Detection and validation of structural variations in bovine whole-genome sequence data
© The Author(s) 2017
Received: 9 August 2016
Accepted: 9 January 2017
Published: 25 January 2017
Several examples of structural variation (SV) affecting phenotypic traits have been reported in cattle. Currently the identification of SV from whole-genome sequence data (WGS) suffers from a high false positive rate. Our aim was to construct a high quality set of SV calls in cattle using WGS data. First, we tested two SV detection programs, Breakdancer and Pindel, and the overlap of these methods, on simulated sequence data to determine their precision and sensitivity. We then identified population SV from WGS of 252 Holstein and 64 Jersey bulls based on the overlapping calls from the two programs. In addition, we validated an overlapped SV set in 28 twice-sequenced Holstein individuals, and in another two validated sets (one for each breed) that were transmitted from sire to son. We also tested whether highly conserved gene sets across eukaryotes and recently expanded gene families in bovine were depleted and enriched, respectively, for SV.
In empirical WGS data, 17,518 SV covering 27.36 Mb were found in the Holstein population and 4285 SV covering 8.74 Mb in the Jersey population, of which 4.62 Mb of SV overlapped between Holsteins and Jerseys. A total of 11,534 candidate SV covering 5.64 Mb were validated in the 28 twice-sequenced individuals, while 3.49 and 0.67 Mb of SV were validated from Holstein and Jersey sire-son transmission, respectively. Only eight of 237 core eukaryotic genes had at least a 50-bp overlap with an SV from our validated sets, suggesting that conserved genes are depleted for SV (p < 0.05). In addition, we observed that recently expanded gene families were significantly more associated with SV than other genes. Long interspersed nuclear elements-1 were enriched for deletions when compared to the rest of the genome (p = 0.0035).
We reported SV from 252 Holstein and 64 Jersey individuals. A considerable proportion of Jersey population SV (53.5%) were also found in Holstein. In contrast, about 76.90% sire-son transmission validated SV were present in Jerseys and Holsteins. The enrichment of SV in expanding gene families suggests that SV can be a source of genetic variation for evolution.
There are several categories of genomic variations within a species. Single nucleotide polymorphisms (SNPs) are the most frequent and have been widely used in genome-wide association and genomic prediction. In the last decade, several studies have detected and verified the existence of large DNA segment mutations in the human genome  and many other species [2–4]. These segment mutations are now described as structural variations (SV), which refer to segments of 1 kilobases (kb) to several megabases (Mb) of deletions, duplications, inversions and translocations in a re-sequenced genome compared to a reference genome [5, 6]. Copy number variations (CNV) are a subset of structural variations including deletions and duplications. As sequencing technology has improved, the resolution of the detection of structural variations has also improved, thus, smaller SV events can now be identified .
In humans, the first paper that reported widespread CNV included evidence that this type of variation plays a significant role in population heritable variation . SV have also been shown to be significantly associated with complex diseases, especially schizophrenia , rheumatoid arthritis  and systemic lupus erythematosus . In cattle, several studies have indicated that SV that span gene coding regions can affect a range of traits . In Angus cattle, 297 CNV were found to be associated with parasite resistance or susceptibility and to overlap with 437 genes enriched for immune function . Recently, a 660-kb deletion was found to be associated with fertility and milk production in Nordic red cattle . In addition, an 80-kb duplication on BTA1 (BTA for Bos taurus chromosome) was shown to be associated with the polled phenotype in Friesian origin cattle, and a 202-bp complex insertion-deletion on BTA21 with polled in Celtic origin cattle [14, 15].
It is plausible that SV are responsible for variation in many complex traits in cattle, including milk production, fertility, and other traits. To test this hypothesis on a genome-wide scale, a genome-wide catalogue of SV in bovine populations must first be developed. Various types of genomic data can be used to detect SV. SNP array data has enabled a rapid high-throughput approach for identifying genetic variants, using signal intensity information. The CNV detection program PennCNV implements a hidden Markov model (HMM) to detect loss or gain of CNV status from SNP arrays . The results are relatively reliable and thus this program has been used in many CNV studies. However, due to limited SNP array density and the high minor allele frequency of these SNPs, identification of smaller and rare CNV, and determination of exact breakpoints are limited. In addition, SNP chip methods cannot capture balanced SV including inversions and translocations.
