Composite
hTERT+tRNA

Part:BBa_K1722010

Designed by: Hao Wang   Group: iGEM15_SZU_China   (2015-09-02)
Revision as of 06:18, 5 September 2015 by How (Talk | contribs)

hTERT+tRNA Composite

Targeted therapy has become the fastest growing subject in research on cancer treatment. Telomerase, which serves as the tumor marker, is activated in most malignancy while it's negatively expressed in normal cells. Because of the high expression of human telomerase reverse transcriptase(hTERT) gene in telomerase positive cancer cells, researchers construct plasmids with hTERT promoter and effector gene to target at cancer cells and kill them.[1] It has been proved that hTERT can regulate the activation and expression of telomerase in transcription level. Research shows that hTERT promoter is rich in GC but lack of TATA box or CAAT box. It's also methylated and deacetylated in different level.

We construct hTERT promoter and tRNA in the same plasmid to produce tRNA. In the unnatural amino acid orthogonal system that we are constructing, hUPll promoter and hTERT promoter can recognise bladder specific RNA polymerase and tumor specific RNA polymerase, respectively. Only when the two promoters are activated simultanuously can both AckRS and tRNA be produced. In this way, Ack can be attached to tRNA that perfectly pair with the mRNA chain to express the protein.


We then performed single digest(EcoRI) and double digest(EcoRI & PstI) to identify our pSB1C3-hTERT-tRNA plasmid.(Fig. 2) From the eletrophoretogram, we have two electrophoresis strips at about 562bp and 2070bp, which are exactly the length of hTERT+tRNA and pSB1C3, respectively in Track 2 and a strip at about 2632bp in Track 3. From this enzyme cutting result, we could make sure the Gene sequence of hTERT+tRNA succeeded in being constructed into pSB1C3 vector.

Figure 3. Identification of recombinant plasmids pSB1C3-hTERT-tRNA by one and two restriction enzymes.
[1:DL2000 DNA Marker 2:pSB1C3-hTERT-tRNA double digest(EcoRI and PstI) 3:pSB1C3-hTERT-tRNA single digest(EcoRI)]
Sequence and Features


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]

Design Notes

Both hTERT promoter and tRNA are achieved from Shenzhen Second People's Hospital. We designed primers and amplified the gene sequences from psi-Check2 vector. Using 3A Assembly method, we constructed hTERT and tRNA in pSB1C3.

Source

Both hTERT promoter and tRNA are achieved from Shenzhen Second People's Hospital.

References

[1] Liu Y. Research Progress in Targeting Human Telomerase Reverse Transcriptase (hTERT) Promoter in Cancer Gene Therapy, Journal of Oncology, 15(3): 150-152


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