Difference between revisions of "Part:BBa K203125"
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<partinfo>BBa_K203125 short</partinfo> | <partinfo>BBa_K203125 short</partinfo> | ||
− | SREBP-upregulated promoter predicted by [http://2009.igem.org/Team:Heidelberg/HEARTBEAT HEARTBEAT] (see also [[Part:BBa_K203125: | + | SREBP-upregulated promoter predicted by [http://2009.igem.org/Team:Heidelberg/HEARTBEAT HEARTBEAT] (see also [[Part:BBa_K203125:Design|Part Design]]). SREBP induction experimentally confirmed. |
Latest revision as of 19:05, 21 October 2009
SREBP regulated promoter, predicted, tested HB8
SREBP-upregulated promoter predicted by [http://2009.igem.org/Team:Heidelberg/HEARTBEAT HEARTBEAT] (see also Part Design). SREBP induction experimentally confirmed.
Usage and Biology
Sterol regulatory element-binding protein (SREBP) is a transcription factor involved in the regulation of sterol metabolism. In cells with high concentration of cholestrol SREBP is present in an inactive form anchored to the endoplasmatic reticulum or the nuclear envelop. If the cholesterol concentration decreases SREBP is cleaved by the proteases site-1 protease and site-2 protease resulting in a release of the aminoterminal domain of SREBP. Two additional proteins (Scap and Insig) are needed to regulate this process in a way that the cleavage occurs exclusively during lack of sterol. The aminoterminal domain of SREBP is translocated into the nucleus and binds to the DNA consensus sequence TCACNCCAC. The binding causes an upregulation of the genes needed for cholesterol synthesis. For references, see [http://2009.igem.org/Team:Heidelberg/Eukaryopedia#SREBP Eukaryopedia].
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Functional Parameters
Underwent rough characterization by automated plate fluorescence reader/TECAN. Shown to be upregulated by Sterol depletion approx. 8-fold, as compared to cells in a surplus of Sterol and LDL. Corresponds to clone HB8.