Fig. 1: Synthetic logic computation and oscillation. | Nature Communications

Fig. 1: Synthetic logic computation and oscillation.

From: Customizing cellular signal processing by synthetic multi-level regulatory circuits

Fig. 1

Recent examples of synthetic logic circuits are shown in (a–e) and oscillators in (f–j). a Four-input AND gates only produce high output signals at the state [1, 1, 1, 1] where four input signals are all present. b The four-input AND gate based on the transcription factor (TF) interaction and layering34. The two-input AND gates relying on the interaction of the transcriptional activator and its cognate chaperone protein are layered into the four-input AND gate. c The four-input AND gate based on recombinase-mediated inversion of promoter and coding sequences, and excision of terminators4,43. d The four-input AND gate based on the assembly of trigger RNAs of the toehold switch12. The trigger RNA complex initiates strand displacement and exposes the RBS and start codon to activate translation. e The four-input AND gate based on the chemical-induced protein assembly84. Four chemical-induced dimerization domains bridge the TF DNA-binding domain and transcription activation (TA) domain. f Oscillators produce periodic, oscillating outputs. g The oscillator based on the CRISPR-dCas9 system32. The upstream sgRNA binds with dCas9 and represses the transcription of the downstream sgRNA. h The oscillator based on plasmid copy number control53. The activator plasmid encodes a self-activating quorum-sensing LuxI synthase and PluxI-driven reporter protein. The repressor plasmid encodes a PluxI-driven endonuclease cleaving the activator plasmid and PluxI-driven RNA mediating repressor plasmid replication. i The oscillator based on the post-translational coupling of genetic circuits85. The quorum clock (driving the yellow protein expression) and constitutively expressed green protein are coupled by sharing ClpXP proteases. j The oscillator based on protein cleavage and degradation87. The upstream protease (e.g., TEV protease) exposes the degron fused to the downstream protease (TVMV protease) and reporter proteins, leading to degradation.

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