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Team:UCSF/Project/Background
From 2013.igem.org
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#opensource {width:306px; float:left; background-color: #F5F5F5; margin-left:8px; padding: 10px; margin-top:8px;} | #opensource {width:306px; float:left; background-color: #F5F5F5; margin-left:8px; padding: 10px; margin-top:8px;} | ||
| - | #rightcontent {width:755px; float:right; background-color: #F5F5F5; margin-left: 8px; margin-top: | + | #rightcontent {width:755px; float:right; background-color: #F5F5F5; margin-left: 8px; margin-top:0px;} |
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| - | <div id="rightcontenttext" style = "width: | + | <div id="rightcontenttext" style = "width:420px; height:200px"align="justify"> |
<font face="arial" size = "3" > | <font face="arial" size = "3" > | ||
| - | Rarely in nature do bacterial strains exist in isolation; they form complex microbial communities that interact with various organisms. | + | Rarely in nature do bacterial strains exist in isolation; they form complex microbial communities that interact with various organisms. These complex, balanced communities - called microbiomes - interact with various organisms and exist almost everywhere from the soil to our own digestive system. Microbiomes play an important role in human and environmental health and disruption of the balance in the microbiome is linked to many diseases. Current methods of manipulating microbiomes, such as antibiotic treatment, are nonspecific and indiscriminately kill both good and bad bacteria. Targeting precise bacterial community strains and controlling their growth, activity, and outputs is difficult and requires many new tools. </font> |
</div> | </div> | ||
<div id="photos"> | <div id="photos"> | ||
| - | <center><img style="margin- | + | <center><img style="width:500px;margin-bottom:10px; margin-top:30px"; padding:0;" |
| - | src="https://static.igem.org/mediawiki/2013/ | + | src="https://static.igem.org/mediawiki/2013/a/a1/UCSF_Background1.png"> </center><br></div> |
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<div id="description" style = "width:920px; height:315px"> | <div id="description" style = "width:920px; height:315px"> | ||
<font face="arial" size = "3" align = "left"> <br> | <font face="arial" size = "3" align = "left"> <br> | ||
| - | At the beginning of this summer, we asked ourselves a question: “What could we introduce to a microbiome which would allow | + | At the beginning of this summer, we asked ourselves a question: “What could we introduce to a microbiome which would allow targeting and eventual gene expression changes in a specific bacteria?” |
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| + | The difficulty faced with this situation is in | ||
<ol> | <ol> | ||
| - | <li> | + | <li>Introduce a targeting system into a defined mixture of bacteria such that you can select and introduce manipulations without negatively affecting other bacteria. </li> |
| - | <li> | + | <li>Creating easy to transfer pathways or circuits that can produce a multitude of outcomes (killing, repressing, upregulating) </li> |
</ol> | </ol> | ||
<br> | <br> | ||
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<br> | <br> | ||
| - | <b><FONT COLOR="#008000"><u> | + | <b><FONT COLOR="#008000"><u>1. Introducing CRISPRi to a bacterial community:</u></font></b><br><br> |
To selectively target and eliminate harmful bacteria, we are utilizing the CRISPRi system, a tool repurposed from a natural adaptive immunity system in bacteria (see diagram below). This tool is comprised of a catalytically dead Cas9 (dCas9) protein that complexes with guide RNAs (gRNA) complementary to the target bacteria’s DNA sequence. This complex binds to DNA complementary to the gRNA and prevents transcription, therefore repressing gene expression. </div> | To selectively target and eliminate harmful bacteria, we are utilizing the CRISPRi system, a tool repurposed from a natural adaptive immunity system in bacteria (see diagram below). This tool is comprised of a catalytically dead Cas9 (dCas9) protein that complexes with guide RNAs (gRNA) complementary to the target bacteria’s DNA sequence. This complex binds to DNA complementary to the gRNA and prevents transcription, therefore repressing gene expression. </div> | ||
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| + | <div id="rightcontenttext" style = "width:400px; height:175px; margin-top:100px"align="justify"> | ||
| + | <font face="arial" size = "3" > | ||
| + | WHY USE CRISPRi? <br><br> 1. CRISPRi utilizes gRNAs which are highly specific and customizable.<br><br> | ||
| + | 2. In principle it could be used to take advantage of unique DNA sequences to target specific bacterial species. | ||
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| + | </div> | ||
<div> | <div> | ||
| - | + | <img style="margin-left:40px; height:400px"; padding:0;" | |
| - | src="https://static.igem.org/mediawiki/2013/ | + | src="https://static.igem.org/mediawiki/2013/5/56/CRISPRi_Background_UCSF.png"> </div> |
| - | <div id="description" style = "width: | + | <div id="description" style = "width:380px; height:20px" align="justify"> |
| - | <font face="arial" size = "2"><center> | + | <font face="arial" size = "2"><center>Amended from: http://www.cell.com/abstract/S0092-8674(13)00211-0?script=true |
| + | </font></center> <br> </div> | ||
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| - | <div id="rightcontenttext" style = "width:400px; height:175px; margin-top: | + | <div id="rightcontenttext" style = "width:400px; height:175px; margin-top:10px"align="justify"> |
<font face="arial" size = "3" > | <font face="arial" size = "3" > | ||
