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Identification of a new Indian camel germplasm by microsatellite markers based genetic diversity and population structure of three camel populations
Camel invokes fascinating chapter of Indian desert history and is integral component of its ecosystem. Camel population has reached a crisis point after three decades of decline (75%) causing major concern to the policy makers. >28% of Indian camel is not yet characterized. It is imperative to de...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7296511/ https://www.ncbi.nlm.nih.gov/pubmed/32565685 http://dx.doi.org/10.1016/j.sjbs.2020.04.046 |
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author | Sharma, Rekha Ahlawat, Sonika Sharma, Himani Prakash, Ved Shilpa Khatak, Sunita Sawal, R.K. Tantia, M.S. |
author_facet | Sharma, Rekha Ahlawat, Sonika Sharma, Himani Prakash, Ved Shilpa Khatak, Sunita Sawal, R.K. Tantia, M.S. |
author_sort | Sharma, Rekha |
collection | PubMed |
description | Camel invokes fascinating chapter of Indian desert history and is integral component of its ecosystem. Camel population has reached a crisis point after three decades of decline (75%) causing major concern to the policy makers. >28% of Indian camel is not yet characterized. It is imperative to describe country’s camel germplasm and its existing diversity for designing conservation plan. One such population is Sindhi, distributed along border with Pakistan. Twenty five microsatellite markers being valuable tool for estimating genetic diversity were selected to elucidate genetic variability and relationship of Sindhi with two registered camel breeds of India- Marwari and Kharai. The standard metrics of genomic diversity detected moderate variability in all the three populations. A total of 303 alleles with a mean of 8.116 ± 0.587 alleles per locus were found in total of 143 animals. Sindhi population had intermediate allelic diversity with 8.522 ± 1.063 alleles per locus. Corresponding values in Marwari and Kharai were 8.783 ± 0.962 and 7.043 ± 1.030, respectively. Genetic variability within the breeds was moderate as evidenced by the mean observed heterozygosity of 0.556 ± 0.025. Sindhi camel population harbors higher genetic variability (Ho = 0.594) as compared to the two registered camel breeds (Marwari, 0.543 and Kharai, 0.531). Mean expected heterozygosity under Hardy-Weinberg equilibrium was higher than the observed values across the three camel groups, indicating deviations from assumptions of this model. In fact, average positive F value of 0.084 to 0.206 reflected heterozygote deficiency in these populations. These Indian camel populations have not experienced serious demographic bottlenecks in the recent past. Differences among populations were medium and accounted for 7.3% of total genetic variability. Distinctness of three camel populations was supported by all the approaches utilized to study genetic relationships such as genetic distances, phylogenetic relationship, correspondence analysis, clustering method based on Bayesian approach and individual assignment. Sindhi camel population was clearly separated from two registered breeds of Indian camel. Results conclude Sindhi to be a separate genepool. Moderate genetic diversity provides an optimistic viewpoint for the survival of severely declining indigenous camel populations with appropriate planning strategies for conserving the existing genetic variation and to avoid any escalation of inbreeding. |
format | Online Article Text |
id | pubmed-7296511 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-72965112020-06-18 Identification of a new Indian camel germplasm by microsatellite markers based genetic diversity and population structure of three camel populations Sharma, Rekha Ahlawat, Sonika Sharma, Himani Prakash, Ved Shilpa Khatak, Sunita Sawal, R.K. Tantia, M.S. Saudi J Biol Sci Article Camel invokes fascinating chapter of Indian desert history and is integral component of its ecosystem. Camel population has reached a crisis point after three decades of decline (75%) causing major concern to the policy makers. >28% of Indian camel is not yet characterized. It is imperative to describe country’s camel germplasm and its existing diversity for designing conservation plan. One such population is Sindhi, distributed along border with Pakistan. Twenty five microsatellite markers being valuable tool for estimating genetic diversity were selected to elucidate genetic variability and relationship of Sindhi with two registered camel breeds of India- Marwari and Kharai. The standard metrics of genomic diversity detected moderate variability in all the three populations. A total of 303 alleles with a mean of 8.116 ± 0.587 alleles per locus were found in total of 143 animals. Sindhi population had intermediate allelic diversity with 8.522 ± 1.063 alleles per locus. Corresponding values in Marwari and Kharai were 8.783 ± 0.962 and 7.043 ± 1.030, respectively. Genetic variability within the breeds was moderate as evidenced by the mean observed heterozygosity of 0.556 ± 0.025. Sindhi camel population harbors higher genetic variability (Ho = 0.594) as compared to the two registered camel breeds (Marwari, 0.543 and Kharai, 0.531). Mean expected heterozygosity under Hardy-Weinberg equilibrium was higher than the observed values across the three camel groups, indicating deviations from assumptions of this model. In fact, average positive F value of 0.084 to 0.206 reflected heterozygote deficiency in these populations. These Indian camel populations have not experienced serious demographic bottlenecks in the recent past. Differences among populations were medium and accounted for 7.3% of total genetic variability. Distinctness of three camel populations was supported by all the approaches utilized to study genetic relationships such as genetic distances, phylogenetic relationship, correspondence analysis, clustering method based on Bayesian approach and individual assignment. Sindhi camel population was clearly separated from two registered breeds of Indian camel. Results conclude Sindhi to be a separate genepool. Moderate genetic diversity provides an optimistic viewpoint for the survival of severely declining indigenous camel populations with appropriate planning strategies for conserving the existing genetic variation and to avoid any escalation of inbreeding. Elsevier 2020-07 2020-05-07 /pmc/articles/PMC7296511/ /pubmed/32565685 http://dx.doi.org/10.1016/j.sjbs.2020.04.046 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Sharma, Rekha Ahlawat, Sonika Sharma, Himani Prakash, Ved Shilpa Khatak, Sunita Sawal, R.K. Tantia, M.S. Identification of a new Indian camel germplasm by microsatellite markers based genetic diversity and population structure of three camel populations |
title | Identification of a new Indian camel germplasm by microsatellite markers based genetic diversity and population structure of three camel populations |
title_full | Identification of a new Indian camel germplasm by microsatellite markers based genetic diversity and population structure of three camel populations |
title_fullStr | Identification of a new Indian camel germplasm by microsatellite markers based genetic diversity and population structure of three camel populations |
title_full_unstemmed | Identification of a new Indian camel germplasm by microsatellite markers based genetic diversity and population structure of three camel populations |
title_short | Identification of a new Indian camel germplasm by microsatellite markers based genetic diversity and population structure of three camel populations |
title_sort | identification of a new indian camel germplasm by microsatellite markers based genetic diversity and population structure of three camel populations |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7296511/ https://www.ncbi.nlm.nih.gov/pubmed/32565685 http://dx.doi.org/10.1016/j.sjbs.2020.04.046 |
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