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Frontiers in Genetics logoLink to Frontiers in Genetics
. 2022 Aug 5;13:910386. doi: 10.3389/fgene.2022.910386

Genome–Environment Associations, an Innovative Tool for Studying Heritable Evolutionary Adaptation in Orphan Crops and Wild Relatives

Andrés J Cortés 1,*,, Felipe López-Hernández 1, Matthew W Blair 2,*
PMCID: PMC9389289  PMID: 35991553

Abstract

Leveraging innovative tools to speed up prebreeding and discovery of genotypic sources of adaptation from landraces, crop wild relatives, and orphan crops is a key prerequisite to accelerate genetic gain of abiotic stress tolerance in annual crops such as legumes and cereals, many of which are still orphan species despite advances in major row crops. Here, we review a novel, interdisciplinary approach to combine ecological climate data with evolutionary genomics under the paradigm of a new field of study: genome–environment associations (GEAs). We first exemplify how GEA utilizes in situ georeferencing from genotypically characterized, gene bank accessions to pinpoint genomic signatures of natural selection. We later discuss the necessity to update the current GEA models to predict both regional- and local- or micro-habitat–based adaptation with mechanistic ecophysiological climate indices and cutting-edge GWAS-type genetic association models. Furthermore, to account for polygenic evolutionary adaptation, we encourage the community to start gathering genomic estimated adaptive values (GEAVs) for genomic prediction (GP) and multi-dimensional machine learning (ML) models. The latter two should ideally be weighted by de novo GWAS-based GEA estimates and optimized for a scalable marker subset. We end the review by envisioning avenues to make adaptation inferences more robust through the merging of high-resolution data sources, such as environmental remote sensing and summary statistics of the genomic site frequency spectrum, with the epigenetic molecular functionality responsible for plastic inheritance in the wild. Ultimately, we believe that coupling evolutionary adaptive predictions with innovations in ecological genomics such as GEA will help capture hidden genetic adaptations to abiotic stresses based on crop germplasm resources to assist responses to climate change.

“I shall endeavor to find out how nature’s forces act upon one another, and in what manner the geographic environment exerts its influence on animals and plants. In short, I must find out about the harmony in nature” Alexander von Humboldt—Letter to Karl Freiesleben, June 1799.

Keywords: gene banks, germplasm collections, landraces, genome–environment associations (GEA), genome-wide environmental scans, genome-wide selection scans (GWSS), genomic prediction (GP), abiotic stress

Introduction—Lack of Crop Genotypes Adapted to Severe Climates

Crop wild relatives (CWR) and landraces are well known for providing new alleles for plant breeding (Tanksley and McCouch, 1997). They also can improve dietary proteins and essential micronutrients for undernourished communities (Blair, 2013). However, their diversity is often unexplored and underutilized (Bronnvik and von Wettberg, 2019; Ramirez-Villegas et al., 2022). Major cultivars typically lack adaptation to abiotic stresses (i.e., heat and drought), jeopardizing worldwide yield stability, given increasing effects of climate change (Cortés et al., 2020a). Luckily, landraces and CWR, as well as orphan crop species, offer novel adaptive alleles (Herron et al., 2020).

For instance, among legumes, bambara groundnut (Vigna subterranea), chickpea (Cicer arietinum), cowpea (V. unguiculata), grass pea (Lathyrus sativus), groundnut (Arachis hypogaea), marama bean (Tylosema esculentum) (Cullis et al., 2018), tarwi (Lupinus mutabilis) (Atchison et al., 2016; Gulisano et al., 2019), and tepary bean—(Phaseolus acutifolius) (Buitrago-Bitar et al., 2021; Burbano-Erazo et al., 2021) constitute genepools of unexplored adaptive diversity for abiotic stresses. Among cereals, orphan crops include teff (Eragrostis tef), sorghum (Sorghum bicolor), and finger millet (Eleusine coracana) or pearl and proso millets (Panicum spp, Pennisetum glaucum). Many of these crops have interesting drought-tolerance traits and some capacity to grow in compacted soils. Cowpeas, groundnuts, and lesser known cereals are already traditional food sources and biocultural components for vulnerable areas, especially in Sub-Saharan Africa and parts of Asia and Latin America (Xiong et al., 2016).

