Introduction
Species differ from each other in many ways, including mating system, ploidy, spatial distribution, life history, size, lifespan, genome size, mutation rate, selective pressure, and population size. These differences make the process of purifying selection more efficient in some species than others. Our understanding of both the causes and consequences of these differences is limited in part by a reliable metric with which to measure them. In the long term, the probability that a gene is fixed for one allele rather than another allele is given by the ratio of fixation and counter-fixation probabilities (Bulmer, 1991). In an idealized population of constant population size and no selection at linked sites, a mutation–selection–drift model describes how this ratio of fixation probabilities depends on the census population size
Figure 1.
The effectiveness of selection, calculated as the long-term ratio of time spent in fixed deleterious: fixed beneficial allele states given symmetric mutation rates, is a function of the product .
Assuming a diploid Wright–Fisher population with
This reasoning has been extended to real populations by positing that species have an ‘effective’ population size,
The amount of neutral polymorphism is the usual property used to empirically estimate
As a practical matter,
An alternative approach to measure the efficiency of selection exploits codon usage bias, which is influenced by weak selection for factors such as translational speed and accuracy (Hershberg and Petrov, 2008; Plotkin and Kudla, 2011; Hunt et al., 2014). The degree of bias in synonymous codon usage that is driven by selective preference offers a more direct way to assess how effective selection is at the molecular level in a given species (Li, 1987; Bulmer, 1991; Akashi, 1996; Subramanian, 2008). Conveniently, it can be estimated from only a single genome, that is, without polymorphism or mutation rate data for that species.
One commonly used metric, the Codon Adaptation Index (CAI) (Sharp and Li, 1987; Sharp et al., 2010) takes the average of Relative Synonymous Codon Usage (RSCU) scores, which quantify how often a codon is used, relative to the codon that is most frequently used to encode that amino acid in that species. While this works well for comparing genes within the same species, it unfortunately means that the species-wide strength of codon bias appears in the normalizing denominator (see Equation 4 and Figure 3—figure supplement 1A). Paradoxically, this can make more exquisitely adapted species have lower rather than higher species-averaged CAI scores (Figure 3—figure supplement 1B; Rocha, 2004; Botzman and Margalit, 2011).
To compare species using CAI, it has been suggested that instead of taking a genome-wide average, one should consider a set of highly expressed reference genes (Sharp et al., 2005; Vicario et al., 2007; Subramanian, 2008; dos Reis and Wernisch, 2009). This approach assumes that the relative strength of selection on those reference genes (often a function of gene expression) remains approximately constant across the set of species considered (red distributions in Figure 2). Its use also requires careful attention to the length of reference genes (Urrutia and Hurst, 2001; Doherty and McInerney, 2013), and some approaches also require information about tRNA gene copy numbers and abundances (dos Reis and Wernisch, 2009).
Figure 2.
More highly adapted species (bottom) have a higher proportion of their sites subject to effective selection on codon bias (blue area).
The Codon Adaptation Index (CAI) attempts to compare the intensity of selection (Figure 1,
Since codon bias varies quantitatively within only a small range of (Figure 1), a promising approach is to measure the proportion of sites at which codon adaptation is effective. We posit that more highly adapted species have a higher proportion of both genes and sites subject to effective selection on codon bias (Figure 2; Galtier et al., 2018). Indeed, CAI might also rely in part on variation in the fraction of sites within the reference genes that is subject to effective selection as a function of species (Figure 2, red). Here we take this logic further, considering all sites in a proteome-wide approach. Averaging across the entire proteome provides robustness to shifts in the expression level of or strength of selection on particular genes. The proteome-wide average depends on the fraction of sites whose selection coefficients exceed the ‘drift barrier’ for that particular species (Figure 2, blue threshold).
In estimating the effects of selection, it is critical to control for other causes of codon bias. In particular, species differ in their mutational bias with respect to the proportion of the genome that consists of guanine-cytosine base pairs (GC), and in the frequency of GC-biased gene conversion (Urrutia and Hurst, 2001; Duret and Galtier, 2009; Doherty and McInerney, 2013; Figuet et al., 2014). Here, we control for %GC, capturing species differences both in mutation and in gene conversion, by calculating the Kullback–Leibler divergence of the observed codon frequencies away from the codon frequencies that we would expect to see given the genomic %GC content of the species. Kullback–Leibler divergence measures the distance of an observed probability distribution from an expected reference distribution, capturing a measure of surprise (Kullback and Leibler, 1951). This method does not require us to specify preferred vs. non-preferred codons, and can thus also accommodate situations in which different genes have different codon preferences (Gingold et al., 2014; Cope et al., 2018).