Massive parallel sequencing or whole-genome sequence data (WGS) is becoming increasingly cost-effective in genotyping studies. WGS data can potentially be used to recover the whole spectrum of SV. Paired-end mapping (PEM), split read (SR), read depth (RD), and de novo assembly are the current four basic strategies used to detect SV from sequence data . Breakdancer  uses PEM information, while Pindel  uses SR information. Both strategies have been applied to cancer genome projects and the 1000 genomes project in humans [20, 21]. No single method is able to detect the entire spectrum of SV events, so studies usually combine two or three strategies to achieve better results depending on the research targets .
Here, we first tested the precision and sensitivity of Breakdancer, Pindel, and a combined strategy to detect SV in simulated bovine WGS data. To expand the catalogue of SV in cattle, with a very high level of confidence, we then detected SV in WGS data from Holstein and Jersey populations using a combination of Breakdancer and Pindel, as well as two novel validation strategies including sire-son transmission and evidence from animals sequenced several times. The overlap of validated SV with those detected by PennCNV was also investigated. Furthermore, we also tested the hypothesis that gene regions that are highly conserved between species should have fewer SV than in less conserved gene regions, while recently expanded gene families in bovine could have more SV than other regions.
We used Breakdancer (version 1.4.4) and Pindel (version 0.2.5a3) programs to detect SV. Since Pindel is not applicable for intra-chromosome duplications (i.e. CTX in Breakdancer), we only used deletions (DEL), insertions (INS), inversions (INV) and tandem duplications (DUP) for comparisons between the two programs.
To gain insight into the power and precision of Pindel and Breakdancer to detect SV, we used a simulated dataset that was generated from simulated short reads based on BTA29 extracted from the UMD3.1 bovine genome reference assembly. Rearranged chromosomes with 300 randomly inserted SV (100 SV each for deletions, inversions and duplications) were generated with the R package RSVSim . Simulation of short reads was achieved by using wgsim .
Parameters for the simulation scenarios
Base error rate
SNP% in SV
SNP% in SV
Number of SV
100 × 3
100 × 3
100 × 3
100 × 3
100 × 3
100 × 3
SD of insert size
Base error rate
For each simulation set, the insert size was set at 500 bp with a 50-bp standard deviation and the indel rate was set at 0.01. In the first two scenarios, in which all SV were either homozygous or heterozygous (HOM, HET), no SV fell into repetitive regions and no SNPs appeared within SV events. For HOM SV, 100 randomly distributed deletions, inversions and duplications, respectively, were inserted into BTA29 to form a rearranged BTA29. Fifty replicate sets of rearranged BTA29 were generated and, based on each rearranged chromosome, 50 replicates of short reads were then simulated with ~tenfold sequence coverage. For HET SV, both the number of SV and coverage per SV were halved to 50 and 5, respectively. One hundred rearranged BTA29 chromosomes were then generated and reads that were simulated from two different rearranged BTA29 chromosomes were pooled together to simulate heterozygous SV and tenfold coverage (see Additional file 1: Figure S1). The third scenario varied the base error rate from 0.001 to 0.025, while for other scenarios the base error rate was set at 0.01. A fourth scenario investigated an extreme case where all SV were in repetitive regions of the genome, i.e. 300 repetitive regions were randomly selected based on the UCSC genome browser database and simulated SV were inserted only into those chosen regions. A fifth scenario considered a range of rates (0.01 to 0.25) of SNPs that occur in SV (number of SNPs divided by the total SV length in bp). Finally, in an attempt to more closely match the real genome structure, we incorporated all the above factors together in one scenario (MIX): all SV were heterozygous with a proportion of SNPs within SV of 0.01, and half of these SV were in repetitive regions. This also included a SNP polymorphism rate calculated from the Holstein animals in the 1000 Bull Genomes project (0.008 per locus).
