46 research outputs found
Evolutionary accessibility of mutational pathways
Functional effects of different mutations are known to combine to the total
effect in highly nontrivial ways. For the trait under evolutionary selection
(`fitness'), measured values over all possible combinations of a set of
mutations yield a fitness landscape that determines which mutational states can
be reached from a given initial genotype. Understanding the accessibility
properties of fitness landscapes is conceptually important in answering
questions about the predictability and repeatability of evolutionary
adaptation. Here we theoretically investigate accessibility of the globally
optimal state on a wide variety of model landscapes, including landscapes with
tunable ruggedness as well as neutral `holey' landscapes. We define a
mutational pathway to be accessible if it contains the minimal number of
mutations required to reach the target genotype, and if fitness increases in
each mutational step. Under this definition accessibility is high, in the sense
that at least one accessible pathwayexists with a substantial probability that
approaches unity as the dimensionality of the fitness landscape (set by the
number of mutational loci) becomes large. At the same time the number of
alternative accessible pathways grows without bound. We test the model
predictions against an empirical 8-locus fitness landscape obtained for the
filamentous fungus \textit{Aspergillus niger}. By analyzing subgraphs of the
full landscape containing different subsets of mutations, we are able to probe
the mutational distance scale in the empirical data. The predicted effect of
high accessibility is supported by the empirical data and very robust, which we
argue to reflect the generic topology of sequence spaces.Comment: 16 pages, 4 figures; supplementary material available on reques
Quantitative analyses of empirical fitness landscapes
The concept of a fitness landscape is a powerful metaphor that offers insight
into various aspects of evolutionary processes and guidance for the study of
evolution. Until recently, empirical evidence on the ruggedness of these
landscapes was lacking, but since it became feasible to construct all possible
genotypes containing combinations of a limited set of mutations, the number of
studies has grown to a point where a classification of landscapes becomes
possible. The aim of this review is to identify measures of epistasis that
allow a meaningful comparison of fitness landscapes and then apply them to the
empirical landscapes to discern factors that affect ruggedness. The various
measures of epistasis that have been proposed in the literature appear to be
equivalent. Our comparison shows that the ruggedness of the empirical landscape
is affected by whether the included mutations are beneficial or deleterious and
by whether intra- or intergenic epistasis is involved. Finally, the empirical
landscapes are compared to landscapes generated with the Rough Mt.\ Fuji model.
Despite the simplicity of this model, it captures the features of the
experimental landscapes remarkably well.Comment: 24 pages, 5 figures; to appear in Journal of Statistical Mechanics:
Theory and Experimen
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Reconstructing Late Holocene North Atlantic atmospheric circulation changes using functional paleoclimate networks
Obtaining reliable reconstructions of long-term atmospheric circulation changes in the North Atlantic region presents a persistent challenge to contemporary paleoclimate research, which has been addressed by a multitude of recent studies. In order to contribute a novel methodological aspect to this active field, we apply here evolving functional network analysis, a recently developed tool for studying temporal changes of the spatial co-variability structure of the Earth's climate system, to a set of Late Holocene paleoclimate proxy records covering the last two millennia. The emerging patterns obtained by our analysis are related to long-term changes in the dominant mode of atmospheric circulation in the region, the North Atlantic Oscillation (NAO). By comparing the time-dependent inter-regional linkage structures of the obtained functional paleoclimate network representations to a recent multi-centennial NAO reconstruction, we identify co-variability between southern Greenland, Svalbard, and Fennoscandia as being indicative of a positive NAO phase, while connections from Greenland and Fennoscandia to central Europe are more pronounced during negative NAO phases. By drawing upon this correspondence, we use some key parameters of the evolving network structure to obtain a qualitative reconstruction of the NAO long-term variability over the entire Common Era (last 2000 years) using a linear regression model trained upon the existing shorter reconstruction
Records and sequences of records from random variables with a linear trend
We consider records and sequences of records drawn from discrete time series
of the form , where the are independent and identically
distributed random variables and is a constant drift. For very small and
very large drift velocities, we investigate the asymptotic behavior of the
