- Research article
- Open Access
Genome wide linkage disequilibrium and genetic structure in Sicilian dairy sheep breeds
© Mastrangelo et al.; licensee BioMed Central Ltd. 2014
- Received: 30 May 2014
- Accepted: 29 September 2014
- Published: 10 October 2014
The recent availability of sheep genome-wide SNP panels allows providing background information concerning genome structure in domestic animals. The aim of this work was to investigate the patterns of linkage disequilibrium (LD), the genetic diversity and population structure in Valle del Belice, Comisana, and Pinzirita dairy sheep breeds using the Illumina Ovine SNP50K Genotyping array.
Average r 2 between adjacent SNPs across all chromosomes was 0.155 ± 0.204 for Valle del Belice, 0.156 ± 0.208 for Comisana, and 0.128 ± 0.188 for Pinzirita breeds, and some variations in LD value across chromosomes were observed, in particular for Valle del Belice and Comisana breeds. Average values of r 2 estimated for all pairwise combinations of SNPs pooled over all autosomes were 0.058 ± 0.023 for Valle del Belice, 0.056 ± 0.021 for Comisana, and 0.037 ± 0.017 for Pinzirita breeds. The LD declined as a function of distance and average r 2 was lower than the values observed in other sheep breeds. Consistency of results among the several used approaches (Principal component analysis, Bayesian clustering, FST, Neighbor networks) showed that while Valle del Belice and Pinzirita breeds formed a unique cluster, Comisana breed showed the presence of substructure. In Valle del Belice breed, the high level of genetic differentiation within breed, the heterogeneous cluster in Admixture analysis, but at the same time the highest inbreeding coefficient, suggested that the breed had a wide genetic base with inbred individuals belonging to the same flock. The Sicilian breeds were characterized by low genetic differentiation and high level of admixture. Pinzirita breed displayed the highest genetic diversity (He, Ne) whereas the lowest value was found in Valle del Belice breed.
This study has reported for the first time estimates of LD and genetic diversity from a genome-wide perspective in Sicilian dairy sheep breeds. Our results indicate that breeds formed non-overlapping clusters and are clearly separated populations and that Comisana sheep breed does not constitute a homogenous population. The information generated from this study has important implications for the design and applications of association studies as well as for development of conservation and/or selection breeding programs.
- OvineSNP50K BeadChip
- Sicilian sheep breeds
- Linkage disequilibrium
- Genome structure
The application of recently developed genomic technology, such as high-density single nucleotide polymorphism (SNP) arrays, has great potential to increase our understanding on the genetic architecture of complex traits, to improve selection efficiency in domestic animals through genomic selection , and to conduct association studies . However, to optimally plan whole-genome association studies, it is crucial to know the extent of linkage disequilibrium (LD), the non-random association of alleles at different loci in the genome. In fact, the extent of LD is often used to determine the optimal number of markers required for fine mapping of quantitative trait loci (QTL) , for genomic selection , and to understand the evolutionary history of the populations . With this in mind, it is important to quantify the extent of LD within different breeds as this is likely to have an impact on the success of gene mapping experiments . Knowledge concerning the extent of genetic diversity, as the level of inbreeding and population structure is critical for each of these applications . Moreover, effective population size (Ne) is an important parameter for the assessment of genetic diversity within a livestock population and its development over time. If pedigree information is not available, LD analysis might offer an alternative perspective for the estimation of Ne. In local breeds, maintaining genetic variability is an important requirement for animal breeding strategies; this guarantees selection response to productive and adaptive traits improvement, to cope with new environmental conditions, changes in market demands, husbandry practices and disease challenges . Currently, with availability of high-density SNP arrays, genetic diversity can be estimated accurately in the absence of pedigree information .
In Sicily, dairy sheep production represents an important resource for the economy of hilly and mountain areas, in which other economic activities are limited . Nowadays, three native dairy sheep breeds are reared in Sicily: Valle del Belice, Comisana and Pinzirita. These breeds present differences both in morphology and production traits, showing excellent adaptability to local environments. The aim of this work was to investigate these breeds from a genetic perspective, including the analysis of: i) genome-wide levels of LD, ii) genetic diversity and population structure using high-density genotyping arrays.
