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Genes2021; 12(4); doi: 10.3390/genes12040546

Genetic Variability and Population Structure of Polish Konik Horse Maternal Lines Based on Microsatellite Markers.

Abstract: The aim of the conservation programme is to maintain the population size of endangered livestock breeds of less economic importance at a level that ensures the survival of the breed, the preservation of genetic diversity, and the preservation of as many pedigree lines as possible. The Polish Konik, a native Polish primitive-type horse breed and is one of the breeds included in such a programme in Poland. Presently, there are only 16 (of the 35 maternal lines known in 1962), some of which are endangered. We examined the genetic variability and structure of the Polish Konik maternal lines (176 individuals) on the basis of the pedigree data and 17 microsatellite markers (STRs) from parentage testing. The overall mean number of alleles was 7.647 (±0.411), the effective number of alleles was 3.935 (±0.271), the mean number of alleles for which the frequency was equal to or lower than 5% was 4.471 (±0.286), and the mean information index was 1.506 (±0.087). The structure of the population and admixture patterns were calculated with the Structure and Structure Harvester software. The structural analysis indicated three likely genetic clusters; as the most optimal K value was estimated as 3, with ∆K of 15.4188. The F-statistics results indicated a low level of inbreeding (average inbreeding coefficient FIT was 0.0188, coefficient of differentiation FST was 0.0304, and mean inbreeding index value FIS was -0.0119). Variability monitoring should be carried out in order to avoid inbreeding depression, while breeding strategies should be designed to prevent the decrease of genetic variability in the Polish horse breed and to sustain the active female lines.
Publication Date: 2021-04-09 PubMed ID: 33918718PubMed Central: PMC8069725DOI: 10.3390/genes12040546Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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This study evaluates the genetic variability and population structure of Polish Konik horse maternal lines, in efforts to support their conservation. The researchers utilized pedigree data and 17 microsatellite markers to analyze 176 individual horses, deriving insights on their genetic clusters and patterns, along with the prevalence of inbreeding.

Study Goals and Context

  • This research aims to support the conservation of Polish Konik horses, a native breed in Poland. Part of a category of livestock breeds of lesser economic importance yet high cultural and biological value, these horse breeds are in danger of disappearing. Of the known 35 maternal lines in 1962, only 16 remain and some of these are under threat.
  • Conservation initiatives strive to maintain populations at a level securing their survival, while also preserving genetic diversity and as many pedigree lines as possible.

Methodology

  • The researchers examined 176 Polish Konik horses from the surviving maternal lines.
  • Their analysis was based on pedigree data and the usage of 17 microsatellite markers or STRs (Short Tandem Repeats), commonly used in parentage testing.
  • They used software like Structure and Structure Harvester to calculate population structure and admixture patterns (the genetic mixing of different populations).

Key Findings

  • From their analysis, the mean number of alleles (which are versions of the same gene) were determined along with the effective number of alleles and the mean information index. The study also noted statistics on alleles with frequency equal to or lower than 5%.
  • The structural analysis suggested the existence of three likely genetic clusters within the breed. The most optimal K value, which determines the number of genetic populations in the data, was estimated as 3.
  • In terms of inbreeding, the levels were deemed low but not absent. Indices such as the average inbreeding coefficient F, the coefficient of differentiation F, and the mean inbreeding index value F were used to gauge this.

Conclusions and Recommendations

  • Overall, the study underscores the need for continued monitoring of genetic variability within the population to prevent inbreeding depression (the reduction of fitness resulting from inbreeding).
  • The authors recommend the design and implementation of breeding strategies aimed at halting the decrease of genetic variability within the Polish Konik horse population and maintaining the active female lines.

Cite This Article

APA
Fornal A, Kowalska K, Zabek T, Piestrzynska-Kajtoch A, Musiał AD, Ropka-Molik K. (2021). Genetic Variability and Population Structure of Polish Konik Horse Maternal Lines Based on Microsatellite Markers. Genes (Basel), 12(4). https://doi.org/10.3390/genes12040546

Publication

ISSN: 2073-4425
NlmUniqueID: 101551097
Country: Switzerland
Language: English
Volume: 12
Issue: 4

Researcher Affiliations

Fornal, Agnieszka
  • Department of Animal Molecular Biology, National Research Institute of Animal Production, 32-083 Krakow, Poland.
Kowalska, Katarzyna
  • Department of Animal Molecular Biology, National Research Institute of Animal Production, 32-083 Krakow, Poland.
Zabek, Tomasz
  • Department of Animal Molecular Biology, National Research Institute of Animal Production, 32-083 Krakow, Poland.
Piestrzynska-Kajtoch, Agata
  • Department of Animal Molecular Biology, National Research Institute of Animal Production, 32-083 Krakow, Poland.
Musiał, Adrianna D
  • Department of Animal Molecular Biology, National Research Institute of Animal Production, 32-083 Krakow, Poland.
Ropka-Molik, Katarzyna
  • Department of Animal Molecular Biology, National Research Institute of Animal Production, 32-083 Krakow, Poland.