The precision and sensitivity of SV calls of Breakdancer and Pindel were then compared. Precision was defined as the number of true positives divided by the number of total calls made by the program. Sensitivity equalled the number of true positives divided by the number of actual variants in the simulations. A true positive SV was defined as an SV call that was detected by the program with at least 50% overlap with a simulated SV.
Genome coverage read depth and insert size of SV for the WGS datasets
Sequence population SV calls
We pooled the Holstein (not including twice-sequenced individuals) and Jersey populations and investigated the SV distribution for the two breeds. For each population, we first ran Breakdancer and Pindel to generate raw SV calls for each SV type (deletion, insertion, inversion and duplication). Picard tools “CollectInsertSizeMetrics.jar” was used to calculate the mean insert size for each bam file. The default parameters were used for both programs. However, we enforced an initial threshold of a minimum of four supporting read pairs and observations of a SV in at least two individuals to classify higher quality SV. SV that spanned chromosome gaps in the reference assembly were also filtered out. We applied an overlap size of at least 25 bp between the two programs to retain smaller SV. We only included SV that were detected by both Breakdancer and Pindel and considered that these overlapping SV had a higher confidence level. The overlapping SV sets were named POP_HOL and POP_JER for Holstein and Jersey populations, respectively. We performed a t test to check whether the overlap of the proportion of genome covered with SV by the two programs was significantly different than expected by chance. For each chromosome, the expected overlap proportion was calculated as the proportion of the genome covered by Breakdancer SV calls multiplied by the proportion of Pindel SV calls. These were contrasted with the actual overlapping genome region across 30 chromosomes (n = 30) and for each SV type separately. A flowchart of the pipeline is in Additional file 1: Figure S2.
Validation of SV
In the Holstein population, 28 individuals were sequenced twice. In theory, for each individual the two independent sequences should support exactly the same SV calls. However, due to random distribution of sequence reads, assembly errors and different depths of coverage, the two generated sequences are not identical, and, thus, programs report different SV. We generated a set of high confidence SV by only reporting the SV that were detected in both sequences (TWICE_SEQ). Furthermore, we also combined the bam files from 21 of the 28 twice-sequenced individuals for which insert sizes did not differ by more than 5 bp (MERGE). The number of SV from the MERGE set was then checked for overlap with the TWICE_SEQ set.
In addition, there were 68 Holstein and 33 Jersey sire-son pairs in the dataset, of which some sons shared the same sire. As SV should be inherited (100% of the time if the sire is homozygous and 50% of the time if the sire is heterozygous for an SV), we only reported SV that were inherited from sire to offspring in at least one pair. The resulting SV sets were named as FAM_HOL and FAM_JER for Holstein and Jersey sire-son pairs, respectively. The two validated sets were further compared between each other and with SV called from SNP chip data. The pipeline for generating validated sets is in Additional file 1: Figures S3 and S4.
Detection of CNV from SNP chip genotype data
One hundred and twenty-eight Holstein and 170 Jersey cattle (the majority of these animals were in the sequenced set as well) were genotyped with the bovine 800 K HD SNP chip. Their converted Log R ratios (LRR) and B allele frequencies (BAF) were used to call SV with PennCNV. Individuals with a standard deviation of LRR higher than 0.35 and BAF higher than 0.2 were discarded, as suggested by Wang et al. . One hundred and twenty-five Holstein and 166 Jersey were retained after this filtering step. The genomic content (GC) model, which incorporates information on GC percentage around each SNP, was used to improve CNV calls. SNP chip methods cannot detect inversions and therefore we excluded inversion events when comparing PennCNV called CNV to validated sets from sequence data.
