4.5 Article

Rapidly mutating Y-STRs in rapidly expanding populations: Discrimination power of the Yfiler Plus multiplex in northern Africa

Journal

FORENSIC SCIENCE INTERNATIONAL-GENETICS
Volume 38, Issue -, Pages 185-194

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.fsigen.2018.11.002

Keywords

Yfiler (R) Plus; E-M81 haplogroup; Northern African populations; Y-STRs

Funding

  1. Region Midi-Pyrenees (Toulouse, France)
  2. CNRS
  3. E.C. Sixth Framework Programme [ERASCT-2003-980409]
  4. Sapienza University of Rome [C26A153PCN]
  5. National Geographic Society [HJ-139-R17]

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The male-specific northern African genetic pool is characterised by a high frequency of the E-M81 haplogroup, which expanded in very recent times (2-3 kiloyears ago). As a consequence of their recent coalescence, E-M81 chromosomes often cannot be completely distinguished on the basis of their Y-STR profiles, unless rapidly-mutating Y-STRs (RM Y-STRs) are analysed. In this study, we used the Yfiler (R) Plus kit, which includes 7 RM Y-STRs and 20 standard Y-STR, to analyse 477 unrelated males coming from 11 northern African populations sampled from Morocco, Algeria, Libya and Egypt The Y chromosomes were assigned to monophyletic lineages after the analysis of 72 stable biallelic polymorphisms and, as expected, we found a high proportion of E-M81 subjects (about 46%), with frequencies decreasing from west to east We found low intra-population diversity indexes, in particular in the populations that experienced long-term isolation. The AMOVA analysis showed significant differences between the countries and between most of the 11 populations, with a rough differentiation between northwestern Africa and northeastern Africa, where the Egyptians Berbers from Siwa represented an outlier population. The comparison between the Yfiler (R) and the Yfiler (R) Plus network of the E-M81 Y chromosomes confirmed the high power of discrimination of the latter kit, thanks to higher variability of the RM Y-STRs: indeed, the number of chromosomes sharing the same haplotype was drastically reduced from 201 to 81 and limited, in the latter case, to subjects from the same population.

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