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Population Genomics of Daphnia pulex .

Authors :
Lynch M
Gutenkunst R
Ackerman M
Spitze K
Ye Z
Maruki T
Jia Z
Source :
Genetics [Genetics] 2017 May; Vol. 206 (1), pp. 315-332. Date of Electronic Publication: 2016 Dec 07.
Publication Year :
2017

Abstract

Using data from 83 isolates from a single population, the population genomics of the microcrustacean Daphnia pulex are described and compared to current knowledge for the only other well-studied invertebrate, Drosophila melanogaster These two species are quite similar with respect to effective population sizes and mutation rates, although some features of recombination appear to be different, with linkage disequilibrium being elevated at short ([Formula: see text] bp) distances in D. melanogaster and at long distances in D. pulex The study population adheres closely to the expectations under Hardy-Weinberg equilibrium, and reflects a past population history of no more than a twofold range of variation in effective population size. Fourfold redundant silent sites and a restricted region of intronic sites appear to evolve in a nearly neutral fashion, providing a powerful tool for population genetic analyses. Amino acid replacement sites are predominantly under strong purifying selection, as are a large fraction of sites in UTRs and intergenic regions, but the majority of SNPs at such sites that rise to frequencies [Formula: see text] appear to evolve in a nearly neutral fashion. All forms of genomic sites (including replacement sites within codons, and intergenic and UTR regions) appear to be experiencing an [Formula: see text] higher level of selection scaled to the power of drift in D. melanogaster , but this may in part be a consequence of recent demographic changes. These results establish D. pulex as an excellent system for future work on the evolutionary genomics of natural populations.<br /> (Copyright © 2017 by the Genetics Society of America.)

Details

Language :
English
ISSN :
1943-2631
Volume :
206
Issue :
1
Database :
MEDLINE
Journal :
Genetics
Publication Type :
Academic Journal
Accession number :
27932545
Full Text :
https://doi.org/10.1534/genetics.116.190611