- Open Access
A genome-wide approach to identify genetic loci with a signature of natural selection in the Irish population
© Mattiangeli et al.; licensee BioMed Central Ltd. 2006
Received: 14 February 2006
Accepted: 11 August 2006
Published: 11 August 2006
In this study we present a single population test (Ewens-Waterson) applied in a genomic context to investigate the presence of recent positive selection in the Irish population. The Irish population is an interesting focus for the investigation of recent selection since several lines of evidence suggest that it may have a relatively undisturbed genetic heritage.
We first identified outlier single nucleotide polymorphisms (SNPs), from previously published genome-wide data, with high FST branch specification in a European-American population. Eight of these were chosen for further analysis. Evidence for selective history was assessed using the Ewens-Watterson's statistic calculated using Irish genotypes of microsatellites flanking the eight outlier SNPs. Evidence suggestive of selection was detected in three of these by comparison with a population-specific genome-wide empirical distribution of the Ewens-Watterson's statistic.
The cystic fibrosis gene, a disease that has a world maximum frequency in Ireland, was among the genes showing evidence of selection. In addition to the demonstrated utility in detecting a signature of natural selection, this approach has the particular advantage of speed. It also illustrates concordance between results drawn from alternative methods implemented in different populations.
Ireland is an island on the western edge of Europe and genetic evidence suggests that its population history may have been relatively (but not absolutely) undisturbed by secondary migrations [1, 2]. This genetic heritage could mean that population genetic signals, such as signatures of recent selection, are more readily detectable in the Irish than in other European populations. Furthermore, Ireland has world frequency extremes (or near extremes) for many variants that are suspected of having undergone selection, including disease-related genes, for example: the cystic fibrosis locus, CFTR [3, 4]; the ABO blood group and the rhesus blood factor ; GALT, associated with galactosemia ; HFE, associated with haemochromatosis ; and PKU, associated with phenyketonuria .
The human genome sequence has provided a resource with enormous medical potential. However, we are as yet ignorant of the majority of genes that are medically important, especially with reference to common diseases, and the variations within those genes that matter. Knowledge of past selection may inform on these key points.
Inference of selection from population genetics
One way to infer evidence of past selection is to compare variation in allele frequency at different loci among different populations. This assumes that geographically variable selective forces favor different variants in different regions. Hence, between-population allele frequency differences may be more extreme in genome portions harboring such variants. An established approach to detecting such genome regions is that of comparing FST values among loci; FST provides an estimate of how much genetic variability partitions between, rather than within, populations.
A particularly promising approach is that of population genomics. Here, the testing of large numbers of loci enables the compiling of an empirical distribution for a summary statistic, such as FST, from which outlying values may be identified as biologically interesting [9, 10]. An empirical approach may confer an additional level of rigor as model-based statistical tests may be sensitive to demographic effects that can produce allele frequency patterns similar to those seen under the presence of selection [11–16]. Importantly, general population demographic history will affect the whole genome but selection will only act on specific loci and these will show unusual deviation from genomic patterns. Human population-specific skews in these distributions have been previously demonstrated. For example, Tajima's D values in humans tend to be skewed towards negative values and this can be attributed to population expansion that occurred to humans post migration from Africa .
In an early genome-level analysis, analyzed 26,530 single nucleotide polymorphisms (SNPs) from 'The SNP Consortium' (TSC) allele frequency project in three populations (African-American, East Asian and European-American). From this three-way comparison, they identified 174 genes associated with SNPs whose extreme deviations in FST values suggested histories of selection. Interestingly, two of these had been implicated in previous studies but another 18 were putative bioinformatically predicted candidate genes. The markers used in this work had been initially discovered by assaying a small number of chromosomes, leading to possible bias toward more common polymorphisms. It should also be noted that these and other results from genome scans are subject to problems arising from multiple testing and the 'winners curse' phenomenon . Therefore, there is a clear and acknowledged need for follow-up analyses to verify the preliminary signatures of selection within this first generation selection map of the human genome.
