Population Genetic Implications from Sequence Variation in Four Y Chromosome Genes

Some insight into human evolution has been gained from the sequencing of four Y chromosome genes. Primary genomic sequencing determined gene SMCY to be composed of 27 exons that comprise 4,620 bp of coding sequence. The unfinished sequencing of the 5′portion of gene UTY1 was completed by primer walk...

Full description

Saved in:
Bibliographic Details
Published in:Proceedings of the National Academy of Sciences - PNAS Vol. 97; no. 13; pp. 7354 - 7359
Main Authors: Shen, Peidong, Wang, Frank, Underhill, Peter A., Franco, Claudia, Yang, Wei-Hsien, Roxas, Adriane, Sung, Raphael, Lin, Alice A., Hyman, Richard W., Vollrath, Douglas, Davis, Ronald W., Cavalli-Sforza, L. Luca, Oefner, Peter J.
Format: Journal Article
Language:English
Published: United States National Academy of Sciences of the United States of America 20-06-2000
National Acad Sciences
National Academy of Sciences
The National Academy of Sciences
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Some insight into human evolution has been gained from the sequencing of four Y chromosome genes. Primary genomic sequencing determined gene SMCY to be composed of 27 exons that comprise 4,620 bp of coding sequence. The unfinished sequencing of the 5′portion of gene UTY1 was completed by primer walking, and a total of 20 exons were found. By using denaturing HPLC, these two 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 found, yielding nucleotide diversity estimates of 2.45 × 10-5, 5.07 × 10-5, and 8.54 × 10-5for the coding regions of SMCY, DFFRY, and UTY1, respectively, with no variant having been observed in DBY. In agreement with most autosomal genes, diversity estimates for the noncoding regions were about 2- to 3-fold higher and ranged from 9.16 × 10-5to 14.2 × 10-5for the four genes. Analysis of the frequencies of derived alleles for all four genes 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 nucleotide mismatch distributions date the occurrence of population expansion to ≈ 28,000 years ago. This estimate is in accord with the spread of Aurignacian technology and the disappearance of the Neanderthals.
Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ObjectType-Article-1
ObjectType-Feature-2
Contributed by L. Luca Cavalli-Sforza
To whom reprint requests should be addressed. E-mail: shen@genome.stanford.edu.
ISSN:0027-8424
1091-6490
DOI:10.1073/pnas.97.13.7354