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Genomic measures of inbreeding in the Norwegian–Swedish Coldblooded Trotter and their associations with known QTL for reproduction and health traits

Genetics Selection Evolution volume 51, Article number: 22 (2019) Cite this article

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Abstract

Background

Since the 1950s, the Norwegian–Swedish Coldblooded trotter (NSCT) has been intensively selected for harness racing performance. As a result, the racing performance of the NSCT has improved remarkably; however, this improved racing performance has also been accompanied by a gradual increase in inbreeding level. Inbreeding in NSCT has historically been monitored by using traditional methods that are based on pedigree analysis, but with recent advancements in genomics, the NSCT industry has shown interest in adopting molecular approaches for the selection and maintenance of this breed. Consequently, the aims of the current study were to estimate genomic-based inbreeding coefficients, i.e. the proportion of runs of homozygosity (ROH), for a sample of NSCT individuals using high-density genotyping array data, and subsequently to compare the resulting rate of genomic-based F (FROH) to that of pedigree-based F (FPED) coefficients within the breed.

Results

A total of 566 raced NSCT were available for analyses. Average FROH ranged from 1.78 to 13.95%. Correlations between FROH and FPED were significant (P < 0.001) and ranged from 0.27 to 0.56, with FPED and FROH from 2000 to 2009 increasing by 1.48 and 3.15%, respectively. Comparisons of ROH between individuals yielded 1403 regions that were present in at least 95% of the sampled horses. The average percentage of a single chromosome covered in ROH ranged from 9.84 to 18.82% with chromosome 31 and 18 showing, respectively, the largest and smallest amount of homozygosity.

Conclusions

Genomic inbreeding coefficients were higher than pedigree inbreeding coefficients with both methods showing a gradual increase in inbreeding level in the NSCT breed between 2000 and 2009. Opportunities exist for the NSCT industry to develop programs that provide breeders with easily interpretable feedback on regions of the genome that are suboptimal from the perspective of genetic merit or that are sensitive to inbreeding within the population. The use of molecular data to identify genomic regions that may contribute to inbreeding depression in the NSCT will likely prove to be a valuable tool for the preservation of its genetic diversity in the long term.

Background

In recent years, there has been a rapid increase in the intensity of selection in many livestock breeding programs with the growing use of elite animals, which ultimately reduces the effective population size (Ne) of some breeds [1,2,3,4,5,6]. Consequently, a small Ne not only reduces genetic variability, but it also increases the effects of inbreeding (F) and genetic drift, and potentially alters the patterns of runs of homozygosity (ROH) in the long term [3,4,5,6,7,8]. While such alterations may not necessarily be of concern for large and highly diverse populations, increased homozygosity at loci with a heterozygous advantage in small native populations reduces furthermore their genetic diversity [7]. Small populations can be particularly vulnerable to inbreeding depression since mating between relatives often decreases individual fitness and can significantly reduce population growth [7, 9]. Moreover, selection programs, while driving favorable alleles to fixation, also allow deleterious alleles to hitchhike along with favorable mutations. In addition to this, more intense selection resulting from combining genomic selection with embryo biotechnologies (e.g. artificial insemination) not only increases rates of genetic gain, but can also increase levels of inbreeding [4, 10].

The Norwegian–Swedish Coldblooded trotter (NSCT) is a domestic breed of horse in Norway and Sweden and is one of the few remaining descendants of the original Nordic coldblooded horse [11]. Since the 1950s, the breed has been intensively selected for harness racing performance with estimated breeding values produced annually since the 1980s [12, 13]. As a result, a remarkable improvement in the racing performance of NSCT has occurred during the last half-century. However, this improved racing performance has also been accompanied by a gradual increase in pedigree-based F levels [14]. Although today NSCT is considered as a relatively healthy breed, the NSCT breeding industry is well aware that increased levels of inbreeding are widely known to increase the expression of recessive deleterious alleles that are linked to genetic diseases. Historically, inbreeding in NSCT has been monitored by using traditional methods that are based on pedigree analysis [14, 15]. While informative, the NSCT industry understands that this classical metric likely underestimates inbreeding within the breed and does not account for the fact that homozygosity at some regions may, in principal, be more or less desirable than at other regions. Two animals that have the same level of inbreeding, may display drastically different unfavorable effects of inbreeding. Even with an extensive and complete pedigree, realized inbreeding levels will likely differ from pedigree-based F levels due to recombination and Mendelian sampling, which is then compounded by the fact that, although the base animals in a pedigree are considered unrelated, they are more often than not, related.

