Difference between revisions of "Part:BBa K782085"

Revision as of 23:57, 26 September 2012

10x[TALA] operator_minimal promoter_TALA:NLS:VP16_t2a_BFP

• TALA labels represents TAL effector 1257 from zebrafish experiments (Sander et al., 2011).
• DNA binding sites for individual TAL effectors are indicated with square brackets [ ].

Introduction

Our construct contains TALA binding sites that are cloned upstream of minimal promoter. Downstream of promoter are TALA:VP16 and blue fluorescent protein.

To enable monitoring level of expression of TAL activator, we linked it with a fluorescent reporter. BFP is a monomeric fluorescent protein with excitation maximum at 402 nm and emision maximum at 457 nm. TAL activator and fluorescent reporter were connected by an intermediate t2A sequence. This sequence causes the ribosome to skip formation of a peptide bond during protein translation, producing the activator and reporter as separate proteins in equimolar amounts (Garg et al., 2012, Kim et al., 2011, de Felipe et al., 2006).

Figure 1: Schematic representation of the construct.

Characterization

We extensively characterized this construct, since it represents essential part of innovative [http://2012.igem.org/Team:Slovenia/TheSwitchPositiveFeedbackLoopSwitch bistable switch based on a positive feedback loop]. Part contains self-activator, necessary for creating a positive feedback loop that improves the classical toggle switch (Gardner et al., 2000) that can only operate with cooperative DNA binding transcription factors. Addition of the autoloop in this part introduces the required nonlinearity into the system and enables the creation of bistable switches from designed DNA binding elements. This switch represents an extremely powerful tool for synthetic biology as we can use its design to prepare numerous orthogonal designed switches differing in the TAL DNA binding domains and operators, which allows creation of complex designed regulatory circuits.

Figure 2:

Left: Addition of Pristinamycine triggers dissociation of PIP:KRAB from its DNA-binding site. Consequently TALB repressor and TALA activator are transcribed. Activator causes transcription of another pair of TALB:KRAB and TALA:VP16, responsible for the positive feedback loop. Meanwhile TALB:KRAB represses the other state of the switch. Right: When the inducer is removed, the inducible repressor binds back to its DNA-binding site, but since TALA:VP16 is still present, auto-activation is achieved, resulting in a stable state.

References

Sander, J. D., Cade, L., Khayter, C., Reyon, D., Peterson, R. T., Joung, J. K., and Yeh, J.-R. J. (2011) Targeted gene disruption in somatic zebrafish cells using engineered TALENs. Nature Biotechnology 29, 697–698.

Kim, J. H., Lee, S.-R., Li, L.-H., Park, H.-J., Park, J.-H., Lee, K. Y., Kim, M.-K., et al. 2011. High cleavage efficiency of a 2A peptide derived from porcine teschovirus-1 in human cell lines, zebrafish and mice. PloS one 6,e18556.

de Felipe, P., Luke, G. a, Hughes, L. E., Gani, D., Halpin, C., Ryan, M. D. 2006. E unum pluribus: multiple proteins from a self-processing polyprotein. Trends in biotechnology 24,68–75.

Sequence and Features