Difference between revisions of "Team:Waterloo/Description"

m
(adds lots of new graphics)
 
(19 intermediate revisions by 2 users not shown)
Line 1: Line 1:
 
{{Waterloo}}
 
{{Waterloo}}
 
<html>
 
<html>
−
<div id ="mainContainer">
+
<div class="container main-container">
−
<div id ="contentContainer">
+
  
−
     <h1>CRISPieR: re-engineering CRISPR-Cas9 with functional applications in eukaryotic systems</h1>
+
     <h1>Project Description</h1>
  
 
     <section id="motivation" title="Motivation">
 
     <section id="motivation" title="Motivation">
 
         <h2>Motivation</h2>
 
         <h2>Motivation</h2>
 
         <p>
 
         <p>
−
             The clustered regularly interspaced short palindromic repeats (CRISPR)-Cas9 system is an astounding tool with many applications in synthetic biology. Since its popularization, CRISPR papers have flooded major journals and many iGEM teams have worked to improve its use as a genome editing tool. The 2015 Waterloo team is taking a three-pronged approach to expand upon previous research for wider, more efficient, and more flexible use of CRISPR-Cas9.
+
             The clustered regularly interspaced short palindromic repeats (CRISPR)-Cas9 system is an exciting tool for synthetic biologists because it can target and edit genomes with unprecedented specificity. The <span class="orangetext">Cas9 Protein</span> binds to a PAM site (NGG), attempts to match its <span class="bluetext">sgRNA target sequence</span> to the adjacent DNA strand and cleaves the DNA if it finds a match. Since its popularization, CRISPR papers have flooded major journals and many iGEM teams have worked to improve its use as a genome editing tool.</p>
 +
      <p>The 2015 Waterloo team is taking a three-pronged approach to expand upon previous research for wider, more efficient, and more flexible use of CRISPR-Cas9: easy testing of sgRNA designs with our <span class="bluetext">Simple sgRNA Exchange</span> design, applying research on new mutations in Cas9's PAM-interacting domain to enable <span class="orangetext">Cas9 PAM Flexibility</span> and applying our work as a <span class="greentext">CRISPR Plant Defense</span> protecting <em>A. thaliana</em> against infection by Cauliflower Mosaic Virus.
 
         </p>
 
         </p>
 +
        <figure>
 +
            <img src="/wiki/images/1/1a/Waterloo_project-overview.png" alt="CRISPR-Cas9 structure and project overview" />
 +
            <figcaption>Overview of CRISPR-Cas9 structure and project sections</figcaption>
 +
        </figure>
 
     </section>
 
     </section>
  
 
     <section id="sgRNA" title="sgRNA Modification" class="sgRNAmod">
 
     <section id="sgRNA" title="sgRNA Modification" class="sgRNAmod">
−
         <h2>sgRNA Modification</h2>
+
         <h2>Simple sgRNA Exchange</h2>
 +
        <figure style="float:left; max-width:30%; width:150px;">
 +
            <img src="/wiki/images/8/85/Waterloo_sgrnaexchangeicon.png" alt="sgRNA Exchange Icon" />
 +
        </figure>
 
         <p>
 
         <p>
−
             We aim to make target selection and guide sequence replacement physically easier in the lab. To target a DNA sequence, a single guide RNA (sgRNA) is used to identify a match <cite ref="Horvath2010"></cite>. Each sgRNA can only have one intended target, however, which forces us to re-synthesize and re-clone the entire sgRNA sequence for each new target we'd like to test. By being able to swap out a 20 base pair section of the sgRNA sequences, instead of synthesizing new targets from scratch, we hope to reduce the turnaround time for using CRISPR to target different sequences.
+
             We aim to make target selection and guide sequence replacement physically easier in the lab. To target a DNA sequence, a single guide RNA (sgRNA) is used to identify a match <cite ref="Horvath2010"></cite>. We modify the sgRNA secondary structure analyzed by Briner et al. <cite ref="Briner2014"></cite> to contain a restriction site. This makes it possible to swap out a 20 base pair section of the sgRNA sequences, instead of synthesizing new targets from scratch, so there is no need to re-synthesize and re-clone the entire sgRNA sequence for each new target we'd like to test. We hope our design reduces the turnaround time for using CRISPR to target different sequences.
 
