De novo creation of protein coding genes involves the formation of short ORFs from noncoding regions; some of these ORFs might then become fixed in the population. These orphan proteins need to, at the bare minimum, not cause serious harm to the organism, meaning that they should for instance not aggregate. Therefore, although the creation of short ORFs could be truly random, the fixation should be subjected to some selective pressure. The selective forces acting on orphan proteins have been elusive, and contradictory results have been reported. In Drosophila young proteins are more disordered than ancient ones, while the opposite trend is present in yeast. To the best of our knowledge no valid explanation for this difference has been proposed. To solve this riddle we studied structural properties and age of proteins in 187 eukaryotic organisms. We find that, with the exception of length, there are only small differences in the properties between proteins of different ages. However, when we take the GC content into account we noted that it could explain the opposite trends observed for orphans in yeast (low GC) and Drosophila (high GC). GC content is correlated with codons coding for disorder promoting amino acids. This leads us to propose that intrinsic disorder is not a strong determining factor for fixation of orphan proteins. Instead these proteins largely resemble random proteins given a particular GC level. During evolution the properties of a protein change faster than the GC level causing the relationship between disorder and GC to gradually weaken.
We show that the GC content of a genome is of great importance for the properties of an orphan protein. GC content affects the frequency of the codons and this affects the probability for each amino acid to be included in a de novo created protein. The codons encoding for Ala, Pro and Gly contain 80% GC, while codons for Lys, Phe, Asn, Tyr and Ile contain 20% or less. The three high GC amino acids are all disorder promoting, while Phe, Tyr and Ile are order promoting. Therefore, random protein sequences at a high GC will be more disordered than the ones created at a low GC. The structural properties of the youngest proteins match to a large degree the properties of random proteins when the GC content is taken into account. In contrast, structural properties of ancient proteins only show a weak correlation with GC content. This suggests that even after fixation in the population, proteins largely resemble random proteins given a certain GC content. Thereafter, during evolution the correlation between structural properties and GC weakens.
Citation: Basile W, Sachenkova O, Light S, Elofsson A (2017) High GC content causes orphan proteins to be intrinsically disordered. PLoS Comput Biol 13(3): e1005375. https://doi.org/10.1371/journal.pcbi.1005375
Editor: Roland L. Dunbrack Jr., Fox Chase Cancer Center, UNITED STATES
Received: July 30, 2016; Accepted: January 21, 2017; Published: March 29, 2017
Copyright: © 2017 Basile et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: All relevant data are within the paper and its Supporting Information files.
Funding: This work was supported by grants from the Swedish Research Council (http://www.vr.se/, VR-NT 2012-5046, VR-M 2010-3555) and the Swedish E-science Research Center (SeRC, www.e-science.se). Computational resources were provided by the Swedish National Infrastructure for Computing (SNIC, http://www.snic.vr.se/). SL was financed by Bioinformatics Infrastructure for Life Science (BILS, www.bils.se). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Proteins without any detectable homology are often referred to as orphans. The presence of orphans can be attributed to several causes; rapid sequence divergence beyond the point of homology recognition [1, 2], lateral transfer of genetic material , and de novo gene creation . The latter is of particular interest, as it is a source of completely novel coding material. Studies of the properties of these proteins might provide unique insights into the fundamental processes in the formation of all proteins, since, in the strict sense, all proteins were once created by a de novo mechanism.
Before the genomic era, the scientific consensus held that de novo creation of new genes was rare—instead it was believed that the vast majority of all genes were generated in an ancient “big bang”. However, when the first complete genomic sequences were initially published, this hypothesis was not supported . In fact, to this day, when analyzing complete genomes from closely related species, a surprisingly high number of orphan proteins is still found [6–8]. It has later been shown that some of these proteins are not de novo created but rather assigned as orphans as a result of limited phylogenetic coverage in earlier studies .
