QST–FST comparisons: evolutionary and ecological insights from genomic heterogeneity
Abstract
Comparative studies of the divergence of quantitative traits and neutral molecular markers, known as Q(ST)-F(ST) comparisons, provide a means for researchers to distinguish between natural selection and genetic drift as causes of population differentiation in complex polygenic traits. The use of Q(ST)-F(ST) comparisons has increased rapidly in the last few years, highlighting the utility of this approach for addressing a wide range of questions that are relevant to evolutionary and ecological genetics. These studies have also provided lessons for the design of future Q(ST)-F(ST) comparisons. Methods based on the Q(ST)-F(ST) approach could also be used to analyse various types of 'omics' data in new and revealing ways.
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By testing whether QST is significantly greater than FST, it is possible to determine whether there is more genetically explained trait variation among populations than expected under neutral evolution.
“Thus, by testing whether QST is significantly greater than FST, it is possible to determine whether there is more genetically explained trait variation among populations than expected under neutral evolution (28–31).”
From Heritability within groups is uninformative about differences among groups: Cases from behavioral, evolutionary, and statistical genetics (2024) · cites this paper as [31]
Under a null model in which phenotypes are selectively neutral, genetic propensity differences contributing to phenotypic differences among populations are predicted to be small, with the expected difference among populations in the trait having comparable magnitude to the classical estimate of the 'apportionment of human genetic diversity'.
“Under a null model in which phenotypes are selectively neutral, genetic propensity differences contributing to phenotypic differences among populations are predicted to be small.”
From Interpreting polygenic scores, polygenic adaptation, and human phenotypic differences (2019) · cites this paper as [43]
Analogous measures of population differences in quantitative phenotypic traits and genetic loci-termed QST and FST, respectively-are approximately equal in neutral evolutionary models that include genetic drift but not natural selection.
“In other words, analogous measures of population differences in quantitative phenotypic traits and genetic loci—termed QST and FST, respectively—are approximately equal in neutral evolutionary models that include genetic drift but not natural selection.”
From Interpreting polygenic scores, polygenic adaptation, and human phenotypic differences (2019) · cites this paper as [43]
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Volis, S., Ormanbekova, D., & Shulgina, I. (2016) · Molecular Ecology · doi:10.1111/mec.13565 · Cited by 54 · see citing works
“Soon after its introduction the QST–FST comparison has become a routine test for adaptive population divergence (reviewed in Leinonen et al. 2008, 2013; De Kort et al. 2013) despite its recognized methodological limitations (Leinonen et al. 2008; Pujol et al. 2008; Whitlock 2008; Whitlock &…”
BackgroundCsilléry, K., Buchmann, N., & Fady, B. (2020) · Evolutionary Applications · doi:10.1111/eva.13029 · Cited by 53 · see citing works
Rathmann, H., & Reyes-Centeno, H. (2020) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.1914330117 · Cited by 53 · see citing works
“To account for stochastic variation inherent to a neutral model of evolution, we calculated r for a given dental trait or trait combination 1,000 times, each time comparing the DP matrix to different DG matrices arrived at by resampling the microsatellite loci data (23, 62).”
BackgroundMethodPerrard, A., Arca, M., Rome, Q., Muller, F. J., Tan, J.-L., Bista, S., Nugroho, H., Baudoin, R., Baylac, M., Silvain, J.-F., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0094162 · Cited by 59 · see citing works
“However, these estimates involve the intra-population variation [57] which can hardly be estimated for lowly sampled populations such as some of ours.”
BackgroundKarhunen, M., Ovaskainen, O., Herczeg, G., & Merilä, J. (2014) · Evolution; international journal of organic evolution · doi:10.1111/evo.12268 · Cited by 51 · see citing works
“…we are able to provide the first formal demonstration of natural selection (but see Shimada et al. 2011) in this extensively studied model system, where earlier studies have provided only indirect indications for adaptive differentiation in a range of quantitative traits (reviewed by Merilä 2013).”
