Part:BBa_K4586001
Mouse notch core
Part Description
This part codes for an enhanced Mouse notch core, which is a notch-derived transmembrane regulatory protein that normally regulates cell fate decisions during a variety of developmental processes. It was first identified in beaded winged flies. The activity of the synthetic notch is determined by the sequential cleavage of its domain carried out by protease enzymes after cell interaction with another cell.
Usage
Mouse notch is implicated in our design as the transmembrane domain of our Syn notch receptor as it transmits the signal that is started by cell-to-cell contact between the external domain and the autoreactive B cells through it’s mechanosensitive quality based on proteolytic cleavage of its domains to release our intra-cellular transcription module (ZF21.16 VP64) that activates the ZF21.16 minCMV promoter controlling the expression of our cargo as shown in figure 1.
Figure 1. shows how the mouse notch core protein within the syn notch receptor is expressed as a transmembrane domain to transmit the signal initiated by interaction between the autoreactive B-cell receptor and our engineered MSC
Literature Characterization
The study used X-Gal staining of brain sections from double transgenic mice to show the effect of active Notch1 signaling in mice. The results suggest that the activation of the N1-Gal4VP16 reporter is consistent with the activity of the endogenous Notch1 receptor. This reporter mouse is a powerful tool for visualizing active Notch1 signaling in embryonic and post-natal development in vivo.
The N1-Gal4VP16 activity in BAC-transgenic reporter mice correlates well with the expected profile of active Notch1 signaling. This is evident from the X-Gal staining of brain sections from double transgenic mice, which shows strong staining in the left lateral ventricle (LV), a region of high Notch1 activity. Immunohistochemistry staining with cleaved Notch1 (Val1744) antibody confirms this finding.
Characterization By Mutational Landscape
In order to optimize the function of our parts, we've used the concept of Directed Evolution through applying different mutations and measuring the effects of these mutations on their evolutionary epistatic fitness. As displayed in the chart below, the mutation (V67E) shows the highest epistatic fitness, while the lowest score was associated with the mutation (S312R).
Figure . An illustration of the effects of different mutations on the Epistatic Fitness of Mouth notch.
References
Generation and characterization of a Notch1 signaling‐specific reporter mouse line - Smith - 2012 - genesis - Wiley Online Library
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI.rc site found at 592
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