Today supported by the vast amount of complete genome sequences available and improved search methods , many of the initially identified orphans have been shown to have distant homologs in other genomes. Still, at least in yeast, a large set of genes appears to have been created through recent de novo formation [11, 12]. These studies indicate that in yeast there is a large set of proto-genes: ORFs that remain on the verge of becoming fixed as protein-coding genes in the population . This provides a possible model of how novel proteins can be generated from noncoding genetic material. In other species than yeast the genomic coverage is more limited and therefore studies have been less detailed.
The availability of many, complete, evenly spaced genomes allows classifying proteins at different evolutionary age [7, 9, 11], using methods such as ProteinHistorian . Here, a protein can be unique to a specific species, or even to a strain; alternatively it can be present pervasively across a taxonomic group [14, 15]. After de novo creation, a gene needs to become fixed in the population. The selective forces governing this process have been studied by examining the properties of orphan proteins. Intrinsic disorder, low complexity, subtelomeric location, high β-sheet preference as well as other features have been associated with orphan proteins [16, 17]. It has also been proposed that with age proteins (i) accumulate interactions, (ii) become more often essential and (iii) obtain lower β-strand content and higher stability . Some aspects of these observations, such as the fact that orphans on average are short, are likely connected to a de novo creation mechanism. However, other features, including intrinsic disorder, are not obviously related to the gene genesis and could instead be the result of the selective pressure acting during fixation.
In yeast, we have earlier reported that the youngest proteins, i.e. the ones unique to S. cerevisiae, are less disordered than older proteins , while in Drosophila the opposite can be seen: the youngest proteins are more disordered than the ancient ones . To the best of our knowledge the origin of this difference has not been explained. Could the selective forces be that disparate between two different eukaryotes? Or is it an artifact caused by limited genomic coverage? One difference between the two organisms is the content of Guanine and Cytosine (GC) nucleotides in the coding regions: Saccharomyces cerevisiae genomes are roughly 40% GC, while in Drosophila melanogaster the GC content is 53%.
To obtain a better understanding of the structural properties of orphan proteins, we determined the age of proteins in 187 eukaryotic genomes and studied a number of intrinsic properties, such as GC content, disorder, hydrophobicity, low complexity, and secondary structure. As expected we find that the most striking difference between young and old proteins is their difference in length. Further, intrinsic disorder and low complexity appear to be higher in orphans, albeit with a much smaller difference than for length, and these differences are not present in all species. The structural features in young proteins differ significantly depending on the GC content: low-GC orphans are much less disordered than high-GC orphans. In older proteins this relationship is much weaker, supporting a model where genes are created de novo starting from random DNA sequences, then their features gradually conform to those of ancient genes through adaptation.
Materials and methods
Protein data for 400 eukaryotic species were obtained from OrthoDB, release 8 , divided into 173 Metazoans and 227 Fungi, for a total of 4,562,743 protein sequences. This initial dataset was then filtered to a final size of 187 species, see below. For each species, a complete proteome was also downloaded from UniProt Knowledge Base .
The ProteinHistorian software pipeline  is aimed at annotating proteins with phylogenetic ages. It requires a phylogenetic tree relating a group of species, and a protein family file representing the orthology relationships between proteins. The pipeline assigns each protein to an age group, depending on the species tree. Here, we used ProteinHistorian with default parameters, the NCBI phylogenetic tree , and protein orthology data obtained from OrthoDB. The OrthoDB method is based on all-against-all protein sequence comparisons using the Smith-Waterman algorithm and requiring a sequence alignment overlap of at least 30 amino acids across all members of an orthologous group. Therefore, the age group can be thought of as the level in the species tree on which a shared sequence of at least 30 amino acids first appeared, i.e. it assigns multi-domain proteins to the age of its oldest domains.
