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Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 1974 Feb;71(2):431–435. doi: 10.1073/pnas.71.2.431

Formation In Vitro of Infective Joint Molecules of λ DNA by T4 Gene-32 Protein

Wilfried Wackernagel 1,2,*, Charles M Radding 1,2
PMCID: PMC388020  PMID: 4521814

Abstract

Half molecules of λ DNA that had been partially digested by λ exonuclease to expose homologous single strands were rejoined by the action of T4 gene-32 protein at 37° in the presence of Mg++. Measurements of infectivity in su- spheroplasts and sedimentation in sucrose demonstrated the formation of sus+ joint molecules from two preparations of sheared λ DNA that carried sus mutations at opposite ends of the genome. The biological activity of joint molecules made by annealing at 75° was diminished by the addition of the gene-32 protein in the absence of Mg++, and largely restored by the subsequent addition of Mg++. The specific infectivity of joint molecules made by gene-32 protein at 37° was similar to that of joint molecules made by annealing at 75°. The experimental system described provides a possible model for simulating early steps in genetic recombination.

Keywords: genetic recombination in vitro, joining reaction, synapsis

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Selected References

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

  1. Alberts B. M., Frey L. T4 bacteriophage gene 32: a structural protein in the replication and recombination of DNA. Nature. 1970 Sep 26;227(5265):1313–1318. doi: 10.1038/2271313a0. [DOI] [PubMed] [Google Scholar]
  2. Anraku N., Anraku Y., Lehman I. R. Enzymic joining of polynucleotides. 8. Structure of hybrids of parental T4 DNA molecules. J Mol Biol. 1969 Dec 28;46(3):481–492. doi: 10.1016/0022-2836(69)90191-0. [DOI] [PubMed] [Google Scholar]
  3. Broker T. R., Lehman I. R. Branched DNA molecules: intermediates in T4 recombination. J Mol Biol. 1971 Aug 28;60(1):131–149. doi: 10.1016/0022-2836(71)90453-0. [DOI] [PubMed] [Google Scholar]
  4. Cassuto E., Lash T., Sriprakash K. S., Radding C. M. Role of exonuclease and beta protein of phage lambda in genetic recombination. V. Recombination of lambda DNA in vitro. Proc Natl Acad Sci U S A. 1971 Jul;68(7):1639–1643. doi: 10.1073/pnas.68.7.1639. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Delius H., Mantell N. J., Alberts B. Characterization by electron microscopy of the complex formed between T4 bacteriophage gene 32-protein and DNA. J Mol Biol. 1972 Jun 28;67(3):341–350. doi: 10.1016/0022-2836(72)90454-8. [DOI] [PubMed] [Google Scholar]
  6. Hotta Y., Stern H. A DNA-binding protein in meiotic cells of Lilium. Dev Biol. 1971 Sep;26(1):87–99. doi: 10.1016/0012-1606(71)90110-2. [DOI] [PubMed] [Google Scholar]
  7. Hotta Y., Stern H. Meiotic protein in spermatocytes of mammals. Nat New Biol. 1971 Nov 17;234(46):83–86. doi: 10.1038/newbio234083a0. [DOI] [PubMed] [Google Scholar]
  8. Josslin R. The lysis mechanism of phage T4: mutants affecting lysis. Virology. 1970 Mar;40(3):719–726. doi: 10.1016/0042-6822(70)90216-3. [DOI] [PubMed] [Google Scholar]
  9. Kozinski A. W., Felgenhauer Z. Z. Molecular recombination in T4 bacteriophage deoxyribonucleic acid. II. Single-strand breaks and exposure of uncomplemented areas as a prerequisite for recombination. J Virol. 1967 Dec;1(6):1193–1202. doi: 10.1128/jvi.1.6.1193-1202.1967. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Kushner S. R., Nagaishi H., Clark A. J. Indirect suppression of recB and recC mutations by exonuclease I deficiency. Proc Natl Acad Sci U S A. 1972 Jun;69(6):1366–1370. doi: 10.1073/pnas.69.6.1366. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Sinha N. K., Snustad D. P. DNA synthesis in bacteriophage T4-infected Escherichia coli: evidence supporting a stoichiometric role for gene 32-product. J Mol Biol. 1971 Nov 28;62(1):267–271. doi: 10.1016/0022-2836(71)90145-8. [DOI] [PubMed] [Google Scholar]
  12. Studier F. W. Effects of the conformation of single-stranded DNA on renaturation and aggregation. J Mol Biol. 1969 Apr;41(2):199–209. doi: 10.1016/0022-2836(69)90385-4. [DOI] [PubMed] [Google Scholar]
  13. Tomizawa J. I. Molecular mechanisms of genetic recombination in bacteriophage: joint molecules and their conversion to recombinant molecules. J Cell Physiol. 1967 Oct;70(2 Suppl):201–213. doi: 10.1002/jcp.1040700414. [DOI] [PubMed] [Google Scholar]
  14. Unger R. C., Clark A. J. Interaction of the recombination pathways of bacteriophage lambda and its host Escherichia coli K12: effects on exonuclease V activity. J Mol Biol. 1972 Oct 14;70(3):539–548. doi: 10.1016/0022-2836(72)90558-x. [DOI] [PubMed] [Google Scholar]
  15. Wackernagel W. An improved spheroplast assay for lambda-DNA and the influence of the bacterial genotype on the transfection rate. Virology. 1972 Apr;48(1):94–103. doi: 10.1016/0042-6822(72)90117-1. [DOI] [PubMed] [Google Scholar]
  16. Wackernagel W., Radding C. M. Transfection by half molecules and inverted molecules of lambda DNA: requirement for exo and -promoted recombination. Virology. 1973 Apr;52(2):425–432. doi: 10.1016/0042-6822(73)90337-1. [DOI] [PubMed] [Google Scholar]

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