Y chromosomal polymorphisms were studied in 502 males from 16 Eurasian ethn
ic groups including the Finns, Saami (Inari Lake area and Skolt Saami), Kar
elians, Mari, Mokshas, Erzas, Hungarians (Budapest area and Csangos), Khant
y, Mansi, Yakuts, Koryaks, Nivkhs, Mongolians, and Latvians. The samples we
re analysed for polymorphisms in the Y chromosome specific Alu insertion (Y
AP) and six microsatellites (DYS19, DYS389-I and II, DYS390, DYS392, DYS393
). The populations were also screened for the recently described Tat polymo
rphism. The incidence of YAP(+) type was highest in the Csangos and in othe
r Hungarians (37.5% and 17.5%, respectively). In the Karelians and the Latv
ians it was present at approximately the same level as commonly found in ot
her European populations, whilst absent in our further samples of Eurasian
populations, including the Finns and the Saami. Aside from the Hungarians,
the C allele of the Tat polymorphism was common in all the Finno-Ugric spea
king populations (from 8.2% to 63.2%), with highest incidence in the Ob-Ugr
ian Khanty. The C allele was also found in the Latvians (29.4%). The haplot
ypes found associated with the Tat C allele showed consistently lower densi
ty than those associated with the T allele, indicating that the T allele is
the original form. The computation of the age of the Tat C suggested that
the mutation might be a relatively recent event giving a maximum likelihood
estimate of 4440years (95% confidence interval about 3140-6200years). The
distribution patterns of the 222 haplotypes found varied considerably among
the populations. In the Finns a majority of the haplotypes could be assign
ed to two distinct groups, one of which harboured the C allele of the Tat p
olymorphism indicating dichotomous primary source of genetic variation amon
g Finnish males. The presence of a bottleneck or founding effect in the mal
e lineages of some of the populations, namely in the Finns and the Saami, w
ould appear to be one likely interpretation for these findings.