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1.
Int J Legal Med ; 135(3): 787-790, 2021 May.
Artículo en Inglés | MEDLINE | ID: mdl-33392656

RESUMEN

In this study, we investigate the forensic and population genetics properties of 21 X-chromosome markers (9 X-Alu insertions and 12 X-STRs) in a dataset composed of 716 individuals from 11 Western Mediterranean populations. The high values of combined forensic parameters indicate that this 21 X-loci panel can complement autosomal or uniparental markers in kinship analysis and complex deficient paternity testing in the populations studied. Population analyses revealed a lower differentiation between Western Mediterranean human groups for X-STRs than for X-Alu insertion polymorphisms. Moreover, X-chromosome markers suggest a sex-biased migration rate, confirming the predominance of patrilocality in this area.


Asunto(s)
Cromosomas Humanos X , Etnicidad/genética , Marcadores Genéticos , Genética de Población , Femenino , Genética Forense , Humanos , Masculino , Región Mediterránea/etnología
2.
Forensic Sci Int Genet ; 31: e5-e11, 2017 11.
Artículo en Inglés | MEDLINE | ID: mdl-28951006

RESUMEN

Population genetic data for 53 X-chromosome markers (32 X-indels, 9 X-Alu insertions and 12 X-STRs) are reported for five populations with Jewish ancestry (Sephardim, North African Jews, Middle Eastern Jews, Ashkenazim, and Chuetas) and Majorca, as the host population of Chuetas. Genetic distances between these populations demonstrated significant differences, except between Sephardic and North African Jews, with the Chuetas as the most differentiated group, in accordance with the particular demographic history of this population. X-chromosome analysis and a comparison with autosomal data suggest a generally sex-biased demographic history in Jewish populations. Asymmetry was found between female and male effective population sizes both in the admixture processes between Jewish communities, and between them and their respective non-Jewish host populations. Results further show that these X-linked markers are highly informative for forensic purposes, and highlight the need for specific databases for differentiated Jewish populations.


Asunto(s)
Elementos Alu , Cromosomas Humanos X , Mutación INDEL , Judíos/genética , Repeticiones de Microsatélite , Dermatoglifia del ADN , Femenino , Frecuencia de los Genes , Marcadores Genéticos , Haplotipos , Humanos , Masculino , Mutagénesis Insercional , Polimorfismo Genético
3.
Int J Legal Med ; 129(2): 253-5, 2015 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-25209717

RESUMEN

Haplotype and allele frequencies of 12 X-STRs included in the Investigator Argus X-12 kit are reported for 255 individuals, representing four Western Mediterranean populations: Valencia (eastern mainland Spain) and the Balearic Islands (Majorca, Minorca, and Ibiza). Ibiza shows the lowest intra-population variability and the highest level of linkage disequilibrium together with an important genetic distance with regard to the geographically close populations, which is consistent with the historical evidence for long-term demographic isolation and its different matrilineal background.


Asunto(s)
Cromosomas Humanos X , Etnicidad/genética , Genética de Población , Repeticiones de Microsatélite , Dermatoglifia del ADN , Femenino , Frecuencia de los Genes , Haplotipos , Humanos , Desequilibrio de Ligamiento , Masculino , España
4.
Meta Gene ; 2: 427-38, 2014 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-25606427

RESUMEN

Detecting population substructure and ancestry is a critical issue for both association studies of health behaviors and forensic genetics. Determining aspects of a population's genetic history as potential sources of substructure can aid in design of future genetic studies. Within this context, fifteen autosomal short tandem repeat (STR), were used to examine population genetic structure and hypotheses of the origin of the modern Moroccan population from individuals belonging to three different ethnical groups from Morocco (Arab, Berber and Sahrawi), by comparing their autosomal STR variation with that of neighboring and non-neighboring populations in North Africa, Europe and Middle East as well as proposed ancestral populations in Morocco (Berber). We report on the results that the gradient of North African ancestry accounts for previous observations of low levels of sharing with Near East and a substantially increased gene flow especially from Morocco and Spain.

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