Difference between revisions of "Part:BBa K2748001"

 
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===Usage and Biology===
 
===Usage and Biology===
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=2019 SYSU-CHINA's characterization=
 
=2019 SYSU-CHINA's characterization=
 
We added some quantitative experimental characterization data on the Tet-On System.
 
We added some quantitative experimental characterization data on the Tet-On System.
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In order to know how many DOX our system needs to work effectively, we do an experiment about the relation between the concentration of DOX and gene expression. The result shows that only 270ng/ml DOX can induce half of the gene expression, which is a really good data. This means a low dose of DOX can achieve the desired effect without considering the side effect of over-dose.
 
In order to know how many DOX our system needs to work effectively, we do an experiment about the relation between the concentration of DOX and gene expression. The result shows that only 270ng/ml DOX can induce half of the gene expression, which is a really good data. This means a low dose of DOX can achieve the desired effect without considering the side effect of over-dose.
 
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[[File:T-SYSU-CHINA-rtTA.jpeg|500px|thumb|left]]
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We also constructed two plasmids which contains the rtTA3 controlled by different promoters. One promoter is pCMV, the other one is hEF1α. The result shows that under the regulate of pCMV, the variance of expression is smaller. While, hEF1α has lower background and higher expression in a high concentration of DOX.
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[[File:T-SYSU-CHINA-pCMEhEF1a rtTA.jpg|500px|thumb|left]]
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<span class='h3bb'>Sequence and Features</span>
 
<span class='h3bb'>Sequence and Features</span>

Latest revision as of 02:10, 20 October 2019


rtTA-advanced (reverse tet-controlled transactivator)

Biology and Usage

rtTA is the transactivator in the Tet-inducible transcription system (tet-ON system) that selectively binds to tet-ON promoter in the presence of tetracycline or doxycycline and activate transcription.

Tet-ON system (Gossen et al., 1995) is a inducible transcription system widely used in mammalian cells. The tet-ON system utilizes the sequence-specific DNA binding property of tet repressor protein (tetR) from Escherichia coli in the presence of tet or dox, and consists of two parts: The Tet-inducible CMV promoter (tet-ON promoter) and reverse tetracycline-controlled transactivator (rtTA). The tet-ON promoter consists of tandem tetracycline-responsive elements (TRE) followed by a minimal CMV promoter. The rtTA protein comprises of reverse-tetR (rtetR, mutant of tetR) and activation domains from herpes simplex virus VP16. When tet or dox is added, the rtTA binds to TRE, and VP16 domain will recruit factors of RNA polymerase II to initiate transcription. In the absence of tet or dox, the rtTA detaches from tetON promoter, and thus no transcription.


Design Considerations

The nucleotide sequence was obtained from our host lab. Biobrick prefix and suffix was added by PCR using the following primers,


rtTA-prefix: 5’ cggaattcgcggccgcttctagatgtcTagGctggacaagagcaaagTC 3’

rtTA-suffix: 5’ AActgcagcggccgctactagtattacccggggagcatgtcaag 3’


and ligated onto the pSB1C3 plasmid backbone obtained from digestion of pSB1C3-lacI-RFP(Part:BBa_J04450). The sequence was comfirmed by Sanger sequencing by IGE Biotechnology LTD using VF2 as the forward primer.

Note that this part comes with an stop codon at the end of the sequence.

Characterization

For more details, please check out our [http://2018.igem.org/Team:SYSU-CHINA#/Demonstrate result page]!

In iGEM 2018, SYSU-CHINA attempted to develop a reversible safe switch for CAR T therapy based on the tet-inducible CMV promoter and U24 protein of Human Herpesvirus 6. Since it is the major part of our project, we conducted extensive research on U24 and obtained valuable results..

In order to determine the optimal concentration of dox for induction, equal amount of HEK293T cells were seeded in 6-well plates and transfected with ptetON-GFP-T2A-U24. Different concentration of dox was added to each well immediately after transfection. For comparison, pEF1a-GFP-T2A-U24 was used as a positive control. 3 fluorescence images of each well were captured and analyzed with ImageJ for fluorescence intensity 24h after introduction of dox. And equal amount of cells were harvested for western blots analysis.

In the absence of Dox, the transient transfected cells exhibited low level of fluorescence, the fluorescence intensity increased as the concentration increase and reached a plateau. In agreement with the fluorescence data, the result from western blot analysis also indicated a rapid increase on expression level at low level of dox and soon reached a plateau after the concentration exceeded 100ng/ml. Thus we reasoned that 100ng/ml is the lowest concentration needed for optimal induction. However, the basal expression level was high, since only 3-fold increase at optimal condition compared to no induction.

Figure 2: Fluorescence and western blot analysis of U24 expression under different concentration of doxycycline


In order to determine the expression time course after adding dox, equal amount of HEK293T cells were seeded in a 6-well plate and transfected with ptetON-GFP-T2A-U24. Dox was added at the same time in all wells and equal number of cells in each well were harvested at the indicated time for western blot analysis. The result was analyzed with ImageJ and the amount of protein of interest was normalized using β-actin as internal controls.

We observed an increase of HA-tagged protein level over the time of 24h and reached a plateau at around 6h, confirming a relatively fast response. However, the fold change was small that a less than 2-fold change was observed, indicating insufficient induction. Due to the time limits, we were unable to conduct additional experiments and more repeats are needed to further validate the results.


Figure 3: Time course of U24 expression


References

Gossen, M., Freundlieb, S., Bender, G., Muller, G., Hillen, W., and Bujard, H. (1995). Transcriptional activation by tetracyclines in mammalian cells. Science 268, 1766-1769.

Usage and Biology


2019 SYSU-CHINA's characterization

We added some quantitative experimental characterization data on the Tet-On System.
In order to know how many DOX our system needs to work effectively, we do an experiment about the relation between the concentration of DOX and gene expression. The result shows that only 270ng/ml DOX can induce half of the gene expression, which is a really good data. This means a low dose of DOX can achieve the desired effect without considering the side effect of over-dose.

T-SYSU-CHINA-rtTA.jpeg



We also constructed two plasmids which contains the rtTA3 controlled by different promoters. One promoter is pCMV, the other one is hEF1α. The result shows that under the regulate of pCMV, the variance of expression is smaller. While, hEF1α has lower background and higher expression in a high concentration of DOX.

T-SYSU-CHINA-pCMEhEF1a rtTA.jpg


Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 409
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal AgeI site found at 347
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal SapI.rc site found at 165