Yet, despite their tolerance to drought and heat plus their high nutritional quality, the utilization of these orphan crops is limited partly because of the poor characterization of their genetic background (Wu et al., 2022). Therefore, a key research area in orphan crop improvement is to expand the use of modern molecular prebreeding tools for them (Ahmad et al., 2020), that is, genome resequencing (Fuentes-Pardo and Ruzzante, 2017; Wu et al., 2020) and genomic prediction (Desta and Ortiz, 2014), to select genotypes for production in dry climates.

Still, a major question to harness crop prebreeding for climate change pressures is whether there is enough heritable variation in traits associated with tolerance to abiotic stress. In this context, genomic characterizations of reference collections comprising CWR, landraces, and orphan crops that span contrasting habitats offer a straightforward scenario to identify natural standing adaptation to abiotic pressures (Ramirez-Villegas et al., 2022).

The spirit behind this novel approach is to detect genomic regions that correlate with habitat heterogeneity as an indication of the natural selection imprint to environmental gradients (Forester et al., 2016). Since these signatures rely on a natural equilibrium between genotypes and their environment (Hancock et al., 2011), the ideal base population must prioritize natural genotypes and landraces and avoid improved cultivars, for which it is not realistic to assume that enough generations have passed as to display divergent selection to environmental heterogeneity. Hence, the goal of the present work is to review key developments to explore and utilize natural adaptation in wild genepools for climate change adaptation.

Modus Operandi to Genomically Assess Natural Evolutionary Adaptation

Coupling ecological genomics innovations (Cortinovis et al., 2020b) with evolutionary adaptive trajectories (Ramírez et al., 2010; López-Hernández and Cortés, 2019; Cortinovis et al., 2020a; Ramirez-Villegas et al., 2020) helps capturing adaptations in CWR and landraces, as shown for teosinte (Pyhäjärvi et al., 2013), rice (Meyer et al., 2016), Glycine (Anderson et al., 2016), and barley (Russell et al., 2016).

The current assortment of genomic pipelines that analyze environmental variation in order to infer the genetic basis of adaptation to natural selection include genome-wide selection scans—GWSS (Zahn and Purnell, 2016), and genome-wide environmental scans—GWES (Rellstab et al., 2015) also known as genome–environment associations—GEAs, a term we prefer based on its simplicity. While GWSS relies on the outlier Bayesian tests contrasted against a genomic background distribution (Antao et al., 2008), GEA uses mixed linear models (MLMs) that incorporate random effects, such as kinship and population stratification (Kruglyak, 2008). GEA behaves like traditional genome-wide association study (GWAS), but instead of modeling a set of phenotypic traits, it considers an environmentally derived variable into its additive genetic factors. These inferences could be misleading (Maher, 2008; Pennisi, 2014) if they overlook the confounding factors (Lambert and Black, 2012; Wolf and Ellegren, 2017) such as demographic (Barton et al., 2019) and genomic (Wray et al., 2013; Huber et al., 2016; Ellegren and Wolf, 2017) constraints also prevalent in GWAS studies. Hence, MLM-based models, which are capable of handling these spurious sources of error, are currently the optimum approach for the use of GEA and environmental variables to unveil the extent and genetic bases of local adaptation in diverse natural populations (Abebe et al., 2015).

In the last decade, the GEA pipeline has been utilized to characterize signatures of environmental adaptation in a rich spectrum of plant species (Table 1). For instance, Eckert et al. (2010) studied environmental associations with aridity across the range of the pine tree Pinus taeda, showing utility of the GEA approach for long-lifecycle, forestry species. This approach proved useful for additional tree species in studies by Holliday et al. (2016) and Pluess et al. (2016), respectively, who demonstrated local adaptation to climate gradients in Populus trichocarpa and Fagus sylvatica. More recently Ingvarsson and Bernhardsson (2020) address climate adaptation in P. tremula under present and future scenarios. With the increasing need for biomass as a fuel source, GEA is likely to continue its important role in the genetic analysis of other trees and woody species.

TABLE 1.

Examples of GEA studies carried out in plant species. This compilation of previous studies explicitly refers to genome–environment association studies (GEA) using the Scopus database https://www.scopus.com/ with the following search parameters: TITLE-ABS-KEY (“Genome – Environment Associations”) AND (LIMIT-TO (DOCTYPE, “ar”)). The table is sorted chronologically. Method abbreviations are shown at the bottom of the table.

