reciprocal sign epistasis between frequently experimentally evolved adaptive mutations causes a rugged fitness landscape相互之间签署上位经常实验进化适应性突变引起的健身景观.pdfVIP
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reciprocal sign epistasis between frequently experimentally evolved adaptive mutations causes a rugged fitness landscape相互之间签署上位经常实验进化适应性突变引起的健身景观
Reciprocal Sign Epistasis between Frequently
Experimentally Evolved Adaptive Mutations Causes a
Rugged Fitness Landscape
Daniel J. Kvitek, Gavin Sherlock*
Department of Genetics, Stanford University, Stanford, California, United States of America
Abstract
The fitness landscape captures the relationship between genotype and evolutionary fitness and is a pervasive metaphor
used to describe the possible evolutionary trajectories of adaptation. However, little is known about the actual shape of
fitness landscapes, including whether valleys of low fitness create local fitness optima, acting as barriers to adaptive change.
Here we provide evidence of a rugged molecular fitness landscape arising during an evolution experiment in an asexual
population of Saccharomyces cerevisiae. We identify the mutations that arose during the evolution using whole-genome
sequencing and use competitive fitness assays to describe the mutations individually responsible for adaptation. In
addition, we find that a fitness valley between two adaptive mutations in the genes MTH1 and HXT6/HXT7 is caused by
reciprocal sign epistasis, where the fitness cost of the double mutant prohibits the two mutations from being selected in the
same genetic background. The constraint enforced by reciprocal sign epistasis causes the mutations to remain mutually
exclusive during the experiment, even though adaptive mutations in these two genes occur several times in independent
lineages during the experiment. Our results show that epistasis plays a key role during adaptation and that inter-genic
interactions can act as barriers between adaptive solutions. These results also provide a new interpretation on the classic
Dobzhansky-Muller model of reproductive isolation and display some surprising parallels with mutations in genes often
associated with tumors.
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