         </p>
 
         </p>
 
         <figure>
 
         <figure>
−
             <img src="/wiki/images/b/b8/Waterloo_cas9_structure.png" alt="CRISPR-Cas9 structure" />
+
             <img src="/wiki/images/7/78/Waterloo_sgrna_scaffold.png" alt="sgRNA scaffold structure" style="width:50%;" />
−
             <figcaption>CRISPR-Cas9 basic structure</figcaption>
+
             <figcaption>sgRNA scaffold structure</figcaption>
 
             <div class="img-att">i
 
             <div class="img-att">i
 
                 <ul class="img-att-bubble">
 
                 <ul class="img-att-bubble">
−
                     <li>Photo &copy; of Cedric Sapet</li>
+
                     <li>Briner et al., 2014 <cite ref="Briner2014"></cite></li>
−
                     <li><a href="http://1.bp.blogspot.com/-2FeBXhYoXy0/VIsXe6UbVRI/AAAAAAAAFfE/YPetkWio-s4/s1600/Cas9%2Bmediated%2BDNA%2Bcleavage%2BPNG.png">Link to Original Photo</a></li>
+
                    <li>Cropped image</li>
 +
                     <li><a href="http://www.sciencedirect.com/science?_ob=MiamiCaptionURL&_method=retrieve&_eid=1-s2.0-S1097276514007515&_image=1-s2.0-S1097276514007515-gr1.jpg&_cid=272198&_explode=defaultEXP_LIST&_idxType=defaultREF_WORK_INDEX_TYPE&_alpha=defaultALPHA&_ba=&_rdoc=1&_fmt=FULL&_issn=10972765&_pii=S1097276514007515&md5=2b34d1b5899d9fa9a88dc9bf04fb8b64">Link to Original Photo</a></li>
 
                 </ul>
 
                 </ul>
 
             </div>
 
             </div>
 
         </figure>
 
         </figure>
 +
        <p class="desc-links" style="text-align:center;">
 +
            <a href="/Team:Waterloo/Lab/sgRNA">Background and Results</a>
 +
        </p>
 
     </section>
 
     </section>
  
−
     <section id="cas9" title="Cas9 Modification" class="cas9mod">
+
     <section id="cas9" title="Cas9 PAM Flexibility" class="cas9mod">
−
         <h2>Cas9 Modification</h2>
+
         <h2>Cas9 PAM Flexibility</h2>
 +
        <figure style="float:left; max-width:30%; width:150px;">
 +
            <img src="/wiki/images/7/72/Waterloo_pamflexeicon.png" alt="Pam Exchange Icon" />
 +
        </figure>
 
         <p>
 
         <p>
−
             By building on recent papers, such as <cite ref="Kleinstiver2015"></cite>, we are trying to make Cas9’s binding to a protospacer adjacent motif (PAM) site more flexible. The standard <i>S. pyogenes</i> type II CRISPR-Cas9 binds to a PAM of length 3, namely NGG. While this is fairly general, requiring that this sequence be next to the target sequence limits where Cas9 can cut. We have produced a model that suggests Cas9 variants and their preferred PAM sites, and we attempted to demonstrate this model’s validity. The overarching goal is to create Cas9 variants that will bind to any desired PAM site, and we hope to take some significant steps forward to make that goal more achievable and directed.
+
             By building on recent papers, such as <cite ref="Kleinstiver2015"></cite>, we are trying to make Cas9’s binding to a protospacer adjacent motif (PAM) site more flexible. The standard <i>S. pyogenes</i> type II CRISPR-Cas9 binds to a PAM of length 3, namely NGG <cite ref="Kleinstiver2015"></cite>. While this is fairly general, requiring that this sequence be next to the target sequence limits where Cas9 can cut. We have produced a model that suggests Cas9 variants and their preferred PAM sites, and we attempted to demonstrate this model’s validity. The overarching goal is to create Cas9 variants that will bind to any desired PAM site, and we hope to take some significant steps forward to make that goal more achievable and directed.
 +
        </p>
 +
        <p class="desc-links" style="text-align:center;">
 +
            <a href="/Team:Waterloo/Lab/dCas9">Lab Design</a>
 +
            <a href="/Team:Waterloo/Modeling/PAM_Flexibility">Modeling</a>
 +
            <a href="/Team:Waterloo/Practices/Human_Practices">IP Laws</a>
 
