Skip to main content
Journal of Virology logoLink to Journal of Virology
. 1972 Sep;10(3):356–361. doi: 10.1128/jvi.10.3.356-361.1972

Plasmid-Controlled Variation in the Content of Methylated Bases in Bacteriophage Lambda Deoxyribonucleic Acid

Stanley Hattman 1
PMCID: PMC356474  PMID: 4561202

Abstract

The N6-methyladenine (MeAde) and 5-methylcytosine (MeC) contents in deoxyribonucleic acid (DNA) of bacteriophage lambda has been analyzed as a function of host specificity. The following facts have emerged: (i) lambda grown on strains harboring the P1 prophage contain ca. 70 more MeAde residues/DNA molecule than lambda grown either in the P1-sensitive parent, or in a P1 immune-defective lysogen which does not confer P1 modification; (ii) lambda grown on strains harboring the N-3 drug-resistance factor contain ca. 60 more MeC residues/DNA molecule than lambda grown on the parental strain lacking the factor; (iii) lambda grown in Escherichia coli B strains is devoid of MeC, whereas lambda grown in a B (N-3) host contains a high level of MeC; (iv) the MeAde content in lambda DNA is not affected by the N-3 factor. These results suggest that P1 controls an adenine-specific DNA methylase, and that the N-3 plasmid controls a cytosine-specific DNA methylase. The N-3 factor has been observed previously to direct cytosine-specific methylation of phage P22 DNA and E. coli B DNA in vivo; in vitro studies presented here demonstrate this activity.

