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Original Article

Analysis of SNP variations in the MSTN gene promoter region between Mongolian and Halla horses

첫 페이지 보기
  • 발행기관
    한국동물생명공학회(구 한국동물번식학회) 바로가기
  • 간행물
    Journal of Animal Reproduction and Biotechnology 바로가기
  • 통권
    Volume. 41 No. 1 (2026.03)바로가기
  • 페이지
    pp.24-30
  • 저자
    Zultsetseg Byambasuren, Khaliunaa Tseveen, Nyambazar Amarsaikhan, Gwang Hyeon Lee, Hong Sik Kong
  • 언어
    영어(ENG)
  • URL
    https://www.earticle.net/Article/A486893

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원문정보

초록

영어
Background: Myostatin (MSTN) gene is a major inhibitor of skeletal muscle growth, and variants within its promoter region may affect transcriptional activity and musclerelated traits. Mongolian native horses have adapted to endurance and harsh environmental conditions, whereas Halla horses exhibit enhanced musculature owing to crossbreeding with Thoroughbreds. MSTN promoter variations in these breeds have not been sufficiently investigated, highlighting a critical research gap that motivated the present study. Methods: Two single nucleotide polymorphisms (SNPs) in the MSTN promoter region were examined in 19 Mongolian and 4 Halla horses using PCR amplification and Sanger sequencing. Additionally, Gene Ontology and Kyoto Encyclopedia of Genes and Genomes pathway annotations were used to characterize gene functions. Results: Two promoter region SNPs were identified in MSTN gene. These distribution patterns represent preliminary observations within the sampled populations, providing a valuable foundation for future investigations. Functional annotation further supported the regulatory relevance of MSTN through its involvement in muscle growth inhibition and the TGF-β/ACVR2B/SMAD pathway. Conclusions: This study provides the first baseline characterization of MSTN promoter polymorphisms in Mongolian and Halla horses. The g.26T>C variant was identified in Mongolian horses, whereas the shared g.156T>C SNP represents a regulatory variant observed in both breeds, pending confirmation in broader populations. However, due to the limited sample size, we consider these findings to be preliminary observations rather than definitive evidence of breed-specific adaptation. The results of this study are expected to serve as fundamental data for establishing future genetic information– based breeding and conservation strategies for Mongolian horses.

목차

ABSTRACT
INTRODUCTION
MATERIALS AND METHODS
Sample collection and DNA extraction
Primer design
PCR amplification and sequencing
In-silico functional annotation of the MSTN gene
RESULTS
MSTN SNP markers and sanger sequencing analysis
In-silico functional annotation of the MSTN gene
DISCUSSION
CONCLUSION
REFERENCES

저자

  • Zultsetseg Byambasuren [ Department of Biotechnology, Hankyong National University, Anseong 17579, Korea ]
  • Khaliunaa Tseveen [ Department of Biotechnology, Hankyong National University, Anseong 17579, Korea ]
  • Nyambazar Amarsaikhan [ Department of Biotechnology, Hankyong National University, Anseong 17579, Korea ]
  • Gwang Hyeon Lee [ Department of Biotechnology, Hankyong National University/Gyeonggi Regional Research Center, Hankyong National University/Genomic Information Center, Hankyong National University/Hankyong and Genetics, Anseong 17579, Korea ]
  • Hong Sik Kong [ Department of Biotechnology, Hankyong National University/Gyeonggi Regional Research Center, Hankyong National University/Genomic Information Center, Hankyong National University/Hankyong and Genetics, Anseong 17579, Korea ] Corresponding Author

참고문헌

자료제공 : 네이버학술정보

간행물 정보

발행기관

  • 발행기관명
    한국동물생명공학회(구 한국동물번식학회) [The Korean Society of Animal Reproduction and Biotechnology]
  • 설립연도
    1976
  • 분야
    농수해양>축산학
  • 소개
    동물번식생리학, 동물생명공학, 수의학, 인공수정 및 수정란이식을 이용한 동물개량에 관한 이론과 기술의 발전을 통해 학계, 연구계, 산업계 및 양축가 상호간의 협력을 도모함으로써 동물과학발전 및 사회일반의 이익에 기여 한다는 목적을 위해 노력해 나가겠습니다.

간행물

  • 간행물명
    Journal of Animal Reproduction and Biotechnology
  • 간기
    계간
  • pISSN
    2671-4639
  • eISSN
    2671-4663
  • 수록기간
    2019~2026
  • 십진분류
    KDC 527 DDC 636

이 권호 내 다른 논문 / Journal of Animal Reproduction and Biotechnology Volume. 41 No. 1

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