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. 2013 Oct 18:8:24.
doi: 10.1186/1745-6150-8-24.

Interaction-based evolution: how natural selection and nonrandom mutation work together

Interaction-based evolution: how natural selection and nonrandom mutation work together

Adi Livnat. Biol Direct. .

Abstract

Background: The modern evolutionary synthesis leaves unresolved some of the most fundamental, long-standing questions in evolutionary biology: What is the role of sex in evolution? How does complex adaptation evolve? How can selection operate effectively on genetic interactions? More recently, the molecular biology and genomics revolutions have raised a host of critical new questions, through empirical findings that the modern synthesis fails to explain: for example, the discovery of de novo genes; the immense constructive role of transposable elements in evolution; genetic variance and biochemical activity that go far beyond what traditional natural selection can maintain; perplexing cases of molecular parallelism; and more.

Presentation of the hypothesis: Here I address these questions from a unified perspective, by means of a new mechanistic view of evolution that offers a novel connection between selection on the phenotype and genetic evolutionary change (while relying, like the traditional theory, on natural selection as the only source of feedback on the fit between an organism and its environment). I hypothesize that the mutation that is of relevance for the evolution of complex adaptation-while not Lamarckian, or "directed" to increase fitness-is not random, but is instead the outcome of a complex and continually evolving biological process that combines information from multiple loci into one. This allows selection on a fleeting combination of interacting alleles at different loci to have a hereditary effect according to the combination's fitness.

Testing and implications of the hypothesis: This proposed mechanism addresses the problem of how beneficial genetic interactions can evolve under selection, and also offers an intuitive explanation for the role of sex in evolution, which focuses on sex as the generator of genetic combinations. Importantly, it also implies that genetic variation that has appeared neutral through the lens of traditional theory can actually experience selection on interactions and thus has a much greater adaptive potential than previously considered. Empirical evidence for the proposed mechanism from both molecular evolution and evolution at the organismal level is discussed, and multiple predictions are offered by which it may be tested.

Reviewers: This article was reviewed by Nigel Goldenfeld (nominated by Eugene V. Koonin), Jürgen Brosius and W. Ford Doolittle.

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Figures

Figure 1
Figure 1
Mutation as a biological process. a) Mutation as a biological process means that genes interact in the determination of mutation. In the schematic figure, information from three different loci (A, B and C) comes together, through cis-acting elements and trans-acting factors, to affect the probability and nature of a genetic change in one of these loci (B). Inputs into this mutational process are shown by the annotated arrows. The downward arrow represents the writing of mutation, for example by components of the so-called “error-repair” machinery, here not restoring but changing the genetic state from what it was previously. In reality, many more pieces of information than depicted here for simplicity may be involved. b) After meiosis, the changed locus (B*) carries in it an information-signature from the combination that participated in the generation of the change, and thus allows the combination as a whole to have a lasting effect, even though its components are no longer all present.
Figure 2
Figure 2
A population-level view. If mutational writing is a biological process, then information flows over the generations from many ancestral combinations into each descendant, and from many loci into each of many single loci, forming a network of information flow across the genome over time. Mutational writing events are shown for the sake of demonstration in three individuals (two parents and an offspring, large boxes), but occur also in other genes and other individuals (to avoid clutter, only one writing event per individual is shown).
Figure 3
Figure 3
A schematic diagram showing the evolution of signals in the Poldi gene, modified from Heinen et al. [11], with permission from Elsevier. The visual presentation follows closely that of Heinen et al. [11]. Exons and introns are not drawn to scale. Observed genes are shown in blue, and a possible history, consistent with the nonfunctional-ancestor consensus view in the literature, is shown in red. Checks and crosses represent presence and absence of signals, respectively. According to a parsimony-based interpretation of the data, a possibility arises that signals have been added on the timescale of millions of years. Note that the total number of signals is monotonically increasing with decreasing phylogenetic distance to Mus musculus (as the clade including M. cypriacus, M. macedonicus, and M. spicilegus can be rotated around its base).

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