To test the hypothesis that SV and CNV are less likely in genes that are highly conserved across species, 248 core eukaryotic genes (CEG) were selected  that were likely to be present in a small number of paralogs in a wide range of species. We downloaded the protein file (fasta format) and used the BLAST program  to detect the most similar proteins and genes in cattle. The search results were further converted into coding nucleotides in bed format with chromosome, strand, start and end position that can be overlapped with our validated SV sets. We required that a minimum of 50 bp of the gene overlapped with the validated SV for the gene to be reported. A Chi squared test (χ 2 = ∑ (E – O)2/E, where E is the expected number of genes assuming that conserved genes and SV are independent and O is the observed number of genes (i.e. conserved or non-conserved, and overlapping or non-overlapping with SV), was performed to test whether these conserved genes contain less SV than expected by chance, with all the other reference genes across the genome downloaded from the UCSC genome browser.
Structural variants in expanded gene families
Gene families are sets of genes that originated from a common ancestor and formed by gene duplication . CNV are considered as a major source of variation for gene family evolution and expansion . First, we searched the literature for expanded gene families in the bovine genome and found five reported expanded gene families: pregnancy-associated glycoprotein , prolactin (PRP) , bovine beta-defensin (DEFB) , cathelicidin (CATHL)  and NK-lysin , with the DEFB family containing four clusters (clusters A to D referring to BTA8, 13, 23 and 27, respectively). We retrieved the coding sequences for these genes from the UCSC genome browser and searched for SV in these regions. We also performed Chi squared tests for these gene families to test whether they contain more SV than expected by chance, as for the conserved genes above.
Some gene family expansions are due to retrotransposons . Long interspersed nuclear elements (LINEs) are abundant retrotransposons in mammals. Although 99.9% of LINEs are not able to mobilize , one subgroup of LINEs, L1, is the only element that is still active in mammalian genomes . L1-mediated retrotransposon events can lead to various structural variations and diseases . We hypothesised that L1 elements were involved with more SV than the other regions that were not under selective constraint (i.e. outside of exons). The L1 regions were retrieved from the UCSC genome browser and were compared with the validated SV sets to check how many SV fall into these regions. We applied a t test to compare the proportion of regions that are affected by SV between the L1 and other regions (excluding exons and L1) in the genome.
In the simulated data, both Breakdancer and Pindel detected similar numbers of homozygous duplications (see Additional file 3: Table S2) and a high proportion of these were true positives. Breakdancer reported more deletions and many more inversions than Pindel. Breakdancer detected a similar proportion of heterozygous and homozygous SV, whereas Pindel detected fewer heterozygous SV than homozygous SV, and the proportion of deletions detected was almost halved for heterozygous SV (see Additional file 3: Table S2).
We attempted to identify situations in which the SV detection programs performed less well than in the ideal conditions simulated above.
Figure 1 shows the precision and sensitivity for each simulation scenario. When data were simulated with higher per base call error rates, we did not observe large decreases in precision. However, when low-complexity regions were simulated, the average precision of SV detection dropped by 19.04, 61.27 and 7.98% when detecting deletions, inversions and duplications, respectively, by Breakdancer, while Pindel had a 8% drop in precision for detecting duplications (see Additional file 3: Table S3). Another more extreme simulation investigated a per locus SNP rate in SV higher than 0.2, in which the precision for detecting deletions with Pindel dramatically fell to 46%. In the MIX scenario (SNP% = 0.01, SNP rate = 0.008 and 50% SV in repetitive regions), we observed a relatively low precision for deletions and a much lower precision for inversions when using Breakdancer. While the precision and sensitivity of SV detection in the simulated data were higher than those that are likely in real studies (in spite of our best efforts to simulate a realistic sequence), the results do demonstrate that the combination of the two programs (Breakdancer and Pindel) yields higher precision, but lower sensitivities, than either program alone under different situations. Therefore, we concluded that the combined approach yielded higher confidence SV calls, which supported our validation strategy in empirical data.