Here we select, using an analysis of locus-specific branch lengths generated from the data of Akey and colleagues , eight SNPs that are good candidates to have undergone selection within European populations. We identify microsatellite markers flanking these loci, and genotype these in an Irish population sample that has previously been genotyped at 372 micrsosatellites throughout the whole genome. This allows a comparison between our test markers and an empirical distribution of the Ewans-Watterson statistic, a summary of within-population allele frequency spectra that is a test for selection. This demonstrates that seven of the SNPs are in the proximity of microsatellite markers with extreme frequency spectra, allowing stronger inference of selective history in north-western Europe at three biologically interesting genes.
Locus specific branch length analysis
Microsatellite diversity at proximal markers
SNPs, genes and microsatellites analysed in this study
Microsatellite distance from SNP (kb)
LRRC7 (leucine rich repeat 7)
CFTR (cystic fibrosis transmembrane conductance regulator)
TOX (thymus high mobility group box protein)
SYT9 (synaptotagmin IX)
PKCη (protein kinase C, eta)
TPSG1 (γ-triptase 1)
p = 0.04
32 kb upstream from the
Two microsatellites proved impossible to genotype due to poor amplification and/or high levels of stuttering. All but one of the microsatellites genotyped did not deviate significantly from Hardy-Weinberg expectations (1 result of p = 0.04 in 15 tests; Table 1), indicating a population in equilibrium and supporting genotyping accuracy .
All microsatellites flanking the same SNP (Table 1) were tested for linkage disequilibrium. With the exception of microsatellites TPSG-1 versus TPSG-2, IVS8CA versus IVS17bTA and IVS17bTA versus CFTR-3, all the other linked markers showed significant values (CFTR-3 versus IVS8CA, p < 0.001; TOX-1 versus TOX-2, p = 0.0017; ng-1 versus ng-2, p = 0.045; SYT9-1 versus SYT9-2, p = 0.015; PRKCH-1 versus PRKCH-2, p < 0.001)
Statistical tests to identify the signature of selection
In the present analysis putative signatures of selection were assessed in two different ways. Firstly, all the genotypes from the microsatellites flanking the eight outlier SNPs were used for a single population statistical test based on simulated values; a development of the Ewens-Watterson test implemented using the program BOTTLENECK. . Secondly, divergences from the heterozygosity values expected under Ewens-Watterson were assessed against an empirical distribution of the same statistic calculated from 372 microsatellites, spread through the entire genome, genotyped on the same panel of individuals.
According to Ewens , under neutrality an expected configuration of allele counts can be calculated from the sample size and the observed number of alleles. Subsequently, a test (Ewens-Watterson) that compares the observed and expected allele configuration to determine departure from neutrality was developed . Changes in allele proportions can be an indication of selection pressure. The differences in allele frequency spectra between that expected under neutrality and that observed can be quantified by the difference between observed gene diversity (equivalent to the Hardy-Weinberg expected heterozygosity) and expected Ewens-Watterson heterozygosity (a DH value) . Each DH value is divided by the standard deviation (sd) of the gene diversity to standardize differences between microsatellite loci (DH/sd) and a significance value is assigned to DH/sd using simulations .
The effects of proximity to coding sequences
We also examined the possibility that the tendency of the microsatellite test markers' DH/sd values to occur in the negative tail of the empirical distribution could be a consequence of bias due to their proximity to coding sequences and, thus, the effects of purifying selection. We constructed a sub-distribution of the empirical null by selecting only those markers that were within genes (introns or exons, n = 174) (Figure 3b). Clearly, a subset of the test markers remain in the tail of this more conservative distribution. A further indication of the neutrality of the gene-associated marker scores from the empirical distribution was that DH/sd values for these microsatellites did not correlate with their distances to the nearest gene (Spearman's rho = 0.08; Pearson correlation = 0.085).
Correlation between divergence and allele frequency spectra
Many methods of assessing non-neutrality using population genetic data are known to be related and thus largely redundant. However, the two employed here belong to two separate approaches: locus-specific FST branch length (LBSL) is based on divergence between populations and DH/sd is an assessment of allele frequency spectra within a single group. To empirically assess the potential complementarity of these approaches, we took a data set composed of 377 microsatellite markers typed in French, Han Chinese and Nigerian Yoruba samples . We calculated two statistics analagous to those we used above: DH/sd in each sample plus the LSBL terminating with the same group. In the European (French) sample the two were negatively correlated (Spearman's Rank correlation: rs = -0.233; p < 0.001). However, LSBL proves a poor predictor of DH/sd; for example, when one examines the top 5% of LSBL score outliers, only 1/19 is also a 5% outlier for DH/sd. Analysis of the rank correlation between LBSL and DH/sd in the Yoruba sample gave a weaker correlation result (rs = -0.155; p < 0.003) and in the Han sample a somewhat stronger correspondence (rs = 0.308; p < 0.001). In the former and the latter, respectively, 3/19 and 5/19 of the top 5% outliers coincided for the two approaches.