An alternative metric, the Effective Number of Codons (ENC) originally quantified how far the codon usage of a sequence departs from equal usage of synonymous codons (Wright, 1990), with lower ENC values indicating greater departure. This approach creates a complex relationship with GC content (Fuglsang, 2008), and so ENC was later modified to correct for GC content (Novembre, 2002). However, a remaining issue with this modified ENC is that differences among species in amino acid composition might act as a confounding factor, even after controlling for GC content. Specifically, species that make more use of an amino acid for which there is stronger selection among codons (which is sometimes the case Vicario et al., 2007) would have higher codon bias, even if each amino acid considered on its own had identical codon bias irrespective of which species it is in. Confounding with amino acid frequencies has been shown to be a problem at the individual protein level (Cope et al., 2018). Neither ENC (Fuglsang, 2004; Fuglsang, 2008) nor the CAI (Sharp and Li, 1987) adequately control for differences in amino acid composition when applied across species. Despite early claims to the contrary (Wright, 1990), this problem is not easy to fix for ENC (Fuglsang, 2004; Fuglsang, 2008).
Here, we extend the CAI, using the information-theory-based Kullback–Leibler divergence, so that it corrects for both GC and amino acid composition (see Methods) to create a new Codon Adaptation Index of Species (CAIS). The availability of a complete genome allows both metrics to be readily calculated without data on polymorphism or mutation rate, without selecting reference genes, and without concerns about demographic history. Our purpose is to find an accessible metric that can quantify the limits to weak selection important to nearly neutral theory; this differs from past evaluations focused on comparing different genes of the same species and recapitulating ‘ground truth’ simulations thereof (Sun et al., 2013; Zhang et al., 2012; Liu et al., 2018). To demonstrate the usefulness of our method, we identify a novel correlation with intrinsic structural disorder (ISD), pointing to what else might be subject to weak selective preferences at the molecular level. While ENC can also identify subtle selection on ISD, CAIS can do so without the risk of confounding with amino acid frequencies.
Results
Both ENC and CAIS solve the GC confounding problem that plagues CAI
CAI is seriously confounded with GC content (Figure 3A). ENC is not confounded with GC content (Figure 3B), while CAIS has only a very weak correlation that is not significant after correction for multiple comparisons (Figure 3C).
Figure 3.
Codon Adaptation Index (CAI) is seriously confounded with GC content (A), while Effective Number of Codons (ENC) and Codon Adaptation Index of Species (CAIS) are not (B and C).
We control for phylogenetic confounding via Phylogenetic Independent Contrasts (PIC) (Felsenstein, 1985); this yields an unbiased
Figure 3—figure supplement 1.
Codon Adaptation Index (CAI) is not appropriate for species-wide effectiveness of selection measurements.
Each CAI value shown is averaged over an entire species’ proteome. (A) The value of CAI is driven by its normalizing denominator term, CAImax. (B) As a result, CAI is inversely proportional to Codon Adaptation Index of Species (CAIS). Each datapoint is one of 118 vertebrate species with ‘Complete’ intergenic genomic sequence available (allowing for %GC correction) and TimeTree divergence dates (allowing for Phylogenetic Independent Contrasts [PIC] correction). p-values shown are for Pearson’s correlation.
Figure 3—figure supplement 2.
The same relationships are shown as in Figure 3, but without correction for phylogenetic confounding, suggesting GC confounding for the Effective Number of Codons (ENC) but not the Codon Adaptation Index of Species (CAIS).
Codon Adaptation Index (CAI) (A) and ENC (B) both correlate with genomic GC, but CAIS (C) does not. Red line shows lm(
Figure 3—figure supplement 3.
Vertebrate Codon Adaptation Index of Species (CAIS) values are not greatly affected by computation for a standardized amino acid composition vs. computation for the amino acid frequencies in the species in question.
