Difference between revisions of "Team:NTU SINGAPORE/Basic Part"

Line 35: Line 35:
 
<img src="https://static.igem.org/mediawiki/2012/c/c1/EdiGEM_gold_medal.png" >
 
<img src="https://static.igem.org/mediawiki/2012/c/c1/EdiGEM_gold_medal.png" >
 
</br>
 
</br>
 +
 +
<div class="ex column full_size" >
 
<img src="https://static.igem.org/mediawiki/2017/3/30/Part1ntu.jpg" >
 
<img src="https://static.igem.org/mediawiki/2017/3/30/Part1ntu.jpg" >
 
</br>
 
</br>
Line 54: Line 56:
 
</div>
 
</div>
 
</div>
 
</div>
 +
  
 
</html>
 
</html>

Revision as of 18:35, 31 October 2017



Basic Part

Functional units of DNA.

Loading…..

Enhanced Part


∆RuvCIII-2 ∆HNH ∆REC2 Sp-dCas9 Enhanced

dCas9 is a catalytically inactive Cas9, which still retains it's ability to bind to DNA. For epigenetic regulation, the dCas9 is highly dependent upon the function of it's fusion partner.


For this part, we have deleted the HNH domain, Rec2 domain and RuvCIII-2 domain of the SP-dCas9. The triple truncation (∆REC2 ∆RuvCIII-2 ∆HNH, referred to as ‘∆3ple’) is especially of interest, since it reduces the size of the dCas9 gene to around 3.2kB which is on par with the size of Sa-Cas9. The ∆3ple truncation has slightly lower activation compared to double truncation. In order to improve the activity of ∆3ple dCas9, quick changes are further performed at various site of dCas9. Combination of quick change at Asn497Lys (QC5), Thr657Lys (QC6) and Ser1109Arg (QC15) show improved activity. It's binding capability was tested by assessing the strength in transcriptional activation via by tagging it with a VP64-p65-Rta tripartite activator.