probability of a record occurring in the th step and the
probability that all entries are records, i.e. that . Our work is motivated by the analysis of temperature time series in
climatology, and by the study of mutational pathways in evolutionary biology.Comment: 21 pages, 7 figure
Harmonization of Neuroticism and Extraversion phenotypes across inventories and cohorts in the Genetics of Personality Consortium : an application of Item Response Theory
Peer reviewe
Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality Consortium
Extraversion is a relatively stable and heritable personality trait associated with numerous psychosocial, lifestyle and health outcomes. Despite its substantial heritability, no genetic variants have been detected in previous genome-wide association (GWA) studies, which may be due to relatively small sample sizes of those studies. Here, we report on a large meta-analysis of GWA studies for extraversion in 63,030 subjects in 29 cohorts. Extraversion item data from multiple personality inventories were harmonized across inventories and cohorts. No genome-wide significant associations were found at the single nucleotide polymorphism (SNP) level but there was one significant hit at the gene level for a long non-coding RNA site (LOC101928162). Genome-wide complex trait analysis in two large cohorts showed that the additive variance explained by common SNPs was not significantly different from zero, but polygenic risk scores, weighted using linkage information, significantly predicted extraversion scores in an independent cohort. These results show that extraversion is a highly polygenic personality trait, with an architecture possibly different from other complex human traits, including other personality traits. Future studies are required to further determine which genetic variants, by what modes of gene action, constitute the heritable nature of extraversion
Meta-analysis of genome-wide association studies for extraversion:Findings from the Genetics of Personality Consortium
Extraversion is a relatively stable and heritable personality trait associated with numerous psychosocial, lifestyle and health outcomes. Despite its substantial heritability, no genetic variants have been detected in previous genome-wide association (GWA) studies, which may be due to relatively small sample sizes of those studies. Here, we report on a large meta-analysis of GWA studies for extraversion in 63,030 subjects in 29 cohorts. Extraversion item data from multiple personality inventories were harmonized across inventories and cohorts. No genome-wide significant associations were found at the single nucleotide polymorphism (SNP) level but there was one significant hit at the gene level for a long non-coding RNA site (LOC101928162). Genome-wide complex trait analysis in two large cohorts showed that the additive variance explained by common SNPs was not significantly different from zero, but polygenic risk scores, weighted using linkage information, significantly predicted extraversion scores in an independent cohort. These results show that extraversion is a highly polygenic personality trait, with an architecture possibly different from other complex human traits, including other personality traits. Future studies are required to further determine which genetic variants, by what modes of gene action, constitute the heritable nature of extraversion
Skewed X-inactivation is common in the general female population
X-inactivation is a well-established dosage compensation mechanism ensuring that X-chromosomal genes are expressed at comparable levels in males and females. Skewed X-inactivation is often explained by negative selection of one of the alleles. We demonstrate that imbalanced expression of the paternal and maternal X-chromosomes is common in the general population and that the random nature of the X-inactivation mechanism can be sufficient to explain the imbalance. To this end, we analyzed blood-derived RNA and whole-genome sequencing data from 79 female children and their parents from the Genome of the Netherlands project. We calculated the median ratio of the paternal over total counts at all X-chromosomal heterozygous single-nucleotide variants with coverage ≥10. We identified two individuals where the same X-chromosome was inactivated in all cells. Imbalanced expression of the two X-chromosomes (ratios ≤0.35 or ≥0.65) was observed in nearly 50% of the population. The empirically observed skewing is explained by a theoretical model where X-inactivation takes place in an embryonic stage in which eight cells give rise to the hematopoietic compartment. Genes escaping X-inactivation are expressed from both alleles and therefore demonstrate less skewing than inactivated genes. Using this characteristic, we identified three novel escapee genes (SSR4, REPS2, and SEPT6), but did not find support for many previously reported escapee genes in blood. Our collective data suggest that skewed X-inactivation is common in the general population. This may contribute to manifestation of symptoms in carriers of recessive X-linked disorders. We recommend that X-inactivation results should not be used lightly in the interpretation of X-linked variants