The DOI matches its Crossref record; 177 of the 177 references it cites were found in a registry or an index.
Genomic signatures of selection at linked sites: unifying the disparity among species
Open accessAbstract
Population genetics theory supplies powerful predictions about how natural selection interacts with genetic linkage to sculpt the genomic landscape of nucleotide polymorphism. Both the spread of beneficial mutations and the removal of deleterious mutations act to depress polymorphism levels, especially in low-recombination regions. However, empiricists have documented extreme disparities among species. Here we characterize the dominant features that could drive differences in linked selection among species — including roles for selective sweeps being 'hard' or 'soft' — and the concealing effects of demography and confounding genomic variables. We advocate targeted studies of closely related species to unify our understanding of how selection and linkage interact to shape genome evolution.
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Cites
Statistical method for testing the neutral mutation hypothesis by DNA polymorphism.
Tajima, F. (1989) · Genetics · doi:10.1093/genetics/123.3.585 · Cited by 13,941
The Comparative Method in Evolutionary Biology
Harvey, P. H., & Pagel, M. D. (1991) · doi:10.1093/oso/9780198546412.001.0001 · Cited by 4,337
Evolutionary Rate at the Molecular Level
KIMURA, M. (1968) · Nature · doi:10.1038/217624a0 · Cited by 3,737
The hitch-hiking effect of a favourable gene
Smith, J. M., & Haigh, J. (1974) · Genetical Research · doi:10.1017/s0016672300014634 · Cited by 3,415
Adaptive protein evolution at the Adh locus in Drosophila
McDonald, J. H., & Kreitman, M. (1991) · Nature · doi:10.1038/351652a0 · Cited by 3,283
The hitch-hiking effect of a favourable gene
MAYNARD, J., & HAIGH, J. (2007) · Genetics Research · doi:10.1017/s0016672308009579 · Cited by 2,643
THE NUMBER OF ALLELES THAT CAN BE MAINTAINED IN A FINITE POPULATION
Kimura, M., & Crow, J. F. (1964) · Genetics · doi:10.1093/genetics/49.4.725 · Cited by 2,620
Rate of de novo mutations and the importance of father’s age to disease risk
Kong, A., Frigge, M. L., Masson, G., Besenbacher, S., Sulem, P., Magnusson, G., Gudjonsson, S. A., Sigurdsson, A., Jonasdottir, A., Jonasdottir, A., et al. (2012) · Nature · doi:10.1038/nature11396 · Cited by 2,134
The effect of linkage on limits to artificial selection
Hill, W. G., & Robertson, A. (1966) · Genetical Research · doi:10.1017/s0016672300010156 · Cited by 1,823
The effect of deleterious mutations on neutral molecular variation.
Charlesworth, B., Morgan, M. T., & Charlesworth, D. (1993) · Genetics · doi:10.1093/genetics/134.4.1289 · Cited by 1,803
Cited by
Cruickshank, T. E., & Hahn, M. W. (2014) · Molecular Ecology · doi:10.1111/mec.12796 · Cited by 1,061
Determinants of genetic diversity
Ellegren, H., & Galtier, N. (2016) · Nature Reviews Genetics · doi:10.1038/nrg.2016.58 · Cited by 874
Coates, D. J., Byrne, M., & Moritz, C. (2018) · Frontiers in Ecology and Evolution · doi:10.3389/fevo.2018.00165 · Cited by 460
Making sense of genomic islands of differentiation in light of speciation
Wolf, J. B. W., & Ellegren, H. (2017) · Nature Reviews Genetics · doi:10.1038/nrg.2016.133 · Cited by 441
Burri, R., Nater, A., Kawakami, T., Mugal, C. F., Olason, P. I., Smeds, L., Suh, A., Dutoit, L., Bureš, S., Garamszegi, L. Z., et al. (2015) · Genome Research · doi:10.1101/gr.196485.115 · Cited by 403
Metadata
- Authors
- Cutter, A. D., & Payseur, B. A.
- Venue
- Nature Reviews Genetics
- Published
- 2013-03-12
- Volume
- 14
- Issue
- 4
- Pages
- 262-274
- ISSN
- 1471-0056 (ISSN-L)
- 1471-0064
- OpenAlex
- W1978025281
- Cited by
- 461
- References
- 177
- FWCI
- 4.56
- Type
- journal article
- Language
- en
- Open access
- green
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