We have found population genetic evidence suggestive of a signature of selection at several markers associated with genes in an Irish sample. Specifically, one microsatellite showed an allele frequency spectrum indicative of balancing selection and eight gave spectra that may support a legacy of positive selection. The use of an empirical distribution of the Ewens-Watterson test (DH/sd) to strengthen the assertion of selection and to distinguish its effects from genome-wide imprints of demographic processes confirms that, in this case, the result has not been confounded by demographic processes in the Irish population. In addition to the demonstrated utility in detecting a signature of natural selection, this approach has the particular advantage of speed. While its relative statistical power to detect selective effects, in comparison to standard tests, has yet to be elucidated, it requires considerably less laboratory effort to perform on a genomic scale, especially when compared with tests that require extensive population re-sequence data.
The genes linked to the markers showing outlying Ewens-Watterson values
On the positive tail of the distribution, suggesting a history of balancing selection, there is 1 of 2 microsatellites (TPSG-1; Table 1 and Figure 3) within the TPSG1 (tryptase gamma 1; MIM:*609341) gene with four common alleles ranging in frequency from 27% to 23% (Additional data file 2). Tryptases have been implicated as mediators in the pathogenesis of asthma and other allergic and inflammatory disorders . The suggestion of balancing selection in this gene is consistent with the expression of multiple tryptase isoforms, some of which are allelic variants; a common feature in genes involved in the immune response, for example, as seen in the major histocompatibility complex (MHC) of vertebrates .
Correlation, although limited, between LSBL and the Ewens-Watterson based statistic used here suggests that there is not complete independence between the two approaches, despite their examining different aspects of allele diversity. However, the TPSG1 outlying result is at the opposite tail to that expected under the correlation, giving stronger inference of underlying adaptive biology. Outlying results at the other tail retain a measure of complementarity given that: the correlation is weak and gives a poor empirical correspondence for outliers; the approaches draw on different aspects of population biology; and the results come from a fresh test population. We discuss two such results below.
Two microsatellites, PRKCH-1 and PRKCH-2 (Table 1 and Figure 3), within the gene PKCη (protein kinase C, eta, MIM *605437), show the most extreme negative DH/sd values. Each of these markers has one predominant allele with frequencies of 50% and 70%, respectively (Additional data file 2), consistent with an allelic configuration expected under positive selection. The majority of the other alleles have a frequency of < 10%. This shared signal was despite a distance between the markers of 79 kb (Table 1 and Figure 3); they were also in significant linkage disequilibrium (p < 0.001). PKC family members phosphorylate a wide variety of protein targets, are known to be involved in diverse cellular signaling pathways  and the protein transcribed by PKCη is involved in processes associated with several medical conditions [29–32]. Interestingly, this protein is highly expressed in the epidermis and inhibits UV-induced apoptosis of keratinocytes. It has been suggested that this mechanism prevents the excessive elimination of differentiated epidermic keratinocytes, cells that are involved in defending the skin from chemical stimulation and UV exposure . A variant in this gene may have featured as part of the selected transition to light skin in the populations ancestral to Europe, although corroborating evidence would be required to assert this. Selective histories at genes related to human pigmentation have been inferred previously .
The next outlying marker in the negative tail of the distribution in a known gene is IVS8CA (Figure 3). This marker is associated with the gene CFTR (cystic fibrosis transmembrane conductance regulator; MIM:*602421), which has been well studied as mutations in it cause the autosomal recessive disorder cystic fibrosis (CF). The CFTR gene product functions as a chloride channel and controls the regulation of other transport pathways. It is also a receptor for bacterial pathogens [35, 36]. There have been several hypotheses as to why CF is present at such a high level in Europe, including that of heterozygote advantage, where a single copy of the main western European disease-causing mutation (ΔF508) increases resistance to typhoid . In this study, only one microsatellite, from the three examined in the gene, showed a significant deviation in the Ewens-Watterson test. Interestingly, this was also the closest to the gene region that encodes the receptor for bacterial pathogens (residues 108 to 117) . The results from our study might be from selection acting on this region with an immune response function, but are unlikely to be associated with CF. The frequency of the disease in Ireland is 1/1,461 . Thus, our 72 Irish samples should have about four carriers, a number too low to profoundly influence the test statistic. Interestingly, a recent analysis has stated evidence of recent selection associated with a variation (V470) that is in linkage disequilibrium with haplotypes that are not associated with the disease .