Identification and definition of orphans
Proteins present in OrthoDB are only those with orthologs in at least one other species, i.e. proteins without orthologs (singletons) are not present in OrthoDB. Therefore, to obtain a set of candidate orphan proteins, the complete proteomes of all species were downloaded from Uniprot. Thereafter, BLAST was used to extract proteins not present in the OrthoDB dataset, obtaining 356,884 candidate orphan proteins. However, a large fraction of these proteins are not orphans but are missing from OrthoDB for other reasons, including that they were not present when the database was created or that they have undergone large domain rearrangements. We would assume that truly de novo created orphans do not contain domains found in other proteins. Therefore to ensure that we have a unique set of orphan proteins we filtered out proteins with hits in the Pfam-A database, by using hmmscan . We believe that, due to the stringent criteria used here, the majority of this remaining set is constituted of de novo created proteins, and we refer to them as orphans throughout the rest of this paper. These proteins are specific to the species taxonomic level, i.e. we expect not to find them in other species in the dataset, even in the same genus. For Saccharomyces cerevisiae, that has 16 strains in the dataset, we also included the strain specific proteins into the orphan group.
Among the OrthoDB proteins, we defined genus orphans those that were assigned age = 1 (2 in the case of S. cerevisiae), while proteins having the maximum age according to ProteinHistorian were defined as ancient: these proteins are thought to be present in the common ancestor of all Fungi (taxon id = 4751) or all Metazoa (taxon id = 33208). Finally, proteins whose estimated age is between genus orphans and ancient were defined as intermediate.
Taxonomic genera represented by a single species in the dataset have by definition no genus orphans; for this reason, we selected for our final dataset only the 187 species that have at least one other species within the same genus. The final dataset amounts to 1,782,675 proteins distributed across 187 species; 0.8% of them are defined orphans and 0.6% as genus orphans, 15% are intermediate and the remaining 84% are ancient.
One problem that exists using the NCBI phylogenetic tree is the presence of many polytomic branches, especially at the genus level, because ProteinHistorian cannot distinguish between proteins being specific to that species and proteins shared among the entire group. To solve this, we forced no polytomy on the terminal branches: multifurcating nodes were converted to a randomly bifurcated topology, transforming the NCBI tree to a fully binary structure. While a binary tree is needed for ProteinHistorian, its algorithm assumes that a protein gain is much more rare than a loss; this means that the most recent common ancestor of a protein will be at the topmost intersection of a group of species. Thus, randomly converting multifurcations to bifurcation might likely underestimate the number of genus-specific orphans, but have no effect on species-specific orphans.
Clades affected by the conversion from multi- to bi-furcating branches include Caenorhabditis (5 species), Drosophila (5 species), Anopheles (5 species), Candida (5 species), Saccharomyces (14 strains), Aspergillus (5 species) and Trichopython (5 species). The taxonomic tree comprising the final set of 187 species is presented in S1 Fig.
Assigning GC content
We could map 1,357,518 out of 1,782,675 proteins (∼76% of the dataset) to their ENA identifiers. This mapping was used to download the Coding Sequence (CDS) data from ENA (https://www.ebi.ac.uk/ena/); the GC content was then calculated for each mapped gene individually.
Gene ontology annotation
Evidence for functionality of the proteins was estimated using annotated Gene Ontology (GO) terms. Using the Uniprot KnowledgeBase mapping data (ftp://ftp.uniprot.org/pub/databases/uniprot/current_release/knowledgebase/idmapping/idmapping.dat.gz) we assigned UniprotKB identifiers to 894,831 out of 1,752,675 proteins (51%). These were then annotated with three terms, one for each main GO category: Molecular Function, Biological Process and Cellular Component. All GO terms are associated with evidence codes; a subset of these codes (‘EXP’,‘IDA’,‘IPI’,‘IMP’,‘IGI’ or ‘IEP’) represents experimentally validated functional annotations. If any of these codes is present we mark the corresponding protein as experimentally characterized.
Predicted properties of proteins
Intrinsic disorder content was predicted for all the proteins by using several disorder predictors; short and long disorder predictions by IUPred , three type of predictions (REM-465, Hotloops and Coils) by DisEMBL  and GlobPlot . In the main figures we only report the prediction by IUPred long; the others are found in the supplementary material (S2 to S7 Figs). It is worth mentioning that these predictors operate with different definitions of disorder, so a consensus should not be expected.
