Different evolutionary patterns of SNPs between domains and unassigned regions in human protein-coding sequences
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- Pang, E., Wu, X. & Lin, K. Mol Genet Genomics (2016) 291: 1127. doi:10.1007/s00438-016-1170-7
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Protein evolution plays an important role in the evolution of each genome. Because of their functional nature, in general, most of their parts or sites are differently constrained selectively, particularly by purifying selection. Most previous studies on protein evolution considered individual proteins in their entirety or compared protein-coding sequences with non-coding sequences. Less attention has been paid to the evolution of different parts within each protein of a given genome. To this end, based on PfamA annotation of all human proteins, each protein sequence can be split into two parts: domains or unassigned regions. Using this rationale, single nucleotide polymorphisms (SNPs) in protein-coding sequences from the 1000 Genomes Project were mapped according to two classifications: SNPs occurring within protein domains and those within unassigned regions. With these classifications, we found: the density of synonymous SNPs within domains is significantly greater than that of synonymous SNPs within unassigned regions; however, the density of non-synonymous SNPs shows the opposite pattern. We also found there are signatures of purifying selection on both the domain and unassigned regions. Furthermore, the selective strength on domains is significantly greater than that on unassigned regions. In addition, among all of the human protein sequences, there are 117 PfamA domains in which no SNPs are found. Our results highlight an important aspect of protein domains and may contribute to our understanding of protein evolution.
KeywordsHuman genome Protein-coding sequence Protein domain SNPs Natural selection
Studying protein evolution is crucial for understanding the evolution of speciation and adaptation, senescence and human genetic disease (Pál et al. 2006). At the sequence level, protein evolution occurs primarily through two processes: the random production of DNA mutations and the fixation of new variations in populations, which is constrained simultaneously by selection and the population size. Single nucleotide polymorphisms (SNPs) are abundant within populations and represent a major form of genomic variation. SNPs are widely exploited as genetic markers for phenotypic differences (Sachidanandam et al. 2001; Suh and Vijg 2005). As a result, SNPs in protein-coding sequences are of particular interest and have been explored extensively in many organisms.
In the pre-whole-genome era, researchers focused on SNPs in different types of proteins. For example, while investigating 182 housekeeping and 148 tissue-specific genes in humans Zhang and Li (2005) found no evidence of positive selection for either gene class, while Cohuet et al. (2008) studied 72 immune related genes and 37 randomly chosen genes in Anopheles gambiae and detected similar patterns and rates of molecular evolution in both categories. The growing numbers of published population genomics studies has increased the availability of genome-scale SNP data sets (Liti et al. 2009; Schacherer et al. 2009; Abecasis et al. 2010; Abecasis et al. 2012), which makes it possible to survey detailed selections from complete genomes. Using more than 11,000 human protein-coding genes, Bustamante et al. (2005) observed that selection acting on genes participating in different biological process and molecular functions varies greatly. In Drosophila simulans, Begun et al. (2007) discovered that adaptive protein evolution is common, while a genome-wide survey of SNPs in Saccharomyces paradoxus, Vishnoi et al. (2011) confirmed that purifying selection within the S. paradoxus lineage is ongoing.