In the present study, the Illumina OvineSNP50K Genotyping BeadChip was used to characterize LD and to analyze genetic diversity and population structure in Sicilian dairy sheep breeds.
Out of a total of 54,241 SNPs genotyped, 378 were unmapped and 1,450 were located on sex chromosomes. Thus, 52,413 SNPs mapped onto 26 sheep autosomes were used, and after filtering (see Methods), the final number of samples and SNPs were 71 and 44,365 for Valle del Belice, 71 and 44,540 for Comisana, and 77 and 45,451 for Pinzirita sheep breeds. The distribution of SNPs per chromosome and breed was reported in Additional file 1: Table S1.
Linkage Disequilibrium (LD)
Average space (bp), Linkage Disequilibrium ( r 2 ) and standard deviation (s.d.) between adjacent single nucleotide polymorphisms (SNPs) on each chromosome (OAR) in the Sicilian sheep breeds
r2 ± s.d.
r2 ± s.d.
r2 ± s.d.
0.162 ± 0.205
0.161 ± 0.213
0.132 ± 0.190
0.182 ± 0.229
0.189 ± 0.237
0.148 ± 0.208
0.170 ± 0.217
0.172 ± 0.224
0.140 ± 0.198
0.171 ± 0.219
0.164 ± 0.216
0.139 ± 0.200
0.150 ± 0.199
0.154 ± 0.205
0.127 ± 0.188
0.158 ± 0.204
0.165 ± 0.216
0.131 ± 0.188
0.151 ± 0.200
0.158 ± 0.209
0.137 ± 0.194
0.164 ± 0.211
0.155 ± 0.206
0.133 ± 0.192
0.167 ± 0.218
0.170 ± 0.222
0.137 ± 0.196
0.168 ± 0.224
0.179 ± 0.230
0.148 ± 0.217
0.155 ± 0.198
0.155 ± 0.208
0.118 ± 0.177
0.165 ± 0.210
0.157 ± 0.207
0.131 ± 0.190
0.151 ± 0.204
0.170 ± 0.219
0.133 ± 0.197
0.133 ± 0.187
0.134 ± 0.188
0.114 ± 0.182
0.149 ± 0.202
0.153 ± 0.209
0.129 ± 0.189
0.149 ± 0.199
0.157 ± 0.212
0.124 ± 0.184
0.155 ± 0.208
0.152 ± 0.208
0.125 ± 0.191
0.149 ± 0.200
0.156 ± 0.205
0.128 ± 0.191
0.156 ± 0.213
0.167 ± 0.217
0.139 ± 0.201
0.150 ± 0.197
0.138 ± 0.187
0.117 ± 0.168
0.152 ± 0.206
0.151 ± 0.205
0.124 ± 0.175
0.154 ± 0.204
0.155 ± 0.209
0.125 ± 0.192
0.156 ± 0.193
0.140 ± 0.189
0.107 ± 0.164
0.134 ± 0.184
0.134 ± 0.187
0.108 ± 0.168
0.141 ± 0.190
0.142 ± 0.202
0.116 ± 0.183
0.143 ± 0.190
0.137 ± 0.178
0.116 ± 0.171
0.155 ± 0.204
0.156 ± 0.208
0.128 ± 0.188
Genetic diversity and population structure
Principal Component Analysis (PCA), Bayesian model-based clustering algorithm, calculation of FST and Neighbor network were used to visualize and explore the genetic relationships among breeds. Genotypes from seven additional sheep breeds belonging to International Sheep Genomics Consortium (Additional file 3: Table S3) were included in the analysis to place the Sicilian sheep breeds in a global context.