We used SCAMPI  to predict the fraction of transmembrane residues in a protein. The fraction of low-complexity residues is predicted using SEG . PSIPRED  was used to predict the secondary structure of all the proteins in the dataset, using only a single sequence and not a profile. This reduces the accuracy but the overall frequencies should not be changed significantly. We annotated each protein with the fraction of residues predicted to be in each type of secondary structure (α-helix, β-strand, coil).
TOP-IDP  is a measure of the disorder-promoting propensity of a single amino acid. For each protein, the average propensity was calculated by averaging the TOP-IDP values of all its residues. Similarly the hydrophobicity of each protein was expressed as the average hydrophobicity using the biological hydrophobicity scale . Finally, we computed the propensity of each amino acid to be in a secondary structure (helix, sheet, coil, turn) in the same manner by using secondary structure propensity scales .
Statistical significance of the results
In order to test the statistical significance of the results, a number of tests were performed. Rank-sum tests between all possible pairs of age groups were performed for the entire dataset and for each studied property. Due to the large number of samples the p-values from these tests are always smaller than 10−141 even when the absolute difference in numbers is minuscule.
To study the difference between young and old proteins on a global level, we performed a rank-sum test for orphan versus ancient proteins within each species. To exclude small variations we only considered the species where the p-value of this test was <0.01.
To determine the relationship between a property and GC we studied the slopes for proteins of different age. If the p-value of a linear regression test is <0.01, the corresponding property is considered significantly correlated with GC.
Random proteins at different GC contents
To test whether the studied intrinsic properties, as well as the frequency of any given amino acid, were solely dependent on GC content, we used a set of 21,000 random ORFs, generated as follows: at each GC content ranging from 20 to 90%, in steps of 1%, a set of 400 ORFs (equally divided into 300, 900, 1,500 and 2,100 bp long) was generated so that its content of GC was fixed. The ORFs were generated by randomly selecting codons among the 61 non-stop codons. The probability to select one codon given a GC content of GCfreq is set accordingly: (1) where Ni is the nucleotide of the codon in position i and δ(N|GC is equal to 1 if the nucleotide N is guanine or cytosine and zero otherwise, etc. Finally, start and stop codons were added. These ORFs were then translated to polypeptides, and all their intrinsic properties, as well as the frequencies of their amino acid were computed, as described above.
The assignment of age to all proteins is based on the ProteinHistorian pipeline . In the youngest, orphan group, only proteins that are (a) not present in any other genome and (b) that do not share any Pfam-A domain with any other eukaryotic protein are present. In the next group, genus orphans, only proteins that are unique to a genus are included. Proteins having the maximum age according to ProteinHisorian are labeled as ancient; the rest is classified as intermediate.
A summary of the age assignment and subsequent grouping into orphans, genus orphans, intermediate and ancient is shown for each species in S1 Table. Orphans and genus orphans constitute each less than 1% of the dataset; intermediate proteins are ∼15% and ancient proteins ∼84%
These results show that for most genomes we do a conservative estimate of the number of orphans and find fewer orphans than in earlier studies. For instance, in Saccharomyces cerevisiae we identified 16 orphans and 5 genus orphans, out of 6466 proteins. As a comparison, in our earlier study we reported 157 species-specific and 125 genus-specific orphans  while Vidal and co-workers reported 143 species-specific (ORFs1) and 609 genus-specific (ORFs2−4) proteins . Similarly, in Drosophila pseudoobscura we could identify only 6 orphan proteins, in comparison to the 228 reported previously . This shows that the exact identification of which proteins are de novo created remains difficult and depends on the genomes included in the study.
However, our primarily aim for this study is not to estimate the exact number of orphans, but to examine properties of proteins of different ages. Therefore, we do believe that our conservative estimate is useful to enhance the fraction of de novo created proteins in the youngest groups.
Next we set out to estimate the functional evidence for our set of proteins; for this we explore their Gene Ontology (GO) annotation. For each main GO category (process, function and component), we computed the fraction of proteins being annotated with at least one GO term in UniProt. In addition we calculated the fraction of proteins having at least one experimentally verified GO annotation, Table 1.
