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- | <!-- ------------------------------------------------From 2011 Macquarie--------------------------------------------- -->
| + | {{:Team:UQ-Australia/Template:Header}} |
- | <!-- ------------------------------ Gets rid of the top and bottom iGEM page bits ------------------------------- -->
| + | {|style="width:100%;" border="0" cellpadding="10" cellspacing="0" |
| + | |rowspan="2"|The human circadian rhythm drives many important processes in the body in accordance with the sleep/wake cycle. A characteristic of this biological clock is the periodic oscillation of gene expression. Current parts in the Registry designed to regulate periodic oscillations of gene expression have shown limited success. |
| + | Here we demonstrate the feasibility a biological clock being standardised as a set of BioBrick parts. |
| | | |
- | <html>
| + | Our network is controlled by an engineered promoter, Plac/ara, which features both an activator and a repressor domain. This controls the production of downstream genes to activate other inducible promoters, pBAD and GlnAp2, eventually leading to the production of a repressor protein, lacI, which inhibits Plac/ara, resulting in oscillatory expression. This project shows the feasibility of standardising the biological clock in E. coli and grounds further development for applications in regulated drug/hormone delivery and ion channel control. |
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| + | |
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| + | |
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- | {|align="justify"
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| + | |
| |- | | |- |
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| | | |
| | | |
- | The human circadian rhythm drives many important processes in the body in accordance with the sleep/wake cycle. A characteristic of this biological clock is the periodic oscillation of gene expression. Current parts in the Registry designed to regulate periodic oscillations of gene expression have shown limited success.
| + | '''NB: wiki best viewed on Chrome, Firefox or Safari.''' |
- | Here we demonstrate a biological clock being standardised as a set of BioBrick parts.
| + | |
- | | + | |
- | Our network is controlled by an engineered promoter, Plac/ara, which features both an activator and a repressor domain. This controls the production of downstream genes to activate other inducible promoters, pBAD and GlnAp2, eventually leading to the production of a repressor protein, lacI, which inhibits Plac/ara, resulting in oscillatory expression. This project shows the feasibility of standardising the biological clock in E. coli and grounds further development for applications in regulated drug/hormone delivery and ion channel control.
| + | |
- | | + | |
- | | + | |
- | | + | |
- | Find us on [http://www.facebook.com/pages/UQ-iGEM-2011/174356539258535 Facebook]!
| + | |
- | | + | |
- | | + | |
- | |[[Image:UQ-Australia_team.png|right|frame|Your team picture]]
| + | |
- | |-
| + | |
- | |
| + | |
- | |align="center"|[[Team:UQ-Australia | Team Example]]
| + | |
- | |}
| + | |