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Originally published as Genetics Published Articles Ahead of Print on October 22, 2006.
Genetics, Vol. 174, 2095-2105, December 2006, Copyright © 2006
doi:10.1534/genetics.106.065102
Multilocus Patterns of Nucleotide Diversity, Linkage Disequilibrium and Demographic History of Norway Spruce [Picea abies (L.) Karst]
Myriam Heuertz*,
,1,2,
Emanuele De Paoli
,1,
Thomas Källman*,1,
Hanna Larsson*,
Irena Jurman
,
Michele Morgante
,
Martin Lascoux*,3 and
Niclas Gyllenstrand*,1
* Program in Evolutionary Functional Genetics, Evolutionary Biology Centre, Uppsala University, 75326 Uppsala, Sweden,
Centre de Recherche Public-Gabriel Lippmann, L-4422 Belvaux, Luxembourg and
Dipartimento di Scienze Agrarie ed Ambientali, Università di Udine, 33100 Udine, Italy
3 Corresponding author: Program in Evolutionary Functional Genetics, Evolutionary Biology Centre, Uppsala University, Norbyvägen 18D, 75326 Uppsala, Sweden.
E-mail: martin.lascoux{at}ebc.uu.se
DNA polymorphism at 22 loci was studied in an average of 47 Norway spruce [Picea abies (L.) Karst.] haplotypes sampled in seven populations representative of the natural range. The overall nucleotide variation was limited, being lower than that observed in most plant species so far studied. Linkage disequilibrium was also restricted and did not extend beyond a few hundred base pairs. All populations, with the exception of the Romanian population, could be divided into two main domains, a BalticoNordic and an Alpine one. Mean Tajima's D and Fay and Wu's H across loci were both negative, indicating the presence of an excess of both rare and high-frequency-derived variants compared to the expected frequency spectrum in a standard neutral model. Multilocus neutrality tests based on D and H led to the rejection of the standard neutral model and exponential growth in the whole population as well as in the two main domains. On the other hand, in all three cases the data are compatible with a severe bottleneck occurring some hundreds of thousands of years ago. Hence, demographic departures from equilibrium expectations and population structure will have to be accounted for when detecting selection at candidate genes and in association mapping studies, respectively.
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