In parentheses is the fraction of proteins having an experimentally validated annotation (i.e. a GO evidence code equal to ‘EXP’,‘IDA’,‘IPI’,‘IMP’,‘IGI’ or ‘IEP’).
The fraction of annotated proteins increases steadily with age, from ∼3-9% in orphans to ∼25% in ancient, Table 1. This is expected, as older proteins have more regulatory, protein-protein, and genetic interactions . However, the fraction of proteins with experimental functional evidence is small (<1% of protein) irrespectively of age. This shows that there exists at least a fraction of proteins of any age that is functionally characterized, but it is difficult to exactly determine how substantial it is.
In most genomes orphan proteins are more disordered
The average length of the proteins increases by age, see Fig 1b. The average length is 100 amino acids in orphans, 150 in genus orphans, 300 for intermediate and 500 for ancient proteins. It can be noted that in the vast majority of the genomes the difference in length is significant between orphan and ancient proteins, Table 2. This highlights the well-established fact that eukaryotic proteins expand during evolution: the expansion can occur by several mechanisms, including domain-fusions , additional secondary structure elements  and expansion within intrinsically disordered regions .
The difference between orphans and ancient is statistically significant for all the considered properties: the p-value of a rank-sum test is always <10−141.
GC content on the other hand does not appear to change by age, see Fig 1c. There is approximately the same number of genomes where a statistically significant increase or decrease exist, Table 2.
Next, we compared predicted structural properties of all proteins, see Figs 1d–1i, S8 and Table 2.
The amount of predicted disorder residues ranges between 20% and 40%, depending on the prediction method. For most disorder predictors the fraction of disordered residues is higher in orphans than in ancient proteins. However, there exists about a handful of genomes where the opposite trend is observed: supporting earlier observations, orphans are significantly more ordered in Candida albicans according to 5 out of 6 methods, in Saccharomyces cerevisiae s288c for 4 methods and in Fusarium pseudograminearum for 3. An interesting case is that of Drosophila pseudoobscura, that appears to have more ordered orphans according to IUPred long, contrary to all others Drosphila species.
The fraction of transmembrane residues is on average ∼2% in orphan proteins, with an increasing trend towards ancient (4%). Similarly the amount of helical residues increase slightly with age, while the fraction of low complexity residues decrease by age. For all these structural predictions the changes are quite small and there are genomes with significant increases and decreases for all measures.
Orphan proteins are more disordered in yeast but less in Drosophila
Above, we noted that on average orphan proteins are more disordered. However, we also noted that in a handful of genomes a statistically significant opposite trend could be observed. To investigate this further we studied the amount of predicted disorder in each genome separately. When studying intrinsic disorder, orphans and genus orphans of S. cerevisiae appear remarkably ordered (∼3% of the amino acids) as shown before  see Fig 2a and 2b. The closely related species Candida albicans shows a similar trend; see Fig 2c. Results from additional disorder predictors are presented in S4–S8 Figs and agree well with these observations.
In contrast, but also consistent with earlier studies , orphans and genus orphans in most Drosophila genomes are more disordered than ancient proteins, see Fig 2d and 2e. In the worm C. elegans (Fig 2f) orphan proteins appear to be consistently more disordered than progressively older ones; this is true across all the considered Caenorhabditis species. These results are consistent in other predictors, see S4–S8 Figs d, e and f.
In general, it is apparent that in most organisms orphans are more disordered than ancient proteins, while in yeast the opposite appears to be the case. What could possibly explain this difference? One possibility is that the more complex regulations in animals require more disordered residues in comparison with yeast. But the average disorder content is similar in all eukaryotic species, contradicting this idea.
We noted that yeasts are among the genomes with lowest GC content (∼40% in S.cerevisiae, 35% in C. glabrata). Therefore, we decided to examine the properties of proteins from different age groups in respect to their GC content.
