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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...

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Autores principales: Ben El Haj, Rafiqua, Salmi, Ayyoub, Regragui, Wafa, Moussa, Ahmed, Bouslam, Naima, Tibar, Houyam, Benomar, Ali, Yahyaoui, Mohamed, Bouhouche, Ahmed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
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).
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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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