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Mitochondrial DNA D‐loop hyper‐variable region 1 variability in Kurdish horse breed
BACKGROUND: Kurdish horse is one of the most valuable horse genetic resources in the Middle East. OBJECTIVES: To assess the genetic diversity of Kurdish horses, Mitochondrial DNA D‐loop hyper‐variable region1 (HVR1) was sequenced in 29 non‐related Kurdish horses which were sampled from diverse geogr...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10029883/ https://www.ncbi.nlm.nih.gov/pubmed/36367719 http://dx.doi.org/10.1002/vms3.996 |
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author | Nikbakhsh, Milad Varkoohi, Sheida Seyedabadi, Hamid Reza |
author_facet | Nikbakhsh, Milad Varkoohi, Sheida Seyedabadi, Hamid Reza |
author_sort | Nikbakhsh, Milad |
collection | PubMed |
description | BACKGROUND: Kurdish horse is one of the most valuable horse genetic resources in the Middle East. OBJECTIVES: To assess the genetic diversity of Kurdish horses, Mitochondrial DNA D‐loop hyper‐variable region1 (HVR1) was sequenced in 29 non‐related Kurdish horses which were sampled from diverse geographic regions of Iran. METHODS: Total DNA was extracted from the collected blood samples by modified salting out method. The HVR1 was amplified by PCR and then sequenced using ABI PRISM BigDyeTM Terminator Cycle Sequencing Ready Reaction Kit. Consequently, the sequences were trimmed to 294 bp using BIOEDIT to become comparable with other reported HVR1 sequences in GeneBank. Sequence alignment was performed using CLUSTALW package. Haplotype and nucleotide diversity were estimated using DNASP5.10 and phylogenetic tree was constructed by neighbour joining method. RESULTS: Fourteen different haplotypes and 22 polymorphic sites were detected. Haplotype diversity, nucleotide diversity and Tajima D values were 0.901 ± 0.001, 0.01153 ± 0.0020 and −1.378, respectively. Kurdish horse showed a high haplotype and low nucleotide diversity. The compositional frequency of consensus sequences for base A was the highest (29.93%) compared to other three nucleotides (C = 28.91%, T = 26.53% and G = 14.63%). As expected, all of the detected Kurdish horse haplotypes belonged to haplogroup K (i.e., Kurdish horses). CONCLUSIONS: According to the phylogenetic analysis, Kurdish horses were genetically more closely related to Tibetan, Chinese, Bulgarian and Iranian native horse breeds, compared to other Asian horse breeds, but some traces of European horse breeds were detected in their maternal lines. |
format | Online Article Text |
id | pubmed-10029883 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-100298832023-03-22 Mitochondrial DNA D‐loop hyper‐variable region 1 variability in Kurdish horse breed Nikbakhsh, Milad Varkoohi, Sheida Seyedabadi, Hamid Reza Vet Med Sci EQUINE BACKGROUND: Kurdish horse is one of the most valuable horse genetic resources in the Middle East. OBJECTIVES: To assess the genetic diversity of Kurdish horses, Mitochondrial DNA D‐loop hyper‐variable region1 (HVR1) was sequenced in 29 non‐related Kurdish horses which were sampled from diverse geographic regions of Iran. METHODS: Total DNA was extracted from the collected blood samples by modified salting out method. The HVR1 was amplified by PCR and then sequenced using ABI PRISM BigDyeTM Terminator Cycle Sequencing Ready Reaction Kit. Consequently, the sequences were trimmed to 294 bp using BIOEDIT to become comparable with other reported HVR1 sequences in GeneBank. Sequence alignment was performed using CLUSTALW package. Haplotype and nucleotide diversity were estimated using DNASP5.10 and phylogenetic tree was constructed by neighbour joining method. RESULTS: Fourteen different haplotypes and 22 polymorphic sites were detected. Haplotype diversity, nucleotide diversity and Tajima D values were 0.901 ± 0.001, 0.01153 ± 0.0020 and −1.378, respectively. Kurdish horse showed a high haplotype and low nucleotide diversity. The compositional frequency of consensus sequences for base A was the highest (29.93%) compared to other three nucleotides (C = 28.91%, T = 26.53% and G = 14.63%). As expected, all of the detected Kurdish horse haplotypes belonged to haplogroup K (i.e., Kurdish horses). CONCLUSIONS: According to the phylogenetic analysis, Kurdish horses were genetically more closely related to Tibetan, Chinese, Bulgarian and Iranian native horse breeds, compared to other Asian horse breeds, but some traces of European horse breeds were detected in their maternal lines. John Wiley and Sons Inc. 2022-11-11 /pmc/articles/PMC10029883/ /pubmed/36367719 http://dx.doi.org/10.1002/vms3.996 Text en © 2022 The Authors. Veterinary Medicine and Science published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | EQUINE Nikbakhsh, Milad Varkoohi, Sheida Seyedabadi, Hamid Reza Mitochondrial DNA D‐loop hyper‐variable region 1 variability in Kurdish horse breed |
title | Mitochondrial DNA D‐loop hyper‐variable region 1 variability in Kurdish horse breed |
title_full | Mitochondrial DNA D‐loop hyper‐variable region 1 variability in Kurdish horse breed |
title_fullStr | Mitochondrial DNA D‐loop hyper‐variable region 1 variability in Kurdish horse breed |
title_full_unstemmed | Mitochondrial DNA D‐loop hyper‐variable region 1 variability in Kurdish horse breed |
title_short | Mitochondrial DNA D‐loop hyper‐variable region 1 variability in Kurdish horse breed |
title_sort | mitochondrial dna d‐loop hyper‐variable region 1 variability in kurdish horse breed |
topic | EQUINE |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10029883/ https://www.ncbi.nlm.nih.gov/pubmed/36367719 http://dx.doi.org/10.1002/vms3.996 |
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