Consequently, the NSCT industry has actively supported a shift towards using genomic data for F calculations in the breed, thus allowing for diversity across the entire genome as well as at specific regions to be evaluated and monitored, and providing not only a more accurate assessment of inbreeding within the breed, but also a much more detailed assessment. As such, the aims of the current study were to provide genomic-based F coefficient estimates (FROH) for a sample of NSCT using a high-density genotyping array and to compare the rate of FROH to that of classical pedigree-based F (FPED) within the breed. Common ROH within the breed were also assessed for overlaps with previously characterized quantitative trait loci (QTL) for health and reproduction traits in the horse, thus providing a first look at genomic regions and traits that may warrant industry intervention in the future.

Methods

Pedigree data

Complete pedigree information on all raced and unraced NSCT were provided by the trotter associations in both Norway and Sweden (Det Norske Travselskap and Svensk Travsport). The pedigree consisted of 112,195 individuals with a median pedigree depth of 15 generations.

Collection of samples

In total, 566 individuals born between 1 January 2000 and 31 December 2009 were selected for this study based on the following criteria: (1) each horse had to have participated in at least one race during its lifetime; this restriction was implemented to allow for a broader use of the data in future analyses that will explore racing performance traits within the breed; (2) hair and/or blood samples had to be readily accessible from the pedigree registration authorities in either Norway (Department of Basic Sciences and Aquatic Medicine, Norwegian University of Life Sciences) or Sweden (Animal Genetics Laboratory, Swedish University of Agricultural Sciences); and (3) a sufficient amount of sample material had to be available to ensure high DNA quality standards.

DNA isolation

DNA was extracted from hair roots using a standard procedure of hair preparation. Briefly, 186 μL of Chelex 100 Resin (Bio-Rad Laboratories, Hercules, CA) and 14 μL of proteinase K (20 mg/mL; Merck KgaA, Darmstadt, Germany) were added to each sample. This mix was incubated at 56 °C for 2 h and proteinase K was inactivated for 10 min at 95 °C. For DNA preparation from blood, DNA from 350-μL blood samples were extracted by using the Qiasymphony instrument and the Qiasymphony DSP DNA mini kit (Qiagen, Hilden, Germany).

Genotyping and quality control

Prior to quality control (QC), the dataset consisted of individuals that were genotyped with the 670K Axiom equine genotyping array (n = 473) and the 670K+ Axiom equine genotyping array (n = 93). Data from the two arrays were subsequently merged based on SNP name, chromosome number and position, which yielded a combined SNP dataset of 611,888 SNPs for 566 horses (SNPs located on chromosomes X and Y were excluded during this process). Then, QC was performed with the PLINK v1.07 software. SNPs were screened based on minor allele frequency (MAF > 0.01), Hardy–Weinberg equilibrium (p > 0.0001), and genotyping rate (> 0.95) with data that did not conform to these criteria and individuals with missing genotypes (> 15%) being removed. Descriptive data for the sample of horses used in the analyses are in Table 1.

Table 1 Descriptive data on the genotyped horses
Full size table

Inbreeding coefficient and runs of homozygosity

Inbreeding coefficients (FPED) were calculated based on the complete pedigree of the breed using the Contribution, Inbreeding (F), Coancestry v1.0 software, which uses a modified algorithm of Sargolzaei et al. [16] to compute inbreeding coefficients that is a fast and accurate tool for FPED calculations.

Inconsistency between ROH-defining criteria in various industries and breeds has been shown to convolute the comparison of studies over time and across population samples [1,2,3,4,5,6, 17,18,19,20,21,22]. Since the criteria to define a ROH continue to remain ambiguous, in our study, we applied a wide range of ROH-defining criteria. Runs of homozygosity were defined in PLINK v1.07 using the sliding windows approach through the homozyg command. The details of each applied threshold setting are in Table S1 (see Additional file 1: Table S1). Genomic inbreeding coefficients (FROH) were estimated for each threshold setting by dividing the summed length of all ROH (per individual) by the length of the genome (2,242,879,462 bp) covered with SNPs. Pearson correlation coefficients between FPED and all FROH were determined using the statistical software R [23]. Paired t-tests between all FROH were also performed.