Orphans are more disordered in high-GC genomes
To identify the origin of the different properties of orphan and ancient proteins in different organisms we studied the distribution of different structural properties, including low complexity, fraction of transmembrane residues, secondary structure frequency and intrinsic disorder) for all genomes against GC of the genomes, see Fig 3.
For clarity only the ancient (blue) and orphan (red) proteins are shown individually, but the linear fitted lines for genus orphans (pink line) and intermediate ones (light blue) are also shown. In the text box three values are presented: rank-sum p-value = p-value of a rank-sum test of orphans versus ancient (only the property on y axis is considered); correlation p-values = p-value of a linear regression test for orphan and ancient.
With the exception of β-sheet frequency, the difference between orphans and ancient proteins for all the considered properties is statistically significant: the p-value of a rank-sum test (a non-parametric equivalent of the t-test) is always < 10−11.
For proteins of all ages, low complexity (SEG) and predicted coil frequency increase with GC, while transmembrane, helix and sheet frequency decrease.
Notable is that intrinsic disorder shows a clear, directly proportional dependency on GC: higher GC corresponds to more disorder. At the extreme (over 60% GC), more than 50% of the residues in orphan proteins are predicted to be disordered, while for ancient proteins the disorder fraction is about 30%. At low GC (below 40%) the fraction of disordered residues is lower and similar in ancient and orphan proteins (15-20%).
Further, the dependency of GC is clearly stronger for younger proteins, indicating that it is related to the creation of the protein and then gradually lost during evolution. To assess the significance of this dependency, we performed a linear regression test for each age group. The p-values of such test is presented for orphans and ancient in the boxes of Fig 3. All the properties, with the exception of low complexity, show a p-value <0.01, indicating that they are significantly correlated with GC in both orphan and ancient proteins.
The GC is not constant over a genome. In complex eukaryotic organisms, the global GC content is heavily determined by the GC composition of isochores: these regions of uniform GC form a mosaic in the genomes of many complex eukaryotes, and their maintenance is likely the result of natural selection . In general coding regions have higher GC than noncoding regions [38, 39]. Further, there are also variation in GC between different regions of a genome, so when a noncoding region is turned into a gene the local GC will decide the amino acid content of the protein.
Therefore, it might be more relevant to study the GC of each protein individually.
A strong relationship between GC and structural properties of orphans
In Fig 4 we show the dependency of structural properties on GC content for individual proteins. In addition, structural properties of a set of proteins generated randomly at all GC levels are shown. Orphans and genus orphans, as well as random proteins, show a definite dependency on GC. In contrast, ancient and intermediate proteins are only loosely dependent on GC.
For each property, colored lines represent proteins of different age: orphans (red), genus orphans (pink), intermediate (light blue) and ancient (blue). The black lines represent randomly generated proteins at different GC frequencies.
In general there is a resemblance between orphans and randomly generated proteins. However, when studying Fig 4 in more detail a few notable differences between them can be observed: orphans are more disordered and contain more low complexity regions but fewer sheets, independently of the GC level.
It should be recalled that what we describe above is based on predicted structural features that are an indirect reflection of the protein sequence. If a certain group of proteins is predicted to be more disordered, or contain more sheets, it is quite likely a consequence of changes in amino acid frequencies.
Next, we studied the proteins using six different amino acid propensity scales. The difference between the scales and predicted features is that scales describe general properties, and are directly calculated from amino acid frequencies, while predicted properties can also include other features. For disorder we use the TOP-IDP scale , for hydrophobicity we use the biological hydrophobicity scale , while sheet, turn, coil and helix propensities are analyzed using the structure-based conformational preferences scales .
In agreement with the predicted values; the average properties in the four age groups of proteins are overlapping, see S8 Fig. However, when taking the GC content into account the properties of the younger proteins show a strong correlation with GC, see Fig 5. To a very large degree the properties of orphan proteins follow what would be expected for random proteins (black line). However, regardless of GC, orphan proteins are more disordered and hydrophobic, have slightly higher turn and helical propensities, and also lower sheet propensities than random.
