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Register a new userSelection first path to the origin of life
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Added by
Nicholas Guttenberg
Publication date
2017
fields
Biology
and research's language is
English
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We propose an alternative to the prevailing two origin of life narratives, one based on a replicator first hypothesis, and one based on a metabolism first hypothesis. Both hypotheses have known difficulties: All known evolvable molecular replicators such as RNA require complex chemical (enzymatic) machinery for the replication process. Likewise, contemporary cellular metabolisms require several enzymatically catalyzed steps, and it is difficult to identify a non-enzymatic path to their realization. We propose that there must have been precursors to both replication and metabolism that enable a form of selection to take place through action of simple chemical and physical processes. We model a concrete example of such a process, repeated sequestration of binary molecular combinations after exposure to an environment with a broad distribution of chemical components, as might be realized experimentally in in a repeated wet-dry cycle. We show that the repeated sequestration dynamics results in a selective amplification of a very small subset of molecular species present in the environment, thus providing a candidate primordial selection process.
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The Wright-Fisher process with selection is an important tool in population genetics theory. Traditional analysis of this process relies on the diffusion approximation. The diffusion approximation is usually studied in a partial differential equations framework. In this paper, I introduce a path integral formalism to study the Wright-Fisher process with selection and use that formalism to obtain a simple perturbation series to approximate the transition density. The perturbation series can be understood in terms of Feynman diagrams, which have a simple probabilistic interpretation in terms of selective events. The perturbation series proves to be an accurate approximation of the transition density for weak selection and is shown to be arbitrarily accurate for any selection coefficient.
We follow up on a companion work that considered growth rates of populations growing at different sites, with different randomly varying growth rates at each site, in the limit as migration between sites goes to 0. We extend this work here to the special case where the maximum average log growth rate is achieved at two different sites. The primary motivation is to cover the case where `sites are understood as age classes for the same individuals. The theory then calculates the effect on growth rate of introducing a rare delay in development, a diapause, into an otherwise fixed-length semelparous life history. Whereas the increase in stochastic growth rate due to rare migrations was found to grow as a power of the migration rate, we show that under quite general conditions that in the diapause model --- or in the migration model with two or more sites having equal individual stochastic growth rates --- the increase in stochastic growth rate due to diapause at rate $epsilon$ behaves like $(log epsilon^{-1})^{-1}$ as $epsilondownarrow 0$. In particular, this implies that a small random disruption to the deterministic life history will always be favored by natural selection, in the sense that it will increase the stochastic growth rate relative to the zero-delay deterministic life history.
We study a continuous-time dynamical system that models the evolving distribution of genotypes in an infinite population where genomes may have infinitely many or even a continuum of loci, mutations accumulate along lineages without back-mutation, added mutations reduce fitness, and recombination occurs on a faster time scale than mutation and selection. Some features of the model, such as existence and uniqueness of solutions and convergence to the dynamical system of an approximating sequence of discrete time models, were presented in earlier work by Evans, Steinsaltz, and Wachter for quite general selective costs. Here we study a special case where the selective cost of a genotype with a given accumulation of ancestral mutations from a wild type ancestor is a sum of costs attributable to each individual mutation plus successive interaction contributions from each $k$-tuple of mutations for $k$ up to some finite ``degree. Using ideas from complex chemical reaction networks and a novel Lyapunov function, we establish that the phenomenon of mutation-selection balance occurs for such selection costs under mild conditions. That is, we show that the dynamical system has a unique equilibrium and that it converges to this equilibrium from all initial conditions.
Understanding the patterns and processes of diversification of life in the planet is a key challenge of science. The Tree of Life represents such diversification processes through the evolutionary relationships among the different taxa, and can be extended down to intra-specific relationships. Here we examine the topological properties of a large set of interspecific and intraspecific phylogenies and show that the branching patterns follow allometric rules conserved across the different levels in the Tree of Life, all significantly departing from those expected from the standard null models. The finding of non-random universal patterns of phylogenetic differentiation suggests that similar evolutionary forces drive diversification across the broad range of scales, from macro-evolutionary to micro-evolutionary processes, shaping the diversity of life on the planet.
The probability distribution of sequences with maximum entropy that satisfies a given amino acid composition at each site and a given pairwise amino acid frequency at each site pair is a Boltzmann distribution with $exp(-psi_N)$, where the total interaction $psi_N$ is represented as the sum of one body and pairwise interactions. A protein folding theory based on the random energy model (REM) indicates that the equilibrium ensemble of natural protein sequences is a canonical ensemble characterized by $exp(-Delta G_{ND}/k_B T_s)$ or by $exp(- G_{N}/k_B T_s)$ if an amino acid composition is kept constant, meaning $psi_N = Delta G_{ND}/k_B T_s +$ constant, where $Delta G_{ND} equiv G_N - G_D$, $G_N$ and $G_D$ are the native and denatured free energies, and $T_s$ is the effective temperature of natural selection. Here, we examine interaction changes ($Delta psi_N$) due to single nucleotide nonsynonymous mutations, and have found that the variance of their $Delta psi_N$ over all sites hardly depends on the $psi_N$ of each homologous sequence, indicating that the variance of $Delta G_N (= k_B T_s Delta psi_N)$ is nearly constant irrespective of protein families. As a result, $T_s$ is estimated from the ratio of the variance of $Delta psi_N$ to that of a reference protein, which is determined by a direct comparison between $DeltaDelta psi_{ND} (simeq Delta psi_N)$ and experimental $DeltaDelta G_{ND}$. Based on the REM, glass transition temperature $T_g$ and $Delta G_{ND}$ are estimated from $T_s$ and experimental melting temperatures ($T_m$) for 14 protein domains. The estimates of $Delta G_{ND}$ agree well with their experimental values for 5 proteins, and those of $T_s$ and $T_g$ are all within a reasonable range. This method is coarse-grained but much simpler in estimating $T_s$, $T_g$ and $DeltaDelta G_{ND}$ than previous methods.
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