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Comparative genomic analysis of inbred rat strains reveals the existence of ancestral polymorphisms
In an alignment of closely related genomic sequences, the existence of discordant mutation sites, which do not reflect the phylogenetic relationship of the genomes, is often observed. Although these discordant mutation sites are thought to have emerged by ancestral polymorphism or gene flow, their f...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7200647/ https://www.ncbi.nlm.nih.gov/pubmed/32166433 http://dx.doi.org/10.1007/s00335-020-09831-7 |
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author | Kim, Hyeonjeong Yoshihara, Minako Suyama, Mikita |
author_facet | Kim, Hyeonjeong Yoshihara, Minako Suyama, Mikita |
author_sort | Kim, Hyeonjeong |
collection | PubMed |
description | In an alignment of closely related genomic sequences, the existence of discordant mutation sites, which do not reflect the phylogenetic relationship of the genomes, is often observed. Although these discordant mutation sites are thought to have emerged by ancestral polymorphism or gene flow, their frequency and distribution in the genome have not yet been analyzed in detail. Using the genome sequences of all protein coding genes of 25 inbred rat strains, we analyzed the frequency and genome-wide distribution of the discordant mutation sites. From the comparison of different substrains, it was found that these loci are not substrain specific, but are common among different groups of substrains, suggesting that the discordant sites might have mainly emerged through ancestral polymorphism. It was also revealed that the discordant sites are not uniformly distributed along chromosomes, but are concentrated at certain genomic loci, such as RT1, major histocompatibility complex of rats, and olfactory receptors, indicating that genes known to be highly polymorphic tend to have more discordant sites. Our results also showed that loci with a high density of discordant sites are also rich in heterozygous variants, even though these are inbred strains. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00335-020-09831-7) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-7200647 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-72006472020-05-07 Comparative genomic analysis of inbred rat strains reveals the existence of ancestral polymorphisms Kim, Hyeonjeong Yoshihara, Minako Suyama, Mikita Mamm Genome Article In an alignment of closely related genomic sequences, the existence of discordant mutation sites, which do not reflect the phylogenetic relationship of the genomes, is often observed. Although these discordant mutation sites are thought to have emerged by ancestral polymorphism or gene flow, their frequency and distribution in the genome have not yet been analyzed in detail. Using the genome sequences of all protein coding genes of 25 inbred rat strains, we analyzed the frequency and genome-wide distribution of the discordant mutation sites. From the comparison of different substrains, it was found that these loci are not substrain specific, but are common among different groups of substrains, suggesting that the discordant sites might have mainly emerged through ancestral polymorphism. It was also revealed that the discordant sites are not uniformly distributed along chromosomes, but are concentrated at certain genomic loci, such as RT1, major histocompatibility complex of rats, and olfactory receptors, indicating that genes known to be highly polymorphic tend to have more discordant sites. Our results also showed that loci with a high density of discordant sites are also rich in heterozygous variants, even though these are inbred strains. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00335-020-09831-7) contains supplementary material, which is available to authorized users. Springer US 2020-03-12 2020 /pmc/articles/PMC7200647/ /pubmed/32166433 http://dx.doi.org/10.1007/s00335-020-09831-7 Text en © The Author(s) 2020 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/. |
spellingShingle | Article Kim, Hyeonjeong Yoshihara, Minako Suyama, Mikita Comparative genomic analysis of inbred rat strains reveals the existence of ancestral polymorphisms |
title | Comparative genomic analysis of inbred rat strains reveals the existence of ancestral polymorphisms |
title_full | Comparative genomic analysis of inbred rat strains reveals the existence of ancestral polymorphisms |
title_fullStr | Comparative genomic analysis of inbred rat strains reveals the existence of ancestral polymorphisms |
title_full_unstemmed | Comparative genomic analysis of inbred rat strains reveals the existence of ancestral polymorphisms |
title_short | Comparative genomic analysis of inbred rat strains reveals the existence of ancestral polymorphisms |
title_sort | comparative genomic analysis of inbred rat strains reveals the existence of ancestral polymorphisms |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7200647/ https://www.ncbi.nlm.nih.gov/pubmed/32166433 http://dx.doi.org/10.1007/s00335-020-09831-7 |
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