Summary
There are many potential problems inherent in trying to regulate multioperon systems. Commonly used strategies include activator proteins that must be present at every promoter in every operon within the system and special sigma factors that activate the otherwise inactive promoters. It is becoming clear that small RNA molecules may also regulate either positively or negatively. As in the case of phage T4, bacteria also sometimes use cascades of sigma factors in which each new sigma factor induces synthesis of yet another sigma factor. The advantage of such a system is its ability to ensure that specific biochemical events occur in a defined sequence. An additional regulatory element that sometimes occurs both in prokaryotes and in eukaryotes is the enhancer, a discrete site to which a protein must bind for a promoter to be fully functional. Multifunctional regulatory proteins are often the subjects of intense study by geneticists because their distinct functions are associated with specific nonoverlapping domains within the molecule. Experimenters can use site-specific mutagenesis to eliminate only one function while preserving others. Examples of genes kept nonfunctional by insertion of extraneous genetic information are now known. Removal of the extra material can occur by protein splicing or recombination prior to transcription.
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References
Generalized
Boos, W., Shuman, H. (1998). Maltose/maltodextrin system of Escherichia coli: Transport, metabolism, and regulation. Microbiology and Molecular Biology Reviews 62: 204–229.
Dixon, R. (1998). The oxygen-responsive NIFL-NIFA complex: A novel two-component regulatory system controlling nitrogenase synthesis in γ-proteobacteria. Archives of Microbiology 169: 371–380.
Geiduschek, E.P. (1997). Paths to activation of transcription. Science 275: 1614–1616.
Gogarten, J.P., Senejani, A.G., Zhaxybayeva, O., Olendzenski, L., Hilario, E. (2002). Inteins: Structure, function, and evolution. Annual Review of Microbiology 56: 263–287.
Gottesman, S. (2004). The small RNA regulators of Escherichia coli: Roles and mechanisms. Annual Review of Microbiology 58: 303–328.
Gruber, T.M., Gross, C.A. (2003). Multiple sigma subunits and the partitioning of bacterial transcription space. Annual Review of Microbiology 57: 441–466.
Hilbert, D.W., Piggot, P.J. (2004). Compartmentalization of gene expression during Bacillus subtilis spore formation. Microbiology and Molecular Biology Reviews 68: 234–262.
Laksanalamai, P., Whitehead, T.A., Robb, F.T. (2004). Minimal protein-folding systems in hyperthermophilic archaea. Nature Reviews: Microbiology 2: 315–324.
Martinez-Argudo, I., Little, R., Shearer, N., Johnson, P., Dixon, R. (2004). The NifL-NifA system: A multidomain transcriptional regulatory complex that integrates environmental signals. Journal of Bacteriology 186: 601–610.
Narberhaus, F. (1999). Negative regulation of bacterial heat shock genes. Molecular Microbiology 31: 1–8.
Wösten, M.M.S.M. (1998). Eubacterial sigma-factors. FEMS Microbiology Reviews 22: 127–150.
Specialized
Govantes, F., Andújar, E., Santero, E. (1999). Mechanism of translational coupling in the nifLA operon of Klebsiella pneumoniae. The EMBO Journal 17: 2368–2377.
Horlacher, R., Xavier, K.B., Santos, H., Diruggiero, J., Kossmann, M., Boos, W. (1998). Archaeal binding protein-dependent ABC transporter: Molecular and biochemical analysis of the trehalose/maltose transport system of the hyperthermophilic archaeon Thermococcus litoralis. Journal of Bacteriology 180: 680–689.
Jack, R., De Zamaroczy, M., Merrick, M. (1999). The signal transduction protein glnK is required for NifL-dependent nitrogen control of nif gene expression in Klebsiella pneumoniae. Journal of Bacteriology 181: 1156–1162.
Joly, N., Danot, O., Schlegel, A., Boos, W., Richet, E. (2002). The Aes protein directly controls the activity of MalT, the central transcriptional activator of the Escherichia coli maltose regulon. The Journal of Biological Chemistry 277: 16606–16613.
Joly, N., Böhm, A., Boos, W., Richet, E. (2004). MalK, the ATP-binding cassette component of the Escherichia coli maltodextrin transporter, inhibits the transcriptional activator MalT by antagonizing inducer binding. The Journal of Biological Chemistry 279: 33123–33130.
Klein, G., Dartigalongue, C., Raina, S. (2003). Phosphorylation-mediated regulation of heat shock response in Escherichia coli. Molecular Microbiology 48: 269–285.
Mogk, A., Deuerling, E., Vorderwülbecke, S., Vierling, E., Bukau, B. (2003). Small heat shock proteins, ClpB and the DnaK system form a functional triade in reversing protein aggregation. Molecular Microbiology 50: 585–595.
Mujacic, M., Bader, M.W., Baneyx, F. (2004). Escherichia coli Hsp31 functions as a holding chaperone that cooperates with the DnaK-DnaJ-GrpE system in the management of protein misfolding under severe stress conditions. Molecular Microbiology 51: 849–859.
Thiel, T., Lyons, E.M., Erker, J.C. (1997). Characterization of genes for a second Mo-dependent nitrogenase in the cyanobacterium Anabaena variabilis. Journal of Bacteriology 179: 5222–5225.
Wu, H., Hu, Z., Liu, X.-Q. (1998). Protein trans-splicing by a split intein encoded in a split dnaE gene of Synechocystis sp. PC 06803. Proceedings of the National Academy of Sciences of the USA 95: 9226–9231.
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(2006). Advanced Regulatory Topics. In: Bacterial and Bacteriophage Genetics. Springer, New York, NY. https://doi.org/10.1007/0-387-31489-X_14
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DOI: https://doi.org/10.1007/0-387-31489-X_14
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