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Exploiting genomic synteny in Felidae: cross-species genome alignments and SNV discovery can aid conservation management
BACKGROUND: While recent advances in genomics has enabled vast improvements in the quantification of genome-wide diversity and the identification of adaptive and deleterious alleles in model species, wildlife and non-model species have largely not reaped the same benefits. This has been attributed t...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8348863/ https://www.ncbi.nlm.nih.gov/pubmed/34362297 http://dx.doi.org/10.1186/s12864-021-07899-2 |
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author | Samaha, Georgina Wade, Claire M. Mazrier, Hamutal Grueber, Catherine E. Haase, Bianca |
author_facet | Samaha, Georgina Wade, Claire M. Mazrier, Hamutal Grueber, Catherine E. Haase, Bianca |
author_sort | Samaha, Georgina |
collection | PubMed |
description | BACKGROUND: While recent advances in genomics has enabled vast improvements in the quantification of genome-wide diversity and the identification of adaptive and deleterious alleles in model species, wildlife and non-model species have largely not reaped the same benefits. This has been attributed to the resources and infrastructure required to develop essential genomic datasets such as reference genomes. In the absence of a high-quality reference genome, cross-species alignments can provide reliable, cost-effective methods for single nucleotide variant (SNV) discovery. Here, we demonstrated the utility of cross-species genome alignment methods in gaining insights into population structure and functional genomic features in cheetah (Acinonyx jubatas), snow leopard (Panthera uncia) and Sumatran tiger (Panthera tigris sumatrae), relative to the domestic cat (Felis catus). RESULTS: Alignment of big cats to the domestic cat reference assembly yielded nearly complete sequence coverage of the reference genome. From this, 38,839,061 variants in cheetah, 15,504,143 in snow leopard and 13,414,953 in Sumatran tiger were discovered and annotated. This method was able to delineate population structure but limited in its ability to adequately detect rare variants. Enrichment analysis of fixed and species-specific SNVs revealed insights into adaptive traits, evolutionary history and the pathogenesis of heritable diseases. CONCLUSIONS: The high degree of synteny among felid genomes enabled the successful application of the domestic cat reference in high-quality SNV detection. The datasets presented here provide a useful resource for future studies into population dynamics, evolutionary history and genetic and disease management of big cats. This cross-species method of variant discovery provides genomic context for identifying annotated gene regions essential to understanding adaptive and deleterious variants that can improve conservation outcomes. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-021-07899-2. |
format | Online Article Text |
id | pubmed-8348863 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-83488632021-08-09 Exploiting genomic synteny in Felidae: cross-species genome alignments and SNV discovery can aid conservation management Samaha, Georgina Wade, Claire M. Mazrier, Hamutal Grueber, Catherine E. Haase, Bianca BMC Genomics Research Article BACKGROUND: While recent advances in genomics has enabled vast improvements in the quantification of genome-wide diversity and the identification of adaptive and deleterious alleles in model species, wildlife and non-model species have largely not reaped the same benefits. This has been attributed to the resources and infrastructure required to develop essential genomic datasets such as reference genomes. In the absence of a high-quality reference genome, cross-species alignments can provide reliable, cost-effective methods for single nucleotide variant (SNV) discovery. Here, we demonstrated the utility of cross-species genome alignment methods in gaining insights into population structure and functional genomic features in cheetah (Acinonyx jubatas), snow leopard (Panthera uncia) and Sumatran tiger (Panthera tigris sumatrae), relative to the domestic cat (Felis catus). RESULTS: Alignment of big cats to the domestic cat reference assembly yielded nearly complete sequence coverage of the reference genome. From this, 38,839,061 variants in cheetah, 15,504,143 in snow leopard and 13,414,953 in Sumatran tiger were discovered and annotated. This method was able to delineate population structure but limited in its ability to adequately detect rare variants. Enrichment analysis of fixed and species-specific SNVs revealed insights into adaptive traits, evolutionary history and the pathogenesis of heritable diseases. CONCLUSIONS: The high degree of synteny among felid genomes enabled the successful application of the domestic cat reference in high-quality SNV detection. The datasets presented here provide a useful resource for future studies into population dynamics, evolutionary history and genetic and disease management of big cats. This cross-species method of variant discovery provides genomic context for identifying annotated gene regions essential to understanding adaptive and deleterious variants that can improve conservation outcomes. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-021-07899-2. BioMed Central 2021-08-06 /pmc/articles/PMC8348863/ /pubmed/34362297 http://dx.doi.org/10.1186/s12864-021-07899-2 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Samaha, Georgina Wade, Claire M. Mazrier, Hamutal Grueber, Catherine E. Haase, Bianca Exploiting genomic synteny in Felidae: cross-species genome alignments and SNV discovery can aid conservation management |
title | Exploiting genomic synteny in Felidae: cross-species genome alignments and SNV discovery can aid conservation management |
title_full | Exploiting genomic synteny in Felidae: cross-species genome alignments and SNV discovery can aid conservation management |
title_fullStr | Exploiting genomic synteny in Felidae: cross-species genome alignments and SNV discovery can aid conservation management |
title_full_unstemmed | Exploiting genomic synteny in Felidae: cross-species genome alignments and SNV discovery can aid conservation management |
title_short | Exploiting genomic synteny in Felidae: cross-species genome alignments and SNV discovery can aid conservation management |
title_sort | exploiting genomic synteny in felidae: cross-species genome alignments and snv discovery can aid conservation management |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8348863/ https://www.ncbi.nlm.nih.gov/pubmed/34362297 http://dx.doi.org/10.1186/s12864-021-07899-2 |
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