architectures

 

There are various set-ups for bacterial tet-regulation. Variables among the involved genetic components include the absolute and relative location of tetR and the target gene (i.e. chromosomal or episomal, cis or trans), the number and position of tetO sites within the target gene promoter (see figure) or the kind of tetR expression ((auto)regulated or constitutive). The tables below schematize architectures described in selected publications. The upper table lists set-ups, in which tetR and the target gene are located adjacent on the same DNA molecule, the table below contains examples of spatially separated tetR and target gene architectures.

 


target gene = grey, tetR = black  
tetR: 1 tetO, target gene: 2 tetO - Geissendörfer und Hillen 1990
tetR: 1 tetO, target gene: 1 tetO - Geissendörfer und Hillen 1990
tetR: no tetO, target gene: 1 tetO - Corrigan and Foster 2009
tetR: 1 tetO, target gene: 2 tetO - Bertram et al. 2005
tetR: 1 tetO, target gene: 1 tetO - Bertram et al. 2005
tetR: no tetO, target gene: 2 tetO - Da Re et al. 2007

 

Among the most often applied target gene promoters for bacterial tet-regulation are Pxyl/tet (with one or two tetO sequences) for low G+C Gram positive bacteria (Geissendörfer and Hillen 1990) and PLtetO-1 for use in Gram negative bacteria (Lutz and Bujard 1997) The figure below illustrates the different locations of the two tetO sequences within the promoters.

 

 

 

target gene (grey, right)
tetR (black, below)

de la Torre et al. 1984      
  Sizemore et al. 1990 Kamionka et al. 2005 Stary et al. 2010
      Transposon Tn10
  Lutz and Bujard 1997   Stary et al. 2010