To better identify population-wide ROH in the breed, custom scripts in R were applied to ROH data from the threshold setting that resulted in the highest correlation between FPED and FROH. These scripts were used to determine which regions of the genome were shared in at least 95% of individuals in the sample [23]. Ultimately, we chose the threshold setting that resulted in the highest correlation between FPED and FROH since not only did it allow the capture of longer ROH that would subsequently be more beneficial when evaluating previously associated QTL, but it also yielded a more conservative estimate of inbreeding within the breed (i.e. an estimate that was more likely to be skewed upwards than downwards). Homozygous regions that were present in at least 95% of the sampled NSCT were then compared to previously reported QTL for reproduction and health traits in the horse (downloaded from the horse QTL database; [24]) using bed file comparisons in BEDOPS [25].

Results

After QC, 360,977 autosomal SNPs and 566 horses were available for analyses. Summary statistics, stratified by country of birth, for FPED are in Table 2. FPED and FROH of Norwegian born horses were higher than those of Swedish born horses, although the highest FPED estimate was found for a Swedish born horse. Median FPED and FROH for the entire cohort of sampled horses, stratified by year, are shown in Fig. 1. Inbreeding in the NSCT population during the 2000–2009 period increased by 1.48 and 3.15% based on FPED and FROH estimates, respectively. Average FROH (%) ranged from 1.78 to 13.95% (see Additional file 1: Table S1). Correlations between FPED and all FROH estimates were significant (P < 0.001) and ranged from 0.27 to 0.56 (see Additional file 2: Table S2) and Fig. 2. The threshold settings as defined below resulted in the highest correlation (R = 0.5629) between FPED and FROH:

  • Size of the sliding window in SNPs: 50 SNPs.

  • Minimum length in kb that a run must have to be called as a ROH: 500.

  • Minimum number of SNPs that a run must have to be called as a ROH: 100.

  • Number of heterozygous SNPs allowed in a ROH: 1.

  • Number of missing calls allowed in a ROH: 5.

  • Pruned for linkage disequilibrium: No.

  • Minimum density to consider a ROH: 1 SNP per 50 kb.

  • Maximum gap allowed between two SNPs: 100 kb.

Table 2 Descriptive results, stratified by country of birth, for average inbreeding coefficient (FPED) and average genomic inbreeding coefficient (FROH) for a sample of raced Norwegian–Swedish Coldblooded trotters born between 1 January 2000 and 31 December 2009
Full size table
Fig. 1
figure1

Median inbreeding levels in the Norwegian–Swedish Coldblooded trotter for horses born between 2000 and 2009. Pop_FPED = pedigree inbreeding for the population (n = 14,547); Sample_FPED = pedigree inbreeding and Sample_FROH = genomic inbreeding for the sample of individuals studied here (n = 566)

Full size image
Fig. 2
figure2

Scatterplot of genomic inbreeding coefficient (FROH) on pedigree inbreeding coefficient (FPED). A = 50snp_500 kb _100snp_1_5; B = 500snp_500 kb _50snp_0_0; C = 50snp_500 kb _100snp_0_1; D = pruned_50snp_500 kb _50snp_1_2 (FORMAT: “sliding window size”_”minimum length (kb) for a run to be called as a ROH”_”minimum number of SNPs for a run to be called as a ROH”_”number of heterozygous SNPs allowed in a ROH”_”number of missing calls allowed in a ROH”)

Full size image

Whereas the above settings resulted in the highest correlation between FPED and FROH, a similarly strong correlation (R = 0.5594) was obtained from the analysis of the pruned data with the same threshold settings except that the minimum number SNPs that a run must have to be called as a ROH was set to 50 SNPs.

Paired t test between all FROH yielded significant differences for most of the FROH threshold settings with only 35 (1.49%) comparisons resulting in no significant difference (see Additional file 3: Table S3). Variations in sliding window size, minimum length in kb and minimum number of SNPs of a run to be called as a ROH clearly altered FROH. The influence of different threshold settings on ROH length and ultimately on FROH is illustrated in Figures S1 and S2 (see Additional file 4: Figure S1 and file 5 Figure S2).