The remaining microsatellites (LRRC, ABCD3-1, SYT9-1), which have significant but less extreme values in the Ewens-Watterson test (PS, Table 1 and Figure 3), are associated with poorly characterized genes. However, they each appear to encode trans-membrane proteins [39–41].
The results presented here provide evidence of a statistically significant deviation (PS) from the expectations of the neutral theory for nine microsatellite markers in the Irish population. Seven of these are associated with six genes, strengthening the likelihood that the elevated FST values shown by some of the SNPs analyzed by previous studies  represent signatures of selection. The CFTR gene is a particularly interesting result given previous discussion of selective history and the global maximum found for the disease allele frequency within Ireland. The simple assay described here provides a means to further validate the presence of recent selection in outlier loci identified in recently published more extensive genome-wide surveys [42, 43].
Materials and methods
Microsatellites were chosen as flanking markers of the eight outlier SNPs. Perfect dinucleotide tandem repeats (according to the definition used in the University of California Santa Cruz Genome Bioinformatics Site ) were identified in the flanking regions of the eight outlier SNPs (Table 1) that were in, or close to, a known gene, using the UC Santa Cruz Genome Assembly (July 2003). Primers (Additional data file 1) were then designed for each microsatellite using the program GeneFisher . All the microsatellite markers were typed using an ABI PRISM 377 DNA sequencer and GENESCAN software (Applied Biosystem, Foster City, California, U.S.A.).
Our sample population was composed of anonymous DNA samples from 72 unrelated Irish individuals that were made available from a previous study on the genetics of bipolar affective disorder , for which participants provided informed consent. The samples were previously genotyped using a commercially available set of microsatellites (ABI PRISM Linkage mapping Set-MD10), distributed throughout the whole genome.
Genotypes at each microsatellite locus were tested for Hardy-Weinberg proportions using GENEPOP . Departure from the expected allele frequency distribution, a potential signature of selection, was tested using the Ewens-Watterson test. The program BOTTLENECK  was used to calculate at each microsatellite locus the expected heterozygosity under neutrality, according to the allelic configuration calculated with Ewens formula . The program also assigned a significance value to DH/sd by completing numerous replicate simulations (PS, Table 1) under a specified mutation model (in this case, stepwise mutation model; 1,000 replicates per locus). A more stringent significant value (PE, Table 1) was also calculated directly from the empirical distribution for each screened microsatellite locus DH/sd value.
Linkage disequilibrium was calculated between linked microsatellite markers using the program ARLEQUIN .
A background genome-wide distribution of DH/sd values for the Irish population was calculated from 372 autosomal microsatellites (ABI-Prism MD-10; the markers on the sex chromosomes were excluded ) typed in the 72 individuals also used in the present study (Figure 3a). The location of each microsatellite from the genome-wide distribution, whether within a gene or not, was determined and consequently a second distribution was generated (Figure 3b). DH/sd values from the microsatellites flanking the outlier SNPs were also interpreted against this second distribution (Figure 3b) to guard against any potential confounding influences, such as the effect of purifying selection for microsatellites within genes. Pearson and Spearman correlations were performed between the distance of microsatellites in base pairs from the closest gene and their DH/sd values.
Additional data files
This material is based on works supported by the Higher Education Authority (HEA), Programme for Research in Third Level Institutions (PRTLI), Cycle 3 - Programme for Human Genomics (PHG), the Dublin Molecular Medicine Centre and Science Foundation Ireland grant No. 02-IN.1-B256. Ross McManus is a Welcome Trust/Health Research Board lecturer. We thank Michael Gill and Ricardo Segurado for providing the Irish DNA samples and the genotypes from the genome-wide screen with the commercially available microsatellites and Brian McEvoy for helpful discussion and proofreading.
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