Proteins in better adapted species evolve more structural disorder
As an example of how correlations with codon adaptation metrics can be used to identify weak selective preferences, we investigate protein ISD. Disordered proteins are more likely to be harmful when overexpressed (Vavouri et al., 2009), and ISD is more abundant in eukaryotic than prokaryotic proteins (Schad et al., 2011; Xue et al., 2012; Basile et al., 2019), suggesting that low ISD might be favored by more effective selection.
However, compositional differences among proteomes might not be driven by differences in how a given protein sequence evolves as a function of the effectiveness of selection. Instead, they might be driven by the recent birth of ISD-rich proteins in animals (James et al., 2021), and/or by differences among sequences in their subsequent tendency to proliferate into many different genes (James et al., 2023). To focus only on the effects of descent with modification, we use a linear mixed model, with each species having a fixed effect on ISD, while controlling for Pfam domain identity as a random effect. We note that once GC is controlled for, codon adaptation can be assessed similarly in intrinsically disordered vs. ordered proteins (Gossmann et al., 2012). Controlling for Pfam identity is supported, with standard deviation in ISD of 0.178 among Pfams compared to residual standard deviation of 0.058, and a p-value on the significance of the Pfam random effect term of 3 × 10−13. Controlling in this way for Pfam identity, we then ask whether the fixed species effects on ISD are correlated with CAIS and with ENC.
Surprisingly, more exquisitely adapted species have more disordered protein domains (Figure 4). Results using ENC and CAIS are similar, with ENC having higher power; the correlation coefficient is 0.36 for CAIS compared to 0.50 for ENC, and the p-value for ENC is 3 orders of magnitude lower. We note, however, that amino acid frequencies strongly influence ISD (Theillet et al., 2013). The CAIS correlation is more reliable than the ENC correlation because by construction, CAIS controls for differences in amino acid frequencies among species.
Figure 4.
Protein domains have higher intrinsic structural disorder (ISD) when found in more exquisitely adapted species, according to (A) the Codon Adaptation Index of Species (CAIS) and (B) the Effective Number of Codons (ENC).
We plot -ENC rather than ENC to more easily compare results with those from CAIS. (C) Correcting for local rather than genome-wide %GC removes the relationship. Each datapoint is one of 118 vertebrate species with ‘complete’ intergenic genomic sequence available (allowing for %GC correction), and TimeTree divergence dates (allowing for Phylogenetic Independent Contrasts [PIC] correction). ‘Effects’ on ISD shown on the
Figure 4—figure supplement 1.
The same relationships are shown as in Figure 4, here without correction for phylogenetic confounding.
As in Figure 4, intrinsic structural disorder (ISD) of protein domains is higher in more highly adapted species, as measured by Codon Adaptation Index of Species (CAIS) (A) and Effective Number of Codons (ENC) (B), but not by CAIS calculated with local GC% rather than genome-wide GC% (C). ISD is calculated as in Figure 4. Red line shows lm(
Different parts of the genome have different GC contents (Bernardi, 2000; Eyre-Walker and Hurst, 2001; Lander et al., 2001), primarily because the extent to which GC-biased gene conversion increases GC content depends on the local rate of recombination (Galtier et al., 2001; Meunier and Duret, 2004; Duret et al., 2006; Duret and Galtier, 2009). We therefore also calculated a version of CAIS whose codon frequency expectations are based on local intergenic GC content. This performed worse (Figure 4C) than our simple use of genome-wide GC content (Figure 4A) with respect to the strength of correlation between CAIS and ISD. If GC-biased gene conversion is a more powerful force than weak selective preferences among codons, then local GC content will evolve more rapidly than codon usage (Kondrashov et al., 2010). In this case, genome-wide GC may serve as an appropriately time-averaged proxy. It is also possible that the local non-coding sequences we used were too short (at 3000 bp or more), creating excessive noise that obscured the signal.
Many vertebrates have higher recombination rates and hence GC-biased gene conversion near genes; in this case genome-wide GC content would misestimate the codon usage expected from the combination of mutation bias and GC-biased gene conversion in the vicinity of genes. If GC-biased gene conversion drove CAIS, we expect high to predict high CAIS. We do not see this relationship (Figure 5), suggesting that gene conversion strength is not a confounding factor impacting CAIS.
Figure 5.
Codon Adaptation Index of Species (CAIS) is not correlated with the degree to which local genomic regions differ in their GC content from global GC content.
