TY - JOUR
T1 - A simple regulatory architecture allows learning the statistical structure of a changing environment
AU - Landmann, Stefan
AU - Holmes, Caroline M.
AU - Tikhonov, Mikhail
N1 - Funding Information:
We thank M Goulian, A Murugan, and B Weiner for helpful discussions. SL was supported by the German Science Foundation under project EN 278/10–1; CMH was supported by the National Science Foundation, through the Center for the Physics of Biological Function (PHY-1734030) and the Graduate Research Fellowship Program.
Publisher Copyright:
© Landmann et al.
PY - 2021/9
Y1 - 2021/9
N2 - Bacteria live in environments that are continuously fluctuating and changing. Exploiting any predictability of such fluctuations can lead to an increased fitness. On longer timescales, bacteria can ‘learn’ the structure of these fluctuations through evolution. However, on shorter timescales, inferring the statistics of the environment and acting upon this information would need to be accomplished by physiological mechanisms. Here, we use a model of metabolism to show that a simple generalization of a common regulatory motif (end-product inhibition) is sufficient both for learning continuous-valued features of the statistical structure of the environment and for translating this information into predictive behavior; moreover, it accomplishes these tasks near-optimally. We discuss plausible genetic circuits that could instantiate the mechanism we describe, including one similar to the architecture of two-component signaling, and argue that the key ingredients required for such predictive behavior are readily accessible to bacteria.
AB - Bacteria live in environments that are continuously fluctuating and changing. Exploiting any predictability of such fluctuations can lead to an increased fitness. On longer timescales, bacteria can ‘learn’ the structure of these fluctuations through evolution. However, on shorter timescales, inferring the statistics of the environment and acting upon this information would need to be accomplished by physiological mechanisms. Here, we use a model of metabolism to show that a simple generalization of a common regulatory motif (end-product inhibition) is sufficient both for learning continuous-valued features of the statistical structure of the environment and for translating this information into predictive behavior; moreover, it accomplishes these tasks near-optimally. We discuss plausible genetic circuits that could instantiate the mechanism we describe, including one similar to the architecture of two-component signaling, and argue that the key ingredients required for such predictive behavior are readily accessible to bacteria.
UR - http://www.scopus.com/inward/record.url?scp=85115980583&partnerID=8YFLogxK
U2 - 10.7554/eLife.67455
DO - 10.7554/eLife.67455
M3 - Article
C2 - 34490844
AN - SCOPUS:85115980583
SN - 2050-084X
VL - 10
JO - eLife
JF - eLife
M1 - e67455
ER -