Full text

PDF
356

Selected References

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

  1. ARBER W., DUSSOIX D. Host specificity of DNA produced by Escherichia coli. I. Host controlled modification of bacteriophage lambda. J Mol Biol. 1962 Jul;5:18–36. doi: 10.1016/s0022-2836(62)80058-8. [DOI] [PubMed] [Google Scholar]
  2. ARBER W., LATASTE-DOROLLE C. [Enlargement of the host area of bacteriophage lambda for Escherichia coli B]. Pathol Microbiol (Basel) 1961;24:1012–1018. [PubMed] [Google Scholar]
  3. ARBER W., MORSE M. L. HOST SPECIFICITY OF DNA PRODUCED BY ESCHERICHIA COLI. VI. EFFECTS ON BACTERIAL CONJUGATION. Genetics. 1965 Jan;51:137–148. doi: 10.1093/genetics/51.1.137. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Arber W., Kühnlein U. Mutationeller Verlust B-spezifischer Restriktion des Bakteriophagen fd. Pathol Microbiol (Basel) 1967;30(6):946–952. [PubMed] [Google Scholar]
  5. Arber W., Linn S. DNA modification and restriction. Annu Rev Biochem. 1969;38:467–500. doi: 10.1146/annurev.bi.38.070169.002343. [DOI] [PubMed] [Google Scholar]
  6. Arber W., Rifat A., Wauters-Willems D., Kühnlein U. Host specificity of DNA produced by Escherichia coli. XVI. Phage lambda DNA carries a single site of affinity for A-specific restriction and modification. Mol Gen Genet. 1972;115(3):195–207. doi: 10.1007/BF00268883. [DOI] [PubMed] [Google Scholar]
  7. Bannister D., Glover S. W. Restriction and modification of bacteriophages by R+ strains of Escherichia coli K12. Biochem Biophys Res Commun. 1968 Mar 27;30(6):735–738. doi: 10.1016/0006-291x(68)90575-5. [DOI] [PubMed] [Google Scholar]
  8. Bannister D., Glover S. W. The isolation and properties of non-restricting mutants of two different host specificities associated with drug resistance factors. J Gen Microbiol. 1970 Apr;61(1):63–71. doi: 10.1099/00221287-61-1-63. [DOI] [PubMed] [Google Scholar]
  9. Boyer H. W. DNA restriction and modification mechanisms in bacteria. Annu Rev Microbiol. 1971;25:153–176. doi: 10.1146/annurev.mi.25.100171.001101. [DOI] [PubMed] [Google Scholar]
  10. Brockes J. P., Brown P. R., Murray K. The deoxyribonucleic acid modification enzyme of bacteriophage P1. Biochem J. 1972 Mar;127(1):1–10. doi: 10.1042/bj1270001. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. DOSKOCIL J., SORMO'VA Z. THE OCCURRENCE OF 5-METHYLCYTOSINE IN BACTERIAL DEOXYRIBONUCLEIC ACIDS. Biochim Biophys Acta. 1965 Mar 15;95:513–515. [PubMed] [Google Scholar]
  12. Doskocil J., Sormová Z. The sequences of 5-methylcytosine in the DNA of Escherichia coli. Biochem Biophys Res Commun. 1965 Jul 26;20(3):334–339. doi: 10.1016/0006-291x(65)90369-4. [DOI] [PubMed] [Google Scholar]
  13. Fujimoto D., Srinivasan P. R., Borek E. On the nature of the deoxyribonucleic acid methylases. Biological evidence for the multiple nature of the enzymes. Biochemistry. 1965 Dec;4(12):2849–2855. doi: 10.1021/bi00888a041. [DOI] [PubMed] [Google Scholar]
  14. Gough M., Lederberg S. Methylated bases in the host-modified deoxyribonucleic acid of Escherichia coli and bacteriophage lambda. J Bacteriol. 1966 Apr;91(4):1460–1468. doi: 10.1128/jb.91.4.1460-1468.1966. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. HATTMAN S. THE CONTROL OF HOST-INDUCED MODIFICATION BY PHAGE P1. Virology. 1964 Jun;23:270–271. doi: 10.1016/0042-6822(64)90291-0. [DOI] [PubMed] [Google Scholar]
  16. Hattman S. DNA methylation of T-even bacteriophages and of their nonglucosylated mutants: its role in P1-directed restriction. Virology. 1970 Oct;42(2):359–367. doi: 10.1016/0042-6822(70)90279-5. [DOI] [PubMed] [Google Scholar]
  17. Hattman S., Gold E., Plotnik A. Methylation of cytosine residues in DNA controlled by a drug resistance factor (host-induced modification-R factors-N 6 -methyladenine-5-methylcytosine). Proc Natl Acad Sci U S A. 1972 Jan;69(1):187–190. doi: 10.1073/pnas.69.1.187. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Hattman S. Variation of 6-methylaminopurine content in bacteriophage P22 deoxyribonucleic acid as a function of host specificity. J Virol. 1971 May;7(5):690–691. doi: 10.1128/jvi.7.5.690-691.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Kelly T. J., Jr, Smith H. O. A restriction enzyme from Hemophilus influenzae. II. J Mol Biol. 1970 Jul 28;51(2):393–409. doi: 10.1016/0022-2836(70)90150-6. [DOI] [PubMed] [Google Scholar]
  20. Kühnlein U., Arber W. Host specificity of DNA produced by Escherichia coli. XV. The role of nucleotide methylation in in vitro B-specific modification. J Mol Biol. 1972 Jan 14;63(1):9–19. doi: 10.1016/0022-2836(72)90518-9. [DOI] [PubMed] [Google Scholar]
  21. LEDERBERG S. Suppression of the multiplication of heterologous bacteriophages in lysogenic bacteria. Virology. 1957 Jun;3(3):496–513. doi: 10.1016/0042-6822(57)90006-5. [DOI] [PubMed] [Google Scholar]
  22. LEDINKO N. OCCURRENCE OF 5-METHYLDEOXYCYTIDYLATE IN THE DNA OF PHAGE LAMBDA. J Mol Biol. 1964 Sep;9:834–835. doi: 10.1016/s0022-2836(64)80191-1. [DOI] [PubMed] [Google Scholar]
  23. Linn S., Arber W. Host specificity of DNA produced by Escherichia coli, X. In vitro restriction of phage fd replicative form. Proc Natl Acad Sci U S A. 1968 Apr;59(4):1300–1306. doi: 10.1073/pnas.59.4.1300. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Mamelak L., Boyer H. W. Genetic control of the secondary modification of deoxyribonucleic acid in Escherichia coli. J Bacteriol. 1970 Oct;104(1):57–62. doi: 10.1128/jb.104.1.57-62.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Meselson M., Yuan R. DNA restriction enzyme from E. coli. Nature. 1968 Mar 23;217(5134):1110–1114. doi: 10.1038/2171110a0. [DOI] [PubMed] [Google Scholar]
  26. Revel H. R., Hattman S. M. Mutants of T2gt with altered DNA methylase activity: relation to restriction by prophage P1. Virology. 1971 Aug;45(2):484–495. doi: 10.1016/0042-6822(71)90348-5. [DOI] [PubMed] [Google Scholar]
  27. Roulland-Dussoix D., Boyer H. W. The Escherichia coli B restriction endonuclease. Biochim Biophys Acta. 1969 Nov 19;195(1):219–229. doi: 10.1016/0005-2787(69)90618-2. [DOI] [PubMed] [Google Scholar]
  28. Smith J. D., Arber W., Kühnlein U. Host specificity of DNA produced by Escherichia coli. XIV. The role of nucleotide methylation in in vivo B-specific modification. J Mol Biol. 1972 Jan 14;63(1):1–8. doi: 10.1016/0022-2836(72)90517-7. [DOI] [PubMed] [Google Scholar]
  29. Takano T., Watanabe T., Fukasawa T. Mechanism of host-controlled restriction of bacteriophage lambda by R factors in Escherichia coli K12. Virology. 1968 Feb;34(2):290–302. doi: 10.1016/0042-6822(68)90239-0. [DOI] [PubMed] [Google Scholar]
  30. Vanyushin B. F., Buryanov Y. I., Belozersky A. N. Distribution of N6-methyladenine in DNA of T2 phage and its host Escherichia coli B. Nat New Biol. 1971 Mar 3;230(1):25–27. doi: 10.1038/newbio230025a0. [DOI] [PubMed] [Google Scholar]
  31. Watanabe T., Takano T., Arai T., Nishida H., Sato S. Episome-mediated Transfer of Drug Resistance in Enterobacteriaceae X. Restriction and Modification of Phages by fi R Factors. J Bacteriol. 1966 Aug;92(2):477–486. doi: 10.1128/jb.92.2.477-486.1966. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Wood W. B. Host specificity of DNA produced by Escherichia coli: bacterial mutations affecting the restriction and modification of DNA. J Mol Biol. 1966 Mar;16(1):118–133. doi: 10.1016/s0022-2836(66)80267-x. [DOI] [PubMed] [Google Scholar]

Articles from Journal of Virology are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES