Difference between revisions of "Part:BBa K607003"
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__NOTOC__ | __NOTOC__ | ||
<partinfo>BBa_K607003 short</partinfo> | <partinfo>BBa_K607003 short</partinfo> | ||
− | GFP with LVA-tag under transcriptional control of a modified Prm(PcI) promoter | + | GFP with LVA-tag under transcriptional control of a modified Prm(PcI) promoter. |
+ | The Prm promotor is induced by cI. For more information on cI, see: https://parts.igem.org/wiki/index.php?title=Part:BBa_K607001<br> | ||
+ | The Prm promotor is part of an operator system where cI or cro can be produced. | ||
+ | <br>[[Image:operatorcI.jpg]] | ||
+ | <br>cI dimers will bind to the first two operators. This will look like this: | ||
+ | <br>[[Image:2operatorcI.jpg]] | ||
+ | <br>The “free” PRM promoter will subsequently be occupied by RNA polymerase which in turn will transcribe cI. This leads to a continuous transcription (DNA to RNA) and subsequent expression (RNA to protein) of cI. This means cI is regulating its own synthesis and simulataneously maintaining the repression of cro. Conversely this auto-regulation can also be obeserved if cro is abundant: cro dimer binding to the operator sites will block binding of RNA polymerase to PRM, but will allow binding to PR, which in turn will lead exclusively to cro transcription. At increasing concentrations of cI the probability of cI binding to OR3 also increases, inhibiting therefore RNA polymerase binding to PRM. This means at higher concentrations cI is inhibiting its own synthesis, acting as a self-repressor. | ||
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<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here |
Revision as of 18:58, 21 September 2011
Prm_GFP-LVA
GFP with LVA-tag under transcriptional control of a modified Prm(PcI) promoter.
The Prm promotor is induced by cI. For more information on cI, see: https://parts.igem.org/wiki/index.php?title=Part:BBa_K607001
The Prm promotor is part of an operator system where cI or cro can be produced.
cI dimers will bind to the first two operators. This will look like this:
The “free” PRM promoter will subsequently be occupied by RNA polymerase which in turn will transcribe cI. This leads to a continuous transcription (DNA to RNA) and subsequent expression (RNA to protein) of cI. This means cI is regulating its own synthesis and simulataneously maintaining the repression of cro. Conversely this auto-regulation can also be obeserved if cro is abundant: cro dimer binding to the operator sites will block binding of RNA polymerase to PRM, but will allow binding to PR, which in turn will lead exclusively to cro transcription. At increasing concentrations of cI the probability of cI binding to OR3 also increases, inhibiting therefore RNA polymerase binding to PRM. This means at higher concentrations cI is inhibiting its own synthesis, acting as a self-repressor.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 752