Moreover, some individuals of Comisana breed were positioned near the cluster of Pinzirita breed. The genetic closeness between these two breeds might be explained considering that they are characterized by a common breeding system and geographical husbandry area, which might have led to genetic exchange between them . The relative contribution of SNPs to population assignment was estimated. In fact, high-throughput genotyping tools make it possible to extract interesting genetic information from animal populations that could be applied to identify useful markers for breed allocation, assignment parentage , and for tracing geographic origin of animal products  as meat and mono-breed cheese. Among the 44,610 SNPs common to the three Sicilian breeds, a subset of 119 SNPs was used to evaluate their ability to cluster individuals belonging to the Sicilian sheep breeds. These SNPs were selected considering their informativeness in pair comparisons that means SNPs with the larger allele frequency differences between pairs of breeds were chosen (fixed alleles in one breed and MAF > 0.25 in the other ones). In fact, differences in allele frequency provide the basis for assignment of individuals into discrete populations. PCA using this subset of SNPs showed lack of ability to discriminate among the breeds and the presence of overlapping areas, in particular between Comisana and Pinzirita sheep breeds (Additional file 4: Figure S1). Kijas et al.  revealed that while 96 of the most informative SNPs (higher average allelic richness and lower average private allelic richness) were insufficient, analysis using a panel of 384 markers successfully sorted individuals into groups. Our results may be due to close relationships among Sicilian sheep breeds that are genetically connected among them ,. Therefore, the subset of SNPs was not useful to assign individuals into discrete clusters and it was insufficient and inadequate for authentication purposes.
Genetic differentiation between population pairs measured using F st.
Estimates of genetic diversity indices for Sicilian sheep breeds
MAF ± s.d.
Ho ± s.d.
He ± s.d.
Valle del Belice
0.290 ± 0.003
0.364 ± 0.126
0.379 ± 0.155
0.055 ± 0.150
0.294 ± 0.004
0.382 ± 0.129
0.382 ± 0.114
0.025 ± 0.031
0.301 ± 0.005
0.388 ± 0.122
0.390 ± 0.108
0.016 ± 0.042
Understanding the relationships among and within populations is an important step to establish conservation priorities and strategies. Consistency of results among the several used approaches (PCA, Bayesian clustering, FST, Neighbor networks) supported the robustness of our conclusions.
Estimates of the genetic diversity in Sicilian sheep breeds
The basic genetic diversity indices within breed were used to compare levels of heterogeneity between Sicilian breeds. Overall average MAF was 0.290 ± 0.003 for Valle del Belice, 0.294 ± 0.004 for Comisana, and 0.301 ± 0.005 for Pinzirita sheep breeds (Table 3). These values were in agreement with those reported by Kijas et al.  in a study on genome-wide analysis of the world¿s sheep breeds for the European-derived populations. Moreover, the distribution of MAF of these SNPs was approximately uniform over the genome in all breeds (Additional file 1: Table S1). Pinzirita breed displayed the highest gene diversity (He = 0.390 ± 0.108), whereas the lowest value was found in Valle del Belice breed (He = 0.379 ± 0.155) (Table 3). These genetic diversity estimates can be compared with those reported by other authors for Southern and Mediterranean European sheep breeds . Similar results for genetic diversity (Ho, He, and MAF) were reported for Sarda sheep breed . We obtained some negative values for inbreeding coefficient F, which corresponded to animals with lower homozygosity than the average population. The highest F, calculated for each individual based upon observed and expected heterozygosity, was found in Valle del Belice breed (0.055 ± 0.150), whereas the lowest value in Pinzirita breed (0.016 ± 0.042). In Valle del Belice breed, the high level of genetic differentiation within breed, with individuals spread out on PC1 (Figure 3), and heterogeneous cluster in Admixture analysis (Figure 4), but at the same time the highest inbreeding coefficient (Table 3), suggested that the breed had a wide genetic base with inbred individuals belonging to the same flock. Rosa et al.  in a study on parentage verification of Valle del Belice breed, reported different values of inbreeding per flock that ranged from 0.017 to 0.165. In fact, in Sicilian farming system natural mating is the