Part:BBa_K415505

VgEcR_2A_RxR L1L2 MammoBlock Entry Vector

Figure 1. Schematic of PonS Induction of the EGSH promoter, leading to transcriptional activation.

Mammalian L1L2 Entry Vector containing VgEcR_2A_RxR construct. retinoid X receptor (RxR) and ecdysone receptors (VgEcR) form a heterodimer to control expression of the EGSH promoter; they can be activated by the addition of the PonS compound. Here they are separated by a viral 2A site that allows for bicistronic expression. (Figure 1)

                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                        

Characterization

Figure 2. Brightfield image of a HEK293FT cell line stably infected with VgEcR_2A_RxR_2A_Hygro.

Figure 2 shows a bright field microscopy image taken of a HEK293FT cell line stably infected with VgEcR_2A_RxR_2A_Hygro, a variant construct (with the same DNA sequence up to the second 2A site as our construct) with a hygromycin selection marker. The marker was added for more efficient selection of the cell line.                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                        

Figure 3. Transcriptional Upregulation of EGSH in Response to PonS addition in the presence of EgVcR and RxR.

HEK293FT cell lines actively transcribing VgEcR, RxR, and Hygromycin under the low level constitutive promoter hEF1a were transfected with EGSH_EGFP constructs via calcium phosphate transient transfection. The micrographs shown in Figure 3 show characterization data for the cell line in the absence and presence of PonS.

Results

Introduction of PonS significantly upregulates the transcription activity of the EGSH_EGFP construct. This confirms the functionality of the EgVcR and RxR proteins.

                                                                                                                         

Sequence and Features

Assembly Compatibility:

• 10
  INCOMPATIBLE WITH RFC[10]

  Illegal XbaI site found at 291
  Illegal PstI site found at 2272
  
• 12
  INCOMPATIBLE WITH RFC[12]

  Illegal NheI site found at 2091
  Illegal PstI site found at 2272
  
• 21
  INCOMPATIBLE WITH RFC[21]

  Illegal BglII site found at 1585
  Illegal BamHI site found at 486
  Illegal BamHI site found at 2962
  Illegal BamHI site found at 3115
  Illegal BamHI site found at 3229
  Illegal XhoI site found at 1578
  Illegal XhoI site found at 1659
  
• 23
  INCOMPATIBLE WITH RFC[23]

  Illegal XbaI site found at 291
  Illegal PstI site found at 2272
  
• 25
  INCOMPATIBLE WITH RFC[25]

  Illegal XbaI site found at 291
  Illegal PstI site found at 2272
  Illegal NgoMIV site found at 1707
  Illegal NgoMIV site found at 2054
  Illegal NgoMIV site found at 3527
  Illegal AgeI site found at 2815
  
• 1000
  INCOMPATIBLE WITH RFC[1000]

  Illegal BsaI.rc site found at 3000
  Illegal SapI.rc site found at 389
  Illegal SapI.rc site found at 521