MeSH Terms

  • Animals
  • Female
  • Genetic Variation
  • Genetics, Population
  • Horses / genetics
  • Inbreeding / methods
  • Male
  • Microsatellite Repeats
  • Poland
  • Population Density

Conflict of Interest Statement

The authors declare no conflict of interest.

References

This article includes 35 references
  1. Mackowski M, Mucha S, Cholewinski G, Cieslak J. Genetic diversity in Hucul and Polish primitive horse breeds.. Arch. Anim. Breed. 2015;58:23–31.
    doi: 10.5194/aab-58-23-2015google scholar: lookup
  2. Pasicka E. Polish konik horse—Characteristics and historical background of native descendants of tarpan.. Acta Sci. Pol. Med. Vet. 2013;12:25–38.
  3. Csizmar N, Mihok S, Javor A, Kusza S. Genetic analysis of the Hungarian draft horse population using partial mitochondrial DNA D-loop sequencing.. PeerJ 2018;6:e4198.
    doi: 10.7717/peerj.4198pmc: PMC5797449pubmed: 29404201google scholar: lookup
  4. Boiko S, Bielinis E, Sierota Z, Zawadzka A, Słupska A, Nasiadko M, Borkowski J. Polish pony changes lower layer biodiversity in old growth scots pine stands.. Forests 2019;10:417.
    doi: 10.3390/f10050417google scholar: lookup
  5. Komosa M, Frackowiak H, Purzyc H, Wojnowska M, Gramacki A, Gramacki J. Differences in exterior conformation between primitive, Half-bred, and Thoroughbred horses: Anatomic-breeding approach.. J. Anim. Sci. 2013;91:1660–1668.
    doi: 10.2527/jas.2012-5367pubmed: 23345554google scholar: lookup
  6. Jaworska J, Ropka-Molik K, Woclawek-Potocka I, Siemieniuch M. Inter- and intrabreed diversity of the major histocompatibility complex (MHC) in primitive and draft horse breeds.. PLoS ONE 2020;15:e0228658.
  7. Pasicka E, Tarnawski K, Chrószcz A, Geringer de Oedenberg H. Morphometric Changes in Polish Konik Mares After Nearly a Hundred Years of the Breed’s Existence.. J. Vet. Med. Ser. C Anat. Histol. Embryol. 2017;46:249–257.
    doi: 10.1111/ahe.12264pubmed: 28105755google scholar: lookup
  8. Jaworski Z. Dlugosc uzytkowania rozplodowego i zycia klaczy konika polskiego w warunkach naturalnych.. Prz. Hod. 1994;62:23–24.
  9. Gorecka-Bruzda A, Jaworski Z, Jaworska J, Siemieniuch M. Welfare of free-roaming horses: 70 years of experience with Konik Polski breeding in Poland.. Animals 2020;10:1094.
    doi: 10.3390/ani10061094pmc: PMC7341202pubmed: 32599935google scholar: lookup
  10. Glazewska I, Wysocka A, Gralak B, Prus R, Sell J. A new view on dam lines in Polish Arabian horses based on mtDNA analysis.. Genet. Sel. Evol. 2007;39:609–619.
    doi: 10.1186/1297-9686-39-5-609pmc: PMC2682809pubmed: 17897600google scholar: lookup
  11. Doboszewski P, Doktor D, Jaworski Z, Kalski R, Kulakowska G, Lojek J, Plachocki D, Rys A, Tylkowska A. Konik polski horses as a mean of biodiversity maintenance in post-agricultural and forest areas: An overview of Polish experiences.. Anim. Sci. Pap. Rep. 2017;35:333–347.
  12. Pluta M, Osinski Z, Cieśla A, Kolstrung R. Genetic and Phenotypic Characteristics of Polish Konik Horses Maintained in the Reserve and Stable System in Central-Eastern Poland.. Acta Sci. Pol. Zootech. 2016;15:59–76.
    doi: 10.21005/asp.2016.15.2.06google scholar: lookup
  13. Polish Horse Breeders Association. [(accessed on 23 January 2021)]; Available online: https://en.pzhk.pl/breeding/breeding-statistics/
  14. Wojciechowska P. Polish Horse Breeders Association. 2021. Unpublished work.
  15. Janczarek I, Pluta M, Paszkowska A. Pochodzenie, hodowla i użytkowanie koników polskich.. Przegląd Hod. 2017;85:6–10.
  16. Jaworski Z. Genealogical Tables of the Polish Primitive Horse.. .
  17. Jaworski Z, Siemieniuch M, Jastrzebska E, Wojciechowska P. Zroznicowanie Genetyczne Populacji Koników Polskich. Proceedings of the LXXXIV Zjazd Naukowy Polskiego Towarzystwa Zootechnicznego w Szczecinie “Osiagniecia i Perspektywy Zootechniki w Aspekcie Zrownowazonego Rolnictwa i Ochrony Srodowiska”; Szczecin, Poland. 18–20 September 2019; p. 123.