common practice, the exchange of rams among flocks is quite unusual, and mating with close relatives can be quite frequent; this led to high level of inbreeding. Analogous results for Valle del Belice breed were reported by Tolone et al. . Therefore, the results (high level of genetic differentiation and high inbreeding coefficient) may be explained considering reduced or absent gene flow between different flocks. It should be noted that Valle del Belice was the most homogeneous breed at the lowest K values, according with higher inbreeding and lower heterozygosity. Moreover, the low level of inbreeding and high genetic diversity in Pinzirita sheep breed reflected the short extent of LD. Average values of LD for 1 Mb bins smoothed with a 50 kb step size were used to estimate the effective population size (Ne). In fact, LD is affected by population history and demography, representing an important tool to be applied to genetic population. Effective population size (Ne) is a general indicator of the risk of genetic erosion, contains relevant information for the monitoring of the genetic diversity, and helps to explain how populations evolved . The highest value of Ne, estimated 50 generations ago, was observed for Pinzirita breed (Ne = 685), whereas the lowest one was observed for Valle del Belice breed (Ne = 369) (Table 3). In fact, high Ne is accompanied with high genetic diversity and low values of LD. Moreover, it is important to remind that LD measures, and therefore Ne, are linked with selection intensity and mating systems. Indeed, high selection pressure and the use of artificial insemination are the main reasons for low Ne values. Ciani et al.  in a study on Italian sheep breeds reported similar results of Ne in Sicilia sheep breeds with 638, 571, and 340 individuals for Pinzirita, Comisana, and Valle del Belice breeds, respectively. Moreover, García-Gámez et al.  in Churra sheep breed reported Ne estimated 50 generation ago of 467 individuals. Our results were consistent with those reported for most European sheep breeds  that showed high Ne. Managing the Ne and F provides a general framework to control loss of variability avoiding or alleviating reductions in viability and fertility; i.e., inbreeding depression .
This study reported for the first time estimates of linkage disequilibrium, genetic diversity and population structure from a genome-wide perspective in Sicilian dairy sheep breeds. Knowledge concerning the behavior of LD is important for performing genomic selection and genome wide association analysis. LD declined as a function of distance and average r 2 was lower than value observed in other sheep breeds. Results indicated that Sicilian sheep breeds formed non-overlapping clusters, with low genetic differentiation and high level of admixture, and that the Comisana breed does not constitute a homogenous population. The different approaches (PCA analysis, Bayesian clustering, FST, NeighborNet) used to assess relationships among breeds showed high degree of congruence and supported the robustness of conclusions. Analysis of genetic diversity indicated high genetic variability and low inbreeding. The identification of genetic relationship and gene flow among livestock breeds/populations is important for breeders and conservationists. In order to maintain the existing genetic diversity, breeding strategies aiming at maintaining effective population size, minimizing inbreeding and genetic drift should be implemented for the Sicilian breeds. The information generated from this study can have important implications for the design and applications of association studies as well as for the development of conservation and/or selection breeding programs.
DNA sampling and genotyping
A total of 221 unrelated animals were collected from several farms in different areas of Sicily, to capture a representative sample of within breed genetic diversity, and were used for the analysis.
The procedures involving animal sample collection followed the recommendation of directive 2010/63/EU. Number of animal sampled per flock ranged from 5 to 10. Samples consisted of 72 Valle del Belice, 72 Comisana and 77 Pinzirita individuals. For these sheep breeds, pedigree data were not available. About 10 ml of blood was collected from jugular vein using tubes with EDTA as anticoagulant. Genomic DNA was extracted from buffy coats of nucleated cells using salting out method . The concentration of extracted DNA was assessed with NanoDrop ND-1000 spectrophotometer (NanoDrop Technologies, Wilmington, DE).