Population SV calls
Number and length of genome regions covered by SV detected in the Holstein and Jersey sets by Breakdancer and Pindel
SV covered region (Mb)
Number and length of genome regions covered by SV detected in the Holstein and Jersey sets and the three validated sets, and in the overlapped set between Holstein and Jersey
Final SV output set
SV covered region (Mb)
Overlap between POP_HOL and POP_JER
Overlap between FAM_HOL and FAM_JER
Validated SV calls
Given the rates of false positives from both Breakdancer and Pindel, only validated SV should be considered further. Based on the overlapped calls from Breakdancer and Pindel, we generated three sets of validated SV calls: twice-sequenced Holstein animals (TWICE_SEQ), and a set of Holstein (FAM_HOL) as well as a set of Jersey (FAM_JER) SV that, as we demonstrated, had Mendelian inheritance (passed from sire to son). Summary statistics for these sets are in Table 4. In the TWICE_SEQ set, most of the SV were detected in both whole-genome sequences, however, some individuals showed large discrepancies between the two sequences (see Additional file 3: Table S5). A total of 5.64 Mb of SV were validated in TWICE_SEQ, while 3.49 Mb and 0.67 Mb of SV were validated in FAM_HOL and FAM_JER. When comparing the SV between FAM sets, 76.90% of the SV that were confirmed in Jersey were also confirmed in Holstein sire-son pairs. Eighty-two percent of the SV were found in both the TWICE_SEQ and the FAM_HOL set. This result suggested fewer false positives and thus higher confidence SV with either validated set compared to non-validated population calls. Figure 2 demonstrates that the size distribution of SV was similar across validated sets. Most deletions and insertions were less than 100 bp (as the maximum size of an insertion is determined by insert size); the size of a large number of inversions was around 900 bp, while that of duplications was around 350 bp. For inversions in FAM_JER, there were two small peaks at 5 kb and 10 kb, respectively. When examining the sires with multiple sons, about 80 kb of the deletions and 90 kb of the duplications on BTA1 were shared in Holstein and 27 kb of the inversions on BTA11 and 16 kb of the duplications on BTA14 were shared in Jersey, which suggests that these regions could be common CNV regions to both breeds.
Comparison of the TWICE_SEQ and MERGE sets for 21 twice-sequenced individuals
The 800 K SNP chip data results from PennCNV indicated a total of 2224 CNV covering 250.5 Mb in Holstein (227 Mb deletions and 23.3 Mb insertions) and 2976 CNV covering 357.4 Mb in Jersey (333 Mb deletions and 24.3 Mb insertions). Since the resolution of the SNP platform is limited, PennCNV cannot detect smaller SV. Therefore, we only compared the PennCNV calls with SV that were larger than 5 kb and detected from the sequence data. As a result, 12.33% of the deletions and 11.59% of the duplications in the validated sets were also found in the Holstein PennCNV analysis, while 14.95% of the deletions and none of the duplications overlapped in Jersey.
The location and length of all validated SV call sets that were pooled and merged across all validations are in Additional file 4: Table S6. Note that INV calls should be treated with some caution, since false INV events can arise from tandem duplications. For example, if one read mapped to one unit and its paired read mapped to another highly similar neighbouring unit, this can be difficult to identify.
Test on conserved genes
Structural variation found in a set of genes that are highly conserved across eukaryotes
Chi squares and p values for the test on conserved genes
Expanded gene families
Expanded gene families in the bovine genome with structural variations
Chi squares and p values for expanded gene families analysis
DEFB cluster B
Other refseq genes
DEFB cluster D
Other refseq genes
Proportion of structural variants in LINE regions, compared with the genome as a whole and other regions
t test p value
First, we detected bovine SV using a stringent pipeline that accepted SV only when there was support from both split read and pair end mapping information. In addition, this overlapping set obtained from combining Breakdancer and Pindel was subjected to two further validations, i.e. SV had to occur (1) in both aligned sequences of animals that were independently sequenced twice, and (2) in inherited sire-son pairs. We found that a large number of SV was shared by Holstein and Jersey populations (53.5% of the SV found in the Jersey genome were also found in the Holstein genome), which suggests that there are some common SV among cattle breeds. Ideally, we should have performed molecular validations to further test our approach. However, this was beyond the scope of our study.