BackgroundSelf-citationThe evolution of group differences in changing environments
Harpak, A., & Przeworski, M. (2021) · PLOS Biology · doi:10.1371/journal.pbio.3001072 · Cited by 50 · see citing works
Ledoux, J., Aurelle, D., Bensoussan, N., Marschal, C., Féral, J., & Garrabou, J. (2015) · Ecology and Evolution · doi:10.1002/ece3.1324 · Cited by 53 · see citing works
“If the trait evolves neutrally, then QST should be equal to FST (Leinonen et al. 2013).”
BackgroundInfluentialEpigenetic plasticity enables copepods to cope with ocean acidification
Lee, Y. H., Kim, M.-S., Wang, M.-H., Bhandari, R., Park, H., Wu, R., & Lee, J.-S. (2022) · Nature Climate Change · doi:10.1038/s41558-022-01477-4 · Cited by 48 · see citing works
Ramírez‐Valiente, J. A., Deacon, N. J., Etterson, J. R., Sparks, J. P., Sparks, K. L., Longwell, T., Pilz, G. E., & Cavender-Bares, J. M. (2018) · Molecular Ecology · doi:10.1111/mec.14566 · Cited by 47 · see citing works
“Only a few studies have analysed QST under contrasting growing conditions (or treatments), most of them in animals (Leinonen et al., 2013).”
BackgroundInfluentialMcDonald, B. A. (2015) · Plant Pathology · doi:10.1111/ppa.12415 · Cited by 60 · see citing works
Firmat, C., Delzon, S., Louvet, J., Parmentier, J., & Kremer, A. (2017) · Journal of Evolutionary Biology · doi:10.1111/jeb.13185 · Cited by 47 · see citing works
“…the QST distribution was compared to the extreme tail of the FST distribution: a 95% upper bound was calculated from the mean FST assuming a chisquare distribution with (npopulations – 1) degrees of freedom, that is the Lewontin–Krakauer distribution (Lewontin & Krakauer, 1973; Whitlock, 2008).”
The evolution of metabolism: How to test evolutionary hypotheses at the genomic level
Scossa, F., & Fernie, A. R. (2020) · Computational and Structural Biotechnology Journal · doi:10.1016/j.csbj.2020.02.009 · Cited by 56 · see citing works
“…[108]; here, suffice to say that F ST , in its sim-plified form, may be expressed as: 2 between þ r 2 within ð 1 Þ where r 2 between is the total genetic variation in a defined locus between populations while r 2 within is the total genetic variation in the same locus within the population [156].”
BackgroundMethodSeeholzer, G., & Brumfield, R. (2018) · Molecular Ecology · doi:10.1111/mec.14429 · Cited by 46
Heritability and quantitative genetic divergence of serotiny, a fire-persistence plant trait
Hernandez‐Serrano, A., Verdú, M., del Blanco, L. S., Climent, J., González‐Martínez, S. C., & Pausas, J. G. (2014) · Annals of Botany · doi:10.1093/aob/mcu142 · Cited by 72 · see citing works
Sun, Y., & Roderick, G. (2019) · Journal of Ecology · doi:10.1111/1365-2745.13198 · Cited by 45
QST–FST comparisons with unbalanced half‐sib designs
Gilbert, K., & Whitlock, M. (2015) · Molecular Ecology Resources · doi:10.1111/1755-0998.12303 · Cited by 45 · see citing works
“QST (Prout & Barker 1993; Spitze 1993) is a commonly used metric of the relative amount of genetic differentiation among populations for quantitative traits (Lynch et al. 1999; Leinonen et al. 2008, 2013; Whitlock 2008).”
BackgroundNeutral and adaptive genomic signatures of rapid poleward range expansion
Swaegers, J., Mergeay, J., Geystelen, A. V., Therry, L., Larmuseau, M., & Stoks, R. (2015) · Molecular Ecology · doi:10.1111/mec.13462 · Cited by 44 · see citing works
“2006), which both may be strong and underlie trait evolution (Leinonen et al. 2013).”