In general, there are many types of evolutionary forces at play during the course of genome sequence evolution; thus, they should impose different and/or subtle constraints on different classes of genomic sequences. For example, constraints on coding-gene sequence, mainly by purifying selection, are stronger than those on most, if not all, non-coding sequences. However, this does not imply that there are uniform constraints across all sequences within a class, and much evidence shows that most sites are differently constrained even within a segment of sequence that constitutes a functional unit (Nielsen 2005; Tian et al. 2008; Koonin and Wolf 2010). For example, Mu et al. (2011) analyzed non-coding elements that were classified into three categories and showed that each had a very distinct variation profile. Most protein sequences are composed of domains, which usually convey distinct functions (Bateman et al. 2002; Koonin et al. 2002; Ponting and Russell 2002). Recently, Yates and Sternberg (2013) analyzed human non-synonymous SNPs to identify disease-resistant and disease-susceptible domains and proteins. In the present study, we explored the distribution of SNPs located in human protein-coding genes (cSNPs) and sought to determine whether there is any significant difference between the distribution patterns of cSNPs when each protein sequence is divided into two groups: the first of which contains PfamA-classified domains, whereas the second group contains unassigned regions (i.e., for each protein, those sequences not annotated by the PfamA database). The SNP dataset was parsed from the newly available genetic variation from 1092 human genomes (Abecasis et al. 2012) according to the GENCODE annotation of protein-coding genes (version 7) (Harrow et al. 2006), whereas the PfamA domain annotation is from the Pfam database, version 27.0. Based on this information, we surveyed the following: (1) the strength of selection acting on SNPs, partitioned into SNPs in domains (doSNPs) and SNPs in unassigned regions (unSNPs); and (2) the density of non-synonymous, and synonymous SNPs, classified into two types. We found that there are significantly different evolutionary patterns between domains and unassigned regions in the human genome. In addition, we found that there are 117 domains for which no SNP has been identified. Our results provide new insight into the existing pool of knowledge regarding the evolution and function of human proteins.
Materials and methods
Overview of our approach
Our analysis is based on a whole-genome set of genetic variations from 1092 human genomes. It involves five steps: (1) mapping SNPs on protein coding sequences; (2) classifying SNPs into non-synonymous (nsSNPs) and synonymous variations (sSNPs); (3) annotating the proteins with PfamA domains; (4) dividing the SNPs into doSNPs and unSNPs; and (5) obtaining the fixed variations in human. We provide the details of data sources and analysis methods for all.
In this study, we mainly used six types of data: genome sequence, genome annotation, genome-wide variations from human populations, principal splice isoforms for human genes (Manuel Rodriguez et al. 2015), PfamA domains and the Enredo-Pecan-Ortheus (EPO) primate alignments (Hubbard et al. 2009).
The genome-wide set of genetic variations from 1092 human genomes (Abecasis et al. 2012) was downloaded from the 1000 Genomes Project (http://www.1000genomes.org/). The human genome sequence used was based on the February 2009 Homo sapiens assembly, GRCh37, downloaded from Ensembl (Flicek et al. 2013) (http://asia.ensembl.org/index.html). Meanwhile, the ancestral sequences with high-confidence calls for H. sapiens (GRCh37) were retrieved from the 1000 Genomes Project (ftp://ftp.1000genomes.ebi.ac.uk/vol1/ftp/phase1/analysis_results/supporting/ancestral_alignments/). The models of the protein-coding genes were retrieved from version 7 of the GENCODE project (December 2010 freeze), whose aim is to annotate all evidence-based gene features in the human genome (Harrow et al. 2006) (http://www.gencodegenes.org/). The 6 way EPO primate alignments were downloaded from Ensembl (ftp://ftp.ensembl.org/pub/release-71/emf/ensembl-compara/epo_6_primate). Based on these datasets, the protein-coding sequences and their related SNPs were extracted using our Perl script. For those genes with multiple transcripts, the principal isoform from APPRIS database (http://appris.bioinfo.cnio.es/#/downloads) was selected; in total, 20,571 protein-coding sequences and their corresponding protein-coding sequences were used for the following analysis.
We used Pfam database (http://pfam.sanger.ac.uk/) (Punta et al. 2012) (Pfam27.0 release, March 2013), which contains 14,831 domains. The proteins were assigned domains using pfam_scan.pl downloaded from Pfam (E value ≤10−3). After this domain annotation, each protein was partitioned into two parts: the domain regions mapped by any Pfam domain and the unassigned regions for the remainder unmapped sequences. All the cSNPs were also divided into two groups: doSNPs if they were within the domain regions and unSNPs when they were not.
Divergence information of protein-coding sequences between humans and their ancestors was identified using our Perl script. The ancestral sequences were from the 1000 Genomes Project, we only used high-confidence call: ancestral state was supported by the other two sequences. A mutation is considered as a fixed divergence if the corresponding site is not polymorphic in human populations and not missing chimp information in the 6 way EPO primate alignments as well.