For each property, colored lines represent proteins of different age: orphans (red), genus orphans (pink), intermediate (light blue) and ancient (blue). The black lines represent randomly generated proteins at different GC frequencies.
Interestingly, the propensities of the two groups of older proteins also change by GC; however, this dependency is less pronounced than for orphan or random proteins. The difference seen between orphan and ancient proteins indicates that, given evolutionary time, the selective pressure to change the GC level is weaker than the selective pressure to change amino acid frequencies.
GC content affects the codon usage in the genome  and it has been argued that GC might be the sole responsible for codon bias . The difference in codon usage causes differences in amino acid frequencies in such a way that some amino acids are more frequent in higher GC for random protein sequences. Also, a preference for some amino acids might cause a change in GC just by a higher frequency of certain codons. In younger proteins the correlation between amino acid frequency and GC is stronger than in older proteins, see Fig 5. This indicates that the selective pressure to change amino acids in a protein is stronger than the one to change the GC content. At low GC ancient proteins are more disordered than expected for random sequence while at high GC they are less.
The influence of GC on amino acid preferences
How do changes in GC content affect proteins? In a random DNA sequence, the frequency of different codons changes depending on GC, and this, in turn, affects the resulting amino acid frequencies. To study the effect of GC content on amino acid frequency we examined the frequency of all 20 amino acids in proteins of different age.
In Fig 6, the expected and observed amino acid frequencies at different GC contents are explored. For most amino acids the observed frequencies are surprisingly well correlated with what is expected from GC alone. However, a few notable exceptions exist:
- For Pro, Arg, Trp, Tyr, Phe and Ile, the frequencies in orphan proteins resemble the random proteins and are strongly dependent on GC content, while the frequencies in ancient proteins are much less dependent on GC content. This suggests that there is a selective pressure to gradually adjust the frequencies of these amino acids to an optimal level.
- Asn and Ala change in both orphans and ancient proteins with GC frequency, indicating that the selective pressure to change the frequency of these amino acids is lower.
- Glu, Gln and Asp are more frequent than expected, at any GC level. Their frequency in orphans is intermediate to what is expected by chance and what is found in ancient proteins, suggesting a gradual increase during evolution. These amino acids are coded by only two codons, i.e. there exists a selective pressure to increase their frequency to a higher level than the 3.3% expected by chance.
- Finally, Cys and His are less frequent, independently of GC content, in real proteins than in random ones, indicating their special roles in protein function and folding as well as their rareness.
A black line represents the expected values. The amino acids are sorted by the GC content in their codons.
In Fig 7 and S2 Table the GC content of the codons of each amino acid is compared with the propensity of that amino acid to be in a certain structural region. Three amino acids, Ala, Gly and Pro are “high GC” amino acids, i.e. they have more than 80% GC in their codons, while five amino acids, Lys, Phe, Asn, Tyr and Ile, are “low GC codons”, with less than 20% GC in their codons.
For each scale the Pearson (R) correlation with GC is also shown.
All three “high GC” amino acids are disorder promoting (high TOP-IDP), and four out of five “low GC” amino acids are order-promoting (low TOP-IDP) residues. Therefore at high GC content, codons coding for hydrophilic, disorder-promoting amino acid are prevalent. Genes low in GC tend to contain codons for hydrophobic amino acids, associated with order.
All scales correlate with the GC frequencies with coefficients ranging from -0.42 to 0.39. The strongest correlations are found with β-sheet propensity (-0.42) and TOP-IDP (0.39) and the weakest with hydrophobicity (0.16).
We have studied the properties of proteins and their age in a large set of eukaryotic genomes. As shown before, orphan proteins are shorter than ancient proteins, but, surprisingly, we do find that on average for other structural features the young and old proteins are rather similar. However, we also observe that the properties of youngest proteins vary significantly with the GC content. At high GC the youngest proteins become more disordered and contain less secondary structure elements, while at low GC the reverse is observed. We show that these properties can be explained by changes in amino acid frequencies caused by the different amount of GC in different codons. The influence of this can be seen in the frequency of the amino acids that have a high or low fraction of GC in their codons, such as Pro.
