size markers up to 4361 nucleotide pairs long. Nucl Acids Res 5:2721–2728

    Google Scholar 

  • Szybaslki EH, Szybalski W (1979) A comprehensive molecular map of bacteriophage lambda. Gene 7:217–270

    Google Scholar 

  • Tu CPD, Cohen SN (1980) 3-end labeling of DNA with [α−32P]cordycepin-5′-triphosphate. Gene 10:177–183

    Google Scholar 

  • Yang HL, Ivashkiv L, Chen HZ, Zubay G, Cashel M (1980) A coupled transcription translation system for cell-free investigation of linear DNA segments. Proc Natl Acad Sci USA 77:7029–7038

    Google Scholar 

  • Yang RC-A, Lis J, Wu R (1979) Elution of DNA from agarose gels after electrophoresis. Methods Enzymol 68:176–182

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Communicated by G. O'Donovan

Rights and permissions

Reprints and permissions

About this article

Cite this article

McGraw, T., Yang, HL. & Mindich, L. Establishment of a physical and genetic map for bacteriophage PRD1. Mol Gen Genet 190, 237–244 (1983). https://doi.org/10.1007/BF00330646

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00330646

Keywords

Navigation