Team:Freiburg/Highlights

From 2013.igem.org

(Difference between revisions)
Line 37: Line 37:
By fusing <b>effector domains</b> to Cas9 we altered the properties it in various ways.</p><p> The <b>activation domain VP16</b> is able to activate transcription of genes. The fusion of the <b>transcriptional repressor domain KRAB</b> leads to synthetic repressor of gene expression. Specific <b>chromatin modification</b> was achieved by fusing a histone methyl transferase G9a to dCas9. With this protein we are able to specifically repress endogenous gene expression. </p> <p> </p> <p>
By fusing <b>effector domains</b> to Cas9 we altered the properties it in various ways.</p><p> The <b>activation domain VP16</b> is able to activate transcription of genes. The fusion of the <b>transcriptional repressor domain KRAB</b> leads to synthetic repressor of gene expression. Specific <b>chromatin modification</b> was achieved by fusing a histone methyl transferase G9a to dCas9. With this protein we are able to specifically repress endogenous gene expression. </p> <p> </p> <p>
   
   
-
We were able to induce our system on light stimulus. This was possible by using photorecetors of higher plants.
+
We were able to induce our system on <b>light stimulus</b>. This was possible by using photorecetors of higher plants.
  </p> <p> </p> <p>
  </p> <p> </p> <p>
By building a plasmid containing the necessary<b> RNAs</b> and <b>insertion sites</b> for targeting we created a modular, BioBrick compatible system for <b>multiple DNA targeting: The RNAimer.</b>
By building a plasmid containing the necessary<b> RNAs</b> and <b>insertion sites</b> for targeting we created a modular, BioBrick compatible system for <b>multiple DNA targeting: The RNAimer.</b>

Revision as of 12:58, 29 September 2013