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1.
PLoS Genet ; 12(10): e1006335, 2016 Oct.
Article de Anglais | MEDLINE | ID: mdl-27760138

RÉSUMÉ

Left-ventricular outflow tract obstructions (LVOTO) encompass a wide spectrum of phenotypically heterogeneous heart malformations which frequently cluster in families. We performed family based whole-exome and targeted re-sequencing on 182 individuals from 51 families with multiple affected members. Central to our approach is the family unit which serves as a reference to identify causal genotype-phenotype correlations. Screening a multitude of 10 overlapping phenotypes revealed disease associated and co-segregating variants in 12 families. These rare or novel protein altering mutations cluster predominantly in genes (NOTCH1, ARHGAP31, MAML1, SMARCA4, JARID2, JAG1) along the Notch signaling cascade. This is in line with a significant enrichment (Wilcoxon, p< 0.05) of variants with a higher pathogenicity in the Notch signaling pathway in patients compared to controls. The significant enrichment of novel protein truncating and missense mutations in NOTCH1 highlights the allelic and phenotypic heterogeneity in our pediatric cohort. We identified novel co-segregating pathogenic mutations in NOTCH1 associated with left and right-sided cardiac malformations in three independent families with a total of 15 affected individuals. In summary, our results suggest that a small but highly pathogenic fraction of family specific mutations along the Notch cascade are a common cause of LVOTO.


Sujet(s)
Sténose pathologique/génétique , Cardiopathies congénitales/génétique , Récepteur Notch1/génétique , Obstacle à l'éjection ventriculaire/génétique , Valve aortique/physiopathologie , Codon non-sens , Sténose pathologique/physiopathologie , Exome/génétique , Femelle , Études d'associations génétiques , Liaison génétique , Génome humain , Cardiopathies congénitales/physiopathologie , Humains , Mâle , Pedigree , Récepteurs Notch/génétique , Délétion de séquence , Transduction du signal/génétique , Obstacle à l'éjection ventriculaire/physiopathologie
2.
Proc Natl Acad Sci U S A ; 111(3): 936-41, 2014 Jan 21.
Article de Anglais | MEDLINE | ID: mdl-24395773

RÉSUMÉ

Linguistic and cultural evidence suggest that Madagascar was the final point of two major dispersals of Austronesian- and Bantu-speaking populations. Today, the Mikea are described as the last-known Malagasy population reported to be still practicing a hunter-gatherer lifestyle. It is unclear, however, whether the Mikea descend from a remnant population that existed before the arrival of Austronesian and Bantu agriculturalists or whether it is only their lifestyle that separates them from the other contemporary populations of South Madagascar. To address these questions we have performed a genome-wide analysis of >700,000 SNP markers on 21 Mikea, 24 Vezo, and 24 Temoro individuals, together with 50 individuals from Bajo and Lebbo populations from Indonesia. Our analyses of these data in the context of data available from other Southeast Asian and African populations reveal that all three Malagasy populations are derived from the same admixture event involving Austronesian and Bantu sources. In contrast to the fact that most of the vocabulary of the Malagasy speakers is derived from the Barito group of the Austronesian language family, we observe that only one-third of their genetic ancestry is related to the populations of the Java-Kalimantan-Sulawesi area. Because no additional ancestry components distinctive for the Mikea were found, it is likely that they have adopted their hunter-gatherer way of life through cultural reversion, and selection signals suggest a genetic adaptation to their new lifestyle.


Sujet(s)
Génétique des populations , Polymorphisme de nucléotide simple , Groupes de population/génétique , Algorithmes , Asiatiques/génétique , /génétique , Culture (sociologie) , Ethnies/génétique , Géographie , Haplotypes , Homozygote , Humains , Linguistique , Madagascar , Mâle , Séquençage par oligonucléotides en batterie
3.
PLoS One ; 8(11): e80932, 2013.
Article de Anglais | MEDLINE | ID: mdl-24278350

RÉSUMÉ

Madagascar is located at the crossroads of the Asian and African worlds and is therefore of particular interest for studies on human population migration. Within the large human diversity of the Great Island, we focused our study on a particular ethnic group, the Antemoro. Their culture presents an important Arab-Islamic influence, but the question of an Arab biological inheritance remains unresolved. We analyzed paternal (n=129) and maternal (n=135) lineages of this ethnic group. Although the majority of Antemoro genetic ancestry comes from sub-Saharan African and Southeast Asian gene pools, we observed in their paternal lineages two specific haplogroups (J1 and T1) linked to Middle Eastern origins. This inheritance was restricted to some Antemoro sub-groups. Statistical analyses tended to confirm significant Middle Eastern genetic contribution. This study gives a new perspective to the large human genetic diversity in Madagascar.


Sujet(s)
Arabes/génétique , Chromosomes Y humains/génétique , ADN mitochondrial/génétique , Ethnies/génétique , Modes de transmission héréditaire/génétique , Islam , Bases de données génétiques , Femelle , Géographie , Haplotypes/génétique , Humains , Madagascar , Mâle , Répétitions microsatellites/génétique , Analyse en composantes principales , Recombinaison génétique/génétique
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