Difference between revisions of "Part:BBa K1150026"
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==Data== | ==Data== | ||
[[File:Freiburg2013_light_results_red2.png|left|300px]]<br> | [[File:Freiburg2013_light_results_red2.png|left|300px]]<br> | ||
| − | '''Figure 1:''' SEAP levels for HEK293T-cells. | + | '''Figure 1:''' SEAP levels for HEK293T-cells. |
| − | The HEK293T-cells were treated as described in the "Experiments" section above. The bars on the left side show SEAP levels of the negative control that was transfected without the targeting plasmid | + | The HEK293T-cells were treated as described in the "Experiments" section above. The bars on the left side show SEAP levels of the negative control that was transfected without the targeting plasmid href="https://parts.igem.org/Part:BBa_K1150034. The bars on the right side show SEAP levels of constructs transfected with target plasmid. Red bars show cell-samples illuminated with activating red-light, white bars show samples illuminated with inactivating far-red light. Error bars show standard deviation of biological triplicates. An increasing SEAP-level after illumination can be observed if target plasmid is present. |
<span class='h3bb'> | <span class='h3bb'> | ||
Revision as of 15:49, 4 October 2013
uniCAS Red Light Switch Part II - Activator
| CMV:PhyB-Linker-VP16-NLS:BGH | |
|---|---|
| Function | Activation domain of red light
induced gene expression control |
| Use in | Mammalian cells |
| RFC standard | RFC 25 |
| Backbone | pSB1C3 |
| Submitted by | [http://2013.igem.org/Team:Freiburg Freiburg 2013] |
Usage and Biology
Fusion protein of PhyB and VP16. This fusion protein PhyB-VP16 is an interaction partner of dCas9-PIF. When crRNA and tracrRNA bind to Cas9, the protein is able to bind complementary DNA. When the system is exposed to red light (660 nm), the Phytochrome B receptor binds to the Phytochrome interaction actor (PIF). So it recruits the dCas9-PIF protein. The PhyB-PIF binding can be abolished by illumination with far-red light (740nm.) This system enables activation of gene expression induced by red light. Have a look at our [http://2013.igem.org/Team:Freiburg/Project/induction#light light project page].
Data
Figure 1: SEAP levels for HEK293T-cells. The HEK293T-cells were treated as described in the "Experiments" section above. The bars on the left side show SEAP levels of the negative control that was transfected without the targeting plasmid href="https://parts.igem.org/Part:BBa_K1150034. The bars on the right side show SEAP levels of constructs transfected with target plasmid. Red bars show cell-samples illuminated with activating red-light, white bars show samples illuminated with inactivating far-red light. Error bars show standard deviation of biological triplicates. An increasing SEAP-level after illumination can be observed if target plasmid is present.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 576
Illegal BglII site found at 1076
Illegal BamHI site found at 1158
Illegal XhoI site found at 1109
Illegal XhoI site found at 1128 - 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI site found at 1325
References
Müller, K. et al. (2013). A red/far-red light-responsive bi-stable toggle switch to control gene expression in mammalian cells. Nucleid Acid Research
Hirai, H. et al. (2010). Structure and functions of powerful transactivators: VP16, MyoD and FoxA. Int. J. Dev. Biol.