If CAIS were driven by GC-biased gene conversion, genomes with more heterogeneous %GC distributions should have higher CAIS scores.
Younger animal-specific protein domains have higher ISD (James et al., 2021). It is possible that selection in favor of high ISD is strongest in young domains, which might use more primitive methods to avoid aggregation (Foy et al., 2019; Bertram and Masel, 2020). To test this, we analyze two subsets of our data: those that emerged prior to the last eukaryotic common ancestor (LECA), here referred to as ‘old’ protein domains, and ‘young’ protein domains that emerged after the divergence of animals and fungi from plants. Young and old domains show equally strong trends of increasing disorder with species’ adaptedness (Figure 6).
Figure 6.
More exquisitely adapted species have higher intrinsic structural disorder (ISD) in both young (A and B) and old (C and D) protein domains, according to both the Codon Adaptation Index of Species (CAIS) (A, C), and the Effective Number of Codons (ENC) (B, D).
Age assignments are taken from James et al., 2021, with vertebrate protein domains that emerged prior to last eukaryotic common ancestor (LECA) classified as ‘old’, and vertebrate protein domains that emerged after the divergence of animals and fungi from plants as ‘young’. ‘Effects’ on ISD shown on the
Figure 6—figure supplement 1.
Without correction for phylogenetic confounding, more highly adapted species have higher intrinsic structural disorder (ISD) in both young (A and B) and old (C and D) protein domains, according to both the Codon Adaptation Index of Species (CAIS) (A, C), and the Effective Number of Codons (ENC) (B, D).
Age assignments and ISD effects are calculated as in Figure 6. Same
Discussion
When different properties are each causally affected by a species’ exquisiteness of adaptation, this will create a correlation between the properties. We use codon adaptation as a reference property, such that correlations with codon adaptation indicate selection. To detect ISD as a novel property under selection, we used a linear mixed model approach that controls for Pfam identity as a random effect. This approach shows that the same Pfam domain tends to be more disordered when found in a well-adapted species (i.e. a species with a higher CAIS or ENC). This is true for both ancient and recently emerged protein domains.
It is important that no additional variable such as GC content or amino acid frequencies creates a spurious correlation by affecting both CAIS and our property of interest. For this reason, we define CAIS as the observed Kullback–Leibler divergence (Kullback and Leibler, 1951) from the codon usage expected given the GC content. The GC content pertinent to this expectation depends primarily on mutation bias and GC-biased gene conversion (Romiguier and Roux, 2017), but potentially also on selection on individual nucleotide substitutions that is hypothesized to favor higher %GC (Long et al., 2018). By controlling for %GC, we exclude all these forces from influencing CAIS or ENC. We thus capture the extent of adaptation in codon bias, including translational speed, accuracy, and any intrinsic preference for GC over AT that is specific to coding regions. These remaining codon-adaptive factors do not create a statistically convincing correlation between CAIS and GC (Figure 3C), nor between ENC and GC (Figure 3B), although CAI is strongly correlated with GC (Figure 3A). Notably, our new CAIS metric of codon adaptation controls for amino acid frequencies, rather than, like ENC, only GC content.
A direct effect of ISD on fitness agrees with studies of random Open Reading Frames (ORFs) in
A more complex metric could control for more than just GC content and amino acid frequencies. First vs. second vs. third codon positions have different nucleotide usage on average, but while correcting for this might be useful for comparing genes (Zhang et al., 2012), correcting for it while comparing species might remove the effect of interest. Similarly, while it might be useful to control for dinucleotide and trinucleotide frequencies (Brbić et al., 2015), to avoid circularity these would need to be taken from intergenic sequences, with care needed to avoid influence from unannotated protein-coding genes or even pseudogenes.
Note that if a species were to experience a sudden reduction in census population size, for example due to habitat loss, leading to less effective selection, it would take some multiple of the neutral coalescent time for CAIS to fully adjust. CAIS thus represents a relatively long-term historical pattern of adaptation. The timescales setting neutral polymorphism-based estimates are likely shorter, based on a single round of coalescence. It is possible that the reason that we obtained correlations when we controlled for genome-wide GC content, but not when we controlled for local GC content, is also that codon adaptation adjusts slowly relative to the timescale of fluctuations in local GC content.
