Some insight into human evolution has been gained from the sequencing of fo
ur Y chromosome genes. Primary genomic: sequencing determined gene SMCY to
be composed of 27 exons that comprise 4,620 bp of coding sequence. The unfi
nished sequencing of the 5' portion of gene UTY1 was completed by primer wa
lking, and a total of 20 exons were found. By using denaturing HPLC these t
wo genes, as well as DBY and DFFRY, were screened for polymorphic sites in
53-72 representatives of the five continents. A total of 98 variants were f
ound, yielding nucleotide diversity estimates of 2.45 x 10(-5), 5.07 x 10(-
5), and 8.54 x 10(-5) for the coding regions of SMCY. DFFRY, and UTY1, resp
ectively, with no variant having been observed in DBY. In agreement with mo
st autosomal genes, diversity estimates for the noncoding regions were abou
t 2- to 3-fold higher and ranged from 9.16 x 10(-5) to 14.2 x 10(-5) for th
e four genes. Analysis of the frequencies of derived alleles for all four g
enes showed that they more closely fit the expectation of a Luria-Delbruck
distribution than a distribution expected under a constant population size
model. providing evidence for exponential population growth. Pairwise nucle
otide mismatch distributions date the occurrence of population expansion to
approximate to 28,000 years ago. This estimate is in accord with the sprea
d of Aurignacian technology and the disappearance of the Neanderthals.