Part:BBa_K1431301
TRE-3G promoter+SV40 PolyA, an ideal controller of mammalian gene expression with Tet-On 3G protein
TRE-3G promoter(PTRE3G) is a kind of eukaryocyte cell promoters that will be switched on after combine with the compound of Tet-On 3G(BBa_K1431101) protein and doxycycline(Dox) mix.
The inducible promoter TRE3G provides for very low basal expression and high maximal expression after induction (Loew et. al., 2010). It consists of 7 repeats of a 19 bp tet operator sequence located upstream of a minimal CMV promoter. In the presence of Dox, Tet-On 3G binds specifically to PTRE3G and activates transcription of the downstream gene of interest (GOI). PTRE3G lacks binding sites for endogenous mammalian transcription factors, so it is virtually silent in the absence of induction.(Source: Clontech)
transactivator undergoes a conformational change allowing it to bind tet operator (tetO) repeats within the
TREG Promoter. The transactivator activates expression through transcription activation domain repeats.
Click here to learn more details about Tet-On and PTRE3G system.
Data
The plasmid transfected into Hela Cell shows below.
Transfect Hela Cell with different doxycycline(Dox) concentration by lipofectamine3000 and get the data after 30hours.
fluorescence microscope
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Flow Cytometry
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We could find that without Dox, TRE-3G promoter hardly be activated because the fluorescent protein do not expressed. The higher concentration of Dox,the higher number of fluorescent protein expressed. But if the concentration reached 1000 ng/ml, the expression become low, that may be toxic to Hela cell for too high concentration.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Improvement:NUDT_CHINA 2021
Our improved part:TCE (Part:BBa_K4016011) is validated to have stronger effect to initiate downstream gene expression with the same dose of doxycycline induction than this part.
Method
We used SEAP assay in vitro to validate the improvement.
SEAP reporter gene was constructed respectively downstream of TRE3G promoter and TCE promoter into two plasmids. ( BBa_K143130-SEAP and BBa_K4016011-SEAP)Meanwhile, we constructed tetR-3G into pcDNA3.1 vector to obtain pcDNA3.1-tetR-3G. TetR-3G can specifically bind to tetO and turn on the transcription of its downstream genes SEAP. The existence of SEAP and therefore the activity of the promotor can be measured by the addition of para-Nitrophenylphosphate (pNPP). The SEAP enzyme catalyzes the reaction from pNPP to para-Nitrophenol, this new product absorbs light at 405 nm and can be measured via photometry which can served as the reporter.
BBa_K143130-SEAP -containing plasmid and BBa_K4016011-SEAP-containing plasmid are simultaneously co-transfected with tetR-3G -expressing plasmid 293T cells. While cells in control group were co-transfected with tetR-3G -expressing plasmid and empty plasmid. Cells were cultured for 24h before adding 2ng/ml doxycycline. SEAP activity was detected 24/48 hours after transfection.
Result
HEK-293T cells co-transfected with BBa_K4016011-SEAP and tetR-3G expressing plasmids showed significantly increased SEAP production upon 24h or 48 h of doxycycline induction comparing to the control group, whose SEAP activity is below detection level. This proves that TCE does initiates the expression of downstream gene. Meanwhile, HEK-293T cells co-transfected with BBa_K4016011-SEAP and tetR-3G expressing plasmids shows ~30 times higher SEAP activity compared to cells transfected with the same dose of BBa_K143130-SEAP and tetR-3G plasmids, demonstrating the successful improvement of BBa_K4016011 in our project.
Figure1. (A)SEAP activity in the culture medium collect from cells 24 hours after 2ng/ml doxycycline induction. (B)SEAP activity in the culture medium collect from cells 48 hours after 2ng/ml doxycycline induction. BDL stands for below detection level.
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