By applying the threshold settings that resulted in the highest correlation between FPED and FROH, the average percentage of a single chromosome covered in ROH ranged from 9.84 to 18.82% (Table 3 Column D). Comparisons of ROH between individuals yielded 1403 regions that were present in at least 95% of the sampled horses (Fig. 3). The length of these regions ranged from 1 bp to 935 kb and overlapped with 35 previously characterized QTL for reproduction and health traits (see Additional file 6: Table S4). A visual representation of overlapping regions is in Fig. 3 with a brief description of each overlapped QTL in Table 4. QTL associated with osteochondrosis accounted for 48.6% of the overlapped QTL with only one of the 35 QTL being associated with fertility (QTL 103450, located on Equus caballus chromosome (ECA) 1).

Table 3 Average percentage of the genome, stratified by chromosome, covered by runs of homozygosity (ROH)
Full size table
Fig. 3
figure3

Location of runs of homozygosity (ROH) across the horse chromosomes tha are common to 95% of the sampled Norwegian–Swedish Coldblooded Trotter population. Regions containing previously characterized QTL for reproduction and health traits are shaded in blue with the shade of blue reflecting the number of QTL in the region (darker as the number of QTL increases)

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Table 4 Previously reported QTL for reproduction and health trait in the horse that overlap with common (> 95% of the sample) ROH regions in the Norwegian–Swedish Coldblooded Trotter
Full size table

Discussion

As expected based on previous studies in other species, the realized FROH in the NSCT population tended to be slightly higher than the FPED estimates [1,2,3,4,5,6,7, 17, 26]. However, in our study, applying strict threshold settings regarding the number of heterozygous SNPs or missing calls allowed in a ROH significantly reduced correlations between FPED and FROH, and drastically altered the ability to capture longer ROH. Since size and frequency of ROH provide evidence for relatedness within and between populations, as well as details on distant and recent ancestry, the ability to capture consistently long ROH is essential for the integration of genomic data into breeding evaluation and preservation protocols for the NSCT breed [4,5,6, 18,19,20]. Shorter ROH (< 1 Mb) tended to be more easily detected regardless of the ROH criteria applied, but longer ROH (> 10 Mb) were more difficult to capture when no heterozygous SNPs or missing calls were allowed in a ROH and at least 100 SNPs were required for a run to be called as a ROH. Although this seems logical since a true ROH does not include any heterozygous SNPs, the high-density equine genotyping array contains more than 670,000 SNPs. Even a genotyping error rate of only 1% could yield 6700 possibly incorrectly genotyped SNPs. Since these incorrectly genotyped SNPs, which are likely attributable to poor sample quality in the current study, tend to be randomly scattered across the entire genome, individual horses can be disproportionately affected simply by chance.

Nevertheless, regardless of the ROH threshold settings applied, FROH in the NSCT breed appears to have steadily increased between 2000 and 2009. While the overall inbreeding level within the breed is slightly underestimated based on classical metrics, the upward trend of inbreeding level revealed by the FPED calculations is clearly supported by the FROH estimates and likely warrants additional exploration by the NSCT breeding industry—particularly in relation to the difference in inbreeding levels between Norwegian born horses and Swedish born horses (Table 2). Furthermore, it is important to note the difference in FPED between the entire population and the sample of individuals used in our study (Fig. 1). Generally speaking, inbreeding is expected to increase by 1% per generation (i.e. 7–9 years in the NSCT). This 1% increase in inbreeding level is clearly seen in the FPED values for the whole population, but is not so obvious for the sample of individuals analyzed here, for which a ~ 1.5% increase was observed instead of the expected 1% over the same time period. Consequently, since the sample of individuals used in our study included only raced horses, although, not certain, it is plausible that the population of raced NSCT is perhaps slightly more inbred than the unraced population.

