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High Diversity at PRDM9 in Chimpanzees and Bonobos
BACKGROUND: The PRDM9 locus in mammals has increasingly attracted research attention due to its role in mediating chromosomal recombination and possible involvement in hybrid sterility and hence speciation processes. The aim of this study was to characterize sequence variation at the PRDM9 locus in...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3388066/ https://www.ncbi.nlm.nih.gov/pubmed/22768294 http://dx.doi.org/10.1371/journal.pone.0039064 |
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author | Groeneveld, Linn Fenna Atencia, Rebeca Garriga, Rosa M. Vigilant, Linda |
author_facet | Groeneveld, Linn Fenna Atencia, Rebeca Garriga, Rosa M. Vigilant, Linda |
author_sort | Groeneveld, Linn Fenna |
collection | PubMed |
description | BACKGROUND: The PRDM9 locus in mammals has increasingly attracted research attention due to its role in mediating chromosomal recombination and possible involvement in hybrid sterility and hence speciation processes. The aim of this study was to characterize sequence variation at the PRDM9 locus in a sample of our closest living relatives, the chimpanzees and bonobos. METHODOLOGY/PRINCIPAL FINDINGS: PRDM9 contains a highly variable and repetitive zinc finger array. We amplified this domain using long-range PCR and determined the DNA sequences using conventional Sanger sequencing. From 17 chimpanzees representing three subspecies and five bonobos we obtained a total of 12 alleles differing at the nucleotide level. Based on a data set consisting of our data and recently published Pan PRDM9 sequences, we found that at the subspecies level, diversity levels did not differ among chimpanzee subspecies or between chimpanzee subspecies and bonobos. In contrast, the sample of chimpanzees harbors significantly more diversity at PRDM9 than samples of humans. Pan PRDM9 shows signs of rapid evolution including no alleles or ZnFs in common with humans as well as signals of positive selection in the residues responsible for DNA binding. CONCLUSIONS AND SIGNIFICANCE: The high number of alleles specific to the genus Pan, signs of positive selection in the DNA binding residues, and reported lack of conservation of recombination hotspots between chimpanzees and humans suggest that PRDM9 could be active in hotspot recruitment in the genus Pan. Chimpanzees and bonobos are considered separate species and do not have overlapping ranges in the wild, making the presence of shared alleles at the amino acid level between the chimpanzee and bonobo species interesting in view of the hypothesis that PRDM9 plays a universal role in interspecific hybrid sterility. |
format | Online Article Text |
id | pubmed-3388066 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-33880662012-07-05 High Diversity at PRDM9 in Chimpanzees and Bonobos Groeneveld, Linn Fenna Atencia, Rebeca Garriga, Rosa M. Vigilant, Linda PLoS One Research Article BACKGROUND: The PRDM9 locus in mammals has increasingly attracted research attention due to its role in mediating chromosomal recombination and possible involvement in hybrid sterility and hence speciation processes. The aim of this study was to characterize sequence variation at the PRDM9 locus in a sample of our closest living relatives, the chimpanzees and bonobos. METHODOLOGY/PRINCIPAL FINDINGS: PRDM9 contains a highly variable and repetitive zinc finger array. We amplified this domain using long-range PCR and determined the DNA sequences using conventional Sanger sequencing. From 17 chimpanzees representing three subspecies and five bonobos we obtained a total of 12 alleles differing at the nucleotide level. Based on a data set consisting of our data and recently published Pan PRDM9 sequences, we found that at the subspecies level, diversity levels did not differ among chimpanzee subspecies or between chimpanzee subspecies and bonobos. In contrast, the sample of chimpanzees harbors significantly more diversity at PRDM9 than samples of humans. Pan PRDM9 shows signs of rapid evolution including no alleles or ZnFs in common with humans as well as signals of positive selection in the residues responsible for DNA binding. CONCLUSIONS AND SIGNIFICANCE: The high number of alleles specific to the genus Pan, signs of positive selection in the DNA binding residues, and reported lack of conservation of recombination hotspots between chimpanzees and humans suggest that PRDM9 could be active in hotspot recruitment in the genus Pan. Chimpanzees and bonobos are considered separate species and do not have overlapping ranges in the wild, making the presence of shared alleles at the amino acid level between the chimpanzee and bonobo species interesting in view of the hypothesis that PRDM9 plays a universal role in interspecific hybrid sterility. Public Library of Science 2012-07-02 /pmc/articles/PMC3388066/ /pubmed/22768294 http://dx.doi.org/10.1371/journal.pone.0039064 Text en Groeneveld et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Groeneveld, Linn Fenna Atencia, Rebeca Garriga, Rosa M. Vigilant, Linda High Diversity at PRDM9 in Chimpanzees and Bonobos |
title | High Diversity at PRDM9 in Chimpanzees and Bonobos |
title_full | High Diversity at PRDM9 in Chimpanzees and Bonobos |
title_fullStr | High Diversity at PRDM9 in Chimpanzees and Bonobos |
title_full_unstemmed | High Diversity at PRDM9 in Chimpanzees and Bonobos |
title_short | High Diversity at PRDM9 in Chimpanzees and Bonobos |
title_sort | high diversity at prdm9 in chimpanzees and bonobos |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3388066/ https://www.ncbi.nlm.nih.gov/pubmed/22768294 http://dx.doi.org/10.1371/journal.pone.0039064 |
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