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Bastian, M.

Publications and source records attributed to Bastian, M..

2 recordsLinked to original sources

Empirical validation of the nearly neutral theory at divergence and population genomic scale using 150 mammals genomes

By limiting the efficacy of selection, random drift is expected to play a major role in genome evolution. Formalizing this idea, the nearly-neutral theory predicts that the ratio of non-synonymous over synonymous polymorphism ({pi}N /{pi}S) within populations, and divergence (dN /dS) between species, should both correlate negatively with Ne. This has previously been tested in mammals and other groups. However, most studies have focused on either dN /dS or on{pi} N /{pi}S, thus not addressing the problem across evolutionary scales. In addition, many studies at the macro scale have used life-history traits (LHT) as a proxy of Ne, assuming that large-bodied organisms have lower Ne than small-bodied species. However, this assumption itself has rarely been validated against more objective measures of Ne, such as genetic diversity{pi} S = 4Ne{micro}, in part because{pi} S estimates are scarce. Here we propose an integrative test of the nearly-neutral predictions on 150 mammalian species, using 6000 orthologous genes, spanning the macro and the micro-evolutionary scale, using for the latter a measure of heterozygosity on each of the assembled diploid genomes. At the micro scale, we observe, for the first time in mammalian nuclear genomes, a relationship between{pi} N /{pi}S and{pi} S. At the macro scale, we confirm the positive correlation between dN /dS and LHT but, more importantly, establish that LHT and dN /dS are correlated with{pi} S, although weakly so. Together, these results provide the first global test of the nearly-neutral theory in mammals across time scales, suggesting all variables are correlated with a single hidden variable: Ne. Significance StatementNatural selection eliminates large-effect deleterious mutations but has limited efficacy for purging mutations of small effects. The effective population size (called Ne) is what determines the cutoff below which selection is inefficient. Since Ne varies between species, the prediction is that more mutations of intermediate effect should segregate and reach fixation in species with small populations. This has been widely studied both between species (macro-evolution) and within species (micro-evolution), although never in a fully integrated manner. Here, we analysed 144 genomes of placental mammals and 6002 orthologous genes, using the original sequence reads produced for genome assembly to estimate within-species genetic diversity based on the heterozygosity of the diploid individual whose genome has been sequenced. We show consistent relationships between genetic diversity within species, life-history traits such as body mass or longevity and selection efficacy simultaneously at the micro- and macro-evolutionary levels. Our analysis provides a globally consistent picture confirming the role of effective population size in tuning selection efficacy in placental mammals.

evolutionary biology↗

Detecting diversifying selection for a trait from within and between-species genotypes and phenotypes

To quantify selection acting on a trait, methods have been developed using either within or between-species variation. However, methods using within-species variation do not integrate the changes at the macro-evolutionary scale. Conversely, current methods using between-species variation usually discard within-species variation, thus not accounting for processes at the micro-evolutionary scale. The main goal of this study is to define a neutrality index for a quantitative trait, by combining within- and between-species variation. This neutrality index integrates nucleotide polymorphism and divergence for normalizing trait variation. As such, it does not require estimation of population size nor of time of speciation for normalization. Our index can be used to seek deviation from the null model of neutral evolution, and test for diversifying selection. Applied to brain mass and body mass at the mammalian scale, we show that brain mass is under diversifying selection. Finally, we show that our test is not sensitive to the assumption that population sizes, mutation rates and generation time are constant across the phylogeny, and automatically adjust for it.

evolutionary biology↗