Abstract
Two late gene am mutants of bacteriophage T4 that can be induced to revert by UV were crossed to a temperature-sensitive ligase mutant. In the double mutants, UV-induced reversion was eliminated at a semirestrictive temperature. When the single am mutants were irradiated and then allowed a single passage in a permissive host, the UV-induced reversion frequency was increased by 15- to 25-fold. This increased mutagenesis was also abolished by the presence of the ligase allele. When the UV-irradiated single am mutants multiply infected a permissive host, allowing multiplicity reactivation to occur, the induced reversion frequency was reduced similarly to the reduction in lethality. The mutagenesis that remained was again abolished by the presence of the ligase allele. It is concluded that UV induces mutations in phage T4 through the action of a pathway that includes polynucleotide ligase. The increase in mutation frequency after growth in a permissive host implies that mutagenesis can occur at more than one stage of the infection rather than only in an early stage before expression of the mutant genome. The process of multiplicity reactivation appears to be error-free since it overcomes lethal lesions without inducing new mutations.
Full text
PDFSelected References
These references are in PubMed. This may not be the complete list of references from this article.
- Averbeck D., Laskowski W., Eckardt F., Lehmann-Brauns E. Four radiation sensitive mutants of Saccharomyces. Survival after UV- and x-ray-irradiation as well as UV-induced reversion rates from isoleucine-valine dependence to independence. Mol Gen Genet. 1970;107(2):117–127. doi: 10.1007/BF00333628. [DOI] [PubMed] [Google Scholar]
- Bernstein C., Morgan D., Gensler H. L., Schneider S., Holmes G. E. The dependence of HNO2 mutagenesis in phage T4 on ligase and the lack of dependence of 2AP mutagenesis on repair functions. Mol Gen Genet. 1976 Oct 18;148(2):213–220. doi: 10.1007/BF00268387. [DOI] [PubMed] [Google Scholar]
- Blanco M., Levine A., Devoret R. IexB: a new gene governing radiation sensitivity and lysogenic induction in Escherichia coli K12. Basic Life Sci. 1975;5A:379–382. doi: 10.1007/978-1-4684-2895-7_50. [DOI] [PubMed] [Google Scholar]
- Castellazzi M., George J., Buttin G. [Prophage induction and cell division in E. coli. II. Linked (recA, zab) and unlinked (lex) suppressors of tif-1-mediated induction and filamentation]. Mol Gen Genet. 1972;119(2):153–174. doi: 10.1007/BF00269134. [DOI] [PubMed] [Google Scholar]
- Chang L. T., Lennox J. E., Tuveson R. W. Induced mutation in UV-sensitive mutants of Aspergillus nidulans and Neurospora crassa. Mutat Res. 1968 Mar-Apr;5(2):217–224. doi: 10.1016/0027-5107(68)90019-5. [DOI] [PubMed] [Google Scholar]
- Clarke C. H., Shankel D. M. Antimutagenesis in microbial systems. Bacteriol Rev. 1975 Mar;39(1):33–53. doi: 10.1128/br.39.1.33-53.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Drake J. W. Ultraviolet mutagenesis in bacteriophage T-4. I. Irradiation of extracellular phage particles. J Bacteriol. 1966 May;91(5):1775–1780. doi: 10.1128/jb.91.5.1775-1780.1966. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Drake J. W. Ultraviolet mutagenesis in bacteriophage T4. II. Photoreversal of mutational lesions. J Bacteriol. 1966 Jul;92(1):144–147. doi: 10.1128/jb.92.1.144-147.1966. [DOI] [PMC free article] [PubMed] [Google Scholar]
- GREEN D. M., KRIEG D. R. The delayed origin of mutants induced by exposure of extracellular phage T4 to ethyl methane sulfonate. Proc Natl Acad Sci U S A. 1961 Jan 15;47:64–72. doi: 10.1073/pnas.47.1.64. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ganesan A. K. Persistence of pyrimidine dimers during post-replication repair in ultraviolet light-irradiated Escherichia coli K12. J Mol Biol. 1974 Jul 25;87(1):103–119. doi: 10.1016/0022-2836(74)90563-4. [DOI] [PubMed] [Google Scholar]
- Green R. R., Drake J. W. Misrepair mutagenesis in bacteriophage T4. Genetics. 1974 Sep;78(1):81–89. doi: 10.1093/genetics/78.1.81. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lawrence C. W., Christensen R. UV mutagenesis in radiation-sensitive strains of yeast. Genetics. 1976 Feb;82(2):207–232. doi: 10.1093/genetics/82.2.207. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lemontt J. F. Induction of forward mutations in mutationally defective yeast. Mol Gen Genet. 1972;119(1):27–42. doi: 10.1007/BF00270441. [DOI] [PubMed] [Google Scholar]
- Lemontt J. F. Mutants of yeast defective in mutation induced by ultraviolet light. Genetics. 1971 May;68(1):21–33. doi: 10.1093/genetics/68.1.21. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Meistrich M. L., Drake J. W. Mutagenic effects of thymine dimers in bacteriophage T4. J Mol Biol. 1972 Apr 28;66(1):107–114. doi: 10.1016/s0022-2836(72)80009-3. [DOI] [PubMed] [Google Scholar]
- Mount D. W., Low K. B., Edmiston S. J. Dominant mutations (lex) in Escherichia coli K-12 which affect radiation sensitivity and frequency of ultraviolet lght-induced mutations. J Bacteriol. 1972 Nov;112(2):886–893. doi: 10.1128/jb.112.2.886-893.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nonn E. M., Bernstein C. Multiplicity reactivation and repair of nitrous acid-induced lesions in bacteriophage T4. J Mol Biol. 1977 Oct 15;116(1):31–47. doi: 10.1016/0022-2836(77)90117-6. [DOI] [PubMed] [Google Scholar]
- Pawl G., Taylor R., Minton K., Friedberg E. C. Enzymes involved in thymine dimer excision in bacteriophage T4-infected Escherichia coli. J Mol Biol. 1976 Nov;108(1):99–109. doi: 10.1016/s0022-2836(76)80097-6. [DOI] [PubMed] [Google Scholar]
- Prakash L. The effect of genes controlling radiation sensitivity on chemical mutagenesis in yeast. Basic Life Sci. 1975;5A:393–395. doi: 10.1007/978-1-4684-2895-7_53. [DOI] [PubMed] [Google Scholar]
- Witkin E. M. The mutability toward ultraviolet light of recombination-deficient strains of Escherichia coli. Mutat Res. 1969 Jul-Aug;8(1):9–14. doi: 10.1016/0027-5107(69)90135-3. [DOI] [PubMed] [Google Scholar]