All animals were genotyped for 54,241 SNPs, using the Illumina OvineSNP50K Genotyping BeadChip following standard operating procedures recommended by the manufacturer. Genotyping was performed by Dipartimento Scienze Agrarie e Forestali, University of Palermo. Raw signal intensities were converted into genotype calls using the Illumina GenomeStudio Genotyping Module v1.0 software (Illumina Inc., San Diego, CA) by applying a no-call threshold of 0.15. Genotyping data were initially tested for quality using the same software. Markers in each breed were filtered to exclude loci assigned to unmapped contigs. Therefore, only SNPs located on autosomes were considered in further analyses. Moreover, quality control included: Call Frequency (proportion of samples with genotype at each locus) ≥ 0.95, minor allele frequency (MAF) ≥ 0.05, and Hardy-Weinberg Equilibrium (HWE) P-value > 0.001. SNPs that did not satisfy these quality criteria were discarded.
A standard descriptive Linkage Disequilibrium (LD) parameter, the squared correlation coefficient of allele frequencies at pair of loci (r 2 ), was used as measure. Pairwise LD between adjacent SNPs was calculated on each chromosome using PLINK . Moreover, r 2 was estimated for all pairwise combinations of SNPs using LD plot function in Haploview v4.2 software , exporting data to text files. For each chromosome, pairwise r 2 was calculated for SNPs between 0 and 50 Mb apart. To visualize the LD pattern per chromosome, r 2 values were stacked and plotted as a function of inter-marker distance categories. Average r 2 for SNP pairs in each interval was estimated as the arithmetic mean of all r 2 .
Analysis of genetic diversity and population structure among breeds
In order to understand the genetic relationship among Sicilian breeds, we performed different analyses. Genotypes from others 7 sheep breeds belonging to International Sheep Genomics Consortium (Additional file 2: Table S2), were included in these analyses. Genotyping data from Sicilian and other breeds were filtered with the same quality criteria reported above. Unlinked SNPs were selected using -indep option of the PLINK , to reduce the impact of the SNP ascertainment bias phenomenon, with the following parameters: 50 SNPs per window, a shift of 5 SNPs between windows, and a variation inflation factor¿s threshold of 2.
First, the average proportion of alleles shared between animals (A s ) was calculated as IBS2 + 0.5*IBS1/N, where IBS1 and IBS2 are the number of loci that share either one or two alleles identical by state (IBS), respectively, and N is the number of loci tested. Genetic distance (D) was calculated as 1-A s . These values were calculated using PLINK  through the use of commands -cluster and -distance-matrix. PCA of D matrix was performed using the multidimensional scaling (MDS) algorithm of pairwise genetic distance implemented in PLINK . It should be noted that when MDS is applied to D matrix, it is numerically identical to PCA . The graphical representation was depicted using the statistical R software (R Development Core Team) with RColorBrewer package.
Extents of population substructure were evaluated through the model-based clustering algorithm implemented in the software Admixture . The most probable number of populations in the dataset (K) was estimated using the default (5-fold) Admixture¿s cross-validation procedure, by which estimated prediction errors are obtained, for each K value, by adopting a kind of `leave one-out¿ approach. K value that minimizes the estimated prediction errors is then assumed to be the most suitable. Graphical representation was visualized using the statistical R software (R Development Core Team).
Genepop  software was used to estimate population relatedness using pair-wise estimates of FST among all breeds. Neighbor networks were constructed from pair-wise estimates of FST using Splitstree .
Estimates of the genetic diversity in Sicilian sheep breeds
PLINK  was also used to estimate basic genetic diversity indices, including observed and expected heterozygosity (Ho and He, respectively), average MAF and coefficient of inbreeding (F) for Sicilian sheep breeds. Files used for basic diversity indices (Ho, He and F) were pruned in PLINK considering 50 SNPs per windows, a shift of 10 SNPs between windows and variation inflation factor¿s threshold of 1.5. Moreover, effective population sizes (Ne) were calculated as Ne = (1/4c)*(1/ r 2 -1) , where r 2 is the value of LD and c is the marker distance in Morgans between SNPs.
This research was financed by PON02_00451_3133441, CUP: B61C1200076005 funded by MIUR.
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