Here, we developed a new metric of species adaptedness at the codon level, capable of quantifying degrees of codon adaptation even among vertebrates. We chose vertebrates partly due to the abundance of suitable data, and partly as a stringent test case, given past studies finding limited evidence for codon adaptation (Kessler and Dean, 2014). It remains to be seen how CAIS behaves among species with stronger codon adaptation. We restricted our analysis to only the best annotated genomes, in part to ensure the quality of intergenic %GC estimates, and in part limited by the feasibility of running linear mixed models with 6 million datapoints. The phylogenetic tree is well resolved for vertebrate species, with an overrepresentation of mammalian species. Despite the focus on vertebrates, we were able to discover new results regarding selection on ISD.
Our finding that more effective selection prefers higher ISD was unexpected, given that lower-
Codon adaptation metrics more directly quantify how species vary in their exquisiteness of adaptation, than do estimates of effective population size that are based on neutral polymorphism. Both CAIS and ENC can also be estimated for far more species because they do not require polymorphism or mutation rate data, nor tRNA gene copy numbers and abundances, but only a single complete genome. CAIS has the additional advantage of not being confounded with amino acid frequencies. This makes CAIS a useful tool for applying nearly neutral theory to protein evolution, as shown by our worked example of ISD.
Methods
Key resources table
Reagent type (species) or resource | Designation | Source or reference | Identifiers | Additional information |
---|---|---|---|---|
Software, algorithm | IUPRED2 | DOI: https://doi.org/10.1093/nar/gky384 | RRID:SCR_014632 | |
Software, algorithm | Codon Adaptation Index of Species | This paper | See Materials and methods | |
Software, algorithm | Codon Adaptation Index | DOI: https://doi.org/10.1093/nar/15.3.1281 | ||
Software, algorithm | ape | DOI: https://doi.org/10.1093/bioinformatics/bty633 | RRID:SCR_017343 | R package |
Software, algorithm | Effective Number of Codons | DOI: https://doi.org/10.1093/oxfordjournals.molbev.a004201 |
Species
Pfam sequences and IUPRED2 estimates of ISD predictions were taken from James et al., 2021, who studied species marked as ‘Complete’ in the GOLD database, with divergence dates available in TimeTree (Kumar et al., 2017). James et al., 2021 applied a variety of quality controls to exclude contaminants from the set of Pfams and assign accurate dates of Pfam emergence. Pfams that emerged prior to LECA are classified here as ‘old’, and Pfams that emerged after the divergence of animals and fungi from plants are classified as ‘young’, following annotation by James et al., 2021. Species list and other information can be found at https://github.com/MaselLab/Codon-Adaptation-Index-of-Species (copy archived at MaselLab, 2024).
Codon Adaptation Index
Sharp and Li, 1987 quantified codon bias through the CAI, a normalized geometric mean of synonymous codon usage bias across sites, excluding stop and start codons. We modify this to calculate CAI including stop and start codons, because of documented preferences among stop codons in mammals (Wangen and Green, 2020). While usually used to compare genes within a species, among-species comparisons can be made using a reference set of genes that are highly expressed (Sharp and Li, 1987). Each codon (1)
where denotes the number of times that codon is used, and the denominator sums over all codons that code for that specific amino acid. RSCU values are normalized to produce a relative adaptiveness values for each codon, relative to the best adapted codon for that amino acid:
(2)
Let be the number of codons across all protein-coding sequences considered. Then
(3)
To understand the effects of normalization, it is useful to rewrite this as:
(4)
where is the geometric mean of the ‘unnormalized’ or observed synonymous codon usages, and is the maximum possible CAI given the observed codon frequencies.
GC content
We calculated total %GC content (intergenic and genic) during a scan of all six reading frames across genic and intergenic sequences available from NCBI with access dates between May and July 2019 (described in James et al., 2023). Of the 170 vertebrates meeting the quality criteria of James et al., 2021, 118 had annotated intergenic sequences within NCBI, so we restricted the dataset further to keep only the 118 species for which total GC content was available.
