Abstract
The induction of λ prophage provokes the constitutive expression of the adjacent gal operon in E. coli. This “escape synthesis” can result from transcription that initiates at a phage promoter and extends into the gal operon. The effect requires the product of the λ gene N. N-mediated transcription not only fails to terminate at the prophage-bacterial junction and at the ends of bacterial operons, but ignores termination signals caused by polar insertions or ochre mutations within gal. Suppression of polarity by N-function is a cis-effect; only transcription initiated at the phage promoter is influenced. We propose that the transcription complex is influenced by N-product to become termination-resistant at a site in the phage genome (juggernaut model). This site appears to be at or near the phage promoter.
Keywords: escape synthesis, juggernaut model, gal operon
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Selected References
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- Adhya S., Echols H. Glucose effect and the galactose enzymes of Escherichia coli: correlation between glucose inhibition of induction and inducer transport. J Bacteriol. 1966 Sep;92(3):601–608. doi: 10.1128/jb.92.3.601-608.1966. [DOI] [PMC free article] [PubMed] [Google Scholar]
- BUTTIN G. M'ECANISMES R'EGULATEURS DANS LA BIOSYNTH'ESE DES ENZYMES DU M'ETABOLISME DU GALACTOSE CHEZ ESCHERICHIA COLI K12. II. LE D'ETERMINISME G'EN'ETIQUE DE LA R'EGULATION. J Mol Biol. 1963 Aug;7:183–205. doi: 10.1016/s0022-2836(63)80045-5. [DOI] [PubMed] [Google Scholar]
- BUTTIN G. M'ECANISMES R'EGULATEURS DANS LA BIOSYNTH'ESE DES ENZYMES DU M'ETABOLISME DU GALACTOSE CHEZ ESCHERICHIA COLI K12. III. L'"EFFET DE D'ER'EPRESSION" PROVOQU'E PAR LE D'EVELOPPEMENT DU PHAGE LAMBDA. J Mol Biol. 1963 Dec;7:610–631. doi: 10.1016/s0022-2836(63)80108-4. [DOI] [PubMed] [Google Scholar]
- Brachet P., Eisen H., Rambach A. Mutations of coliphage lambda affecting the expression of replicative functions O and P. Mol Gen Genet. 1970;108(3):266–276. doi: 10.1007/BF00283357. [DOI] [PubMed] [Google Scholar]
- CAMPBELL A. Sensitive mutants of bacteriophage lambda. Virology. 1961 May;14:22–32. doi: 10.1016/0042-6822(61)90128-3. [DOI] [PubMed] [Google Scholar]
- Cohen S. N., Hurwitz J. Genetic transcription in bacteriophage lambda: studies of lambda m RNA synthesis in vivo. J Mol Biol. 1968 Nov 14;37(3):387–406. doi: 10.1016/0022-2836(68)90110-1. [DOI] [PubMed] [Google Scholar]
- Court D., Campbell A. Gene regulation in N mutants of bacteriophage lambda. J Virol. 1972 Jun;9(6):938–945. doi: 10.1128/jvi.9.6.938-945.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Couturier M., Dambly C., Thomas R. Control of development in temperate bacteriophages. V. Sequential activation of the viral functions. Mol Gen Genet. 1973 Feb 2;120(3):231–252. doi: 10.1007/BF00267155. [DOI] [PubMed] [Google Scholar]
- De Crombrugghe B., Adhya S., Gottesman M., Pastan I. Effect of Rho on transcription of bacterial operons. Nat New Biol. 1973 Feb 28;241(113):260–264. doi: 10.1038/newbio241260a0. [DOI] [PubMed] [Google Scholar]
- Geiduschek E. P., Haselkorn R. Messenger RNA. Annu Rev Biochem. 1969;38:647–676. doi: 10.1146/annurev.bi.38.070169.003243. [DOI] [PubMed] [Google Scholar]
- Georgopoulos C. P. Bacterial mutants in which the gene N function of bacteriophage lambda is blocked have an altered RNA polymerase. Proc Natl Acad Sci U S A. 1971 Dec;68(12):2977–2981. doi: 10.1073/pnas.68.12.2977. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ghysen A., Pironio M. Relationship between the N function of bacteriophage lambda and host RNA polymerase. J Mol Biol. 1972 Mar 28;65(2):259–272. doi: 10.1016/0022-2836(72)90281-1. [DOI] [PubMed] [Google Scholar]
