Team:UCSF

From 2009.igem.org

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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>
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<p  align="center" class="style2">CHROMATIN MEMORIES<br></br>A new tool for Synthetic Biology</p>
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      <h2 align="left">Epigenetic control of gene expression</h2>
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      <p align="left">The cells of higher eukaryotes utilize chromatin state to encode &quot;permanent&quot; 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 &quot;silenced&quot; 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>
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      <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>
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      <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>
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    <p align="right"><a href="https://2008.igem.org/Team:UCSF/Project">More...</a></p>
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      <p align="right">&nbsp;</p>
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          <td width="202" height="208"><img src="https://static.igem.org/mediawiki/2008/b/b6/Our_project.jpg" alt="" width="200" height="201" /></td>
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          <td width="650"><h3>&nbsp;</h3>
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            <blockquote>
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              <h3>OUR PROJECT</h3>
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              <blockquote>
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                <h4><a href="https://2008.igem.org/Team:UCSF/Project">Synthetic Chromatin Bit</a></h4>
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                <ul>
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                  <ul>
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                    <li><a href="https://2008.igem.org/Team:UCSF/Synthetic Chromatin Design">Design</a></li>
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                    <li><a href="https://2008.igem.org/Team:UCSF/Synthetic Chromatin Properties">Properties</a></li>
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                    <li><a href="https://2008.igem.org/Team:UCSF/Modeling">Modeling</a></li>
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                    <li><a href="https://2008.igem.org/Team:UCSF/Strengthening Silencing">Strengthening Silencing</a></li>
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                    <li><a href="https://2008.igem.org/Team:UCSF/Higher_order_systems">Higher-Order Systems</a></li>
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                    <li><a href="https://2008.igem.org/Team:UCSF/Materials and Methods">Materials and Methods</a></li>
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                  </ul>
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                </ul>
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                <h4><a href="https://2008.igem.org/FAQs_about_our_Project">FAQs about our Project</a></h4>
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                <h4><a href="https://2008.igem.org/Team:UCSF/Human Practices">Human Practices</a></h4>
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              </blockquote>
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            </blockquote>
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          <p>&nbsp;</p></td>
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          <td width="202" height="208"><img src="https://static.igem.org/mediawiki/2008/f/f5/Our_team.jpg" alt="" width="200" height="200" /></td>
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          <td width="650"><h3>&nbsp;</h3>
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              <blockquote>
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                <h3>OUR TEAM</h3>
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                <blockquote>
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                  <h4><a href="https://2008.igem.org/Team:UCSF/Team">Team Members</a></h4>
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                  <h4><a href="https://2008.igem.org/Team:UCSF/Summer Experience">Summer Experience</a></h4>
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                  <h4><a href="https://2008.igem.org/Team:UCSF/Notebook">Notebooks</a></h4>
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                  <h4><a href="https://2008.igem.org/Everything_you_ever_wanted_to_know_about_AarI">Aar1 Cloning System</a></h4>
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                  <h4><a href="https://2008.igem.org/Team:UCSF/Parts">Parts submitted to the Registry</a></h4>
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                  <h4><a href="https://2008.igem.org/FAQs_about_our_Team">FAQs about our Team</a></h4>
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                </blockquote>
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              </blockquote>
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          <p>&nbsp;</p></td>
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      </table>
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<br><br></br></br>
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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>

Revision as of 21:12, 19 October 2009

Engineering the Movement of Cellular Robots

Some eukaryotic cells, such as white blood cells, have the amazing ability to sense specific external chemical signals, and move toward those signals. This behavior, known as chemotaxis, is a fundamental biological process crucial to such diverse functions as development, wound healing and immune response. Our project focuses on using a synthetic biology approach to manipulate signaling pathways that mediate chemotaxis in two model organisms: HL-60 (neutrophil-like) cells and the slime mold, Dictyostelium discoideum. We are attempting to reprogram the movements that the cells undergo by altering the guidance and movement machinery of these cells in a modular way. For example, can we make cells move faster? Slower? Can we steer them to migrate toward new signals?

Through our manipulations, we hope to better understand how these systems work, and eventually to build or reprogram cells that can perform useful tasks. Imagine, for example, therapeutic nanorobots that could home to a directed site in the body and execute complex, user-defined functions (e.g., kill tumors, deliver drugs, guide stem cell migration and differentiation). Alternatively, imagine bioremediation nanorobots that could find and retrieve toxic substances. Such cellular robots could be revolutionary biotechnological tools.

'


Home The Team The Project Parts Submitted to the Registry Our summer experience Notebook Human Practices

(Or you can choose different headings. But you must have a team page, a project page, and a notebook page.)

Untitled Document

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.

More...

 

 

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...


Retrieved from "http://2009.igem.org/Team:UCSF"