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Autoregulation of the rho gene of Escherichia coli K-12

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Summary

It has previously been proposed, based on indirect evidence, that the Rho protein may control the expression of the rho gene. Using an in vitro system for the transcription and translation of the rho gene cloned into plasmid pBR322, we tested this hypothesis directly by monitoring the effect in vitro of excess or limiting Rho protein. The addition of purified Rho protein suppresses Rho synthesis in vitro. The addition of antibody to Rho specifically stimulates Rho synthesis in vitro. The stimulation of Rho factor synthesis by antibody to Rho is reversed by Rho protein. Rho factor purified from a strain with a mutationally altered rho gene (rho-115) does not suppress Rho synthesis in vitro. These results provide convincing evidence that the rho gene is subject to autoregulation.

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References

  • Adhya S, Gottesman M, DeCrombrugghe B (1974) Release of polarity in Escherichia coli by gene N of phage lambda: Termination of transcription. Proc Natl Acad Sci USA 71:2534–2538

    Google Scholar 

  • Brown S, Albrechtsen B, Petersen S, Klemm K (1982) Localization and regulation of the structural gene for transcription-termination factor rho of Escherichia coli. J Mol Biol 162:283–298

    Google Scholar 

  • Calhoun DH, Hatfield GW (1975) Autoregulation of gene expression. Annu Rev Microbiol 29:275–299

    Google Scholar 

  • Casadaban M (1976) Regulation of the regulatory gene for the arabinose pathway, araC. J Mol Biol 104:556–557

    Google Scholar 

  • Gray JE, Patin DW, Calhoun DH (1981) Identification of the protein products of the rrnC, ilv, rho region of the Escherichia coli K-12 chromosome. Mol Gen Genet 183:428–436

    Google Scholar 

  • Greeblaatt J, McLimont M, Hanly S (1981) Termination of transcription by NusA gene protein of Escherichia coli. Nature 292:215–220

    Google Scholar 

  • Guterman SK, Howitt CL (1979) Rifampicin supersensitivity of rho strains of E. coli, and suppression by sur mutation. Mol Gen Genet 169:27–34

    Google Scholar 

  • Housley PR, Leavitt AD, Whitfield HJ (1981) Genetic analysis of a temperature sensitive Salmonella typhimurium rho mutant with an altered Rho associated polytidylate dependent adenosine triphosphate activity. J Bacteriol 147:13–24

    Google Scholar 

  • Imai M, Shigesada K (1978) Studies on the altered Rho factor in nitA mutants of Escherichia coli defective in transcription termination. I. Characterization and quantitative determination of Rho in cell extracts. J Mol Biol 120:451–466

    Google Scholar 

  • Kelley RL, Yanofsky C (1982) trp aporepressor production is controlled by autogenous regulation and inefficient translation. Proc Natl Acad Sci USA 79:3120–3124

    Google Scholar 

  • Kent RB, Guterman SK (1981) A mutant Rho ATPase from Escherichia coli that is temperature sensitive in the presence of RNA. Mol Gen Genet 181:367–372

    Google Scholar 

  • Kung H-F, Morrissey J, Revel M, Spears C, Weissbach H (1975) Studies on the lactose operon. The control of DNA directed in vitro protein synthesis by interfereon factor i-a. J Biol Chem 250:8780–8784

    Google Scholar 

  • Lemaire G, Gold L, Yarus M (1978) Autogenous translational repression of bacteriophate T4 gene 32 expression in vitro. J Mol Biol 126:73–90

    Google Scholar 

  • Lindahl L, Zengel JM (1982) Expression of ribosomal genes in bacteria. Adv Genet 21:53–121

    Google Scholar 

  • Platt T (1981) Termination of transcription and its regulation in the tryptophan operon of E. coli. Cell 24:10–23

    Google Scholar 

  • Ptashne M, Jeffrey A, Johnson AD, Maurer R, Meyer BJ, Pabo CO, Roberts TM, Sauer RT (1980) How the lambda repressor and cro work. Cell 19:1–11

    Google Scholar 

  • Ratner D (1976) Evidence that mutations in the suA polarity suppressing gene directly affect termination factor Rho. Nature 259:151–153

    Google Scholar 

  • Reyes O, Gottesman M, Adhya S (1976) Suppression of polarity of insertion mutations in the gal operon and N mutations in bacteriophage lambda. J Bacteriol 126:1108–1112

    Google Scholar 

  • Richardson JP, Grimley C, Lowry C (1975) Transcription termination factor Rho activity is altered in Escherichia coli with suA gene mutations. Proc Natl Acad Sci USA 72:1725–1728

    Google Scholar 

  • Roberts JW (1969) Termination factor for RNA synthesis. Nature 224:1168–1174

    Google Scholar 

  • Yanofsky C (1981) Attenuation in the control of expression of bacterial operons. Nature 289:751–758

    Google Scholar 

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Communicated by G.A. O'Donovan

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Kung, Hf., Bekesi, E., Guterman, S.K. et al. Autoregulation of the rho gene of Escherichia coli K-12. Molec Gen Genet 193, 210–213 (1984). https://doi.org/10.1007/BF00330669

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  • DOI: https://doi.org/10.1007/BF00330669

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