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. 1964 Jan;87(1):86–96. doi: 10.1128/jb.87.1.86-96.1964

GENETIC LINKAGE OF MUTATIONAL SITES AFFECTING SIMILAR CHARACTERS IN PNEUMOCOCCUS AND STREPTOCOCCUS

Arnold W Ravin 1, Joscelyn D H De Sa 1
PMCID: PMC276966  PMID: 14102878

Abstract

Ravin, Arnold W. (University of Rochester, Rochester, N.Y.), and Joscelyn D. H. De Sa. Genetic linkage of mutational sites affecting similar characters in pneumococcus and streptococcus. J. Bacteriol. 87:86–96. 1964.—By interspecific transformation, deoxyribonucleic acid (DNA) determinants conferring resistance to high levels of streptomycin in pneumococcus were found to be allelic with DNA determinants conferring low levels of streptomycin resistance in the Challis and NBSI strains of streptococcus. The reciprocal transformation (low resistance pneumococcus × high resistance streptococcus) led to the same conclusion. In addition, determinants controlling resistance to erythromycin in pneumococcus and the Challis strain of streptococcus were found to become closely linked after interspecific transformation. Modifier genes influencing the phenotype conferred by mutations at the streptomycin-resistance locus differentiate species to a certain extent. The results demonstrate that transformations between pneumococcus and streptococcus are not due to episomes, but involve recombinational events in which genetic material of the host species is replaced by homologous material that performed a similar function in the donor species.

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Selected References

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

  1. BRACCO R. M., KRAUSS M. R., ROE A. S., MACLEOD C. M. Transformation reactions between Pneumococcus and three strains of Streptococci. J Exp Med. 1957 Aug 1;106(2):247–259. doi: 10.1084/jem.106.2.247. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. BRYAN B. E. Genetic modifiers of streptomycin resistance in Pneumococcus. J Bacteriol. 1961 Oct;82:461–470. doi: 10.1128/jb.82.4.461-470.1961. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. GUILD W. R. Evidence for intramolecular heterogeneity in pneumococcal DNA. J Mol Biol. 1963 Mar;6:214–229. doi: 10.1016/s0022-2836(63)80071-6. [DOI] [PubMed] [Google Scholar]
  4. Iyer V. N. APPLICATION OF THE MEMBRANE FILTER FOR THE QUANTITATIVE STUDY OF TRANSFORMATIONS WITH PARTICULAR REFERENCE TO PHENOTYPIC EXPRESSION OF AN ERYTHROMYCIN-RESISTANCE MUTATION. J Bacteriol. 1962 Aug;84(2):326–330. doi: 10.1128/jb.84.2.326-330.1962. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. LERMAN L. S., TOLMACH L. J. Genetic transformation. I. Cellular incorporation of DNA accompanying transformation in Pneumococcus. Biochim Biophys Acta. 1957 Oct;26(1):68–82. doi: 10.1016/0006-3002(57)90055-0. [DOI] [PubMed] [Google Scholar]
  6. MARMUR J., FALKOW S., MANDEL M. NEW APPROACHES TO BACTERIAL TAXONOMY. Annu Rev Microbiol. 1963;17:329–372. doi: 10.1146/annurev.mi.17.100163.001553. [DOI] [PubMed] [Google Scholar]
  7. PERRY D., SLADE H. D. Transformation of streptococci to streptomycin resistance. J Bacteriol. 1962 Mar;83:443–449. doi: 10.1128/jb.83.3.443-449.1962. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. RAVIN A. W., IYER V. N. Genetic mapping of DNA: influence of the mutated configuration on the frequency of recombination along the length of the molecule. Genetics. 1962 Oct;47:1369–1384. doi: 10.1093/genetics/47.10.1369. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. RAVIN A. W., IYER V. N. The genetic relationship and phenotypic expression of mutations endowing Pneumococcus with resistance to erythromycin. J Gen Microbiol. 1961 Oct;26:277–301. doi: 10.1099/00221287-26-2-277. [DOI] [PubMed] [Google Scholar]
  10. RAVIN A. W. The origin of bacterial species. Genetic recombination and factors limiting it between bacterial populations. Bacteriol Rev. 1960 Jun;24(2):201–220. doi: 10.1128/br.24.2.201-220.1960. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. ROGER M., HOTCHKISS R. D. Selective heat inactivation of pneumococcal transforming deoxyribonucleate. Proc Natl Acad Sci U S A. 1961 May 15;47:653–669. doi: 10.1073/pnas.47.5.653. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. ROLFE R., EPHRUSSI-TAYLOR H. Density differences between genetic markers in Pneumococcal transforming principle. Proc Natl Acad Sci U S A. 1961 Sep 15;47:1450–1461. doi: 10.1073/pnas.47.9.1450. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. ROTHEIM M. B., RAVIN A. W. The mapping of genetic loci affecting streptomycin resistance in Pneumococcus. Genetics. 1961 Dec;46:1619–1634. doi: 10.1093/genetics/46.12.1619. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. SCHAEFFER P. Interspecific reactions in bacterial transformation. Symp Soc Exp Biol. 1958;12:60–74. [PubMed] [Google Scholar]
  15. SCHAEFFER P. La pénétration de l'acide nucleique dans les bactéries réceptrices au cours des transformations interspécifiques. C R Hebd Seances Acad Sci. 1957 Jul 17;245(3):375–377. [PubMed] [Google Scholar]
  16. ZINDER N. D. Hybrids of Escherichia and Salmonella. Science. 1960 Mar 18;131(3403):813–815. doi: 10.1126/science.131.3403.813. [DOI] [PubMed] [Google Scholar]

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