Difference between revisions of "Part:BBa K2295001"

Revision as of 14:42, 31 October 2017

CRE (cAMP response element)

Overview

This part is a cAMP dependent promoter. Being one of the main downstream signaling pathways of Gs coupled GPCRs (G protein coupled receptors), this BioBrick supports the combination with a wide range of other parts. The iGEM BioBrick library already contains several Gs coupled GPCRs. Depending on the GPCR, different inputs can be used for ligand dependent gene expression.

G protein coupled receptors

Figure 1:

G protein-coupled receptors (GPCRs), also known as seven-transmembrane domain receptors or heptahelical receptors, are a large family of integral membrane proteins that respond to many different extracellular stimuli. The two principal signal transduction pathways involving GPCRs are the cAMP signal pathway as well as the phosphatidylinositol signal pathway.

Mechanism

Due to the fact that this BioBrick is mainly used for cAMP dependent transcription, only the cAMP cascade will be described, which is characteristical for Gs coupled GPCRs. Being activated by its extracellular ligand (Figure 1: H+ ions), a conformational change is induced in the receptor. This change is transmitted to an attached intracellular heterotrimeric G protein complex (Figure 1: Gs).

GPCRs that increase intracellular cAMP are Gs coupled. This also applies to the heptahelical receptor TDAG8 (BBa_K2295000) seen in Figure 1.

Freiburg 2017's Promoter characterization

The cAMP response element-containing promoter (pCRE), which is pH responsive, was characterized in vitro in Jurkat and HEK293T cell lines. For this purpose, the pH of the media had to be adjusted.

In order to characterize the CRE promoter, stably transduced HEK293T and Jurkat lines were created expressing eCFP under a minimal promoter with multiple CRE sites. Induction was performed with pH adjusted media. Constitutively expressed mCherry was used as transduction marker. For analysis in HEK293T, PEI transfection of the pH receptor TDAG8, which is not expressed in these cells, was performed. (Ausländer et al., 2014). To generate a high expression by activating the signaling cascade downstream of the receptor, the stable cell lines were induced with forskolin and IBMX. Forskolin activates the cAMP-producing enzyme adenylyl cyclase and IBMX inhibits cAMP-hydrolyzing phosphodiesterases (Bittinger et al., 2004). Fluorescence was measured by flow cytometry after 24 h of treatment (Fig. 1).

Figure 2: Flow cytometry of hypoxia response element promoter analysis. a)</b> Jurkat cells stably transduced with 4xCRE-pTal:eCFP were incubated 24 h in pH adjusted RPMI 1640. b) The experiment was repeated inducing with Forskolin (10 µM) and IBMX (10 µM). c) and d) HEK293T cells stably transduced with 4xCRE-pTal:eCFP with and without transient TDAG8 were induced similarly to a) and b). Results show the represent the amount of eCFP positive cells c) and the d) mean fluorescence intensity. All data points are mean values of triplicates, error bars represent standard deviation. Significant differences in a) and b) were determined using ANOVA, for c) and d) significant differences were determined using one-tailed student’s t-test (Excel 2017); * p < 0.05, ** p < 0.01, *** p < 0.001, non-significant differences are not marked.

Sequence and Features