         </p>
 
         </p>
 
     </section>
 
     </section>
  
−
     <section id="plants" title="Plant Defence" class="plantmod">
+
     <section id="plants" title="CRISPR Plant Defense" class="plantmod">
−
         <h2>Plant Viral Defence</h2>
+
         <h2>CRISPR Plant Defense</h2>
 +
        <figure style="float:left; max-width:30%; width:150px;">
 +
            <img src="/wiki/images/7/73/Waterloo_plantdefenseicon.png" alt="Plant Defense Icon" />
 +
        </figure>
 
         <p>
 
         <p>
−
             Finally, CRISPR originated as a viral defence mechanism for bacteria, for specific and targeted immunity. Multi-cellular organisms have developed their own defenses to achieve this goal, but from our research it appears that groups have not publicly attempted to introduce CRISPR as an antiviral mechanism in multicellular organisms. Our team is attempting to use the CRISPR system in plants to discover whether it can defend against a class of double-stranded DNA viruses.
+
             Finally, CRISPR originated as a viral defence mechanism for bacteria, for specific and targeted immunity <cite ref="Horvath2010"></cite>. Multi-cellular organisms have developed their own defenses to achieve this goal, but from our research it appears that groups have not publicly attempted to introduce CRISPR as an antiviral mechanism in multicellular organisms. Our team is attempting to use the CRISPR system in plants to discover whether it can defend against a class of double-stranded DNA viruses.
 +
        </p>
 +
        <br>
 +
        <p class="desc-links" style="text-align:center;">
 +
            <a href="/Team:Waterloo/Modeling/CaMV_Biology">CaMV Background</a>
 +
            <a href="/Team:Waterloo/Lab/Plants">Lab Design</a>
 +
            <a href="/Team:Waterloo/Modeling/CaMV_Replication">Modeling CaMV Replication</a>
 +
            <a href="/Team:Waterloo/Modeling/Intercellular_Spread">Modeling Intercellular Spread</a>
 +
            <a href="/Team:Waterloo/Practices/Commercialization">Commercialization</a>
 
         </p>
 
         </p>
 
     </section>
 
     </section>
  
−
     <section>
+
     <section id="references" title="References">
 
         <h2>References</h2>
 
         <h2>References</h2>
 
         <ol id="reflist">
 
         <ol id="reflist">
Line 50: Line 80:
 
     </section>
 
     </section>
  
−
 
−
    <div class="prevHighlightBox">
 
−
        <h5>What should this page contain?</h5>
 
−
        <ul>
 
−
            <li> A clear and concise description of your project.</li>
 
−
            <li>A detailed explanation of why your team chose to work on this particular project.</li>
 
−
            <li>References and sources to document your research.</li>
 
−
            <li>Use illustrations and other visual resources to explain your project.</li>
 
−
        </ul>
 
−
 
−
 
−
        <br />
 
−
        <h4>Advice on writing your Project Description</h4>
 
−
 
−
        <p>We encourage you to put up a lot of information and content on your wiki, but we also encourage you to include summaries as much as possible. If you think of the sections in your project description as the sections in a publication, you should try to be consist, accurate and unambiguous in your achievements.</p>
 
−
 
−
        <p>Judges like to read your wiki and know exactly what you have achieved. This is how you should think about these sections; from the point of view of the judge evaluating you at the end of the year.</p>
 
