Team:Heidelberg/Project Highlights

From 2009.igem.org

Project Highlights

We are able to predict functional mammalian promoter sequences

We created HEARTBEAT, a model portfolio based upon genome-wide bioinformatic analysis and fuzzy logic. We used these tools to predict promoter sequences and subsequently synthesized those sequences. We found that promoters most closely matching the model predictions work, whereas others do not (Fig 1). Read more about these results on the "HEARTBEAT database" page. We also present a GUI which enables the users to design the promoter of their needs.

Fig 1: HEARTBEAT describes the spatial distribution of Transcription Factor Binding Sites along a mammalian promoter. The diagram on the top shows this distribution for SREBP. HEARTBEAT also describes Transcription Factors co-occurring with a given TF, which, for SREBP, is Sp1. We placed SREBP and Sp1 Binding sites according to the predicted distribution and found only promoters which resemble the distribution closest to be induced by SREBP (see small diagram). Other promoter sequences are not functional (not shown).

We have created a functional biochemical synthesis method for the generation of promoters libraries

We developed RA-PCR, a biochemical method for the generation of randomized promoter libraries (Fig. 2). Using this method we created a library of constitutive promoters (Fig. 3), an NF-κB responsive promoter which was subjected to extensive characterization (Fig. 4) as well as some other regulated promoters .

Fig. 2: The method of RA-PCR. Oligos and transcription factor binding sites (TFBS) and mutually annealing sequences are combined in a single PCR reaction. Randomized repeats of such TFBSs were generated at random spacing, making it likely to produce functional promoters at different strength.
Fig. 3: A library of constitutive promoters of different strength created by RA-PCR.
Fig. 4: NF-κB regulated promoter created by RA-PCR.It is activated, which is detected by the green fluorescence of the reporterprotein if NF-κB localizes to the nucleus detected by p65-mCherry fusion protein (red fluorescence within the nucleus)

We have developed novel standards for measurement of promoters in mammalian cells

Applying both qRT-PCR and flow cytometry, we developed two new relative units in analogy to bacterial RPU for use in mammalians: Relative Expression Units (Fig. 5) and Relative Mammalian Promoter Units (Fig. 6). We applied these units to the characterization of our promoters, as well as an [http://partsregistry.org/Part:BBa_I712004 existing promoter from the registry]. Read more about our Measurement subproject...

Fig. 5 :Strength of the CMV promoter in different cell lines in REU. Relative Expression Units (REU) were determined by three independent flow cytometry measurements on three different days. This measurement was confirmed by an independent technique - image analysis.
Fig. 6: Real-time RT-PCR data of CMV promoter. Twelve replicates of HeLa cells were transfected with a plasmid containing the CMV promoter coupled to GFP. Another set of twelve replicates was transfected with the JeT promoter coupled to GFP served as reference. Total amount of RNA generated by CMV was divided by the total amount of RNA generated by JeT to obtain RMPU.

4 RFCs, well characterized parts

According to the standards required by synthetic biology we submitted all the methods and units we developed as RFCs (Request for Comments). By introducing new standards for synthetic biology in mammalian cells, we hope to initiate a process that will allow the number of mammalian parts in the registry to skyrocket within the next years:

  • [http://hdl.handle.net/1721.1/49501 RCF 41]: Units for Promoter Measurement in Mammalian Cells
  • [http://hdl.handle.net/1721.1/49502 RFC 42]: RA-PCR, a method for the generation of randomized promoter libraries
  • RFC 43: Design of specific mammalian promoters by in silico prediction
  • [http://hdl.handle.net/1721.1/49503 RFC 45]: Cloning Standard for Mammalian BioBrick Parts and Devices

We also submit more than 10 well-characterized parts to the registry (see Parts Characterization). Also, we submit several other parts, for which we offer at least a rough characterization (Find our full parts list here)