Difference between revisions of "Part:BBa K2406071"

Latest revision as of 11:31, 29 October 2017

Rox-Term-Slox Measurement Construct

Introduction

This measurement construct was used to test the cross-reactivity of Rox and Slox (BBa_K2406000, BBa_K2406003). The theory behind the function of this measurement construct is summarised in the adjacent figure. Essentially, when two recombination sites cannot be recognised by a single recombinase, the terminator (represented as parallel lines in the diagram) will not be excised and there will be no RFP reporter outlook. This part is useful because it tests the cross-reactivity of the target sites in question. In order to catalyse two independent, distinct recombination events in one cell with two recombinase systems, it is vital that there is no cross-reactivity. Thus, this measurement construct tests the suitability for using Dre/Rox and SCre/Slox in one cell.

Schematic outlining principle of all measurement constructs used by Edinburgh_UG 2017

Results

All assays performed using this measurement construct are summarised to the right. For reference, cross-reactivity and fluorescence output is compared to other measurement constructs in the context of DreBBa_K2406081 and SCre BBa_K2406084. We observed no cross-reactivity within this construct, as fluorescence output was negligible when Dre and Scre were present and not present.

All measurements performed involving Vika

All measurements performed involving SCre

Discussion

The target sites involved in this construct were previously discovered as being potentially orthogonal to other recombinases [1][2]. It is therefore important to test their cross-reactivity extensively to fully understand what recombinases can be used within one cell. This had not been done extensively before. Our results demonstrate no cross reactivity between the two target sites, BBa_K2406001, BBa_K2406003. This is because negligible RFP output was seen compared to control. Therefore, the Dre/Rox and SCre/Slox can be used in an orthogonal manner within a single cell.

References

[1] Anastassiadis, K., Fu, J., Patsch, C., Hu, S., Weidlich, S., Duerschke, K., Buchholz, F., Edenhofer, F., and Stewart A.F. 2009. “Dre recombinase, like Cre, is a highly efficient site-specific recombinase in E. coli, mammalian cells and mice.” Disease Models and Mechanisms: Sep-Oct; 2(9-10):508-515. [2]Suzuki E. and Nakayama, M. 2011. “VCre/VloxP and SCre/SloxP: new site-specific recombination systems for genome engineering.” Nucleic Acids Research 39(8):e49.

Sequences

File below confirms sequence of all target sites, generators and measurement constructs used. Media:File:Sequencing Results Edinburgh UG.zip

Sequence and Features