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Prdm9 Polymorphism Unveils Mouse Evolutionary Tracks
PR/SET domain containing 9 (Prdm9) mediates histone modifications such as H3K4me3 and marks hotspots of meiotic recombination. In many mammalian species, the Prdm9 gene is highly polymorphic. Prdm9 polymorphism is assumed to play two critical roles in evolution: to diversify the spectrum of meiotic...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4060951/ https://www.ncbi.nlm.nih.gov/pubmed/24449848 http://dx.doi.org/10.1093/dnares/dst059 |
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author | Kono, Hiromitsu Tamura, Masaru Osada, Naoki Suzuki, Hitoshi Abe, Kuniya Moriwaki, Kazuo Ohta, Kunihiro Shiroishi, Toshihiko |
author_facet | Kono, Hiromitsu Tamura, Masaru Osada, Naoki Suzuki, Hitoshi Abe, Kuniya Moriwaki, Kazuo Ohta, Kunihiro Shiroishi, Toshihiko |
author_sort | Kono, Hiromitsu |
collection | PubMed |
description | PR/SET domain containing 9 (Prdm9) mediates histone modifications such as H3K4me3 and marks hotspots of meiotic recombination. In many mammalian species, the Prdm9 gene is highly polymorphic. Prdm9 polymorphism is assumed to play two critical roles in evolution: to diversify the spectrum of meiotic recombination hotspots and to cause male hybrid sterility, leading to reproductive isolation and speciation. Nevertheless, information about Prdm9 sequences in natural populations is very limited. In this study, we conducted a comprehensive population survey on Prdm9 polymorphism in the house mouse, Mus musculus. Overall M. musculus Prdm9 displays an extraordinarily high level of polymorphism, particularly in regions encoding zinc finger repeats, which recognize recombination hotspots. Prdm9 alleles specific to various M. musculus subspecies dominate in subspecies territories. Moreover, introgression into other subspecies territories was found for highly divergent Prdm9 alleles associated with t-haplotype. The results of our phylogeographical analysis suggest that the requirement for hotspot diversity depends on geographical range and time span in mouse evolution, and that Prdm9 polymorphism has not been maintained by a simple balanced selection in the population of each subspecies. |
format | Online Article Text |
id | pubmed-4060951 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-40609512014-06-18 Prdm9 Polymorphism Unveils Mouse Evolutionary Tracks Kono, Hiromitsu Tamura, Masaru Osada, Naoki Suzuki, Hitoshi Abe, Kuniya Moriwaki, Kazuo Ohta, Kunihiro Shiroishi, Toshihiko DNA Res Full Papers PR/SET domain containing 9 (Prdm9) mediates histone modifications such as H3K4me3 and marks hotspots of meiotic recombination. In many mammalian species, the Prdm9 gene is highly polymorphic. Prdm9 polymorphism is assumed to play two critical roles in evolution: to diversify the spectrum of meiotic recombination hotspots and to cause male hybrid sterility, leading to reproductive isolation and speciation. Nevertheless, information about Prdm9 sequences in natural populations is very limited. In this study, we conducted a comprehensive population survey on Prdm9 polymorphism in the house mouse, Mus musculus. Overall M. musculus Prdm9 displays an extraordinarily high level of polymorphism, particularly in regions encoding zinc finger repeats, which recognize recombination hotspots. Prdm9 alleles specific to various M. musculus subspecies dominate in subspecies territories. Moreover, introgression into other subspecies territories was found for highly divergent Prdm9 alleles associated with t-haplotype. The results of our phylogeographical analysis suggest that the requirement for hotspot diversity depends on geographical range and time span in mouse evolution, and that Prdm9 polymorphism has not been maintained by a simple balanced selection in the population of each subspecies. Oxford University Press 2014-06 2014-01-20 /pmc/articles/PMC4060951/ /pubmed/24449848 http://dx.doi.org/10.1093/dnares/dst059 Text en © The Author 2014. Published by Oxford University Press on behalf of Kazusa DNA Research Institute. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Full Papers Kono, Hiromitsu Tamura, Masaru Osada, Naoki Suzuki, Hitoshi Abe, Kuniya Moriwaki, Kazuo Ohta, Kunihiro Shiroishi, Toshihiko Prdm9 Polymorphism Unveils Mouse Evolutionary Tracks |
title | Prdm9 Polymorphism Unveils Mouse Evolutionary Tracks |
title_full | Prdm9 Polymorphism Unveils Mouse Evolutionary Tracks |
title_fullStr | Prdm9 Polymorphism Unveils Mouse Evolutionary Tracks |
title_full_unstemmed | Prdm9 Polymorphism Unveils Mouse Evolutionary Tracks |
title_short | Prdm9 Polymorphism Unveils Mouse Evolutionary Tracks |
title_sort | prdm9 polymorphism unveils mouse evolutionary tracks |
topic | Full Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4060951/ https://www.ncbi.nlm.nih.gov/pubmed/24449848 http://dx.doi.org/10.1093/dnares/dst059 |
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