Codon Adaptation Index of Species
Controlling for GC bias in synonymous codon usage
Consider a sequence region within species where each nucleotide has an expected probability of being G or C = . For our main analysis, we consider just one region encompassing the entire genome of a species . In a secondary analysis, we break the genome up and use local values of in the non-coding regions within and surrounding a gene or set of overlapping genes. To annotate the boundaries of these local regions, we first selected 1500 base pairs flanking each side of every coding sequence identified by NCBI annotations. Coding sequence annotations are broken up according to exon by NCBI. When coding sequences of the same gene did not fall within 3000 base pairs of each other, they were treated as different regions. When two coding sequences, whether from the same gene or from different genes, had overlapping 1500 bp catchment areas, we merged them together. was then calculated based on the non-coding sites within each region, including both genic regions such as promoters and non-genic regions such as introns and intergenic sequences.
With no bias between C vs. G, nor between A vs. T, nor patterns beyond the overall composition taken one nucleotide at a time, the expected probability of seeing codon in a triplet within is
(5)
where total positions in codon . The expected probability that amino acid in region is encoded by codon is
(6)
We can then measure the degree to which the observed codon frequencies diverge from these expected probabilities using the Kullback–Leibler divergence. This gives a CAIS metric for a species where is the observed frequency of codon (7)
Controlling for amino acid composition
Some amino acids may be more intrinsically prone to codon bias. We want a metric that quantifies effectiveness of selection (not amino acid frequency), so we re-weight CAIS on the basis of a standardized amino acid composition, to remove the effect of variation among species in amino acid frequencies.
Let be the frequency of amino acid across the entire dataset of 118 vertebrate genomes. We want to re-weight on the basis of to ensure that differences in amino acid frequencies among species do not affect CAIS, while preserving relative codon frequencies for the same amino acid. We do this by solving for so that
(8)
We then define to obtain an amino acid frequency adjusted CAIS:
(9)
The values for our species set are at https://github.com/MaselLab/Codon-Adaptation-Index-of-Species/blob/main/CAIS_ENC_calculation/Total_amino_acid_frequency_vertebrates.txt. Use of the standardized set of amino acid frequencies has only a small effect on computed CAIS values relative to using each vertebrate species’ own amino acid frequencies (Figure 3—figure supplement 3).
CAIS corrected for local intergenic GC content but not species-wide amino acid composition is
(10)
where is the number of times codon appears in region of species , is the expected number of times codon would appear in region of species given the local intergenic GC content, is the number of regions, and is the total number of codons in the genome. Rewritten for greater computational ease:
(11)
Given the limited impact of amino acid frequency correction, we used Equation 11 for the local GC results, but we could correct for amino acid composition by replacing the prefactor with , or even .
Novembre’s ENC controlled for total GC content
The expected number of codons is based on the squared deviations of the frequencies of the codons for each amino acid from null expectations:
(12)
where is the total number of times that amino acid appears. Novembre, 2002 defines the corrected ‘ (13)
and
(14)
where each is the average of the ‘ (15)
Statistical analysis
All statistical modeling was done in R 3.5.1. Scripts for calculating CAI and CAIS were written in Python 3.7.
Phylogenetic Independent Contrasts
Spurious phylogenetically confounded correlations can occur when closely related species share similar values of both metrics. One danger of such pseudoreplication is Simpson’s paradox, where there are negative slopes within taxonomic groups, but a positive slope among them might combine to yield an overall positive slope. We avoid pseudoreplication by using Phylogenetic Independent Contrasts (PIC) (Felsenstein, 1985) to assess correlation. PIC analysis was done using the R package ‘ape’ (Paradis and Schliep, 2019).
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
© 2023, Weibel, Wheeler et al. This work is published under https://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
Abstract
The nearly neutral theory of molecular evolution posits variation among species in the effectiveness of selection. In an idealized model, the census population size determines both this minimum magnitude of the selection coefficient required for deleterious variants to be reliably purged, and the amount of neutral diversity. Empirically, an ‘effective population size’ is often estimated from the amount of putatively neutral genetic diversity and is assumed to also capture a species’ effectiveness of selection. A potentially more direct measure of the effectiveness of selection is the degree to which selection maintains preferred codons. However, past metrics that compare codon bias across species are confounded by among-species variation in %GC content and/or amino acid composition. Here, we propose a new Codon Adaptation Index of Species (CAIS), based on Kullback–Leibler divergence, that corrects for both confounders. We demonstrate the use of CAIS correlations, as well as the Effective Number of Codons, to show that the protein domains of more highly adapted vertebrate species evolve higher intrinsic structural disorder.
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer