Your browser doesn't support javascript.
loading
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.
Afiliación
  • Ben El Haj R; Research Team in Neurology and Neurogenetics, Genomics Center of Human Pathologies, Medical School and Pharmacy, Mohammed V University, Rabat, Morocco.
  • Salmi A; Laboratory of Information and Communication Technologies, National School of Applied Sciences, Abdelmalek Essaadi University, Tanger, Morocco.
  • Regragui W; Research Team in Neurology and Neurogenetics, Genomics Center of Human Pathologies, Medical School and Pharmacy, Mohammed V University, Rabat, Morocco.
  • Moussa A; Department of Neurology and Neurogenetics, Specialties Hospital, IBN Sina University Hospital Center, Rabat, Morocco.
  • Bouslam N; Laboratory of Information and Communication Technologies, National School of Applied Sciences, Abdelmalek Essaadi University, Tanger, Morocco.
  • Tibar H; Department of Neurology and Neurogenetics, Specialties Hospital, IBN Sina University Hospital Center, Rabat, Morocco.
  • Benomar A; Research Team in Neurology and Neurogenetics, Genomics Center of Human Pathologies, Medical School and Pharmacy, Mohammed V University, Rabat, Morocco.
  • Yahyaoui M; Department of Neurology and Neurogenetics, Specialties Hospital, IBN Sina University Hospital Center, Rabat, Morocco.
  • Bouhouche A; Research Team in Neurology and Neurogenetics, Genomics Center of Human Pathologies, Medical School and Pharmacy, Mohammed V University, Rabat, Morocco.
PLoS One ; 12(7): e0181335, 2017.
Article en En | MEDLINE | ID: mdl-28723952
ABSTRACT
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).
Asunto(s)

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Enfermedad de Parkinson / Haplotipos / Árabes / Proteína 2 Quinasa Serina-Treonina Rica en Repeticiones de Leucina Límite: Adult / Aged / Aged80 / Humans / Middle aged País/Región como asunto: Africa Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2017 Tipo del documento: Article País de afiliación: Marruecos

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Enfermedad de Parkinson / Haplotipos / Árabes / Proteína 2 Quinasa Serina-Treonina Rica en Repeticiones de Leucina Límite: Adult / Aged / Aged80 / Humans / Middle aged País/Región como asunto: Africa Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2017 Tipo del documento: Article País de afiliación: Marruecos