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Team:TU Munich/Project/Light Switchable Promoter
From 2012.igem.org
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Light Switchable Promoter
The Reinheitsgebot or Bavarian Beer Purity Law forbids the use of any ingredients other than water, barley and hops. Hence, to be able to control the expression of our pathways in yeast, a promoter which does not rely on any chemical additive is needed.
The light switchable promoter, does not only comply with these needs, it also is easy, cheap and very precisely applicable. Furthermore, as the expression of the downstream gene can be upregulated as well as downregulated by red light and far red light respectively
Hence it allows high spatio-temporal control over the genes downstream of the promoter.
Background and principles
This system bases on the yeast two-hybrid system which was originally created for exploring protein-protein interactions. One candidate of a potential protein-interaction pair is fused to the DNA-binding domain of a transcription factor and the other candidate to the activation domain of the transcription factor. If the proteins candidates are really physically interacting with each other, this event will starts the transcription of downstream reporter genes.
This light-inducible system contains two proteins, phytochrome B (PhyB) and phytochrome interacting factor 3 (Pif3), which only interacts together when the PhyB is in it's active conformer (Pfr-form). PhyB, a phytochrome containing a essential chromophore phycocyanobilin B (PCB), is naturally synthesized in it's inactive form (Pr; r stand for red-light sensitive form). So it cannot bound to Pif3 once synthesized. PhyB first has to be activated by red light (λ = 660 nm) which causes a Z-E conformer isomerization to the active form Pfr (fr stands for far-red light senstive form). Relaxation (E-Z conformation change) is induced by far-red light (λ = 750 nm); the high energy form Pfr has a half-life of 30–60 min resulting that after this time half of the Pfr species is spontanously relaxed into the low-energy form Pr. This allows us to generate time-stable light-switchable promoter systems. It is also possible not only have a discret genetic switch. By varying freqrency of red/far-red light pulses one should be able to control the strength of gene-expression or the strength-ratio between two expressed genes.
Idea
General remarks and issues
- A yeast strain with GAL4/GAL80 deletion is required to avoid interference by endogenous GAL4 and GAL80 proteins. Disadvantage of GAL4/GAL80 deletion is that the cells are growing more slowly compared to strains with the wildtype alleles of these genes. Use of prokaryotic LexA instead of the DNA-binding domain of GAL4 avoids that. In this case the UAS (upstream activation sequence) of GAL1 has to be replaced by a prokaryotic upstream LexA operator.
- For a perfect light-switchable system I need an idea for inactivating/degrading LacI fastly because the half-life of LacI is about 10 min. Is it fast enough?
- Check for avaible Nuclear Localization Signals (NLS) for nuclear localized proteins!
- Better we synthesize the DNA of some promoters including UAS and operators.
- The first ~650 N-terminal amino acids are only needed for a functional PhyB.
- The first ~100 N-terminal amino acids are only needed for a fucntional Pif3.
- I asked Roman, if he can get all the elements for Yeast-two-hybrid-system including the GAL4/GAL80 deletion strain from Professor Schwab. May be he also has the modifed Yeast-two-hybrid-sytem with LexA.
Biobricks and sequences
Synthesis of chromophore phycocyanobilin B (PCB)
As described phycocyanobilin is a essential chromophore for a functional phytochrome B. PCB can be synthesized in two steps from heme. First, heme is converted to biliverdin IXα (BV) and second, BV is converted to 3Z-phycocyanobilin (PCB).
