Literature DB >> 24843135

Inferring fitness landscapes by regression produces biased estimates of epistasis.

Jakub Otwinowski1, Joshua B Plotkin2.   

Abstract

The genotype-fitness map plays a fundamental role in shaping the dynamics of evolution. However, it is difficult to directly measure a fitness landscape in practice, because the number of possible genotypes is astronomical. One approach is to sample as many genotypes as possible, measure their fitnesses, and fit a statistical model of the landscape that includes additive and pairwise interactive effects between loci. Here, we elucidate the pitfalls of using such regressions by studying artificial but mathematically convenient fitness landscapes. We identify two sources of bias inherent in these regression procedures, each of which tends to underestimate high fitnesses and overestimate low fitnesses. We characterize these biases for random sampling of genotypes as well as samples drawn from a population under selection in the Wright-Fisher model of evolutionary dynamics. We show that common measures of epistasis, such as the number of monotonically increasing paths between ancestral and derived genotypes, the prevalence of sign epistasis, and the number of local fitness maxima, are distorted in the inferred landscape. As a result, the inferred landscape will provide systematically biased predictions for the dynamics of adaptation. We identify the same biases in a computational RNA-folding landscape as well as regulatory sequence binding data treated with the same fitting procedure. Finally, we present a method to ameliorate these biases in some cases.

Entities:  

Keywords:  experimental evolution; molecular evolution; penalized regression

Mesh:

Year:  2014        PMID: 24843135      PMCID: PMC4050575          DOI: 10.1073/pnas.1400849111

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  64 in total

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4.  Experiments on the role of deleterious mutations as stepping stones in adaptive evolution.

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Journal:  Proc Natl Acad Sci U S A       Date:  2013-08-05       Impact factor: 11.205

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Journal:  Evolution       Date:  2013-05-22       Impact factor: 3.694

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Authors:  Daniel B Weissman; Michael M Desai; Daniel S Fisher; Marcus W Feldman
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8.  The spatial architecture of protein function and adaptation.

Authors:  Richard N McLaughlin; Frank J Poelwijk; Arjun Raman; Walraj S Gosal; Rama Ranganathan
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9.  Reciprocal sign epistasis between frequently experimentally evolved adaptive mutations causes a rugged fitness landscape.

Authors:  Daniel J Kvitek; Gavin Sherlock
Journal:  PLoS Genet       Date:  2011-04-28       Impact factor: 5.917

10.  An epistatic ratchet constrains the direction of glucocorticoid receptor evolution.

Authors:  Jamie T Bridgham; Eric A Ortlund; Joseph W Thornton
Journal:  Nature       Date:  2009-09-24       Impact factor: 49.962

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  27 in total

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Authors:  Jakub Otwinowski; David M McCandlish; Joshua B Plotkin
Journal:  Proc Natl Acad Sci U S A       Date:  2018-07-23       Impact factor: 11.205

3.  Biophysical Inference of Epistasis and the Effects of Mutations on Protein Stability and Function.

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Journal:  Mol Biol Evol       Date:  2018-10-01       Impact factor: 16.240

4.  Approaching protein design with multisite λ dynamics: Accurate and scalable mutational folding free energies in T4 lysozyme.

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6.  Detecting epistasis from an ensemble of adapting populations.

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7.  On the sparsity of fitness functions and implications for learning.

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Authors:  Craig R Miller; James T Van Leuven; Holly A Wichman; Paul Joyce
Journal:  Theor Popul Biol       Date:  2017-12-02       Impact factor: 1.570

Review 9.  The causes of evolvability and their evolution.

Authors:  Joshua L Payne; Andreas Wagner
Journal:  Nat Rev Genet       Date:  2019-01       Impact factor: 53.242

10.  Network of epistatic interactions within a yeast snoRNA.

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