Predicting mutational routes to new adaptive phenotypes

Author:

Lind Peter A12ORCID,Libby Eric134,Herzog Jenny1,Rainey Paul B156ORCID

Affiliation:

1. New Zealand Institute for Advanced Study, Massey University at Albany, Auckland, New Zealand

2. Department of Molecular Biology, Umeå University, Umeå, Sweden

3. Santa Fe Institute, New Mexico, United States

4. Department of Mathematics, Umeå University, Umeå, Sweden

5. Department of Microbial Population Biology, Max Planck Institute for Evolutionary Biology, Plön, Germany

6. Ecole Supérieure de Physique et de Chimie Industrielles de la Ville de Paris, ESPCI Paris-Tech, CNRS UMR 8231, PSL Research University, Paris, France

Abstract

Predicting evolutionary change poses numerous challenges. Here we take advantage of the model bacterium Pseudomonas fluorescens in which the genotype-to-phenotype map determining evolution of the adaptive ‘wrinkly spreader’ (WS) type is known. We present mathematical descriptions of three necessary regulatory pathways and use these to predict both the rate at which each mutational route is used and the expected mutational targets. To test predictions, mutation rates and targets were determined for each pathway. Unanticipated mutational hotspots caused experimental observations to depart from predictions but additional data led to refined models. A mismatch was observed between the spectra of WS-causing mutations obtained with and without selection due to low fitness of previously undetected WS-causing mutations. Our findings contribute toward the development of mechanistic models for forecasting evolution, highlight current limitations, and draw attention to challenges in predicting locus-specific mutational biases and fitness effects.

Funder

Royal Society of New Zealand

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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