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. 1987 Jan;115(1):3–10. doi: 10.1093/genetics/115.1.3

Synthesis of a trans-Acting Inhibitor of DNA Maturation by Prohead Mutants of Phage λ

Helios Murialdo 1, Wendy L Fife 1
PMCID: PMC1203060  PMID: 2951296

Abstract

Bacteriophage λ with mutations in genes that control prohead assembly and other head precursors cannot mature their DNA. In this paper we present evidence that the failure of these phage mutants to mature DNA is a reflection of a mechanism that modulates terminase nicking activity during normal phage development. We have constructed plasmids that contain the λ-cohesive end site (cos) and the genes that code for DNA terminase, the enzyme that matures DNA by cutting at cos. The DNA terminase genes are under control of a thermosensitive cI repressor. These plasmids lack most of the genes involved in prohead morphogenesis and other head precursors. However, when repression is lifted by destruction of the thermosensitive repressor, the terminase synthesized is able to cut almost 100% of the plasmids. Therefore, these plasmids can mature in the absence of proheads and other head gene products. The plasmids are also able to complement mutants of λ deficient in terminase and DNA maturation. However, in these complementation experiments, if the phage carry mutations in prohead genes E or B, not only is phage DNA maturation blocked, but the plasmid also fails to mature. These experiments show that, in the absence of proheads, phage λ produces a trans-acting inhibitor of maturation. The genetic determinant of this inhibitor maps in a region extending from the middle of gene B to the end of gene C. A model is proposed in which the nicking activity of DNA-bound terminase is inhibited by the trans-acting inhibitor. Prohead (and other factors) binding to this complex would release the block to allow DNA cleavage and packaging.

