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2008 | 57 | 2 |

Tytuł artykułu

The delayed early gene G23 of temperate mycobacteriophage L1 regulates the expression of deoxyribonuclease, the product of another delayed early gene of the phage

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
To get clues about the genes as well as the gene regulatory circuit controlling the lytic development of temperate mycobacteriophage L1, previously we screened several conditional lethal mutants of L1 and characterized some of them to an extent. One of the mutants, L1 G23ts23, was found defective in both growth and late gene transcription at 42°C but not at 32°C. Here we show that the above phage mutant is also defective in the expression of phage-coded deoxyribonuclease (DNase) at 42°C but not at 32°C. The G23 gene however does not code for the above enzyme. Further analyses using the L1 G23ts23 mutant suggest that synthesis of DNase is also not regulated by G23 at transcriptional level. Expression of functional DNase in fact requires de novo protein synthesis. Among the 25 revertants isolated from the L1 G23ts23 mutant, which are capable of growing at 42°C (by overcoming the ts defect in late transcription), two, R4 and R22, have been shown to retain the ts defect in the expression of the above enzyme and R4, to retain also the G23ts23 mutation. This suggests that R4 (R22 was not tested for the presence of G23ts23 mutation) carries an extragenic suppressor of G23ts23 mutation in a different gene (we call this putative gene as Gx), which now helps bypass the requirement of G23 for late gene transcription. Possible role of G23 on the regulation of L1-coded Gx and deoxyribonuclease has been discussed at length.

Wydawca

-

Rocznik

Tom

57

Numer

2

Opis fizyczny

p.113-119,fig.,ref.

Twórcy

autor
  • Bose Institute, P1/12 CIT Scheme VII M, Kolkata 700 054, West Bengal, India
autor
autor
autor

Bibliografia

  • Chattopadhyay D.J. and N.C. Mandal. 1982. Studies on polylysogens containing λNcΙ prophages. Ι . Control of synthesis and maintenance of a large number of integrated λ genomes. Virology 118: 439-448.
  • Chaudhuri B., S. Sau, H.J. Datta and N.C. Mandal. 1993. Isolation, characterization, and mapping of temperature-sensitive mutations in the genes essential for lysogenic and lytic growth of the mycobacteriophage L1. Virology 194: 166-173.
  • Clark A.J. 1973. Recombination-deficient mutants of E. coli and other bacteria. Annu. Rev. Genet. 7: 67-86.
  • Datta H.J. and N.C. Mandal. 1998. Identification of an early positive regulatory gene of mycobacteriophage L1. J. Gen. Virol. 79: 205-210.
  • Datta H.J., P. Mandal, R. Bhattacharyya, N. Das, S. Sau and N.C. Mandal. 2007. The G23 and G2J genes of temperate mycobacteriophage L1 are essential for the transcription of its late genes. J. Biochem. Mol. Biol. 40: 156-162.
  • Doke S. 1960. Studies on mycobacteriophages and lysogenic mycobacteria. Kumamoto Med. J. 34, 1360-1373.
  • Harshey R.M. and T. Ramakrishnan. 1976. Purification and properties of DNA-dependent RNA polymerase from Mycobacterium tuberculosis H37RV. Biochim. Biophys. Acta 432: 49-59.
  • Hartmann G., K.O. Honikel, F. Knusel and J. Nuesch. 1967. The specific inhibition of the DNA-directed RNA synthesis by rifamycin. Biochim. Biophys. Acta 145: 843-844.
  • Hatfull G.F. 2000. Molecular genetics of mycobacteriophages. In: Molecular Genetics of Mycobacteria. Ed by Hatfull, G. F. and Jacobs, W. R.,Jr. ASM Press (Washington D.C.).
  • Kuzminov A. 2001. DNA replication meets genetic exchange: chromosomal damage and its repair by homologous recombination. Proc. Natl. Acad. Sci. USA 98: 8461-8.
  • Krüger D.H. and C. Schroeder. 1981. Bacteriophage T3 and bacteriophage T7 virus-host cell interactions. Microbiol. Rev. 45: 9-51.
  • Levin N.C. and G.F. Hatfull. 1993. Mycobacterium smegmatis RNA polymerase: RNA supercoiling, action of rifampicin and mechanism of rifampicin resistance. Mol. Microbiol. 8: 277-285.
  • Little J.W. 1967. An exonuclease induced by bacteriophage lambda. II. Nature of the enzymatic reaction. J. Biol. Chem. 242: 679-686.
  • Mandal N.C, R. Bhattacharyya, S. Sau and B. Chaudhuri. 2004. Studies on temperate mycobacteriophage L1: Its physical map, site of deletion in one of its mutants, and organization of early, delayed early and late genes. In Perspectives in Cytology and Genetics (Eds: Manna, G.K. and Roy, S. C.) Vol. 11: 81-100.
  • Marmur J. 1961. A procedure for the isolation of deoxyribonucleic acid from microorganisms. J. Mol. Biol. 3: 208-218.
  • Miller E.S., E. Kutter, G. Mosig, F. Arisaka, T. Kunisawa and W. Ruger. 2003. Bacteriophage T4 genome. Microbiol. Mol. Biol. Rev. 67: 86-156.
  • Radding CM. 1964. Nuclease activity in defective lysogens of phage lambda. Biochem. Biophys. Res. Commun. 15: 8-12.
  • Renzo R. and S. Ochoa. 1962. Effect of chloramphenicol on protein synthesis in cell-free preparations of Escherichia coli. Cell 78: 317-324.
  • Sambrook J., E.F. Fritsch and T. Maniatis. 1989. Molecular Cloning: A Laboratory Manual, 2nd edn. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory.
  • Sharpies G.J., L.M. Corbett and P. McGlynn. 1999. DNA structure specificity of Rap endonuclease. Nucl. Acids Res. 27: 4121-4127.
  • Walker G.C 1985. Inducible DNA repair systems. Annu. Rev. Biochem. 54: 425-457.

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Bibliografia

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