Team:Hong Kong HKUST/characterization/cmv

From 2013.igem.org

(Difference between revisions)
Line 422: Line 422:
The positive control was pEGFP-N1 (Clontech) that contains CMV promoter and EGFP reporter. The negative control was the same as the experimental construct, but minus the promoter.
The positive control was pEGFP-N1 (Clontech) that contains CMV promoter and EGFP reporter. The negative control was the same as the experimental construct, but minus the promoter.
The <a href="https://2013.igem.org/Team:Hong_Kong_HKUST/protocols">detailed protocols</a> employed for our characterization work can be accessed via the link.</p>
The <a href="https://2013.igem.org/Team:Hong_Kong_HKUST/protocols">detailed protocols</a> employed for our characterization work can be accessed via the link.</p>
-
<br>
 
-
 
-
<p>
 
-
CMV promoter was characterized by obtaining <i>in vivo</i> expression of green fluorescence protein in mammalian liver cell. To do so, we have built a CMV promoter characterization construct by fusing it with green fluorescence protein (GFP) and hGH polyadenylation sequence (hGH pA) in pSB1C3 backbone. The construct was transfected in HEK293FT cells along with GFP – pSB1C3 construct for negative control and pEGFP-N1 for positive control. We have cloned CMV promoter out from pEGFP-N1 (Addgene), which contains CMV promoter and EGFP reporter. The green fluorescence was observed under confocal microscope.
 

Revision as of 22:33, 27 September 2013

CMV Promoter

Introduction

CMV (Cytomegalovirus) promoter is a constitutive mammalian promoter.


For this promoter's characterization we assembled it with GFP reporter (BBa_K648013) and hGH polyA terminator (BBa_K404108). The Pcmv-GFP was then transfected into HEK293FT cells and in vivo green fluorescence signal was observed under confocal microscope. The positive control was pEGFP-N1 (Clontech) that contains CMV promoter and EGFP reporter. The negative control was the same as the experimental construct, but minus the promoter. The detailed protocols employed for our characterization work can be accessed via the link.

Characterization Procedure

1. Build:

- CMV characterization construct: CMV promoter – Green Fluorescence Protein (GFP) – hGH polyadenylation sequence (hGH pA) - pSB1C3 (BBa_K1119006 – BBa_K648013 – BBa_K404108 – pSB1C3)

- Negative control construct: GFP – hGH pA - pSB1C3 (BBa_K648013 – BBa_K404108 – pSB1C3)

2. Culture HEK293FT cell line (see below)

3. Transfect CMV characterization (CMV – GFP – hGH pA – pSB1C3), negative control (GFP – hGH pA – pSB1C3) and positive control (pEGFP-N1) plasmids in HEK293FT cell line. *We cloned CMV promoter out from pEGFP-N1 (Addgene) that contains CMV promoter and enhanced green fluorescence protein (EGFP). We used this plasmid as our positive control for CMV promoter characterization.

4. Observe GFP signal under confocal microscope

Cell Culture and Transfection

We cultured HEK293FT cells following ATCC’s standard procedure, except that we have used DMEM with 10% FBS and 1% penicillin/streptomycin for culture medium. For transfection, we have followed the manufacturer’s protocol of LipofectamineTM 2000 (Invitrogen). We have used serum free and antibiotics free DMEM to form DNA-lipofectamine complex.

Result



Figure 1. CMV promoter drives expression of GFP. HEK293FT cells transfected with Pcmv-GFP gave GFP signals. HEK cells transfected with the commercial pEGFP-N1 showed similar results, while the same construct without any promoter did not give any GFP signals. Scale bar = 10 microns


Conclusion

CMV Promoter has drived expression of GFP in HEK293FT cells and green signal was obtained under confocal microscope.

Reference

BD Biosciences Clontech.(2002).pEGFP-N1 Vector Information.Retrieved from http://www.staff.ncl.ac.uk/p.dean/pEGFP-N1_map.pdf