ABSTRACT The first cell fate decisions in the developing fly embryo are made very rapidly: hunchback genes decide in a few minutes whether a given nucleus follows the anterior or the posterior developmental blueprint by reading out the positional information encoded in the Bicoid morphogen. This developmental system constitutes a prototypical instance of the broad spectrum of regulatory decision processes that combine speed and accuracy. Traditional arguments based on fixed-time sampling of Bicoid concentration indicate that an accurate readout is not possible within the short times observed experimentally. This raises the general issue of how speed-accuracy tradeoffs are achieved. Here, we compare fixed-time sampling strategies to decisions made on-the-fly, which are based on updating and comparing the likelihoods of being at an anterior or a posterior location. We found that these more efficient schemes can complete reliable cell fate decisions even within the very short embryological timescales. We discuss the influence of promoter architectures on the mean decision time and decision error rate and present concrete promoter architectures that allow for the fast readout of the morphogen. Lastly, we formulate explicit predictions for new experiments involving Bicoid mutants.

hunchbackPromoters Can Readout Morphogenetic Positional Information in Less Than a Minute