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. 1974 Dec;78(4):989–1014. doi: 10.1093/genetics/78.4.989

Partial Exclusion between T-Even Bacteriophages; an Incipient Genetic Isolation Mechanism

Richard L Russell 1, Robert J Huskey 1
PMCID: PMC1213253  PMID: 4455560

Abstract

Conditional lethal mutant systems developed in T-even bacteriophages T2, T4 and T6 have been used to study the partial exclusion which characterizes mixed infections of these phages. In bacteria mixedly infected with T2 and T4, the dominant phage (T4) acts against localized exclusion sensitivity determinants in the genome of the excluded phage (T2). These determinants are clustered near genes controlling early functions; the determinants themselves do not appear among the progeny, but markers located close to them appear infrequently, by recombination. The excluding action of T4 does not depend on the action of any gene so far identified by conditional lethal mutations, nor does it depend on differences in DNA glucosylation between infecting phages. Regardless of mechanism, the genetic consequence of this partial exclusion is to limit genetic exchange between T2 and T4 in the region of the genome controlling early functions, while retaining the capacity for extensive exchange in other regions; in short, partial exclusion constitutes a localized genetic isolating mechanism. Related forms of partial exclusion characterize mixed infections of other T-even phages, including those of some phages newly isolated from nature.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. ADAMS M. H. Classification of bacterial viruses: characteristics of the T5 species and of the T2, C16 species. J Bacteriol. 1952 Sep;64(3):387–396. doi: 10.1128/jb.64.3.387-396.1952. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Beckendorf S. K., Kim J. S., Lielausis I. Structure of bacteriophage T4 genes 37 and 38. J Mol Biol. 1973 Jan;73(1):17–35. doi: 10.1016/0022-2836(73)90156-3. [DOI] [PubMed] [Google Scholar]
  3. Beckendorf S. K., Wilson J. H. A recombination gradient in bacteriophage T4 gene 34. Virology. 1972 Nov;50(2):315–321. doi: 10.1016/0042-6822(72)90382-0. [DOI] [PubMed] [Google Scholar]
  4. Bigger C. H., Murray K., Murray N. E. Recognition sequence of a restriction enzyme. Nat New Biol. 1973 Jul 4;244(131):7–10. doi: 10.1038/newbio244007a0. [DOI] [PubMed] [Google Scholar]
  5. Boyer H. W., Chow L. T., Dugaiczyk A., Hedgpeth J., Goodman H. M. DNA substrate site for the EcoRII restriction endonuclease and modification methylase. Nat New Biol. 1973 Jul 11;244(132):40–43. doi: 10.1038/newbio244040a0. [DOI] [PubMed] [Google Scholar]
  6. Cowie D. B., Avery R. J., Champe S. P. DNA homology among the T-even bacteriophages. Virology. 1971 Jul;45(1):30–37. doi: 10.1016/0042-6822(71)90109-7. [DOI] [PubMed] [Google Scholar]
  7. Delbrück M. Interference Between Bacterial Viruses: III. The Mutual Exclusion Effect and the Depressor Effect. J Bacteriol. 1945 Aug;50(2):151–170. [PMC free article] [PubMed] [Google Scholar]
  8. EDGAR R. S., LIELAUSIS I. TEMPERATURE-SENSITIVE MUTANTS OF BACTERIOPHAGE T4D: THEIR ISOLATION AND GENETIC CHARACTERIZATION. Genetics. 1964 Apr;49:649–662. doi: 10.1093/genetics/49.4.649. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. EISERLING F. A., BOYDELATOUR E. CAPSOMERES AND OTHER STRUCTURES OBSERVED ON SOME BACTERIOPHAGES. Pathol Microbiol (Basel) 1965;28:175–180. [PubMed] [Google Scholar]
  10. FUKASAWA T., SAITO S. THE COURSE OF INFECTION WITH T-EVEN PHAGES ON MUTANTS OF ESCHERICHIA COLI K12 DEFECTIVE IN THE SYNTHESIS OF URIDINE DIPHOSPHOGLUCOSE. J Mol Biol. 1964 Feb;8:175–183. doi: 10.1016/s0022-2836(64)80127-3. [DOI] [PubMed] [Google Scholar]
  11. Georgopoulos C. P., Revel H. R. Studies with glucosyl transferase mutants of the T-even bacteriophages. Virology. 1971 May;44(2):271–285. doi: 10.1016/0042-6822(71)90259-5. [DOI] [PubMed] [Google Scholar]
  12. HATTMAN S., FUKASAWA T. HOST-INDUCED MODIFICATION OF T-EVEN PHAGES DUE TO DEFECTIVE GLUCOSYLATION OF THEIR DNA. Proc Natl Acad Sci U S A. 1963 Aug;50:297–300. doi: 10.1073/pnas.50.2.297. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. JESAITIS M. A. The inheritance of the glucose component of the phage nucleic acids. J Gen Physiol. 1961 Jan;44:585–603. doi: 10.1085/jgp.44.3.585. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Levinthal C, Visconti N. Growth and Recombination in Bacterial Viruses. Genetics. 1953 Sep;38(5):500–511. doi: 10.1093/genetics/38.5.500. [DOI] [PMC free article] [PubMed] [Google Scholar]

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