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Selected References

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  1. ADLER J., TEMPLETON B. THE AMOUNT OF GALACTOSE GENETIC MATERIAL IN LAMBDA-DG BACTERIOPHAGE WITH DIFFERENT DENSITIES. J Mol Biol. 1963 Dec;7:710–720. doi: 10.1016/s0022-2836(63)80118-7. [DOI] [PubMed] [Google Scholar]
  2. Casjens S., Horn T., Kaiser A. D. Head assembly steps controlled by genes F and W in bacteriophage lambda. J Mol Biol. 1972 Mar 14;64(3):551–563. doi: 10.1016/0022-2836(72)90082-4. [DOI] [PubMed] [Google Scholar]
  3. Dove W. F. Action of the lambda chromosome. I. Control of functions late in bacteriophage development. J Mol Biol. 1966 Aug;19(1):187–201. doi: 10.1016/s0022-2836(66)80060-8. [DOI] [PubMed] [Google Scholar]
  4. Emmons S. W. Bacteriophage lambda derivatives carrying two copies of the cohesive end site. J Mol Biol. 1974 Mar 15;83(4):511–525. doi: 10.1016/0022-2836(74)90511-7. [DOI] [PubMed] [Google Scholar]
  5. Feinberg A. P., Vogelstein B. A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity. Anal Biochem. 1983 Jul 1;132(1):6–13. doi: 10.1016/0003-2697(83)90418-9. [DOI] [PubMed] [Google Scholar]
  6. Feiss M., Margulies T. On maturation of the bacteriophage lambda chromosome. Mol Gen Genet. 1973 Dec 31;127(4):285–295. doi: 10.1007/BF00267099. [DOI] [PubMed] [Google Scholar]
  7. Fuerst C. R., Bingham H. Genetic and physiological characterization of the J gene of bacteriophage lambda. Virology. 1978 Jun 15;87(2):437–458. doi: 10.1016/0042-6822(78)90146-0. [DOI] [PubMed] [Google Scholar]
  8. Georgopoulos C. P., Hendrix R. W., Casjens S. R., Kaiser A. D. Host participation in bacteriophage lambda head assembly. J Mol Biol. 1973 May 5;76(1):45–60. doi: 10.1016/0022-2836(73)90080-6. [DOI] [PubMed] [Google Scholar]
  9. Goldberg A. R., Howe M. New mutations in the S cistron of bacteriophage lambda affecting host cell lysis. Virology. 1969 May;38(1):200–202. doi: 10.1016/0042-6822(69)90148-2. [DOI] [PubMed] [Google Scholar]
  10. Hohn B., Wurtz M., Klein B., Lustig A., Hohn T. Phage lambda DNA packaging, in vitro. J Supramol Struct. 1974;2(2-4):302–317. doi: 10.1002/jss.400020220. [DOI] [PubMed] [Google Scholar]
  11. Hohn T., Flick H., Hohn B. Petit lambda, a family of particles from coliphage lambda infected cells. J Mol Biol. 1975 Oct 15;98(1):107–120. doi: 10.1016/s0022-2836(75)80104-5. [DOI] [PubMed] [Google Scholar]
  12. Imber R., Tsugita A., Wurtz M., Hohn T. Outer surface protein of bacteriophage lambda. J Mol Biol. 1980 May 25;139(3):277–295. doi: 10.1016/0022-2836(80)90131-x. [DOI] [PubMed] [Google Scholar]
  13. Laski F., Jackson E. N. Maturation cleavage of bacteriophage P22 DNA in the absence of DNA packaging. J Mol Biol. 1982 Feb 5;154(4):565–579. doi: 10.1016/s0022-2836(82)80015-6. [DOI] [PubMed] [Google Scholar]
  14. Mackinlay A. G., Kaiser A. D. DNA replication in head mutants of bacteriophage lambda. J Mol Biol. 1969 Feb 14;39(3):679–683. doi: 10.1016/0022-2836(69)90155-7. [DOI] [PubMed] [Google Scholar]
  15. McClure S. C., Gold M. Intermediates in the maturation of bacteriophage lambda DNA. Virology. 1973 Jul;54(1):19–27. doi: 10.1016/0042-6822(73)90110-4. [DOI] [PubMed] [Google Scholar]
  16. Murialdo H., Becker A. A genetic analysis of bacteriophage lambda prohead assembly in vitro. J Mol Biol. 1978 Oct 15;125(1):57–74. doi: 10.1016/0022-2836(78)90254-1. [DOI] [PubMed] [Google Scholar]
  17. Murialdo H., Becker A. Assembly of biologically active proheads of bacteriophage lambda in vitro. Proc Natl Acad Sci U S A. 1977 Mar;74(3):906–910. doi: 10.1073/pnas.74.3.906. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Murialdo H., Fife W. L., Becher A., Feiss M., Yochem J. Bacteriophage lambda DNA maturation. The functional relationships among the products of genes Nul, A and FI. J Mol Biol. 1981 Jan 15;145(2):375–404. doi: 10.1016/0022-2836(81)90211-4. [DOI] [PubMed] [Google Scholar]
  19. Murialdo H., Fife W. L. The maturation of coliphage lambda DNA in the absence of its packaging. Gene. 1984 Oct;30(1-3):183–194. doi: 10.1016/0378-1119(84)90119-7. [DOI] [PubMed] [Google Scholar]
  20. Rackwitz H. R., Zehetner G., Murialdo H., Delius H., Chai J. H., Poustka A., Frischauf A., Lehrach H. Analysis of cosmids using linearization by phage lambda terminase. Gene. 1985;40(2-3):259–266. doi: 10.1016/0378-1119(85)90048-4. [DOI] [PubMed] [Google Scholar]
  21. Sanger F., Coulson A. R., Hong G. F., Hill D. F., Petersen G. B. Nucleotide sequence of bacteriophage lambda DNA. J Mol Biol. 1982 Dec 25;162(4):729–773. doi: 10.1016/0022-2836(82)90546-0. [DOI] [PubMed] [Google Scholar]
  22. Southern E. M. Detection of specific sequences among DNA fragments separated by gel electrophoresis. J Mol Biol. 1975 Nov 5;98(3):503–517. doi: 10.1016/s0022-2836(75)80083-0. [DOI] [PubMed] [Google Scholar]
  23. Sternberg N., Weisberg R. Packaging of coliphage lambda DNA. II. The role of the gene D protein. J Mol Biol. 1977 Dec 15;117(3):733–759. doi: 10.1016/0022-2836(77)90067-5. [DOI] [PubMed] [Google Scholar]
  24. Takahashi S. Role of genes O and P in the replication of bacteriophage lambda DNA. J Mol Biol. 1975 May 25;94(3):385–396. doi: 10.1016/0022-2836(75)90209-0. [DOI] [PubMed] [Google Scholar]
  25. Wake R. G., Kaiser A. D., Inman R. B. Isolation and structure of phage lambda head-mutant DNA. J Mol Biol. 1972 Mar 14;64(3):519–540. doi: 10.1016/0022-2836(72)90080-0. [DOI] [PubMed] [Google Scholar]

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