Team:Edinburgh/Introduction/Metal promoters

Fur transcription factor and the fur box

In Bacillus subtilis iron recognition is achieved via the Ferric Uptake Regulator (Fur). Fur normally forms a dimer and interacts with a specific operator named the fur box to repressor genes further down-stream. At higher intra-cellular iron concentrations, Fur binds to iron to form a holo-repressor and then binds to the fur box and represses gene transcription. Genes controlled by the fur box usually code for iron binding protein and gate mechanisms within the cell (about 40 genes are controlled by the fur box). In the absence of significant iron levels, the apo-repressor fur does not bind to the fur box and the relevant genes can be coded for.

There are two iron binding site per Fur, so 4 overall sites overall in the dimer. (Pohl et al., 2003) The upper binding site (S2) regularly has a zinc ion for structural integrity. The lower binding site (S1) typically has a zinc ion, which is replaced by iron when intracellular iron concentration rises (figure 1).

The fur box pattern that is conserved by in all different fur boxes is the palyndromic sequence: TGATAAT-N-ATTATCA (N being any base). Most fur boxes are 19 to 21 base pairs and always contain this 7-1-7 palyndromic sequence. Different theories exist as to how the Fur dimer binds to the fur box. The classical model states that a Fur dimer binds to one fur box and represses the downstream gene. Another states that the hexameric GATAAT pattern is recognized by three different fur dimers (Fuangthong and Helmann, 2003). The most recent one posits that the minimal binding site for the Fur dimer is TGATAAT-N-ATTATCA and that most fur boxes contain two repeats of this pattern, such as TGATAATGATAATCATTATCA (figure 2).

We decided to assess the minimal binding site for the fur box to work (TGATAAT-N-ATTATCA) in a synthetic construct and assay the effect of iron on a fluorescent protein located downstream.