Although NSCT is not currently considered an at risk breed, it represents unique Norwegian and Swedish genetic resources and is present on the department of agriculture’s list of horse breeds that should be preserved [27]. The NSCT industry has historically been at the forefront regarding the application of emerging genetic technologies in racehorses, and is currently providing FPED estimates, as well as estimated breeding values (EBV) for breeders and owners to use as part of their criteria for determining sire/dam pairing [28, 29]. While this information has undoubtedly proved valuable over the last half-century, genomic information provides the opportunity to manage NSCT breeding more effectively - particularly if it is used to produce genomic EBV. In addition, the use of genomic information to determine both inbreeding levels and relationships between individuals is also likely to have a knock-on effect on performance, increasing the accuracy of the industry’s current EBV and therefore increasing the industry’s ability to improve the performance and health of their horses.

As with other species and breeds, opportunities exist for the NSCT industry to develop software programs that provide breeders with easily interpretable feedback on regions of the genome that are suboptimal from the perspective of genetic merit or that are sensitive to inbreeding within the population. Overall, 1403 common ROH regions were identified within the sample of raced horses used here. There were few overlaps with known QTL for health and reproduction traits, which indicates that perhaps only a small percentage of these regions may warrant concern, at this time [24]. Whereas multiple ROH regions (n = 17) contained QTL that are associated with osteochondrosis (OC) [30,31,32,33], it is possible that homozygosity in these regions may be optimal rather than detrimental when one considers the widely heralded robustness of the breed and that only raced horses were evaluated in our study. It is likely that both the draught horse origins of NSCT and the breeding industry’s emphasis on continued production of robust, tractable horses through artificial selection, have resulted in the breed displaying a strong resistance to the development of OC with increasing homozygosity in specific areas of the genome over time. A similar observation can also be made for the common ROH that overlap with QTL associated with recurrent exertional rhabdomyolysis (RER), which is another condition rarely seen in NSCT [34]. However, additional research is required to confirm this.

Increased inbreeding within a population also tends to impact fertility traits unfavorably; however, only one of the common ROH regions overlapped with a known QTL related to reproduction [35], which suggests that, at present, poor fertility may not be a major concern in the NSCT breed. Nevertheless, it is strongly recommended that future genomic studies in this breed should consider the inclusion of data on fertility traits, since it will likely prove to be highly beneficial in subsequent efforts to preserve the breed’s genetic variability in the long term [5, 36].

Conclusions

In the current study, both FPED and FROH were calculated for a sample of raced NSCT with FROH resulting in higher inbreeding coefficients, and both methods showing a gradual increase in inbreeding between 2000 and 2009. Stricter ROH threshold criteria regarding the number of heterozygous SNPs and missing calls allowed in a ROH significantly reduced correlations between FPED and FROH and noticeably altered the chances of capturing long ROH. While the exact reasons behind this decrease in correlations are not known with certainty, the established associations between classical F estimates and recent inbreeding within a pedigree (characterized by long ROH) in other species provide some insight. Since retaining genetic variation is important to allow populations to adapt to changing environments, the integration of genomic data into their EBV and the use of molecular data to identify both genomic regions contributing to inbreeding depression and pedigree errors will likely prove invaluable as the NSCT industry moves forward in its conservation and selection efforts.

Availability of data and materials

The data that support the findings of this study are available from the Swedish Trotter Association (Stockholm, Sweden) and the Norwegian Trotter Association (Oslo, Norway), but restrictions apply to the availability of these data, which were used under license for the current study, and so are not publicly available. However, data are available from the authors upon reasonable request and with permission of the Swedish Trotter Association (Stockholm, Sweden) and the Norwegian Trotter Association (Oslo, Norway).

References

  1. 1.

    Solé M, Gori A, Faux P, Bertrand A, Farnir F, Gautier M, et al. Age-based partitioning of individual genomic inbreeding levels in Belgian Blue cattle. Genet Sel Evol. 2017;49:92.

  2. 2.

    Luan T, Yu X, Dolezal M, Bagnato A, Meuwissen THE. Genomic prediction based on runs of homozygosity. Genet Sel Evol. 2014;46:64.

  3. 3.

    Pryce JE, Haile-Mariam M, Goddard ME, Hayes BJ. Identification of genomic regions associated with inbreeding depression in Holstein and Jersey dairy cattle. Genet Sel Evol. 2014;46:71.

  4. 4.