−
 
−
 
−
        <br />
 
−
        <h4>References</h4>
 
−
        <p>iGEM teams are encouraged to record references you use during the course of your research. They should be posted somewhere on your wiki so that judges and other visitors can see how you though about your project and what works inspired you.</p>
 
−
 
−
 
−
 
−
        <h4>Inspiration</h4>
 
−
        <p>See how other teams have described and presented their projects: </p>
 
−
 
−
        <ul>
 
−
            <li><a href="https://2014.igem.org/Team:Imperial/Project"> Imperial</a></li>
 
−
            <li><a href="https://2014.igem.org/Team:UC_Davis/Project_Overview"> UC Davis</a></li>
 
−
            <li><a href="https://2014.igem.org/Team:SYSU-Software/Overview">SYSU Software</a></li>
 
−
        </ul>
 
−
    </div>
 
−
 
−
</div>
 
 
</div>
 
</div>
 
</html>
 
</html>
 
{{Waterloo_Footer}}
 
{{Waterloo_Footer}}

Latest revision as of 17:01, 20 November 2015

Project Description

Motivation

The clustered regularly interspaced short palindromic repeats (CRISPR)-Cas9 system is an exciting tool for synthetic biologists because it can target and edit genomes with unprecedented specificity. The Cas9 Protein binds to a PAM site (NGG), attempts to match its sgRNA target sequence to the adjacent DNA strand and cleaves the DNA if it finds a match. Since its popularization, CRISPR papers have flooded major journals and many iGEM teams have worked to improve its use as a genome editing tool.

The 2015 Waterloo team is taking a three-pronged approach to expand upon previous research for wider, more efficient, and more flexible use of CRISPR-Cas9: easy testing of sgRNA designs with our Simple sgRNA Exchange design, applying research on new mutations in Cas9's PAM-interacting domain to enable Cas9 PAM Flexibility and applying our work as a CRISPR Plant Defense protecting A. thaliana against infection by Cauliflower Mosaic Virus.

CRISPR-Cas9 structure and project overview
Overview of CRISPR-Cas9 structure and project sections

Simple sgRNA Exchange

sgRNA Exchange Icon

We aim to make target selection and guide sequence replacement physically easier in the lab. To target a DNA sequence, a single guide RNA (sgRNA) is used to identify a match . We modify the sgRNA secondary structure analyzed by Briner et al. to contain a restriction site. This makes it possible to swap out a 20 base pair section of the sgRNA sequences, instead of synthesizing new targets from scratch, so there is no need to re-synthesize and re-clone the entire sgRNA sequence for each new target we'd like to test. We hope our design reduces the turnaround time for using CRISPR to target different sequences.

sgRNA scaffold structure
sgRNA scaffold structure
i

Background and Results

Cas9 PAM Flexibility

Pam Exchange Icon

By building on recent papers, such as , we are trying to make Cas9’s binding to a protospacer adjacent motif (PAM) site more flexible. The standard S. pyogenes type II CRISPR-Cas9 binds to a PAM of length 3, namely NGG . While this is fairly general, requiring that this sequence be next to the target sequence limits where Cas9 can cut. We have produced a model that suggests Cas9 variants and their preferred PAM sites, and we attempted to demonstrate this model’s validity. The overarching goal is to create Cas9 variants that will bind to any desired PAM site, and we hope to take some significant steps forward to make that goal more achievable and directed.

Lab Design Modeling IP Laws

CRISPR Plant Defense

Plant Defense Icon

Finally, CRISPR originated as a viral defence mechanism for bacteria, for specific and targeted immunity . Multi-cellular organisms have developed their own defenses to achieve this goal, but from our research it appears that groups have not publicly attempted to introduce CRISPR as an antiviral mechanism in multicellular organisms. Our team is attempting to use the CRISPR system in plants to discover whether it can defend against a class of double-stranded DNA viruses.


CaMV Background Lab Design Modeling CaMV Replication Modeling Intercellular Spread Commercialization

References

Top