Regulatory

Part:BBa_K123002

Designed by: Jason Gardiner   Group: iGEM08_University_of_Alberta   (2008-10-27)
Revision as of 19:49, 21 October 2021 by Lovasz1rf (Talk | contribs) (Improvement of ERE controlled TetR Expression - Alma 2021)

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LacIQ ERE TetR

This composite part contains LacIQ (BBa_I14032) and Estrogen Receptor Element (ERE) and TetR (BBa_C0040). The Estrogen Responsive element is to be used in conjunction with ER (Estrogen Receptor). This design involves ER binding to the ERE and disrupting the constitutive promoter LacIQ from producing TetR via physically getting in the way of the polymerase.

Improvement of ERE controlled TetR Expression - Alma 2021

When we thought we had succeeded in improving K123002, we sent 2 colonies for sequencing and learned that we had added a stronger promoter (Part BBa_J23100) and the human estrogen receptor element (Part BBa_K3737003). Although it showed that we were not able to include the ribosome binding site (RBS), we continued with qPCR to further compare parts K3737004 and K123002.

When comparing K123002 to K3737004 via qPCR, we used the difference between CT values of the strains with and without reverse transcriptase (RT) to calculate the amount of RNA present. We used two clones of K3737004; both clones showed lower CT values with RT than without. This proves that more DNA was made from the RNA present in clones with RT compared to the clones without RT.

Alma qPCR.jpeg

K123002 had very similar CT values. This means that converting the RNA present did not make any more DNA, and there was no transcription of TetR in the K123002 part. Because we used tet_seqR and tet_seqF primers, we know that the TetR gene was present in K3737004 and not present in K123002.

The amplification plot made from the qPCR is a visual representation of our data. We also made amplification plots to show the difference in amplification between K123002 and K3737004.

Alma qpcramplification.png Alma amplificationK3737004.png Alma amplificationK123002.png


The dissociation curve shows only one peak, proving that there is only 1 type of DNA in the qPCR samples. This proves that the tet_seqR and tet_seqF were the only primers that were able to bind any genes in the samples. This is promising because it indicates that clone 1 and clone 2 are the same sequence. Based on this data, we have successfully improved upon K123002.

File:Alma qpcrdissociation Sequence and Features


Barcodes are discontinued, but one was appended to the sequence of this part. Composite parts using this part will include the barcode. More ...

Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


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