In a random sequence, Pro only represents less than 5% of the amino acids at 40% GC, but 10% at 60% GC. This actually agrees well with what is observed in orphan proteins: 5% at 40% GC vs. 9% at 60% GC, see Fig 6. Similar changes in frequencies can be observed for several amino acids.
On average, young proteins are more disordered than ancient proteins, but this property is strongly related to the GC content. In a low-GC genome the disorder content of an orphan protein is ∼30% while in a high-GC genome it is over 50%, see Fig 3.
Here we show that GC content of a genome strongly affects the amino acid distribution in de novo created proteins. It appears as if de novo created proteins that become fixed in the population are very similar to random proteins given a certain GC content. Codons coding for disorder-promoting residues are on average richer in GC, explaining the earlier contrasting observations between the low disorder among orphans in yeast (a low GC organism) and the high disorder among orphans in Drosophila (a high GC organism).
Finally, it can be observed that older proteins show a lower dependency of their structural properties on GC, but have a GC content similar to the one of orphans. This can lead to the speculation that selective pressure acts less on GC levels and more on structural features of proteins.
S1 Table. Summary of the numbers (with percentages in parentheses) of orphans, genus orphans, intermediate and ancient proteins for each of the 187 considered eukaryotic species.
S2 Table. For each amino acid we show the GC content of its codons, its value in the TOP-IDP scale, its hydrophobicity (Hessa scale), as well as its value in the secondary structure scales for Alpha, Beta, Coil and Turn propensity.
S1 Fig. Phylogenetic tree of the final set of 187 eukaryotic species.
S2 Fig. Violin plots showing intrinsic disorder as predicted by (a) IUPred (short), (b) DisEMBL Coils, (c) DisEMBL Rem465, (d) DisEMBL Hotloops and (e) GlobPlot for all the 187 species.
S3 Fig. For six selected species (two strains of S. cerevisiae, C. Albicans, D. melanogaster, D. sechellia and C. elegans), intrinsic disorder (% of amino acid predicted as disordered by IUpred short) is shown as violin plots for proteins in the different age groups.
S4 Fig. For six selected species (two strains of S. cerevisiae, C. Albi ans, D. melanogaster, D. sechellia and C. elegans), intrinsic disorder (% of amino acid predicted as disordered by DisEMBL Coils) is shown as violin plots for proteins in the different age groups.
S5 Fig. For six selected species (two strains of S. cerevisiae, C. Albicans, D. melanogaster, D. sechellia and C. elegans), intrinsic disorder (% of amino acid predicted as disordered by DisEMBL REM-465) is shown as violin plots for proteins in the different age groups.
S6 Fig. For six selected species (two strains of S. cerevisiae, C. Albicans, D. melanogaster, D. sechellia and C. elegans), intrinsic disorder (% of amino acid predicted as disordered by DisEMBL Hotloops) is shown as violin plots for proteins in the different age groups.
S7 Fig. For six selected species (two strains of S. cerevisiae, C. Albicans, D. melanogaster, D. sechellia and C. elegans), intrinsic disorder (% of amino acid predicted as disordered by GlobPlot is shown as violin plots for proteins in the different age groups.
S8 Fig. Violin plots showing several properties calculated from propensity scales, as average score.
(a) Intrinsic disorder using the TOP-IDP scale, (b) hydrophobicity using the Hessa scale, (c-f) secondary structure preferences.
- Conceptualization: AE SL WB.
- Data curation: AE WB.
- Formal analysis: AE WB.
- Funding acquisition: AE.
- Investigation: AE WB SL OS.
- Methodology: AE WB.
- Project administration: AE.
- Resources: AE.
- Software: WB OS.
- Supervision: AE.
- Validation: AE WB OS SL.
- Visualization: AE WB.
- Writing – original draft: WB.
- Writing – review & editing: AE WB SL.
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