BackgroundBarnes, A. C., Rodríguez-Zapata, F., Juárez-Núñez, K. A., Gates, D. J., Janzen, G. M., Kur, A., Wang, L., Jensen, S., Estévez-Palmas, J. M., Crow, T. M., et al. (2022) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.2100036119 · Cited by 43 · see citing works
Chung, M. Y., Son, S., Herrando‐Moraira, S., Tang, C. Q., Maki, M., Kim, Y.-D., López-Pujol, J., Hamrick, J., & Chung, M. (2020) · Conservation Biology · doi:10.1111/cobi.13467 · Cited by 43 · see citing works
“…in several tree species among-population differentiation at several quantitative (morphological and physiological) traits (mean measured as QST, the among-population differentiation at quantitative, adaptive traits) is higher than GST (Lamy et al. 2012; De Kort et al., 2013; Leinonen et al. 2013).”
BackgroundTibblin, P., Forsman, A., Koch‐Schmidt, P., Nordahl, O., Johannessen, P., Nilsson, J., & Larsson, P. (2015) · American Naturalist · doi:10.1086/681597 · Cited by 43 · see citing works
“To establish whether differentiation among subpopulations was adaptive, we compared phenotypic differentiation estimated from the common-garden experiment (QST) with the neutral expectation based on microsatellite loci (FST; Leinonen et al. 2013).”
BackgroundMethodHaguenauer, A., Zuberer, F., Ledoux, J., & Aurelle, D. (2013) · Journal of Experimental Marine Biology and Ecology · doi:10.1016/j.jembe.2013.10.010 · Cited by 58 · see citing works
Roux, F., & Bergelson, J. (2016) · Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2016.03.001 · Cited by 42
Detecting Adaptive Differentiation in Structured Populations with Genomic Data and Common Gardens
Josephs, E. B., Berg, J. J., Ross-Ibarra, J., & Coop, G. (2018) · Genetics · doi:10.1534/genetics.118.301786 · Cited by 41 · see citing works
Guo, B., Lu, D., Liao, W. B., & Merilä, J. (2016) · Molecular Ecology · doi:10.1111/mec.13722 · Cited by 47 · see citing works
“…the outlier approaches were able to pick up footprints of directional selection; in general, it becomes more difficult to detect signals of adaptive differentiation as the neutral genetic baseline increases (e.g. O’Hara & Meril€a 2005; Leinonen et al. 2008, 2013; Whitlock & Guillaume 2009).”
BackgroundSelf-citationCamarretta, N., Harrison, P., Lucieer, A., Potts, B., Davidson, N., & Hunt, M. (2020) · Remote Sensing · doi:10.3390/rs12193184 · Cited by 40
“Traits exhibiting a significant QST > FST signaled evidence for divergent selection driving among provenance variation [26].”
BackgroundMíguez-Soto, B., Fernández-Cruz, J., & Fernández-López, J. (2019) · PLoS ONE · doi:10.1371/journal.pone.0211315 · Cited by 40 · see citing works
Causes and consequences of intra-specific variation in vertebral number
Tibblin, P., Berggren, H., Nordahl, O., Larsson, P., & Forsman, A. (2016) · Scientific Reports · doi:10.1038/srep26372 · Cited by 40
Barley, A. J., Monnahan, P. J., Thomson, R. C., Grismer, L. L., & Brown, R. M. (2015) · Molecular Ecology · doi:10.1111/mec.13151 · Cited by 39 · see citing works
“Although comparisons of distributions of FST versus PST represent a primary source of evidence for morphological selection (Leinonen et al. 2013), there is little consensus and/ or justification for estimating the necessary confidence intervals.”
BackgroundEvolution of plant drought strategies and herbivore tolerance after two decades of climate change
Rauschkolb, R., Li, Z., Godefroid, S., Dixon, L., Durka, W., Májeková, M., Bossdorf, O., Enßlin, A., & Scheepens, J. F. (2022) · New Phytologist · doi:10.1111/nph.18125 · Cited by 51 · see citing works
“The Q ST of onset of flowering was larger than the F ST in three species ( M. tricuspidata , C. vulgare and L. hispidus ), suggesting directional selection as the most likely responsible evolutionary process (Leinonen et al ., 2013).”
