Difference between revisions of "Part:BBa K3861022"

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hilA, together with hilC and hilD, are global regulators and control the expression of the Salmonella pathogenicity island I (SPI-1) genes in <i>S</i>. typhimurium on which the SPI-1 T3SS injectisome is encoded.<sup>1</sup> Over 25 genes that are needed for host invasion are located on the SPI-1.<sup>2</sup> Also, hilA activates the SPI-1 operon mediated by the prg and inv promoters.<sup>3,4</sup> Thus, hilA controls SPI genes in response to enviromental needs like pH and oxygen levels.<sup>4–6</sup>
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hilA, together with hilC and hilD, are global regulators and control the expression of the <i>Salmonella</i> pathogenicity island I (SPI-1) genes in <i>S</i>. typhimurium on which the SPI-1 T3SS injectisome is encoded.<sup>1</sup> Over 25 genes that are needed for host invasion are located on the SPI-1.<sup>2</sup> Also, hilA activates the SPI-1 operon mediated by the prg and inv promoters.<sup>3,4</sup> Thus, hilA controls SPI-1 genes in response to enviromental needs like pH and oxygen levels.<sup>4–6</sup>
 
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As a part of our project “TargteTaxi”, we require the SPI-1 T3SS to be present in the minicells membrane. For assembly of the SPI-1 T3SS in the minicells we must overexpress the SPI-1 encoded genes, as it has been shown previously by Caerlton et al. (2013)<sup>7</sup>. The overexpression of the T3SS genes can be achieved by overexpressing its master regulator, hilA. In our bacterial strain, hilA expression is going to be regulated by the arabinose inducible promoter of Salmonella Typhimurium, allowing us to control the expression of the SPI-1 enconded genes.
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As a part of our project “TargteTaxi”, we require the SPI-1 T3SS to be present in the minicells membrane. For assembly of the SPI-1 T3SS in the minicells, we must overexpress the SPI-1 encoded genes as it has been shown previously by Carleton et al. (2013)<sup>7</sup>. The overexpression of the T3SS genes can be achieved by overexpressing its master regulator, hilA. In our bacterial strain, hilA expression is going to be regulated by the arabinose inducible promoter of <i>S</i>. Typhimurium, allowing us to control the expression of the SPI-1 encoded genes.
  
 
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6. Main-Hester, K. L., Colpitts, K. M., Thomas, G. A., Fang, F. C. & Libby, S. J. Coordinate regulation of Salmonella pathogenicity island 1 (SPI1) and SPI4 in Salmonella enterica serovar Typhimurium. <i>Infect. Immun. 76</i>, 1024–1035 (2008).
 
6. Main-Hester, K. L., Colpitts, K. M., Thomas, G. A., Fang, F. C. & Libby, S. J. Coordinate regulation of Salmonella pathogenicity island 1 (SPI1) and SPI4 in Salmonella enterica serovar Typhimurium. <i>Infect. Immun. 76</i>, 1024–1035 (2008).
 
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7.      Carleton, H. A., Lara-Tejero, M., Liu, X. & Galán, J. E. Engineering the type III secretion system in non-replicating bacterial minicells for antigen delivery. Nat. Commun. (2013) doi:10.1038/ncomms2594.

Latest revision as of 15:32, 21 October 2021


hilA transcriptional regulator

hilA, together with hilC and hilD, are global regulators and control the expression of the Salmonella pathogenicity island I (SPI-1) genes in S. typhimurium on which the SPI-1 T3SS injectisome is encoded.1 Over 25 genes that are needed for host invasion are located on the SPI-1.2 Also, hilA activates the SPI-1 operon mediated by the prg and inv promoters.3,4 Thus, hilA controls SPI-1 genes in response to enviromental needs like pH and oxygen levels.4–6
As a part of our project “TargteTaxi”, we require the SPI-1 T3SS to be present in the minicells membrane. For assembly of the SPI-1 T3SS in the minicells, we must overexpress the SPI-1 encoded genes as it has been shown previously by Carleton et al. (2013)7. The overexpression of the T3SS genes can be achieved by overexpressing its master regulator, hilA. In our bacterial strain, hilA expression is going to be regulated by the arabinose inducible promoter of S. Typhimurium, allowing us to control the expression of the SPI-1 encoded genes.

Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal PstI site found at 1112
    Illegal PstI site found at 1309
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal PstI site found at 1112
    Illegal PstI site found at 1309
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 1635
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal PstI site found at 1112
    Illegal PstI site found at 1309
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal PstI site found at 1112
    Illegal PstI site found at 1309
    Illegal NgoMIV site found at 151
    Illegal AgeI site found at 1258
  • 1000
    COMPATIBLE WITH RFC[1000]


References

1. Widmaier, D. M. et al. Engineering the Salmonella type III secretion system to export spider silk monomers. Mol. Syst. Biol. 5, 309 (2009).
2. Heran Darwin, K. & Miller, V. L. InvF Is Required for Expression of Genes Encoding Proteins Secreted by the SPI1 Type III Secretion Apparatus in Salmonella typhimurium. J. Bacteriol. 181, 4949–4954 (1999).
3. Bajaj, V., Hwang, C. & Lee, C. A. hilA is a novel ompR/toxR family member that activates the expression of Salmonella typhimurium invasion genes. Mol. Microbiol. 18, 715–727 (1995).
4. Bajaj, V., Lucas, R. L., Hwang, C. & Lee, C. A. Co-ordinate regulation of Salmonella typhimurium invasion genes by environmental and regulatory factors is mediated by control of hilA expression. Mol. Microbiol. 22, 703–714 (1996).
5. Ahmer, B. M., van Reeuwijk, J., Watson, P. R., Wallis, T. S. & Heffron, F. Salmonella SirA is a global regulator of genes mediating enteropathogenesis. Mol. Microbiol. 31, 971–982 (1999).
6. Main-Hester, K. L., Colpitts, K. M., Thomas, G. A., Fang, F. C. & Libby, S. J. Coordinate regulation of Salmonella pathogenicity island 1 (SPI1) and SPI4 in Salmonella enterica serovar Typhimurium. Infect. Immun. 76, 1024–1035 (2008).
7. Carleton, H. A., Lara-Tejero, M., Liu, X. & Galán, J. E. Engineering the type III secretion system in non-replicating bacterial minicells for antigen delivery. Nat. Commun. (2013) doi:10.1038/ncomms2594.