Coding
TF-KRAB-1

Part:BBa_K2446037

Designed by: Yijie Pan   Group: iGEM17_Fudan   (2017-10-21)
Revision as of 19:00, 29 October 2017 by Pyj6060 (Talk | contribs)


ZF_GAl4_KRAB

This part is one of our mammalian synthetic transcription factors (SynTFs) based on Gal4 DNA binding domain [1]. Gal4-KRAB (or TF-KRAB-1 in our project) containing three core domains from N-terminal to C-terminal: GAL4 DNA binding domain, nuclear location sequence and KRAB transcription regulating domain [2].And a (G4S) linker was added between DBD and NLS for providing region flexibility [3]. GAL4DBD enable binding to specific DNA sequences, so that we can use Gal4-KRAB as a specific transcription factors to repress the expression of our mammalian synthetic promoter Sv40-UAS (BBa_K2446036).

The information of other SynTF-SynPro is showed in the table below.

SynTFs SynPros
Gal4-KRAB(TF-KRAB-1) BBa_K2446037 Sv40-UAS(Sv40-UAS) BBa_K2446036
ZF_PIP_KRAB(TF-KRAB-2) BBa_K2446045 SV40_2/4/8_PIP BBa_K2446033/BBa_K2446034/BBa_K2446035
ZF_21-16KRAB(TF-KRAB-3) BBa_K2446039 SV40_8_ZF_21-16 BBa_K2446030
ZF_42-10_KRAB(TF-KRAB-4) BBa_K2446040 SV40_8_ZF_42-10 BBa_K2446025
ZF_43-8_KRAB(TF-KRAB-5) BBa_K2446041 SV40_2/4/8_ZF_43-8 BBa_K2446026/BBa_K2446027/BBa_K2446028
ZF_54-8_KRAB(TF-KRAB-6) BBa_K2446042 SV40_8_ZF_54-8 BBa_K2446029
ZFHD1_KRAB(TF-KRAB-7) BBa_K2446043 SV40_4_ZFHD1 BBa_K2446032

Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal PstI site found at 256
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal PstI site found at 256
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal PstI site found at 256
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal PstI site found at 256
    Illegal NgoMIV site found at 41
    Illegal NgoMIV site found at 176
  • 1000
    COMPATIBLE WITH RFC[1000]


Experiments

SynTF-SynPro Pairs


Figure 1: the testing circuits of GAL4-KRAB& Sv40 UAS pair

Figure 2:The results of GAL4-KRAB&SV40 testing: (A) The red points is the cells before co-transfecting GAL4-KRAB and the blue points is the cells after co-transfecting GAL4-KRAB. It’s easy to see that the red points depart from the diagonal and higher than the blue pints. So the expression of mCherry silenced after the expression of GAL4-KRAB;(B) The red area is the fluorescence intensity of mCherry before co-transfecting GAL4-KRAB and the blue area is the intensity after co-transfecting GAL4-KRAB.(C) The statistical result of all of the SynTFs-SynPros pairs: GAL4-KRAB can silence the expression intensity of Sv40-UAS in 25 folds


To make sure the SynTF-SynPro pairs work in mammalian cells, we use the circuits above to test if the Gal4-KRAB can repress the expression of Sv40-UAS indeed. Gal4-KRAB is linked to the C terminal of EGFP by the link of P2A. And mCherry expressions is controlled by corresponding SynPro (Sv40 UAS). These circuits are both inserted in to the mammalian expression vactor pML2. We transfect pML2-Sv40-UAS into Hela cells and measure the fluorescence intensity of mCherry by flow cytometer to get the basic expression intensity of Sv40-UAS. We also co-transfect the pML2-GAL4-KRAB with pML2-Sv40-UAS into Hela cells at the same time. Then measure the fluorescence intensity of mCherry again to get the expression intensity of Sv40-UAS influenced by GAL4-KRAB. The results of the experiment is showed below. The SynTF GAL4 can silence the expression of the SynPro Sv40-UAS in 25 folds.


SynTF-SynPro Orthogonality

<p> To construct our Strip module, more than one SynTF-SynPro pairs would be applied. Thus, the interaction between the pairs would influence or ruin our construction. We did massive orthogonality experiments to avoid that. We observed all of the 5 pairs were actually orthogonal, as you could see the grids on the diagonal were always the darkest. The three DBDs commonly used in previous works were didn’t let us down. However, the expression level of these RE loaded SynPros were relative low compared to SynPro(S)-ZF serials. As the blue rectangle in the lower right corner of the orthogonality may showed the SynPro(S)-ZF has high basic expression with unpaired SynTFs, but could be silenced to the similar fold of commonly used DBDs corresponding SynPros. The SynPro(S)-ZF was likely won’t be target by other unpaired DBD, hence the purple appeared on the bottom rows.

Figure 3: the SynTF-SynPro pairs’ Orthogonality. Grids in blue rectangle showed that SynTF-SynPro pairs constructed by using SynZF as DBD with well orthogonality. Grids in pink rectangles replaced our favorite SynTF-SynPro pairs. At least 20,000 cells were analyzed for each condition in both histogram and each grid in heat map. Data are recorded by FACS at 24h after cotransfecting.

References

[1] Morsut, L. et al. Engineering Customized Cell Sensing and Response Behaviors Using Synthetic Notch Receptors. Cell 164, 780--791 (2016).

[2] Witzgall, R., O'Leary, E., Leaf, A., Onaldi, D. & Bonventre, J. V. The Krüppel-associated box-A (KRAB-A) domain of zinc finger proteins mediates transcriptional repression. Proceedings of the National Academy of Sciences 91, 4514-4518 (1994).

[3] Chen, X., Zaro, J. L. & Shen, W.-C. Fusion protein linkers: property, design and functionality. Advanced drug delivery reviews 65, 1357-1369 (2013).

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