Mucopolysaccharidosis type I: founder effect of the p.P533R mutation in North Africa.

Autor: Chkioua L; Research Laboratory of Human Genome and Multifactorial Diseases (LR12ES07), Faculty of Pharmacy, University of Monastir, Monastir, Tunisia. chkioualatifa2002@yahoo.fr., El Fissi H; Department of Biology, Laboratory of Biotechnologies and Valorization of Natural Resources, School of Sciences, IBN Zohr University, Agadir, Morocco., Amri Y; Laboratory of Biochemistry (LR 00SP03), Bechir Hamza Children's Hospital, Tunis, Tunisia.; Department of Educational Sciences, Higher Institute of Applied Studies in Humanity Le Kef, University of Jendouba, Le Kef, Tunisia., Sahli C; Laboratory of Biochemistry (LR 00SP03), Bechir Hamza Children's Hospital, Tunis, Tunisia., Bouzid F; Department of Biology, Laboratory of Biotechnologies and Valorization of Natural Resources, School of Sciences, IBN Zohr University, Agadir, Morocco., Boudabous H; Laboratory of Pediatrics, La Rabta Hospital, Tunis, Tunisia., Tbib N; Laboratory of Pediatrics, La Rabta Hospital, Tunis, Tunisia., Ferchichi S; Laboratory of Biochemistry, Farhat Hached Hospital, Sousse, Tunisia., Massoud T; Laboratory of Biochemistry (LR 00SP03), Bechir Hamza Children's Hospital, Tunis, Tunisia., Alif N; Department of Biology, Laboratory of Biotechnologies and Valorization of Natural Resources, School of Sciences, IBN Zohr University, Agadir, Morocco., Laradi S; The Eurofins biomedical laboratory -Interlab, Toulouse, 31000, France., Ben Abdennebi H; Research Laboratory of Human Genome and Multifactorial Diseases (LR12ES07), Faculty of Pharmacy, University of Monastir, Monastir, Tunisia.
Jazyk: angličtina
Zdroj: BMC genomics [BMC Genomics] 2024 Oct 09; Vol. 25 (1), pp. 948. Date of Electronic Publication: 2024 Oct 09.
DOI: 10.1186/s12864-024-10724-1
Abstrakt: Background: Mucopolysaccharidosis type I is a lysosomal storage disease resulting from a deficiency in alpha-L-iduronidase (IDUA), which causes the accumulation of partially degraded dermatan sulfate and heparan sulfate. This retrospective study, spanning eight years, analyzed data from 45 MPSI patients. The report aimed to explore the potential origin of the p.P533R mutation in the Maghrebin population by constructing a single-nucleotide polymorphism haplotype around the IDUA gene, in order to propose a molecular proof of a founder effect of the MPSI/p.P533R allele.
Patients and Methods: All of the studied patients were from Libya (2), Mauritania (1) Morocco (21) and Tunisia (21) with first cousins being the most frequent union. The diagnosis of MPSI patients often involves the combination of urinary screening, leukocyte IDUA activity determination, and DNA molecular analysis. In our study, to identify the common p.P533R mutation, we performed both DNA sequencing and tetra-primer ARMS PCR assay. Additionally, Haploview was used to determine the specific haplotype that cosegregates with the p.P533R mutation. Controls were genotyped to ensure that all the SNPs were in Hardy-Weinberg equilibrium.
Results: In the present report we confirmed the very strong impact of consanguinity on the incidence of MPSI disease. Furthermore, studied families of mixed ancestry shared common and specific haplotype, which was observed in studied populations, suggesting the presence of a founder effect in the North Africa.
Conclusion: The p.P533R missense mutation was identified in each patient originated from Libya, Mauritania, Morocco and Tunisia. Furthermore, these MPSI patients exhibited the same IDUA haplotype. The occurrence of a shared AAGGGTG haplotype, among North African populations may be attributed to substantial historical gene exchange between these groups, likely stemming from migration, inter-ethnic marriage, or other forms of interaction throughout history.
(© 2024. The Author(s).)
Databáze: MEDLINE
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