| - | < | + | As a means <a href="https://2013.igem.org/Team:UCSF/Project/Conjugation/Design" >to introduce our CRISPRi system into a microbial community we’ve opted to utilize conjugation</a><span> - a naturally occurring mechanism bacteria use to transfer DNA. By utilizing this mechanism, we are able to target specific strains of bacteria and affect gene expression. This will have a potential for future applications that require targeting individual strains in a bacterial community. </div> |
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<div id="photos"> | <div id="photos"> | ||
| - | <center><img style="margin-left:20px; | + | <center><img style="margin-left:20px;margin-top:20px; width: 390px"; padding:0;" |
| - | src="https://static.igem.org/mediawiki/2013/ | + | src="https://static.igem.org/mediawiki/2013/e/e7/Conjugation_Bkgrd_UCSF.png"> </center><br></div> |
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| - | <div id="rightcontenttext" style = "width:900px; height: | + | <div id="rightcontenttext" style = "width:900px; height:75px; margin-top:10px"align="justify"> |
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<b><center><FONT COLOR="#008000"> | <b><center><FONT COLOR="#008000"> | ||
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</div> | </div> | ||
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| + | <div id="description" style = "width:920px; height:315px"> | ||
| + | <font face="arial" size = "3" align = "left"> <br> | ||
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| + | <b><FONT COLOR="#008000"><u>2. Creating scalable CRISPRi circuits that can choose between outcomes based on the input</u></font></b><br><br> | ||
| + | In addition to our conjugation project, we have developed a <a href="https://2013.igem.org/Team:UCSF/Project/Circuit/Design" >CRISPRi circuit</a><span>, which could be delivered by the same conjugation system, that could apply to future regulatory applications (upregulation of bacterial growth, bacterial activity and behavior, gene expression, and other bacterial processes, etc.). Our circuit is multi-functional, eliciting different responses with the presence of different inducers and is scalable by incorporating additional designed plasmids or guide RNAs. The circuit relies on the use of CRISPRi gRNAs to provide scalability - several genes can be targeted for silencing, upregulation, or other needs. </div> | ||
</html> | </html> | ||
Latest revision as of 23:43, 27 October 2013
Rarely in nature do bacterial strains exist in isolation; they form complex microbial communities that interact with various organisms. These complex, balanced communities - called microbiomes - interact with various organisms and exist almost everywhere from the soil to our own digestive system. Microbiomes play an important role in human and environmental health and disruption of the balance in the microbiome is linked to many diseases. Current methods of manipulating microbiomes, such as antibiotic treatment, are nonspecific and indiscriminately kill both good and bad bacteria. Targeting precise bacterial community strains and controlling their growth, activity, and outputs is difficult and requires many new tools.
At the beginning of this summer, we asked ourselves a question: “What could we introduce to a microbiome which would allow targeting and eventual gene expression changes in a specific bacteria?” The difficulty faced with this situation is in
- Introduce a targeting system into a defined mixture of bacteria such that you can select and introduce manipulations without negatively affecting other bacteria.
- Creating easy to transfer pathways or circuits that can produce a multitude of outcomes (killing, repressing, upregulating)
1. Introducing CRISPRi to a bacterial community:
To selectively target and eliminate harmful bacteria, we are utilizing the CRISPRi system, a tool repurposed from a natural adaptive immunity system in bacteria (see diagram below). This tool is comprised of a catalytically dead Cas9 (dCas9) protein that complexes with guide RNAs (gRNA) complementary to the target bacteria’s DNA sequence. This complex binds to DNA complementary to the gRNA and prevents transcription, therefore repressing gene expression.
WHY USE CRISPRi?
1. CRISPRi utilizes gRNAs which are highly specific and customizable.
2. In principle it could be used to take advantage of unique DNA sequences to target specific bacterial species.
1. CRISPRi utilizes gRNAs which are highly specific and customizable.
2. In principle it could be used to take advantage of unique DNA sequences to target specific bacterial species.
As a means to introduce our CRISPRi system into a microbial community we’ve opted to utilize conjugation - a naturally occurring mechanism bacteria use to transfer DNA. By utilizing this mechanism, we are able to target specific strains of bacteria and affect gene expression. This will have a potential for future applications that require targeting individual strains in a bacterial community.
2. Creating scalable CRISPRi circuits that can choose between outcomes based on the input
In addition to our conjugation project, we have developed a CRISPRi circuit, which could be delivered by the same conjugation system, that could apply to future regulatory applications (upregulation of bacterial growth, bacterial activity and behavior, gene expression, and other bacterial processes, etc.). Our circuit is multi-functional, eliciting different responses with the presence of different inducers and is scalable by incorporating additional designed plasmids or guide RNAs. The circuit relies on the use of CRISPRi gRNAs to provide scalability - several genes can be targeted for silencing, upregulation, or other needs.