The proportion of the genome displaying SV, which we found in this study, is lower than that reported in humans. In the human 1000 genome pilot phase project, population-scale CNV mapping with 185 individuals revealed a total of 22,025 deletions and 6000 additional SV . Recently, the human 1000 genome project released phase III integrated SV data. A total of 330.3 Mb of CNV gains (duplications) and 350.2 Mb of CNV losses (deletions) were reported, with 3.63 Mb inversions, 5.6 kb small insertions and 1.54 Mb indels. The fact that, in cattle, we identified a lower proportion of the genome involved in SV may reflect the stringent filters, which we adopted, and the smaller number of total sequence reads in our data set, rather than species differences.
There is some overlap between our SV set and that reported in other bovine SV studies. Hou et al.  reported 3438 CNV regions (CNVR) that cover 146.9 Mb on the UMD 3.1 assembly from 630 cattle of 27 breeds using BovineHD BeadChip information, of which 1360 were unique to only one sample. Thirty-six percent of the identified variable sequence space were also reported in their previous study . Compared to our SNP chip results, we found 1295 CNVR that covered 53.2 Mb and overlapped with the Hou et al.  set, from which 774 of the 2135 CNVR (33.4 Mb/243.9 Mb, ~ 13.7%) and 1023 of the 2833 CNVR (42 Mb/346.3 Mb, 12.13%) were also found in the Holstein and Jersey sets, respectively. We also found that about 36% of the CNVR reported by Hou et al. overlapped with our genome sequence set. Jiang et al.  reported 358 CNVR that covered 34.45 Mb of the 29 bovine autosomes using the BovineHD BeadChip on 96 Chinese Holstein cattle. Two hundred and eighty of the 358 (78.2%) CNVR that covered 21.33 Mb were also confirmed by our SNP chip results. Several comparative genomic hybridization array (array-CGH) based studies have reported CNV. Liu et al.  reported CNV that spanned 28.1 Mb of the genome from 90 animals using array-CGH and Kijas et al.  reported 51 CNV that spanned about 1.33 Mb of the genome from 10 animals. Since we did not use an array-CGH based method for SV detection, we did not compare our specific SV locations with those reported in these two latter studies.
Among the other sequence-based SV studies, Zhan et al.  reported 8596 SV that covered 6.28 Mb using Breakdancer and 1416 SV that covered 1.15 Mb using Pindel from one Holstein bull, and Bickhart et al.  detected 55.6 Mb of the bovine genome that encompassed SV from five individuals using a RD-based method. Our population SV calls (27.36 Mb in Holstein and 8.64 Mb in Jersey) represent a smaller proportion of the genome, although the sample size was larger in our study. As described in the Method section, this is likely the result of the very stringent pipeline used for SV detection and validation, which has the advantage that SV were called with lower false positive rates, but false negatives undoubtedly do occur.
The comparison between our PennCNV calls and large SV (larger than 5 kb) suggested a low overlapping rate (only 12 to 15%). This low percentage is mainly due to the different spectrums of detection: RP and SR methods are sensitive to small and medium-sized SV because of the limit set on insert size while SNP chip data only capture large SV. One potential better comparison would be to use an RD method such as CNVnator  and jointSLM  that target large SV events and then to compare them with SV from SNP chip data.
Another consideration is that SV detection from WGS data relies on differences with a reference genome, thus the quality of the bovine reference genome assembly is very important. Compared with the human genome, the quality of the bovine genome assembly is lower, which makes it more difficult to detect SV in the bovine genome than in the human genome, and perhaps resulting in a higher rate of false positive SV . Furthermore, the mean coverage of most individuals in our study was not as high as for the human 1000 genome project (20 to 60×), thus limiting the power of the detection methods. With a higher coverage, both the accuracy and sensitivity can be improved and an additional strategy such as the read depth method could be used for SV analysis.