Calculation of the direction of selection
Direction of selection (DoS) provides a statistic to estimate the patterns of selection based on numbers of non-synonymous polymorphism (Pn), synonymous polymorphism (Ps), non-synonymous substitutions (Dn), and synonymous institutions (Ds) (Stoletzki and Eyre-Walker 2011). DoS was defined as Dn/(Dn + Ds) − Pn/(Pn + Ps).
Inference of the strength of purifying selection acting on domains and unassigned regions
The method proposed by Eyre-Walker et al. (2006) was used to infer the strength of purifying selection. The software was downloaded from http://www.lifesci.sussex.ac.uk/home/Adam_Eyre-Walker/Website/Software.html.
The density of sSNPs (or nsSNPs)
The density of sSNPs (or nsSNPs) is the number of synonymous (or non-synonymous) polymorphisms per synonymous (or non-synonymous) site. We counted the number of synonymous (or non-synonymous) SNPs and the number of synonymous (or non-synonymous) sites for domains and unassigned regions, respectively. The odd ration of them is defined as the density of sSNPs (or nsSNP).
Assessment of differences in amino acid compositions between domains and unassigned regions
For the proteins, we counted the number of each type of amino acids (total 20 types of amino acids) in domains and unassigned regions, respectively. We considered the result to indicate significant differences in amino acid composition between domains and unassigned regions if the 20 types of amino acids had significant difference according to Chi square tests (p value <0.05).
Assessment of codon usage bias
To assess the codon usage bias, we calculated effective number of codons (ENC) with CodonW (http://codonw.sourceforge.net/). The reported value of ENC is always between 20 (when only one codon is effectively used for each amino acid) and 61 (when codons are used randomly). In this work, genes have no significant codon bias when the ENC value is more than 50.
A randomization process was used to measure whether the number of domains without any SNPs is statistically significant. First, we randomly assigned all their N observed SNPs to positions in the human proteins. This randomization process was repeated 1000 times. Then we counted how many times the number of domains without SNPs is greater or equal than 117, and how many times the average occurrences of domains without SNPs is higher or equal than the one observed for the origin 117 domains. Finally, we can obtain empirical p-values, which are the ratios of the times that the value of domains without SNPs is greater or equal that the one observed for the origin 117 domains.
Fisher’s exact test was used to test difference of the density of SNPs. The difference of amino acid compositions was tested by Chi square test. Mann–Whitney test was used to test the difference of lengths of two groups of domains. Spearman’s rank test was used to test correlation between paired samples. All statistical tests were performed using the R statistical package.
Classification of SNPs within human protein-coding sequences
Using the human genome based on the GRCh37 assembly and genome annotation version 7, 20,571 protein-coding genes were identified (excluding genes on the Y chromosome and in the mitochondrial genome). Because 92–94 % of the genes undergo alternative splicing (Wang et al. 2008), we extracted the principal splice isoform for each protein-coding gene basing on APPRIS database, which designated one of the isoforms as the principal isoform integrating protein structural information, functionally important residues, conservation of function domains and evidence of cross-species conservation (Manuel Rodriguez et al. 2015). By mapping the SNPs from 1092 human genomes (Abecasis et al. 2012) onto these genes, we identified 19,909 genes with cSNPs. We observed 492,826 polymorphic nucleotides, of which 291,485 altered the amino acid sequences and 201,341 were synonymous.
Summary of polymorphisms and divergence
Rare (MAF <0.5 %)
Low (0.5 % ≤ MAF ≤ 5 %)
Common (MAF >5 %)
Polymorphism 19,909 genes
Divergence (fixed) 15,649 genes
Using high-quality ancestral sequences filtering the sites chimp missing, we identified 15,649 genes with fixed mutations. In all, we found 74,577 fixed changes derived from humans; 31,963 were non-synonymous and 42,614 were synonymous. These changes were divided into four types (Table 1).