- Gottesman M. E., Yarmolinsky M. B. Integration-negative mutants of bacteriophage lambda. J Mol Biol. 1968 Feb 14;31(3):487–505. doi: 10.1016/0022-2836(68)90423-3. [DOI] [PubMed] [Google Scholar]
- Greenblatt J. Regulation of the expression of the N gene of bacteriophage lambda. Proc Natl Acad Sci U S A. 1973 Feb;70(2):421–424. doi: 10.1073/pnas.70.2.421. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Guha A., Tabaczyński M., Szybalski W. Orientation of transcription for the galactose operon as determined by hybridization of gal mRNA with the separated DNA strands of coliphages lambda-dg. J Mol Biol. 1968 Jul 14;35(1):207–213. doi: 10.1016/s0022-2836(68)80048-8. [DOI] [PubMed] [Google Scholar]
- Hill C. W., Echols H. Properties of a mutant blocked in inducibility of messenger RNA for the galactose operon of Escherichia coli. J Mol Biol. 1966 Aug;19(1):38–51. doi: 10.1016/s0022-2836(66)80048-7. [DOI] [PubMed] [Google Scholar]
- Hiraga S., Yanofsky C. Hyper-labile messenger RNA in polar mutants of the tryptophan operon of Escherichia coli. J Mol Biol. 1972 Dec 14;72(1):103–110. doi: 10.1016/0022-2836(72)90072-1. [DOI] [PubMed] [Google Scholar]
- Kayajanian G., Campbell A. The relationship between heritable physical and genetic properties of selected gal- and gal+ transducing lambda dg. Virology. 1966 Nov;30(3):482–492. doi: 10.1016/0042-6822(66)90124-3. [DOI] [PubMed] [Google Scholar]
- Kourilsky P., Marcaud L., Sheldrick P., Luzzati D., Gros F. Studies of the messenger RNA of bacteriophage lambda, I. Various species synthesized early after induction of the prophage. Proc Natl Acad Sci U S A. 1968 Nov;61(3):1013–1020. doi: 10.1073/pnas.61.3.1013. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Luzzati D. Regulation of lambda exonuclease synthesis: role of the N gene product and lambda repressor. J Mol Biol. 1970 Apr 28;49(2):515–519. doi: 10.1016/0022-2836(70)90261-5. [DOI] [PubMed] [Google Scholar]
- Miller Z., Varmus H. E., Parks J. S., Perlman R. L., Pastan I. Regulation of gal messenger ribonucleic acid synthesis in Escherichia coli by 3',5'-cyclic adenosine monophosphate. J Biol Chem. 1971 May 10;246(9):2898–2903. [PubMed] [Google Scholar]
- Nakanishi S., Adhya S., Gottesman M. E., Pastan I. In vitro repression of the transcription of gas operon by purified gal repressor. Proc Natl Acad Sci U S A. 1973 Feb;70(2):334–338. doi: 10.1073/pnas.70.2.334. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nakanishi S., Adhya S., Gottesman M., Pastan I. Studies on the mechanism of action of the gal repressor. J Biol Chem. 1973 Sep 10;248(17):5937–5942. [PubMed] [Google Scholar]
- Perlman R., Pastan I. Cyclic 3'5-AMP: stimulation of beta-galactosidase and tryptophanase induction in E. coli. Biochem Biophys Res Commun. 1968 Mar 27;30(6):656–664. doi: 10.1016/0006-291x(68)90563-9. [DOI] [PubMed] [Google Scholar]
- Roberts J. W. Termination factor for RNA synthesis. Nature. 1969 Dec 20;224(5225):1168–1174. doi: 10.1038/2241168a0. [DOI] [PubMed] [Google Scholar]
- Saedler H., Gullon A., Fiethen L., Starlinger P. Negative control of the galactose operon in E. coli. Mol Gen Genet. 1968;102(1):79–88. doi: 10.1007/BF00341872. [DOI] [PubMed] [Google Scholar]
- Signer E. R., Manly K. F., Brunstetter M. A. Deletion mapping of the c-3-N region of bacteriophage. Virology. 1969 Sep;39(1):137–141. doi: 10.1016/0042-6822(69)90356-0. [DOI] [PubMed] [Google Scholar]
- Varmus H. E., Perlman R. L., Pastan I. Regulation of lac messenger ribonucleic acid synthesis by cyclic adenosine 3',5'-monophosphate and glucose. J Biol Chem. 1970 May 10;245(9):2259–2267. [PubMed] [Google Scholar]
- Yarmolinsky M. B., Wiesmeyer H. REGULATION BY COLIPHAGE LAMBDA OF THE EXPRESSION OF THE CAPACITY TO SYNTHESIZE A SEQUENCE OF HOST ENZYMES. Proc Natl Acad Sci U S A. 1960 Dec;46(12):1626–1645. doi: 10.1073/pnas.46.12.1626. [DOI] [PMC free article] [PubMed] [Google Scholar]
