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Frank J. Poelwijk

Publications and source records attributed to Frank J. Poelwijk.

3 recordsLinked to original sources

The relation between alignment covariance and background-averaged epistasis

Epistasis, or the context-dependence of the effects of mutations, limits our ability to predict the functional impact of combinations of mutations, and ultimately our ability to predict evolutionary trajectories. Information about the context-dependence of mutations can essentially be obtained in two ways: First, by experimental measurement the functional effects of combinations of mutations and calculating the epistatic contributions directly, and second, by statistical analysis of the frequencies and co-occurrences of protein residues in a multiple sequence alignment of protein homologs. In this manuscript, we derive the mathematical relationship between epistasis calculated on the basis of functional measurements, and the covariance calculated from a multiple sequence alignment. There is no one-to-one mapping between covariance and epistatic terms: covariance implies epistasis, but epistasis does not necessarily lead to covariance, indicating that covariance in itself is not the directly relevant quantity for functional prediction. Having calculated epistatic contributions from the alignment, we can directly obtain a functional prediction from the alignment statistics by applying a Walsh-Hadamard transform, fully analogous to the transformation that reconstructs functional data from measured epistatic contributions. This embedding into the Hadamard framework is directly relevant for solidifying our theoretical understanding of statistical methods that predict function and three-dimensional structure from natural alignments.

q-bio.QM↗

Quantification of the effect of mutations using a global probability model of natural sequence variation

Modern biomedicine is challenged to predict the effects of genetic variation. Systematic functional assays of point mutants of proteins have provided valuable empirical information, but vast regions of sequence space remain unexplored. Fortunately, the mutation-selection process of natural evolution has recorded rich information in the diversity of natural protein sequences. Here, building on probabilistic models for correlated amino-acid substitutions that have been successfully applied to determine the three-dimensional structures of proteins, we present a statistical approach for quantifying the contribution of residues and their interactions to protein function, using a statistical energy, the evolutionary Hamiltonian. We find that these probability models predict the experimental effects of mutations with reasonable accuracy for a number of proteins, especially where the selective pressure is similar to the evolutionary pressure on the protein, such as antibiotics.

q-bio.BM↗

The context-dependence of mutations: a linkage of formalisms

Defining the extent of epistasis - the non-independence of the effects of mutations - is essential for understanding the relationship of genotype, phenotype, and fitness in biological systems. The applications cover many areas of biological research, including biochemistry, genomics, protein and systems engineering, medicine, and evolutionary biology. However, the quantitative definitions of epistasis vary among fields, and its analysis beyond just pairwise effects remains obscure in general. Here, we show that different definitions of epistasis are versions of a single mathematical formalism - the weighted Walsh-Hadamard transform. We discuss that one of the definitions, the backgound-averaged epistasis, is the most informative when the goal is to uncover the general epistatic structure of a biological system, a description that can be rather different from the local epistatic structure of specific model systems. Key issues are the choice of effective ensembles for averaging and to practically contend with the vast combinatorial complexity of mutations. In this regard, we discuss possible approaches for optimally learning the epistatic structure of biological systems.

q-bio.QM↗