BackgroundParallel Speciation of Wild Rice Associated with Habitat Shifts
Cai, Z., Zhou, L., Ren, N., Xu, X., Liu, R., Huang, L., Zheng, X., Meng, Q., Du, Y.-S., Wang, M., et al. (2019) · Molecular Biology and Evolution · doi:10.1093/molbev/msz029 · Cited by 40 · see citing works
“…between species is an adaptive response to divergent habitats, we performed QST–FST analysis, a method that has been widely used to examine whether natural selection or genetic drift is the main cause of population differentiation in phenotypic traits (McKay and Latta 2002; Leinonen et al. 2013).”
MethodResultInfluentialHäkli, K., Østbye, K., Kahilainen, K., Amundsen, P., & Præbel, K. (2018) · Ecology and Evolution · doi:10.1002/ece3.3876 · Cited by 38
Reyes‐Centeno, H., Ghirotto, S., & Harvati, K. (2017) · American Journal of Physical Anthropology · doi:10.1002/ajpa.23060 · Cited by 37 · see citing works
Population genetics revisited – towards a multidisciplinary research field
Habel, J., Zachos, F., Dapporto, L., Rödder, D., Radespiel, U., Tellier, A., & Schmitt, T. (2015) · Biological Journal of the Linnean Society · doi:10.1111/bij.12481 · Cited by 37 · see citing works
“Thus, the distinction between fitness-related and peripheral (often morphological) traits is not general as the forms of natural selection are different (directional vs. stabilizing) and of different magnitudes (e.g. critically reflected in the QST–FST debate, Leinonen et al., 2013).”
BackgroundClo, J., Gay, L., & Ronfort, J. (2019) · Evolution; international journal of organic evolution · doi:10.1111/evo.13789 · Cited by 36 · see citing works
“More data have been published for numerous plant species since this literature review (Lavergne and Molofsky 2007; Leinonen et al. 2013; Wood et al. 2016), making it timely to conduct a new and more precise study.”
MethodHigh degree of genetic differentiation in marine three‐spined sticklebacks (Gasterosteus aculeatus)
Defaveri, J., Shikano, T., Shimada, Y., & Merilä, J. (2013) · Molecular Ecology · doi:10.1111/mec.12430 · Cited by 36
“…this heterogeneous differentiation is consistent with the view that has emerged from a totally independent body of work comparing levels of differentiation in neutral marker genes with those in quantitative traits (reviewed in: Meril€a & Crnokrak 2001; Cano et al. 2008; Leinonen et al. 2008, 2013).”
BackgroundResultInfluentialSelf-citation
- Authors
- Leinonen, T., McCairns, R. J. S., O'Hara, R. B., & Merilä, J.
- Affiliations
- University of Helsinki (FI)
- Corresponding author
- Merilä, Juha
- Venue
- Nature Reviews Genetics
- Published
- 2013-02-05
- Volume
- 14
- Issue
- 3
- Pages
- 179-190
- ISSN
- 1471-0056 (ISSN-L)
- 1471-0064
- OpenAlex
- W2018112412
- Cited by
- 422
- References
- 122
- Citations by year
- 2026: 16 · 2025: 22 · 2024: 16 · 2023: 24 · 2022: 34 · 2021: 34 · 2020: 34 · 2019: 47 · 2018: 46 · 2017: 28 · 2016: 40 · 2015: 42 · 2014: 20 · 2013: 18
- FWCI
- 4.92
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Reviews Genetics (publishedVersion)
- PubMed (publishedVersion)
- HAL (submittedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic diversity and population structure
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Evolution and Genetic Dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Mapping and Diversity in Plants and Animals
- Keywords
- QST-FST comparison, natural selection, genetic drift, genetic differentiation, polygenic traits, genomic heterogeneity, evolutionary genetics, ecological genetics, omics data analysis
- MeSH terms
- Animals, Ecology, Genetic Markers, Genetics, Population, Humans, Selection, Genetic, Genetic Variation, Genetic Heterogeneity, Evolution, Molecular, Genomics, Quantitative Trait Loci, Genetic Drift
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