    Howard JT, Pryce JE, Baes C, Maltecca C. Inbreeding in the genomics era: inbreaeding, inbreeding depression, and management of genomic variability. J Dairy Sci. 2017;100:6009–24.

  5. 5.

    Peripolli E, Munari DP, Silva MVGB, Lima ALF, Irgang R, Baldi F. Runs of homozygosity: current knowledge and applications in livestock. Anim Genet. 2017;48:255–71.

  6. 6.

    Kim ES, Sonstegard TS, Van Tassell CP, Wiggans G, Rothschild MF. The relationship between runs of homozygosity and inbreeding in Jersey cattle under selection. PLoS One. 2015;10:e0129967.

  7. 7.

    Kardos M, Akesson M, Fountain T, Flagstad O, Liberg O, Olason P, et al. Genomic consequences of intensive inbreeding in an isolated wolf population. Nat Ecol Evol. 2018;2:124–31.

  8. 8.

    Ayroles JF, Hughes KA, Rowe KC, Reedy MM, Rodriguez-Zas SL, Drnevich JM, et al. A genomewide assessment of inbreeding depression: gene number, function, and mode of action. Conserv Biol. 2009;23:920–30.

  9. 9.

    Charlesworth D, Willis JH. The genetics of inbreeding depression. Nat Rev Genet. 2009;10:783–96.

  10. 10.

    Ponsart C, Le Bourhis D, Knijn H, Fritz S, Guyader-Joly C, Otter T, et al. Reproductive technologies and genomic selection in dairy cattle. Reprod Fertil Dev. 2013;26:12–21.

  11. 11.

    Jäderkvist Fegraeus K, Velie BD, Axelsson J, Ang R, Hamilton NA, Andersson L, et al. A potential regulatory region near the EDN3 gene may control both harness racing performance and coat color variation in horses. Physiol Rep. 2018;6:e13700.

  12. 12.

    Klemetsdal G. Norwegian trotter breeding and estimation of breeding values. In: State of breeding evaluation in trotters. In Proceedings of the European Federation of Animal Science Symposium of the Commission on Horse Production: 27 June–1 July 1988; Helsinki.; 1989. pp 95–105.

  13. 13.

    Arnason T, Bendroth M, Philipsson J, Henriksson K, Darenius A. Genetic evaluation of Swedish trotters. In State of breeding evaluation in trotters. In Proceedings of the European Federation of Animal Science Symposium of the Commission on Horse Production: 27 June–1 July 1988; Helsinki.; 1989. pp 106–30.

  14. 14.

    Svensk Travsport. 2018. https://www.travsport.se/wicket/bookmarkable/se.atg.web.travsport.page.polopoly.ArticlePage?6&cid=2.255. Accessed 1 Sept 2018.

  15. 15.

    Klemetsdal G. The effect of inbreeding on racing performance in Norwegian cold-blooded trotters. Genet Sel Evol. 1998;30:351–66.

  16. 16.

    Sargolzaei M, Iwaisaki H, Colleau JJ. CFC, A tool for monitoring genetic diversity. In: Proceedings of the 8th World Congress on Genetics Applied to Livestock Production: 13–18 August 2006; Belo Horizonte; 2006.

  17. 17.

    Forneris NS, Steibel JP, Legarra A, Vitezica ZG, Bates RO, Ernst CW, et al. A comparison of methods to estimate genomic relationships using pedigree and markers in livestock populations. J Anim Breed Genet. 2016;133:452–62.

  18. 18.

    Druml T, Neuditschko M, Grilz-Seger G, Horna M, Ricard A, Mesaric M, et al. Population networks associated with runs of homozygosity reveal new insights into the breeding history of the Haflinger horse. J Hered. 2018;109:384–92.

  19. 19.

    Keller MC, Visscher PM, Goddard ME. Quantification of inbreeding due to distant ancestors and its detection using dense single nucleotide polymorphism data. Genetics. 2011;189:237–49.

  20. 20.

    Ferencakovic M, Solkner J, Curik I. Estimating autozygosity from high-throughput information: effects of SNP density and genotyping errors. Genet Sel Evol. 2013;45:42.

  21. 21.

