Difference between revisions of "Part:BBa K5317003"
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===Theoretical Part Design=== | ===Theoretical Part Design=== | ||
| − | The MREwt promoter was synthesized and please visit the | + | The MREwt promoter was synthesized and please visit the K53170xx registry entry for functionality analysis . |
===Sequence and Features=== | ===Sequence and Features=== | ||
Revision as of 09:46, 13 September 2024
MREwt promoter
Usage and Biology
The MRE-sites containing promoter enables the metal-dependent expression of a downstream positioned reporter gene via the metal ion-dependent transcription factor MTF-1 (BBa_K5317007) for cell-based metal-detection.
The varying Metal Responsive Elements (MREs) upstream of the eukaryotic metallothionein (MT) gene were discovered in the early 80s (Carter et al. 1984, Stuart et al. 1985). All MREs a-d carry core consensus sites (TGCRCNC) to which the primary MRE-binding transcription factor MTF-1 can bind after binding to heavy metal ions and translocating into the nucleus. Physiologically, this leads to the expression of metallothionein, a protein capable of binding metals such as zinc, cadmium, copper and others for metal homeostasis and detoxification (Cousins 1983).
Cloning
Theoretical Part Design
The MREwt promoter was synthesized and please visit the K53170xx registry entry for functionality analysis .
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]