Population genomic footprints of fine-scale differentiation between habitats in Mediterranean blue tits

Linking population genetic variation to the spatial heterogeneity of the environment is of fundamental interest to evolutionary biology and ecology, in particular when phenotypic differences between populations are observed at biologically small spatial scales. Here, we applied restriction‐site asso...

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Published inMolecular ecology Vol. 25; no. 2; pp. 542 - 558
Main Authors Szulkin, M., Gagnaire, P.-A., Bierne, N., Charmantier, A.
Format Journal Article
LanguageEnglish
Published England Blackwell Publishing Ltd 01.01.2016
Wiley
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Summary:Linking population genetic variation to the spatial heterogeneity of the environment is of fundamental interest to evolutionary biology and ecology, in particular when phenotypic differences between populations are observed at biologically small spatial scales. Here, we applied restriction‐site associated DNA sequencing (RAD‐Seq) to test whether phenotypically differentiated populations of wild blue tits (Cyanistes caeruleus) breeding in a highly heterogeneous environment exhibit genetic structure related to habitat type. Using 12 106 SNPs in 197 individuals from deciduous and evergreen oak woodlands, we applied complementary population genomic analyses, which revealed that genetic variation is influenced by both geographical distance and habitat type. A fine‐scale genetic differentiation supported by genome‐ and transcriptome‐wide analyses was found within Corsica, between two adjacent habitats where blue tits exhibit marked differences in breeding time while nesting < 6 km apart. Using redundancy analysis (RDA), we show that genomic variation remains associated with habitat type when controlling for spatial and temporal effects. Finally, our results suggest that the observed patterns of genomic differentiation were not driven by a small proportion of highly differentiated loci, but rather emerged through a process such as habitat choice, which reduces gene flow between habitats across the entire genome. The pattern of genomic isolation‐by‐environment closely matches differentiation observed at the phenotypic level, thereby offering significant potential for future inference of phenotype‐genotype associations in a heterogeneous environment.
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ArticleID:MEC13486
OSU-OREME
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Part I - Supplementary Figures: Fig. S1. The number of sequence reads per individual blue tit increases the number of RAD tags detected in that individual (n = 202). Fig. S2. Marker-derived IBS plotted against expected relatedness. Fig. S3. Graphical representation of PCA for (a) Corsica Island (n = 140, 5567 SNPs) and (b) the valley of Muro (n = 57, 4010 SNPs), MAF 5% and 90% call rate for each dataset. Fig. S4. Left: Plots of partial RDA analyses for habitat (top), latitude (middle), and birth year (bottom), after conditionning on other constraining variables to remove their confounding effects. PART II - Controlling for family effects - the "No family ties" dataset: Fig. S5. PCA in the "no family ties" dataset for (a) all four populations from the French mainland and Corsica (6164 SNPs), (b) Corsica Island (5170 SNPs) and (c) the valley of Muro (4081 SNPs). Table S1. Percentage of genotypic variance explained by PCA axes 1-5 at three different level of analysis (A - all four populations, B - Corsica Island, C - Muro Valley) for the entire dataset and the "no family ties" dataset presented in brackets. Table S2. Spatial PCA global test P-values testing for global structures such as distinct spatial groups or clines. PART III - Controlling for birth year and sample size - the "symmetrical minimal dataset": Table S3. Results of RDA significance tests (P-values, 1000 permutations), detailed for the global RDA analysis (full model) and the marginal effect of each constraining variable in the model. Fig. S6. RDA analysis of the "symmetrical minimal" dataset (90% MAF 2% 8347 SNPs) for (a) all four populations, (b) Corsican birds only and (c) partial RDA analysis for habitat after conditioning on other constraining variables to remove their confounding effects. Table S4. Pairwise FST values for the symmetrical minimal dataset (n = 36, 5% MAF, 95% call rate).
ANR BioAdapt - No. ANR-12-ADAP-0006-02-PEPS
APEGE
IEF Marie Curie Fellowship
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0962-1083
1365-294X
DOI:10.1111/mec.13486