  18. Cieslak J, Wodas L, Borowska A, Cothran E.G., Khanshour A.M., Mackowski M. Characterization of the Polish Primitive Horse (Konik) maternal lines using mitochondrial D-loop sequence variation.. PeerJ 2017;5:e3714.
    doi: 10.7717/peerj.3714pmc: PMC5572418pubmed: 28852595google scholar: lookup
  19. Fornal A, Kowalska K, Zabek T, Piestrzynska-Kajtoch A, Musiał A.D., Ropka-Molik K. Genetic diversity and population structure of polish konik horse based on individuals from all the male founder lines and microsatellite markers.. Animals 2020;10:1569.
    doi: 10.3390/ani10091569pmc: PMC7552212pubmed: 32899310google scholar: lookup
  20. Pritchard J.K., Stephens P, Donnelly P. Inference of population structure using multilocus genotype data.. Genetics 2000;155:945–959.
    pmc: PMC1461096pubmed: 10835412
  21. Earl D.A., VonHoldt B.M. Structure Harvester: A website and program for visualizing Structure output and implementing the Evanno method.. Conserv. Genet. Resour. 2012;4:359–361.
    doi: 10.1007/s12686-011-9548-7google scholar: lookup
  22. Peakall R., Smouse P.E. GenALEx 6.5: Genetic analysis in Excel. Population genetic software for teaching and research—An update.. Bioinformatics 2012;28:2537–2539.
  23. Peakall R., Smouse P.E. GENALEX 6: Genetic analysis in Excel. Population genetic software for teaching and research.. Mol. Ecol. Notes 2006;6:288–295.
  24. Goudet J. FSTAT, a program to estimate and test gene diversities and fixation indices (version 2.9. 3). Department of Ecology and Evolution, University of Lausanne, Switzerland.. J. Hered. 2001;149:507–526.
  25. Paradis E. Pegas: An R package for population genetics with an integrated-modular approach.. Bioinformatics 2010;26:419–420.
    doi: 10.1093/bioinformatics/btp696pubmed: 20080509google scholar: lookup
  26. Jombart T. adegenet: A R package for the multivariate analysis of genetic markers.. Bioinformatics 2008;24:1403–1405.
    doi: 10.1093/bioinformatics/btn129pubmed: 18397895google scholar: lookup
  27. Radko A, Zalewski D, Rubis D, Szumiec A. Genetic differentiation among 6 populations of red deer (Cervus elaphus L.) in Poland based on microsatellite DNA polymorphism.. Acta Biol. Hung. 2014;65:414–427.
    doi: 10.1556/ABiol.65.2014.4.6pubmed: 25475981google scholar: lookup
  28. Pablo Gómez M, Landi V, Martínez A.M., Gómez Carpio M, Nogales Baena S, Delgado Bermejo J.V., Oom M.D.M., Luis C, Ouragh L, Vega-Pla J.L. Genetic diversity of the semi-feral Marismeño horse breed assessed with microsatellites.. Ital. J. Anim. Sci. 2017;16:14–21.
  29. Gralak B, Niemczewski C, Jaworski Z. Genetic polymorphism of 12 micorsatellite markers in Polish Primitive Horse.. Anim. Sci. Pap. Rep. 2001;19:277–283.
  30. Szwaczkowski T, Greguła-Kania M, Stachurska A, Borowska A, Jaworski Z, Gruszecki T.M. Inter- and intra-genetic diversity in the Polish Konik horse: Implications for the conservation program.. Can. J. Anim. Sci. 2016;96:570–580.
    doi: 10.1139/cjas-2015-0173google scholar: lookup
  31. Castaneda C, Juras R, Khanshour A, Randlaht I, Wallner B, Rigler D, Lindgren G, Raudsepp T, Cothran E.G. Population Genetic Analysis of the Estonian Native Horse Suggests Diverse and Distinct Genetics, Ancient Origin and Contribution from Unique Patrilines.. Genes 2019;10:629.
    doi: 10.3390/genes10080629pmc: PMC6722507pubmed: 31434327google scholar: lookup
  32. Georgescu S.E., Manea M.A., Costache M. The genetic structure of indigenous Romanian Hucul horse breed inferred from microsatellite data.. Roum. Biotechnol. Lett. 2008;13:4030–4036.
  33. DAD-IS (Domestic Animal Diversity Information System Hosted by FAO) [(accessed on 23 January 2021)]; Available online: http://dad.fao.org.
  34. Zabek T, Fornal A. Evaluation of the 17-plex STR kit for parentage testing of polish Coldblood and Hucul horses.. Ann. Anim. Sci. 2009;9:363–372.
  35. Kusza S, Priskin K, Ivankovic A, Jedrzejewska B, Podgorski T, Javor A, Mihok S. Genetic characterization and population bottleneck in the Hucul horse based on microsatellite and mitochondrial data.. Biol. J. Linn. Soc. 2013;109:54–65.
    doi: 10.1111/bij.12023google scholar: lookup