Difference between revisions of "Part:BBa K3179100"
Line 13: | Line 13: | ||
[[File:T--SYSU-CHINA--sensor.png|500px|thumb|left]] | [[File:T--SYSU-CHINA--sensor.png|500px|thumb|left]] | ||
− | + | <br style="clear:both;"> | |
<!-- --> | <!-- --> | ||
<span class='h3bb'>Sequence and Features</span> | <span class='h3bb'>Sequence and Features</span> |
Revision as of 05:31, 21 October 2019
pTREK
This part consists of Vector pTRE, miR663b-target, 2kt-EGFP and miR885-5p-target. There is a CMV promoter on pTRE that can transcribe mRNAs containing miR663b-target, 2kt-EGFP and miR885-5p-target. The translation of this mRNA is regulated by L7Ae and the amount of intracellular free miRNA663b and miRNA885-5p. When miRNA663b, miRNA885-5p and L7Ae exist, the translation of this mRNA is suppressed. The mRNA’s translation product is EGFP, and green fluorescence can be observed to facilitate observation of gene expression results.
In our design, pTRE-miR663b-2kt-EGFP-miR885-5p is used for co-transduction with pTRE-L7Ae-miR592, and the compatibility and effectiveness of L7Ae-Kturn system and Tet-On system can be tested by measuring the expression amount of EGFP.
Usage and Biology
We placed the miRNA sensor downstream of the pTRE promoter to detect if Tet on could work compatibly with it. miRNA-592 mimics were transported to switch off the miRNA sensor, while miRNA-885-5p inhibitor were transported to switch on the miRNA sensor. Experimental result shows that the two systems are well compatible.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 195
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 201
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 857