Stronger purifying selection pressure on domains than on unassigned regions
Direction of selections for domain and unassigned regions
Type of regions in 15,649 genes
Direction of selection
Direction of selection
Greater constraint on the synonymous SNPs in unassigned regions than on those in domains
There is another question of whether there is any difference between domains and unassigned regions in human protein-coding sequences for non-synonymous/synonymous SNPs. In order to answer the question, the cSNPs were partitioned into four types: non-synonymous doSNPs, non-synonymous unSNPs, synonymous doSNPs, and synonymous unSNPs basing on all SNPs being classified as either doSNPs or unSNPs. We then calculated the density for each of them (see “Materials and methods” for details).
Next, we surveyed the synonymous SNPs. As described in Fig. 2a, there was a different pattern with that of the non-synonymous SNPs. The density of synonymous doSNPs was significantly greater (Fisher’s exact test: ρ = 1.13, p < 2.2 × 10−16) than that of unSNPs. We further analyzed the densities of different MAF synonymous SNPs and found that the densities of different MAF synonymous doSNPs were all significantly greater than those of synonymous unSNPs (Fisher’s exact test, ρ = 1.14, p < 2.2 × 10−16, ρ = 1.07, p < 3.27 × 10−10, and ρ = 1.14, p < 2.2 × 10−16, respectively for rare, low and common SNPs, Fig. 2c).
We recognized that these results could stem from the different amino acid compositions between the two types of sequences. To control for this, we did not consider genes with significant differences in amino acid compositions of two parts (Chi square tests, p < 0.05) (see “Materials and methods”). After filtering, 5480 proteins remained, at which point we repeated the analysis and found similar patterns with the whole protein set (Fisher’s exact test, ρ = 0.86, p < 2.2 × 10−16 and ρ = 1.09, p < 2.2 × 10−16, respectively for non-synonymous SNPs and synonymous SNPs) (Supplementary Figure S1).
The codon usage bias of proteins might affect on our results. To remove the potential influence of codon usage bias, we excluded proteins with ENC less than or equal to 50 (see “Materials and methods”). We obtained 9768 proteins in which codon usage has no bias. We analyzed the protein set, and the patterns were also consistent (Fisher’s exact test, ρ = 0.88, p < 2.2 × 10−16 and ρ = 1.08, p < 2.2 × 10−16, respectively for non-synonymous SNPs and synonymous SNPs) (Supplementary Figure S2).
These results implied that our observation was affected by many factors. Synonymous mutations have been found to be the causes and consequences of codon bias (Plotkin and Kudla 2010; Weatheritt and Babu 2013) and to affect protein translation and folding (Kimchi-Sarfaty et al. 2007; Poliakov et al. 2014). Recently, Lawrie et al. found strong purifying selection at synonymous sites in Drosophila melanogaster (Lawrie et al. 2013). Based on these observations, we speculate that the codon usage bias, different evolutionary constraint, among others, may cause the pattern we observed.
Domains without SNPs
Annotation of domains without any variation
Frequency of occurrences
Category IDa, category nameb
GO:0005185, neurohypophyseal hormone activity
GO:0003723, RNA binding
GO:0003735, structural constituent of ribosome
GO:0005133, interferon-gamma receptor binding
GO:0003735, structural constituent of ribosome
GO:0003899, DNA-directed RNA polymerase activity
GO:0003677, DNA binding
GO:0003735, structural constituent of ribosome
GO:0003723, RNA binding
GO:0000287, magnesium ion binding
GO:0008897, holo-[acyl-carrier-protein] synthase activity
GO:0003676, nucleic acid binding
GO:0003700, sequence-specific DNA binding transcription factor activity
GO:0003677, DNA binding
GO:0003713, transcription coactivator activity
GO:0004129, cytochrome-c oxidase activity
GO:0005524, ATP binding
GO:0004812, aminoacyl-tRNA ligase activity
GO:0005179, hormone activity
GO:0042030, ATPase inhibitor activity
GO:0005246, calcium channel regulator activity
GO:0004057, arginyltransferase activity
GO:0030234, enzyme regulator activity
GO:0008270, zinc ion binding
GO:0005515, protein binding
GO:0051539, 4 iron, 4 sulfur cluster binding
GO:0004519, endonuclease activity
GO:0003910, DNA ligase (ATP) activity
GO:0043130, ubiquitin binding
GO:0048040, UDP-glucuronate decarboxylase activity
GO:0046983, protein dimerization activity
GO:0003723, RNA binding
To verify the number of domains without any SNPs is statistically significant, we randomly assigned all their N observed SNPs to positions in the human proteins, repeated this random assignment 1000 times (see “Materials and methods”). We obtained two p values: the proportion of times that the number of domains without SNPs is greater or equal 117, and the proportion of times that the average of occurrences of domains without SNPs is higher or equal than the one observed for the original 117 domains. Both of them are 0. These indicate that there are significantly greater domains without SNPs than expected at random, and the domains without SNPs are not rare domains.
