"
Team:UCSF
From 2013.igem.org
| (26 intermediate revisions not shown) | |||
| Line 105: | Line 105: | ||
font-family: Myriad Pro, Gill Sans MT, Trebuchet MS, Arial, Sans-Serif; | font-family: Myriad Pro, Gill Sans MT, Trebuchet MS, Arial, Sans-Serif; | ||
border: 0; | border: 0; | ||
| - | |||
} | } | ||
| Line 112: | Line 111: | ||
font-weight: normal; | font-weight: normal; | ||
color: black; | color: black; | ||
| - | margin-bottom: | + | margin-bottom: 0px; |
padding-left: 5px; | padding-left: 5px; | ||
} | } | ||
| Line 161: | Line 160: | ||
h2{ | h2{ | ||
font-size: 1.7em; | font-size: 1.7em; | ||
| + | line-height: 1.2em; | ||
} | } | ||
h3{ | h3{ | ||
| Line 168: | Line 168: | ||
#box1{ | #box1{ | ||
width: 980px; | width: 980px; | ||
| - | margin-top: | + | margin-top: 10px; |
background: #fffff; | background: #fffff; | ||
float: left; | float: left; | ||
| - | padding-bottom: | + | padding-bottom: 20px; |
margin-bottom: 5px; | margin-bottom: 5px; | ||
} | } | ||
| - | |||
| - | |||
#box1 p{ | #box1 p{ | ||
font-size: 1.2em; | font-size: 1.2em; | ||
| Line 197: | Line 195: | ||
background-color: #fffff; | background-color: #fffff; | ||
margin-top: 10px; | margin-top: 10px; | ||
| - | padding-bottom: | + | padding-bottom: 0px; |
| - | margin-bottom: | + | margin-bottom: 0px; |
text-align:justify; | text-align:justify; | ||
} | } | ||
| Line 246: | Line 244: | ||
float:left; | float:left; | ||
border-radius:4px; | border-radius:4px; | ||
| + | margin-top:10px; | ||
margin-right:10px; | margin-right:10px; | ||
} | } | ||
| Line 264: | Line 263: | ||
<h2><center>Operation CRISPR: Deploying precision guided tools to target unique species in a complex microbiome</h2></center> <p> | <h2><center>Operation CRISPR: Deploying precision guided tools to target unique species in a complex microbiome</h2></center> <p> | ||
In microbial communities, bacterial populations are commonly controlled using indiscriminate, broad range antibiotics. There are few ways to target specific strains effectively without disrupting the entire microbiome and local environment. The goal of our project is to take advantage of a natural horizontal gene transfer mechanism in bacteria to precisely affect gene expression in selected strains. We combine bacterial conjugation with CRISPRi, an RNAi-like repression system developed from bacteria, to regulate gene expression in targeted strains within a complex microbial community. One possible application is to selectively repress pathogenic genes in a microbiome, leaving the community makeup unaffected. In addition, we use CRISPRi to lay the groundwork for transferring large circuits that enable complex functionality and decision-making in cells. </p> | In microbial communities, bacterial populations are commonly controlled using indiscriminate, broad range antibiotics. There are few ways to target specific strains effectively without disrupting the entire microbiome and local environment. The goal of our project is to take advantage of a natural horizontal gene transfer mechanism in bacteria to precisely affect gene expression in selected strains. We combine bacterial conjugation with CRISPRi, an RNAi-like repression system developed from bacteria, to regulate gene expression in targeted strains within a complex microbial community. One possible application is to selectively repress pathogenic genes in a microbiome, leaving the community makeup unaffected. In addition, we use CRISPRi to lay the groundwork for transferring large circuits that enable complex functionality and decision-making in cells. </p> | ||
| + | </div> | ||
| + | <div class="line"> | ||
| + | <br> | ||
</div> | </div> | ||
| Line 304: | Line 306: | ||
</div> | </div> | ||
| - | + | ||
<!--Sponsors--> | <!--Sponsors--> | ||
Latest revision as of 16:41, 28 October 2013
Operation CRISPR: Deploying precision guided tools to target unique species in a complex microbiome
In microbial communities, bacterial populations are commonly controlled using indiscriminate, broad range antibiotics. There are few ways to target specific strains effectively without disrupting the entire microbiome and local environment. The goal of our project is to take advantage of a natural horizontal gene transfer mechanism in bacteria to precisely affect gene expression in selected strains. We combine bacterial conjugation with CRISPRi, an RNAi-like repression system developed from bacteria, to regulate gene expression in targeted strains within a complex microbial community. One possible application is to selectively repress pathogenic genes in a microbiome, leaving the community makeup unaffected. In addition, we use CRISPRi to lay the groundwork for transferring large circuits that enable complex functionality and decision-making in cells.
TeamMeet our dedicated team of under-graduates who conceived of, planned, and carried out the whole project. |
ProjectDiscover our precision guided tools to target unique species in a complex microbiome and our groundwork for transferring large circuits that enable complex functionality and decision-making in cells. |
ModelingTake a look at how we use mathematical modeling to facilitate the design and construct of our project. |
Human PracticeExamine how we teach Synthetic Biology to the general public through night event at Exploratorium and to high school students through a collaboration with Lincoln High School. |
Special Thanks to Our 2013 iGEM Team Sponsors!
