Difference between revisions of "Part:BBa K1150032"
(One intermediate revision by one other user not shown) | |||
Line 29: | Line 29: | ||
This part contains the protein [https://parts.igem.org/Part:BBa_K1150007 COP1] fused to the Methyl-Tranferase [https://parts.igem.org/Part:BBa_K1150003 G9a]. It's an interaction partner of [https://parts.igem.org/Part:BBa_K1150029 dCas9-UVR8] and part of the UVB light controlled mechanism to repress gene expression. You will be able to repress any desired gene by a short UV-light pulse. | This part contains the protein [https://parts.igem.org/Part:BBa_K1150007 COP1] fused to the Methyl-Tranferase [https://parts.igem.org/Part:BBa_K1150003 G9a]. It's an interaction partner of [https://parts.igem.org/Part:BBa_K1150029 dCas9-UVR8] and part of the UVB light controlled mechanism to repress gene expression. You will be able to repress any desired gene by a short UV-light pulse. | ||
− | For more information and experimental data have a look at our [http://2013.igem.org/Team:Freiburg/Project/induction#light light] and [http://2013.igem.org/Team:Freiburg/Project/effector# | + | For more information and experimental data have a look at our [http://2013.igem.org/Team:Freiburg/Project/induction#light light] and [http://2013.igem.org/Team:Freiburg/Project/effector#epigenetics epigenetic] project page. |
==Biology & Usage== | ==Biology & Usage== | ||
− | COP1 is a protein that was first described in the model organism ''Arabidopsis thaliana''. It will bind to the UV-light receptor UVR8 after illumination [1]. Thereby recruiting G9a to its target locus. Subsequently the local DNA-expression will be repressed by DNA-methylation. For this UVB light controled gene repression system you need a combination of these BioBricks: [https://parts.igem.org/Part:BBa_K1150029 | + | COP1 is a protein that was first described in the model organism ''Arabidopsis thaliana''. It will bind to the UV-light receptor UVR8 after illumination [1]. Thereby recruiting G9a to its target locus. Subsequently the local DNA-expression will be repressed by DNA-methylation. For this UVB light controled gene repression system you need a combination of these BioBricks: [https://parts.igem.org/Part:BBa_K1150029 dCas9-UVR8], [https://parts.igem.org/Part:BBa_K1150032 COP1-G9a] and [https://parts.igem.org/Part:BBa_K1150034 RNaimer]. |
Latest revision as of 23:14, 4 October 2013
uniCAS UV Light Switch Part II - Histone Modifier
CMV:COP1-Linker-G9a-NLS:BGH | |
---|---|
Function | Histone modification domain
of UVB light induced gene expression control |
Use in | Mammalians |
RFC standard | RFC 25 |
Backbone | pSB1C3 |
Submitted by | [http://2013.igem.org/Team:Freiburg Freiburg 2013] |
Introduction
This part contains the protein COP1 fused to the Methyl-Tranferase G9a. It's an interaction partner of dCas9-UVR8 and part of the UVB light controlled mechanism to repress gene expression. You will be able to repress any desired gene by a short UV-light pulse.
For more information and experimental data have a look at our [http://2013.igem.org/Team:Freiburg/Project/induction#light light] and [http://2013.igem.org/Team:Freiburg/Project/effector#epigenetics epigenetic] project page.
Biology & Usage
COP1 is a protein that was first described in the model organism Arabidopsis thaliana. It will bind to the UV-light receptor UVR8 after illumination [1]. Thereby recruiting G9a to its target locus. Subsequently the local DNA-expression will be repressed by DNA-methylation. For this UVB light controled gene repression system you need a combination of these BioBricks: dCas9-UVR8, COP1-G9a and RNaimer.
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 2231 - 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 1373
Illegal BsaI.rc site found at 1450
Illegal SapI.rc site found at 962
References
[1] Müller, K.; Engesser, R.; Schulz, S.; Steinberg, T.; Tomakidi, P.; Weber, C. C. et al. (Nucleid Acids Research 2013): Multi-chromatic control of mammalian gene expression and signaling