Sign in
Synthetic BiologybioRxiv
Preprint

Engineering the smallest transcription factor: accelerated evolution of a 63-amino acid peptide dual activator-repressor

Andreas K. BrödeliD, Rui RodriguesiD, Alfonso JaramilloiD, Mark IsalaniD

Abstract

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 {lambda} is the smallest known repressor (66 amino acids; a.a.) but activators are typically much larger (e.g. {lambda} cI, 237 a.a.). Indeed, previous efforts to engineer a minimal activator from Cro resulted in no activity in vivo. In this study, we show that directed evolution results in a new Cro activator-repressor that functions as efficiently as {lambda} cI, in vivo. To achieve this, we develop Phagemid-Assisted Continuous Evolution: PACEmid. We find that a peptide as small as 63-a.a. functions efficiently as an activator and/or repressor. To our knowledge, this is the smallest protein gene regulator reported to date, highlighting the capacity of transcription factors to evolve from very short peptide sequences.

PDFDOI

02 /Specification & Classification

Click any tag to browse matching papers

Reproducibility ledger

Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.

Sign in to file a reproducibility report.