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Temporal FST genome scans: the case of partially selfing populations

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Submitted on 5 Jun 2020

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Temporal FST genome scans: the case of partially selfing populations

Miguel Navascués, Arnaud Becheler, Laurène Gay, Joelle Ronfort, Renaud Vitalis

To cite this version:

Miguel Navascués, Arnaud Becheler, Laurène Gay, Joelle Ronfort, Renaud Vitalis. Temporal FST genome scans: the case of partially selfing populations. 2. Joint Congress on Evolutionary Biology (EVOLUTION 2018), Aug 2018, Montpellier, France. 2018. �hal-02786861�

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Temporal F

ST

genome scans: the case of partially

selfing populations

Miguel Navascu´es

Arnaud Becheler

Laur`ene Gay

Jo¨

elle Ronfort

Renaud Vitalis

miguel.navascues@inra.fr

Background

Temporal change in allele frequency, which may be characterized by a

measure of genetic differentiation between two or more samples, is generally used to infer the effective size of a population (Waples 1989; Genetics

121:379–91).

Because some loci may be targeted by other evolutionary forces than genetic drift, it has been proposed to test for the homogeneity of

locus-specific estimates of temporal differentiation to detect outlier loci that may be targeted by natural selection (Goldringer & Bataillon 2004;

doi:10.1534/genetics.103.025908).

Self-fertilization, however, reduces the effective size of populations, and therefore the effective recombination rate between loci, which promotes hitch-hiking over long chromosome stretches, and may jeopardize the detection of loci under selection.

Evaluation of the method: simulations

Simulations were carried out with SLiM (Messer 2013,

doi:10.1534/genetics.113.152181). Simulated populations consisted of

N = 500 diploid individuals with a genome of 2 chromosomes (500Mb

total) with µ = 10−8 and r = 10−8 per bp. Two samples of 50 individuals

genotyped at 10,000 SNPs were obtained 25 generations apart. A new advantageous mutation appears, or existing neutral allele becomes

advantageous (s = 0.5), at first sampled generation. FST for each locus was

calculated as in the example below (outcrossing population). Position of

locus under selection.

F ST 0.0 0.2 0.4 0.6 0.8 chr 1 chr 2

Footprints of selection acting on new mutations

Neutral markers in the vicinity of the site under selection have a higher probability to be called positive in our temporal FST test, due to

hitch-hiking. This extended footprint of selection improves our chances to characterize the genomic region under selection. With larger selfing rates, however, the footprint of selection vanishes, as the whole genome is

affected by selection. 0.01 0.05 0.50 5.00 50.00 0.0 0.2 0.4 0.6 0.8 1.0

distance to selected locus (cM)

Propor tion of positiv es ● ● ● ● ● ● ● ● σ=0 σ=0.5 σ=0.9 σ=0.99

Conclusion

Temporal FST scans are powerful to detect footprints of selection on regions around loci under selection. In predominant selfing populations, low

effective recombination strongly limits the detection of selection, unless it is based on standing variation.

Temporal F

ST

genome scan

We extended the method proposed by Goldringer & Bataillon (2004). In our method, genomic differentiation between two temporal samples is

measured by multilocus FST, which is then used to infer effective population size ( ˆNe). We simulate alleles frequencies conditionnally on the initial

frequency at a focal locus and ˆNe we then evaluate whether the observed

FST at a focal locus is expected under the null hypothesius of neutral

evolution: we compute the p-value of our test as the proportion of

simulated FST values larger than the observed FST.

0 5 10 15 20 25 0.0 0.1 0.2 0.3 0.4 0.5 Time Allele frequency ● ● 0.00 0.05 0.10 0.15 0.20 0 5 10 15 20 25 30 FST Probability density observed FST=0.09 p−value=0.03

Hitch-hiking along the chromosome

Genetic differentiation along the chromosome, as a function of the distance from the selected site, shows the extent of hitch-hiking. Selfing increases the length of the region affected by selection. How does this affect the probability to detect selection using our genome-scan approach? Does it increase the size of the genomic region for which we detect selection or does it reduce power?

distance to selected site (bp)

F S

T

0 1e+07 2e+07 3e+07 4e+07

0.0 0.2 0.4 0.6 Selfing rate: σ = 0, σ = 0.5, σ = 0.9, σ = 0.99 ——— mean FST - - - - expected FSTτ +4Nτ e under neutrality

Footprints of selection acting on standing variation

In highly selfing populations (σ = 0.95), recombination events occurring before the selective sweep allow to distinguish between the region around the site under selection and the rest of the genome. Advantageous alleles that start at a low frequency are almost as easy to detect as new

advantageous mutations in outcrossing populations. Ancestral

advantageous alleles have a higher probability of detection because they had longer time to recombine with the genetic background.

0.01 0.05 0.50 5.00 50.00 0.0 0.2 0.4 0.6 0.8 1.0

distance to selected locus (cM)

Propor tion of positiv es ● ● ● ● ● ● ancestral allele, π0=0.1 derived allele, π0=0.1 ancestral allele, π0=0.9 derived allele, π0=0.9 Acknowledgements

This work was funded by INRA’s meta-program ACCAF (SELFADAPT project).

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