    Metzger J, Karwath M, Tonda R, Beltran S, Agueda L, Gut M, et al. Runs of homozygosity reveal signatures of positive selection for reproduction traits in breed and non-breed horses. BMC Genomics. 2015;16:764.

  22. 22.

    Kaminski S, Hering DM, Jaworski Z, Zabolewicz T, Rusc A. Assessment of genomic inbreeding in Polish Konik horses. Pol J Vet Sci. 2017;20:603–5.

  23. 23.

    R Development Core Team: R-A Language and environment for statistical computing; 2018 https://www.r-project.org/. Accessed 1 April 2018.

  24. 24.

    Hu ZL, Park CA, Reecy JM. Developmental progress and current status of the Animal QTLdb. Nucleic Acids Res. 2016;44:D827–33.

  25. 25.

    Neph S, Kuehn MS, Reynolds AP, Haugen E, Thurman RE, Johnson AK, et al. BEDOPS: high-performance genomic feature operations. Bioinformatics. 2012;28:1919–20.

  26. 26.

    Kardos M, Luikart G, Allendorf FW. Measuring individual inbreeding in the age of genomics: marker-based measures are better than pedigrees. Heredity (Edinb). 2015;115:63–72.

  27. 27.

    Department of Agriculture. Delmål för husdjursgenetiska resurser åren 2010 till 2020; 2009. http://www.jordbruksverket.se/download/18.2958036f1211efb32978000308/rapport%2B070511.pdf. Accessed 1 Sept 2018.

  28. 28.

    Svensk Travsport; 2018 https://www.travsport.se/artikel/kvalificerings-_&_premielopp. Accessed 1 Sept 2018.

  29. 29.

    Det Norske Travselskap; 2018 https://www.travsport.no. Accessed 1 Sept 2018.

  30. 30.

    Dierks C, Komm K, Lampe V, Distl O. Fine mapping of a quantitative trait locus for osteochondrosis on horse chromosome 2. Anim Genet. 2010;41:S87–90.

  31. 31.

    Orr N, Hill EW, Govindarajan P, Conroy J, van Grevenhof EM, Ducro BJ, et al. Genome-wide association study of osteochondrosis in the tarsocrural joint of Dutch Warmblood horses identifies susceptibility loci on chromosomes 3 and 10. Anim Genet. 2013;44:408–12.

  32. 32.

    Lykkjen S, Dolvik NI, McCue ME, Rendahl AK, Mickelson JR, Roed KH. Genome-wide association analysis of osteochondrosis of the tibiotarsal joint in Norwegian Standardbred trotters. Anim Genet. 2010;41:S111–20.

  33. 33.

    Lampe V, Dierks C, Distl O. Refinement of a quantitative gene locus on equine chromosome 16 responsible for osteochondrosis in Hanoverian warmblood horses. Animal. 2009;3:1224–31.

  34. 34.

    Fritz KL, McCue ME, Valberg SJ, Rendahl AK, Mickelson JR. Genetic mapping of recurrent exertional rhabdomyolysis in a population of North American Thoroughbreds. Anim Genet. 2012;43:730–8.

  35. 35.

    Gottschalk M, Metzger J, Martinsson G, Sieme H, Distl O. Genome-wide association study for semen quality traits in German Warmblood stallions. Anim Reprod Sci. 2016;171:81–6.

  36. 36.

    de Simoni Gouveia JJ, da Silva MVGB, Paiva SR, de Oliveira SMP. Identification of selection signatures in livestock species. Genet Mol Biol. 2014;37:330–42.

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Acknowledgements

We want to thank Christina Olsson, Annica Edberg, Knut Larsen, Chameli Lilja Lawrence, Thorvaldur Árnason, the Swedish Trotter Association, and the Norwegian Trotter Association for providing their support and the data/samples for the study.

Funding

This work was supported by the Swedish-Norwegian Foundation for Equine Research, H-15-47-075, http://hastforskning.se (GL, ES). The funders had no role in the design of the study, data collection and analysis, decision to publish, or preparation of the manuscript.

