Difference between revisions of "Part:BBa K415509:Design"
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* Tissue Factor: Sp1 site isolated from the Tissue Factor promoter and has sequence GGGGCGGGGCG. | * Tissue Factor: Sp1 site isolated from the Tissue Factor promoter and has sequence GGGGCGGGGCG. | ||
* MCP-1: the TRE site isolated from the promoter of teh MCP-1 gene. It has the sequence TGACTCC. | * MCP-1: the TRE site isolated from the promoter of teh MCP-1 gene. It has the sequence TGACTCC. | ||
− | + | * SV40: Minimal promoter | |
===Source=== | ===Source=== |
Latest revision as of 20:44, 28 October 2010
pNR1NR2_SV40 Shear Stress Responsive Promoter
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 6
- 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 6
- 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 6
Illegal BglII site found at 81
Illegal XhoI site found at 77 - 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 6
- 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 6
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 42
Illegal BsaI.rc site found at 62
Design Notes
MIT iGEM 2010 Mammalian Promoter Part.
Preliminary data suggests that this synthetic promoter lends transcriptional sensitivity to fluid shear stress in the HEK293FT cell line. The schematic for the construction of this part, based on Silberman et al., Angiogenesis, 2009, is shown below. The promoter consists of a concatenation of three different shear stress responsive motifs isolated from different genes in front of the SV40 minimal promoter.
Of these:
- PDGF/B: the original shear stress responsive element (SSRE) isolated from the platelet derived growth factor B promoter and has sequence GAGACC.
- Tissue Factor: Sp1 site isolated from the Tissue Factor promoter and has sequence GGGGCGGGGCG.
- MCP-1: the TRE site isolated from the promoter of teh MCP-1 gene. It has the sequence TGACTCC.
- SV40: Minimal promoter
Source
MIT iGEM 2010 Mammalian Part
References
Silberman et al. "Shear Stress-induced Transcriptional Regulation via Hybrid Promoters as a Potential Tool for Promoting Angiogenesis." Angiogenesis 12.3 (2009): 231-42. Print.