6533b85afe1ef96bd12b8b83

RESEARCH PRODUCT

Accelerated evolution of a minimal 63–amino acid dual transcription factor

Rui RodriguesAlfonso JaramilloAlfonso JaramilloAlfonso JaramilloAndreas K. BrödelMark Isalan

subject

RepressorPeptide03 medical and health sciences0302 clinical medicineGene expressionQDMolecular BiologyTranscription factorResearch ArticlesPolymerase030304 developmental biologychemistry.chemical_classification0303 health sciencesMultidisciplinarybiologyActivator (genetics)SciAdv r-articlesDirected evolutionQPAmino acidCell biologychemistrybiology.proteinSynthetic Biology030217 neurology & neurosurgeryResearch Article

description

Transcription factors control gene expression in all life. This raises the question of what is the smallest protein that can support such activity. In nature, Cro from bacteriophage λ is one of the smallest known repressors (66 amino acids), and activators are typically much larger (e.g., λ cI, 237 amino acids). Previous efforts to engineer a minimal activator from λ Cro resulted in no activity in vivo in cells. In this study, we show that directed evolution results in a new Cro activator-repressor that functions as efficiently as λ cI in vivo. To achieve this, we develop phagemid-assisted continuous evolution (PACEmid). We find that a peptide as small as 63 amino acids functions efficiently as an activator and/or repressor. To our knowledge, this is the smallest protein activator that enables polymerase recruitment, highlighting the capacity of transcription factors to evolve from very short peptide sequences.

10.1126/sciadv.aba2728http://hdl.handle.net/10261/220820