Team:UCSF
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+ | <p align="center"><img src="https://static.igem.org/mediawiki/2008/0/0e/UCSF2008logo2.jpg" width="276" height="288" align="middle" /></p> | ||
+ | <p align="center" class="style2">CHROMATIN MEMORIES<br></br>A new tool for Synthetic Biology</p> | ||
+ | <blockquote> | ||
+ | <br> | ||
+ | <br> | ||
+ | <br> | ||
+ | <h2 align="left">Epigenetic control of gene expression</h2> | ||
+ | <p align="left">The cells of higher eukaryotes utilize chromatin state to encode "permanent" epigenetic changes in gene expression. For example, signals received by a cell during the course of development can induce the partitioning of the genome into accessible (euchromatin) and inaccessible (heterochromatin) regions that specify the fate of that cell. This epigenetic profile, in which blocks of gene are "silenced" by heterochromatin, is stably maintained and inherited by daughter cells. Thus, chromatin state provides a higher level of gene expression control that is regional (acting on many genes at once), dominant over transcription factors, ultra-cooperative (all or none), and highly stable (memory). Engineerable control over chromatin state would clearly be a powerful tool for Synthetic Biology. </p> | ||
+ | <p align="left"><strong>We have constructed and characterized a synthetic silencing system in <em>S. cerevisiae</em> in which we can inducibly silence specific loci in the genome. </strong></p> | ||
+ | <p align="left">This foundational technology will facilitate the construction of complex genetic circuits with memory, and has potential application in the engineering of cell differentiation in higher eukaryotes.</p> | ||
+ | <p align="right"><a href="https://2008.igem.org/Team:UCSF/Project">More...</a></p> | ||
+ | <p align="right"> </p> | ||
+ | <table width="870" border="0" cellpadding="3"> | ||
+ | <tr> | ||
+ | <td width="202" height="208"><img src="https://static.igem.org/mediawiki/2008/b/b6/Our_project.jpg" alt="" width="200" height="201" /></td> | ||
+ | <td width="650"><h3> </h3> | ||
+ | <blockquote> | ||
+ | <h3>OUR PROJECT</h3> | ||
+ | <blockquote> | ||
+ | <h4><a href="https://2008.igem.org/Team:UCSF/Project">Synthetic Chromatin Bit</a></h4> | ||
+ | <ul> | ||
+ | <ul> | ||
+ | <li><a href="https://2008.igem.org/Team:UCSF/Synthetic Chromatin Design">Design</a></li> | ||
+ | <li><a href="https://2008.igem.org/Team:UCSF/Synthetic Chromatin Properties">Properties</a></li> | ||
+ | <li><a href="https://2008.igem.org/Team:UCSF/Modeling">Modeling</a></li> | ||
+ | <li><a href="https://2008.igem.org/Team:UCSF/Strengthening Silencing">Strengthening Silencing</a></li> | ||
+ | <li><a href="https://2008.igem.org/Team:UCSF/Higher_order_systems">Higher-Order Systems</a></li> | ||
+ | <li><a href="https://2008.igem.org/Team:UCSF/Materials and Methods">Materials and Methods</a></li> | ||
+ | </ul> | ||
+ | </ul> | ||
+ | <h4><a href="https://2008.igem.org/FAQs_about_our_Project">FAQs about our Project</a></h4> | ||
+ | <h4><a href="https://2008.igem.org/Team:UCSF/Human Practices">Human Practices</a></h4> | ||
+ | </blockquote> | ||
+ | </blockquote> | ||
+ | <p> </p></td> | ||
+ | </tr> | ||
+ | </table> | ||
+ | <table width="870" border="0" cellpadding="3"> | ||
+ | <tr> | ||
+ | <td width="202" height="208"><img src="https://static.igem.org/mediawiki/2008/f/f5/Our_team.jpg" alt="" width="200" height="200" /></td> | ||
+ | <td width="650"><h3> </h3> | ||
+ | <blockquote> | ||
+ | <h3>OUR TEAM</h3> | ||
+ | <blockquote> | ||
+ | <h4><a href="https://2008.igem.org/Team:UCSF/Team">Team Members</a></h4> | ||
+ | <h4><a href="https://2008.igem.org/Team:UCSF/Summer Experience">Summer Experience</a></h4> | ||
+ | <h4><a href="https://2008.igem.org/Team:UCSF/Notebook">Notebooks</a></h4> | ||
+ | <h4><a href="https://2008.igem.org/Everything_you_ever_wanted_to_know_about_AarI">Aar1 Cloning System</a></h4> | ||
+ | <h4><a href="https://2008.igem.org/Team:UCSF/Parts">Parts submitted to the Registry</a></h4> | ||
+ | <h4><a href="https://2008.igem.org/FAQs_about_our_Team">FAQs about our Team</a></h4> | ||
+ | </blockquote> | ||
+ | </blockquote> | ||
+ | <p> </p></td> | ||
+ | </tr> | ||
+ | </table> | ||
+ | <br><br></br></br> | ||
+ | </blockquote> | ||
+ | </body> | ||
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+ | '''UCSF iGEM 2008 is sponsored by...''' | ||
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- | + | <p align="center"><img src="https://static.igem.org/mediawiki/2008/1/16/Sponsors.png" width="650" height="129" align="middle" /></p></html> | |
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Latest revision as of 03:11, 30 October 2008
CHROMATIN MEMORIES
A new tool for Synthetic Biology
Epigenetic control of gene expression
The cells of higher eukaryotes utilize chromatin state to encode "permanent" epigenetic changes in gene expression. For example, signals received by a cell during the course of development can induce the partitioning of the genome into accessible (euchromatin) and inaccessible (heterochromatin) regions that specify the fate of that cell. This epigenetic profile, in which blocks of gene are "silenced" by heterochromatin, is stably maintained and inherited by daughter cells. Thus, chromatin state provides a higher level of gene expression control that is regional (acting on many genes at once), dominant over transcription factors, ultra-cooperative (all or none), and highly stable (memory). Engineerable control over chromatin state would clearly be a powerful tool for Synthetic Biology.
We have constructed and characterized a synthetic silencing system in S. cerevisiae in which we can inducibly silence specific loci in the genome.
This foundational technology will facilitate the construction of complex genetic circuits with memory, and has potential application in the engineering of cell differentiation in higher eukaryotes.
OUR PROJECT
Synthetic Chromatin Bit
FAQs about our Project
Human Practices
OUR TEAM
Team Members
Summer Experience
Notebooks
Aar1 Cloning System
Parts submitted to the Registry
FAQs about our Team
UCSF iGEM 2008 is sponsored by...