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Team:EPF-Lausanne
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{{EPF-Lausanne09}} | {{EPF-Lausanne09}} | ||
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| + | <br><br> | ||
| + | ==Concept== | ||
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| + | <div style="text-align:justify;"> | ||
| + | [[Image:LovTAP_dimer.png|right|300px|thumb|LovTAP dimer bound to DNA]] | ||
| + | Recent discoveries of photoreceptors in many organisms got us excited about the possibility of using light-responsive genetic tools in synthetic biology. Indeed, such tools could in principle induce phenotypic changes in a more localized, preciser and faster fashion than currently available chemical-based methods. To evaluate the biotechnological potential of such tools, we specifically aimed to induce a change in gene expression, more specifically to directly turn a gene on or off, in a living organism, in response to a light stimulus. | ||
| - | + | For this purpose, we used a light-sensitive DNA binding protein "LovTAP" (for Light, Oxygen, Voltage Tryptophan-Activated Protein) to convert a light input into a chosen output, here fluorescence generated by the RFP reporter gene. | |
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| - | + | The results clearly show that this light-induced gene switch tool works ''in vivo'', demonstrating the feasibility of implementing such powerful technology for a diverse range of bio(techno)logical applications. | |
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! scope=col | [[Image:Logo_Novartis.png|100 px]] | ! scope=col | [[Image:Logo_Novartis.png|100 px]] | ||
! scope=col | [[Image:Logo_Syngenta.png|80 px]] | ! scope=col | [[Image:Logo_Syngenta.png|80 px]] | ||
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! scope=col | [[Image:Logo_ciba.jpg|80 px]] | ! scope=col | [[Image:Logo_ciba.jpg|80 px]] | ||
! scope=col | [[Image:Logo_nikon.jpg|60 px]] | ! scope=col | [[Image:Logo_nikon.jpg|60 px]] | ||
Latest revision as of 22:45, 21 October 2009
Concept
Recent discoveries of photoreceptors in many organisms got us excited about the possibility of using light-responsive genetic tools in synthetic biology. Indeed, such tools could in principle induce phenotypic changes in a more localized, preciser and faster fashion than currently available chemical-based methods. To evaluate the biotechnological potential of such tools, we specifically aimed to induce a change in gene expression, more specifically to directly turn a gene on or off, in a living organism, in response to a light stimulus.
For this purpose, we used a light-sensitive DNA binding protein "LovTAP" (for Light, Oxygen, Voltage Tryptophan-Activated Protein) to convert a light input into a chosen output, here fluorescence generated by the RFP reporter gene.
The results clearly show that this light-induced gene switch tool works in vivo, demonstrating the feasibility of implementing such powerful technology for a diverse range of bio(techno)logical applications.
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