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Abstract

A genetic perspective of human history in Europe was derived from 22 binary markers of the nonrecombining Y chromosome (NRY). Ten lineages account for >95% of the 1007 European Y chromosomes studied. Geographic distribution and age estimates of alleles are compatible with two Paleolithic and one Neolithic migratory episode that have contributed to the modern European gene pool. A significant correlation between the NRY haplotype data and principal components based on 95 protein markers was observed, indicating the effectiveness of NRY binary polymorphisms in the characterization of human population composition and history.

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We thank all the men who donated DNA, K. Kyriakou for the Syrian samples, H. Cann for the French samples, A. Piazza for some of the Italian samples, and G. Brumat for helping us in some blood sample collections. We are also grateful to the anonymous reviewers for their constructive criticisms. Supported by NIH grants GM 28428 and GM 55273 to L.L.C.-S. and by funds from the Italian Ministry of the University “Progetti di ricerca ad interesse Nazionale” and PF “Beni culturali” to A.S.S.-B.

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Published In

Science
Volume 290 | Issue 5494
10 November 2000

Submission history

Received: 5 April 2000
Accepted: 25 September 2000
Published in print: 10 November 2000

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Authors

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Ornella Semino*,
Dipartimento di Genetica e Microbiologia, Università di Pavia, Via Ferrata 1, 27100 Pavia, Italy.
Department of Genetics, Stanford University School of Medicine, 300 Pasteur Drive, Stanford, CA 94305–5120, USA.
Giuseppe Passarino
Department of Genetics, Stanford University School of Medicine, 300 Pasteur Drive, Stanford, CA 94305–5120, USA.
Dipartimento di Biologia Cellulare, Università della Calabria, 87030 Rende, Italy.
† Peter J. Oefner
Stanford Genome Technology Center, 855 California Avenue, Palo Alto, CA 94304, USA.
Alice A. Lin
Department of Genetics, Stanford University School of Medicine, 300 Pasteur Drive, Stanford, CA 94305–5120, USA.
Svetlana Arbuzova
International Medico-Genetic Centre, Hospital Nol, 57 Artem Str, 340000 Donetsk, Ukraine.
Lars E. Beckman
Department of Oncology, Pathology and Medical Genetics, University of Umeå, S-901 85 Umeå, Sweden.
Giovanna De Benedictis
Dipartimento di Biologia Cellulare, Università della Calabria, 87030 Rende, Italy.
Paolo Francalacci
Dipartimento di Zoologia e Antropologia Biologica, Università di Sassari, Via Regina Margherita, 15, 07100 Sassari, Italy.
Anastasia Kouvatsi
Department of Genetics, Development and Molecular Biology, Aristotle University, 54006 Thessaloniki, Macedonia, Greece.
Svetlana Limborska
Institute of Molecular Genetics, Russian Academy of Sciences, Kurchatov Square, 2, Moscow 123182, Russia.
Mladen Marcikiæ
Clinical Hospital Center Osijek, Department of Pathology Medical School, J Huttlera 4, 31000 Osijek, Croatia.
Anna Mika
Regionalne Centrum Krwiodawstwa i Krwiolecznictwa w Lublinie–Oddzial w, Zamosciu, ul Legionow 10, 22400 Zamosc, Poland.
Barbara Mika
Samodzielny Publiczny Szpital Wojwodzki im. Papieza Jona Pawla II w, Zamosciu, ul Legionow 10, 22400 Zamosc, Poland.
Dragan Primorac
University Hospital Split, Department of Pediatrics, Laboratory for Clinical and Forensic Genetics, Spinèiæeva 1, 21000 Split, Croatia.
A. Silvana Santachiara-Benerecetti
Dipartimento di Genetica e Microbiologia, Università di Pavia, Via Ferrata 1, 27100 Pavia, Italy.
L. Luca Cavalli-Sforza
Department of Genetics, Stanford University School of Medicine, 300 Pasteur Drive, Stanford, CA 94305–5120, USA.
Peter A. Underhill
Department of Genetics, Stanford University School of Medicine, 300 Pasteur Drive, Stanford, CA 94305–5120, USA.

Notes

*
To whom correspondence should be addressed. E-mail: [email protected]
These authors contributed equally to this work.

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