Our simulation results suggested that combining two methods (e.g. Breakdancer and Pindel, paired read mapping information and split read mapping information) can detect higher quality SV calls with less false positives. Although we aimed at mimicking real sequence data in the simulation by considering sequencing and alignment errors and repetitive regions, we do expect more false positives in the empirical than in the simulation data. To minimize miss-calls from low-complexity regions and poorly mapped regions, we also set a threshold in Pindel that allowed a maximum number of supporting reads (twice the genome coverage for deletions, insertions and inversions and four times for duplications) to report an SV event. In the end, pursuing validation in empirical data seemed a better strategy to define a SV set, than further refining simulations.
A potential limitation of our study is that we used alignment (BAM) files that were created with BWA , as provided to the 1000 Bull Genomes project. The project guidelines specify that reads are uniquely mapped and trimmed for base quality, which is likely to reduce the number of SV detected, especially in repetitive regions where unique positions are difficult to define. However, unfiltered raw reads may be associated with higher base and mapping error rates, which could lead to more false positives. Our primary aim was not to identify all possible putative SV, but rather to identify a subset of SV that have a high probability of being true SV.
When we tested the hypothesis that the number of SV spanning genes should be smaller in genes that are highly conserved across species, we found that eight of the 237 CEG were encompassed by SV of at least 50 bp. The Chi squared test results indicated that SV were less common in the regions of genes that are highly conserved across eukaryotes. One of the eight genes, DENR on BTA29, was completely covered by a deletion SV. We further looked into the individuals that harbor this deletion and found that they were all heterozygous deletions.
We also identified several gene families that were expanded in the bovine genome and were associated with SV. Within the beta-defensin gene family, nine of the 34 (26.5%) genes were spanned by different types of SV. In cluster B, both deletions and insertions were located within DEFB122 and DEFB125, two genes that bear a closer similarity to each other than to any other defensin genes in the bovine genome . Interestingly, the expression of DEFB122 differs significantly between Norwegian Red and Holstein cattle; DEFB125 was expressed in the mature bull epididymis and vas deferens, but was absent from immature male and female individuals . In cluster D of the beta-defensin gene family, Bickhart et al.  showed that DEFB and DEFB1 harboured SV and that the copy number of DEFB1 varied between Bos indicus and B. taurus and among Angus, Holstein and Hereford breeds. We also identified SV in the cathelicidin, PAG and PRP gene families, with CATHL2 from the cathelicidin family being entirely encompassed by an SV.
L1-mediated retrotransposons are associated with various forms of SV and with human genetic diseases , which suggests that they may be a major source of genetic structural variation and evolution . In our study, we detected more deletions in the L1 regions than in the other non-exonic regions, whereas there was no significant difference for the three other SV. In general, our findings support the hypothesis that recent expansions of gene families derived from SV/CNV have provided another source of genetic variation during evolution.
Using information from split reads and pair-end mapping, as well as stringent filtering of data from twice-sequenced animals and evidence of sire-son transmissions, we were able to identify a catalogue of higher confidence SV in two bovine breeds (Holstein and Jerseys). A large proportion of the SV were shared between these two breeds, which suggests that at least some SV are common across breeds. We found that SV were depleted in genes that are highly conserved across eukaryotes and enriched in gene families that are expanded in the bovine genome and L1 regions. Three immune-related genes, DEFB, DEFB1 and CATHL2 were completely encompassed by SV, which confirms results from other studies. The set of SV described here could be useful for the identification of potential causative variants in QTL regions . Furthermore, the incorporation of SV genotypes into genomic prediction may increase the accuracy of genome estimated breeding values for some traits and lead to additional genetic gain.
BH and HD designed the study. AC and CR generated, quality controlled, and processed genomic data. LC performed all other analyses. LC, HD and BH wrote the manuscript. All authors read and approved the final manuscript.
The authors are very grateful to all members of the 1000 Bull Genomes Consortium for provision of data.
The authors declare that they have no competing interests.
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