Author information

Affiliations

  1. School of Life and Environmental Sciences, University of Sydney, Sydney, Australia

    • Brandon D. Velie

  2. Department of Animal Breeding and Genetics, Swedish University of Agricultural Sciences, Uppsala, Sweden

    • Brandon D. Velie
    • , Marina Solé
    • , Kim Jäderkvist Fegraeus
    • , Maria K. Rosengren
    •  & Gabriella Lindgren

  3. Department of Basic Sciences and Aquatic Medicine, Norwegian University of Life Sciences, Oslo, Norway

    • Knut H. Røed

  4. Department of Companion Animal Clinical Sciences, Norwegian University of Life Sciences, Oslo, Norway

    • Carl-Fredrik Ihler
    •  & Eric Strand

  5. Livestock Genetics, Department of Biosystems, KU Leuven, Leuven, Belgium

    • Gabriella Lindgren

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Contributions

BDV, KJF, CI, ES, and GL conceived and designed the experiments; KJF, MKR, and KHR contributed to sampling. GL and ES contributed the reagents and MKR extracted the DNA; BDV analyzed the data and drafted the manuscript; KJF, MS, CI, ES, and GL discussed and contributed to data analysis. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Brandon D. Velie.

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Ethics approval and consent to participate

All experimental procedures and sample collection methods were approved by the Ethics Committee for Animal Experiments in Uppsala, Sweden [Number: C 121/14]. Samples used in this study were already available at either the Animal Genetics Laboratory at SLU in Uppsala, Sweden or the Department of Basic Sciences and Aquatic Medicine at the Norwegian University of Life Sciences in Oslo, Norway, since they had been previously used for parentage testing. Permission to use the samples was granted from the Swedish Trotting Association and the Norwegian Trotting Association (the owners of the samples per the rules/guidelines of the industry).

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Not applicable.

Competing interests

The authors have the following interests: GL is a co-inventor on a granted patent concerning commercial testing of the DMRT3 mutation: A method to predict the pattern of locomotion in horses. PCT EP 12,747,875.8. European patent registration date: 2011-05-05, US patent registration date: 2011-08-03. There are no further patents, products in development, or marketed products to declare.

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Additional files

12711_2019_465_MOESM1_ESM.xlsx

Additional file 1: Table S1. Threshold settings used to define runs of homozygosity in PLINK and the corresponding average FROH for a sample of raced Norwegian-Swedish Coldblooded trotters born between 1 January 2000 and 31 December 2009.

12711_2019_465_MOESM2_ESM.xlsx

Additional file 2: Table S2. Correlation matrix between FPED and all FROH estimates.

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Additional file 3: Table S3. Results of the paired t-test (P-values) between FPED and all FROH estimates.

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Additional file 4: Figure S1. Histograms for run of homozygosity (ROH) lengths based on four different threshold combinations in PLINK v 1.07. A = 50snp_500kb _100snp_0_0; B = 50snp_500kb _100snp_0_2; C = 50snp_500kb _100snp_1_2; D = 50snp_500kb _100snp_1_5 (FORMAT: “sliding window size”_”minimum length (kb) to be called as homozygous”_”minimum number of SNPs to be called as homozygous”_”number of heterozygotes allowed”_”number of missing calls allowed”).

12711_2019_465_MOESM5_ESM.tif

Additional file 5: Figure S2. Histograms for run of homozygosity (ROH) lengths based on varying window size thresholds in PLINK v 1.07. A = 50snp_500kb _15snp_0_1; B = 50snp_500kb _50snp_0_1; C = 500snp_500kb _50snp_0_1; D = pruned_50snp_500kb _50snp_0_1 (FORMAT: “sliding window size”_”minimum length (kb) for a run to be called as a ROH”_”minimum number of SNPs for a run to be called as a ROH”_”number of heterozygous SNPs allowed in a ROH”_”number of missing calls allowed in a ROH”).

12711_2019_465_MOESM6_ESM.xlsx

Additional file 6: Table S4. Homozygous regions of the genome that are shared by at least 95% of the sample of Norwegian-Swedish Coldblooded Trotters (n = 566).

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Velie, B.D., Solé, M., Fegraeus, K.J. et al. Genomic measures of inbreeding in the Norwegian–Swedish Coldblooded Trotter and their associations with known QTL for reproduction and health traits. Genet Sel Evol 51, 22 (2019) doi:10.1186/s12711-019-0465-7

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Genetics Selection Evolution

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