Literature DB >> 23961977

An investigation of the genetic diversity of the Kerkennah islands and Mahdia (Tunisia) using biparental markers.

Sabeh Frigi1, Amel Ben Ammar El Gaaied, Lotfi Cherni.   

Abstract

BACKGROUND: Kerkennah is one of the main inhabited islands of Tunisia. The origin of the population of Kerkennah has not been established and no well-defined ethnic groups have been identified nor are genetic studies available. Mahdia, a Tunisian coastal city, has a long history dating back to ancient times. AIM: To discover the genetic diversity of the two studied populations and analyse their relationships with other Mediterranean populations. SUBJECT AND METHODS: Seven human-specific Alu insertion polymorphisms were typed in 99 individuals born in Kerkennah and Mahdia.
RESULTS: A neighbour-joining tree and MDS multidimensional scaling analysis showed that these Tunisian populations are scattered amongst North African and Europeans populations, indicating their high genetic diversity and mosaic aspect. The important finding of this study was the proximity of Kerkennah to Moroccans. Hence, the actual gene pool of this insular population may descend from the ancestral population known to be of Moroccan origin. Concerning Mahdia, its closeness to Eurasian populations and some Tunisian groups reflected a high Eurasian genetic component for North African populations and confirmed their heterogeneity.
CONCLUSION: The strategic location of the two studied populations and their fortifications have allowed them to play a leading role in the Mediterranean basin.

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Year:  2013        PMID: 23961977     DOI: 10.3109/03014460.2013.824025

Source DB:  PubMed          Journal:  Ann Hum Biol        ISSN: 0301-4460            Impact factor:   1.533


  1 in total

1.  New Insight into the human genetic diversity in North African populations by genotyping of SNPs in DRD3, CSMD1 and NRG1 genes.

Authors:  Souhir Mestiri; Sami Boussetta; Andrew J Pakstis; Sarra El Kamel; Amel Ben Ammar El Gaaied; Kenneth K Kidd; Lotfi Cherni
Journal:  Mol Genet Genomic Med       Date:  2022-02-07       Impact factor: 2.183

  1 in total

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