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Evidence for prehistoric origins of the G2019S mutation in the North African Berber population
The most common cause of the monogenic form of Parkinson’s disease known so far is the G2019S mutation of the leucine-rich repeat kinase 2 (LRRK2) gene. Its frequency varies greatly among ethnic groups and geographic regions ranging from less than 0.1% in Asia to 40% in North Africa. This mutation h...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5517005/ https://www.ncbi.nlm.nih.gov/pubmed/28723952 http://dx.doi.org/10.1371/journal.pone.0181335 |
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author | Ben El Haj, Rafiqua Salmi, Ayyoub Regragui, Wafa Moussa, Ahmed Bouslam, Naima Tibar, Houyam Benomar, Ali Yahyaoui, Mohamed Bouhouche, Ahmed |
author_facet | Ben El Haj, Rafiqua Salmi, Ayyoub Regragui, Wafa Moussa, Ahmed Bouslam, Naima Tibar, Houyam Benomar, Ali Yahyaoui, Mohamed Bouhouche, Ahmed |
author_sort | Ben El Haj, Rafiqua |
collection | PubMed |
description | The most common cause of the monogenic form of Parkinson’s disease known so far is the G2019S mutation of the leucine-rich repeat kinase 2 (LRRK2) gene. Its frequency varies greatly among ethnic groups and geographic regions ranging from less than 0.1% in Asia to 40% in North Africa. This mutation has three distinct haplotypes; haplotype 1 being the oldest and most common. Recent studies have dated haplotype 1 of the G2019S mutation to about 4000 years ago, but it remains controversial whether the mutation has a Near-Eastern or Moroccan-Berber ancestral origin. To decipher this evolutionary history, we genotyped 10 microsatellite markers spanning a region of 11.27 Mb in a total of 57 unrelated Moroccan PD patients carrying the G2019S mutation for which the Berber or Arab origin was established over 3 generations based on spoken language. We estimated the age of the most recent common ancestor for the 36 Arab-speaking and the 15 Berber-speaking G2019S carriers using the likelihood-based method with a mutation rate of 10(−4). Data analysis suggests that the shortest haplotype originated in a patient of Berber ethnicity. The common founder was estimated to have lived 159 generations ago (95% CI 116–224) for Arab patients, and 200 generations ago (95% CI 123–348) for Berber patients. Then, 29 native North African males carrying the mutation were assessed for specific uniparental markers by sequencing the Y-chromosome (E-M81, E-M78, and M-267) and mitochondrial DNA (mtDNA) hypervariable regions (HV1 and HV2) to examine paternal and maternal contributions, respectively. Results showed that the autochthonous genetic component reached 76% for mtDNA (Eurasian and north African haplogroups) and 59% for the Y-chromosome (E-M81 and E-M78), suggesting that the G2019S mutation may have arisen in an autochthonous DNA pool. Therefore, we conclude that LRRK2 G2019S mutation most likely originated in a Berber founder who lived at least 5000 years ago (95% CI 3075–8700). |
format | Online Article Text |
id | pubmed-5517005 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-55170052017-08-07 Evidence for prehistoric origins of the G2019S mutation in the North African Berber population Ben El Haj, Rafiqua Salmi, Ayyoub Regragui, Wafa Moussa, Ahmed Bouslam, Naima Tibar, Houyam Benomar, Ali Yahyaoui, Mohamed Bouhouche, Ahmed PLoS One Research Article The most common cause of the monogenic form of Parkinson’s disease known so far is the G2019S mutation of the leucine-rich repeat kinase 2 (LRRK2) gene. Its frequency varies greatly among ethnic groups and geographic regions ranging from less than 0.1% in Asia to 40% in North Africa. This mutation has three distinct haplotypes; haplotype 1 being the oldest and most common. Recent studies have dated haplotype 1 of the G2019S mutation to about 4000 years ago, but it remains controversial whether the mutation has a Near-Eastern or Moroccan-Berber ancestral origin. To decipher this evolutionary history, we genotyped 10 microsatellite markers spanning a region of 11.27 Mb in a total of 57 unrelated Moroccan PD patients carrying the G2019S mutation for which the Berber or Arab origin was established over 3 generations based on spoken language. We estimated the age of the most recent common ancestor for the 36 Arab-speaking and the 15 Berber-speaking G2019S carriers using the likelihood-based method with a mutation rate of 10(−4). Data analysis suggests that the shortest haplotype originated in a patient of Berber ethnicity. The common founder was estimated to have lived 159 generations ago (95% CI 116–224) for Arab patients, and 200 generations ago (95% CI 123–348) for Berber patients. Then, 29 native North African males carrying the mutation were assessed for specific uniparental markers by sequencing the Y-chromosome (E-M81, E-M78, and M-267) and mitochondrial DNA (mtDNA) hypervariable regions (HV1 and HV2) to examine paternal and maternal contributions, respectively. Results showed that the autochthonous genetic component reached 76% for mtDNA (Eurasian and north African haplogroups) and 59% for the Y-chromosome (E-M81 and E-M78), suggesting that the G2019S mutation may have arisen in an autochthonous DNA pool. Therefore, we conclude that LRRK2 G2019S mutation most likely originated in a Berber founder who lived at least 5000 years ago (95% CI 3075–8700). Public Library of Science 2017-07-19 /pmc/articles/PMC5517005/ /pubmed/28723952 http://dx.doi.org/10.1371/journal.pone.0181335 Text en © 2017 Ben El Haj 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Ben El Haj, Rafiqua Salmi, Ayyoub Regragui, Wafa Moussa, Ahmed Bouslam, Naima Tibar, Houyam Benomar, Ali Yahyaoui, Mohamed Bouhouche, Ahmed Evidence for prehistoric origins of the G2019S mutation in the North African Berber population |
title | Evidence for prehistoric origins of the G2019S mutation in the North African Berber population |
title_full | Evidence for prehistoric origins of the G2019S mutation in the North African Berber population |
title_fullStr | Evidence for prehistoric origins of the G2019S mutation in the North African Berber population |
title_full_unstemmed | Evidence for prehistoric origins of the G2019S mutation in the North African Berber population |
title_short | Evidence for prehistoric origins of the G2019S mutation in the North African Berber population |
title_sort | evidence for prehistoric origins of the g2019s mutation in the north african berber population |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5517005/ https://www.ncbi.nlm.nih.gov/pubmed/28723952 http://dx.doi.org/10.1371/journal.pone.0181335 |
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