In the human genome, there are three sources of genome-wide SNP data sets: the Single Nucleotide Polymorphism Database (dbSNPs) (Sherry et al. 2001), HapMap (Altshuler et al. 2010), and the 1000 Genome Project. Half of the reported SNPs in dbSNPs are only candidate SNPs and are not validated in a population (Musumeci et al. 2010). For HapMap, certain genome loci were selected for sequence analysis, so the variations are biased. The 1000 Genome Project reports the genomes of 1092 individuals from 14 populations using whole-genome and exome sequencing. This is a powerful and cost-effective design for discovering variants (Abecasis et al. 2012). Our analysis is based on data from the 1000 Genome Project, which bolsters the accuracy and comprehensiveness of our investigation. Using this data set, we also observed the relationship between the length of protein-coding sequences and variation.
Spearman’s ρ and p between the number of different MAF SNPs and the length of proteins
Spearman’s ρ, p of rare MAF SNPs
Spearman’s ρ, p of low MAF SNPs
Spearman’s ρ, p of common MAF SNPs
0.83, <2.2 × 10−16
0.65, <2.2 × 10−16
0.43, <2.2 × 10−16
0.82, <2.2 × 10−16
0.70, <2.2 × 10−16
0.53, <2.2 × 10−16
Synonymous mutations do not alter amino acids and are therefore not considered to alter the function of the protein where they occur. Thus, such mutations have long been thought to lack functional effect or evolutionary importance. Recent research has contradicted this notion (Singh et al. 2007; Weatheritt and Babu 2013). In our studies, we found that synonymous density is less frequent in unassigned regions compared to that in human domains. This may be caused by codon usage bias or different evolutionary constraints between on the synonymous unSNPs and on the synonymous doSNPs.
We must note that our results might be affected by the quality of the datasets upon which our analyses are based. First, in 1000 Genomes pilot data, SNPs have been identified within each population, but allele frequency information are applied to all the populations. Second, although deep (50–100×) exome sequencing strategy was taken in 1000 Genomes project, there are only 1092 individuals and may miss coding sites. Third, the classification of domains and unassigned regions are based on PfamA version 27.0.
In summary, protein evolution is crucial for species evolution. Previous studies have focused on whole proteins, while less attention has been paid to differences within a protein. To our knowledge, this is the first study exploring evolution at the protein domain level within species. The results presented here imply that substitutions in domains and synonymous mutations in other unassigned regions must be taken into consideration for coding sequences. This research may help to further understand human protein evolution and disease.
The authors thank two anonymous reviews for their constructive comments. They thank Professor Dengke Niu for his helpful discussion. This work was supported by the National Natural Science Foundation of China (Grant 31171235 and 31571361), the State Key Laboratory of Earth Surface Processes and Resource Ecology, the Fundamental Research Funds for the Central Universities.
Compliance with ethical standards
This work was funded by the National Natural Science Foundation of China (Grant 31171235 and 31571361), the State Key Laboratory of Earth Surface Processes and Resource Ecology, and the Fundamental Research Funds for the Central Universities.
Conflict of interest
The authors declare that they have no conflict of interest.
This article does not contain any studies with human participants performed by any of the authors.
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