Speciesapproach Sampling data Genotypic data Targeted stress Environmental data Analytical Main finding References
GLM Tolerance to aridity Pinus taeda 3,059 SNPs and 23 SSRs Aridity index and Thornthwaite index using biovariables http://worldclim.org/version2 622 trees Environmental and genetic data for the identification of functionally important genetic variation within natural populations Eckert et al. (2010)
Genome-wide scans Local adaptation to climate gradients Arabidopsis ∼215,000 SNPs Aridity, temperature, precipitation, radiation, and day length http://www.sciencemag.org/content/suppl/2011/10/05/334.6052.83.DC1.html 948 accessions Natural adaptive genetic variation in Arabidopsis at a continental scale Hancock et al. (2011)
Redundancy analysis (RDA) Local adaptation to climate gradients Arabidopsis 214,051 SNPs Potential evapotranspiration using annual precipitation and a measure of aridity http://worldclim.org/version2, variability in precipitation http://esrl.noaa.gov/psd/, and photosynthetically active radiation http://eosweb.larc.nasa.gov/PRODOCS/srb/table_srb.html 1,003 accessions The climatic structure of SNP correlations is due to changes in coding sequence that may underlie local adaptation Lasky et al. (2012)
MLM Drought and heat stress Medicago truncatula 1,918,637 SNPs Biovariables http://worldclim.org/current 202 accessions Genetic basis of adaptation to drought and heat stress disclosed in M. truncatula Yoder et al. (2014)
EMMA Tolerance to aluminum toxicity and drought stress Sorghum bicolor 404,627 SNPs Potential evapotranspiration using annual precipitation and a measure of aridity http://worldclim.org/version2, variability in precipitation http://esrl.noaa.gov/psd/, photosynthetically active radiation https://eosweb.larc.nasa.gov/project/srb/srb_table, and edaphic data http://daac.ornl.gov/SOILS/guides/DunneSoil.html, http://www.fao.org/nr/water/docs/harm-world-soil-dbv7cv.Pdf 1,943 accessions Genomic signatures of environmental adaptation may be useful for crop improvement, enhancing germplasm identification, and marker-assisted selection Lasky et al. (2015)
BayeScan Local adaptation to climate gradients Populus trichocarpa ∼170,000 SNPs Variables from Holliday et al. (2016) 391 trees Physical proximity of genes in coadapted complexes may buffer against the movement of maladapted alleles from geographically proximal but climatically distinct populations Holliday et al. (2016)
LFMMs, GLM Local adaptation to climate gradients Fagus sylvatica 144 SNPs—12 SSRs Environmental index from raw variables in Pluess et al. (2016) and references herein 79 natural populations Local adaptation to climate gradients Pluess et al. (2016)
Bayenv, Bayescan Local adaptation to climate gradients Cenchrus americanus 87,218 SNPs Variables from Berthouly-Salazar et al. (2016) 762 trees Outlier loci putatively under selection detected in populations at the extremity of climatic gradients, and tested ad hoc in populations along the gradients Berthouly-Salazar et al. (2016)
MLM, GLM Drought stress Phaseolus vulgaris 22,845 SNPs Drought index using Thornthwaite model and annual precipitation http://worldclim.org/version2 86 accessions Genomic signatures of adaptation are useful for germplasm characterization, potentially enhancing future marker-assisted selection, and crop improvement Cortés and Blair (2018a)
BayPass Abiotic stresses Arabidopsis 1,638,649 SNPs Mean annual temperature; mean coldest month temperature; and precipitations in winter, spring, summer, and autumn https://sites.ualberta.ca/∼ahamann/data/climateeu.html 168 natural populations The identification of climate-adaptive genetic loci at a micro-geographic scale also highlights the importance to include within-species genetic diversity in ecological niche models for projecting potential species distributional shifts Frachon et al. (2018)
LFMMs and GLM Drought stress Beta vulgaris subsp. vulgaris 14,409 SNPs Aridity index using biovariables http://worldclim.org/version2 1,249 accessions Wild individuals have higher ability to resist stress-aridity conditions and could be used to improve the resistance of cultivated varieties Manel et al. (2018)
LFMMs and MSOD-MSR Drought stress Medicago truncatula 43,515 SNPs Biovariables http://worldclim.org/version2, atmospheric nitrogen deposition https://daac.ornl.gov/, and soil variables https://library.wur.nl/WebQuery/wurpubs/510208 202 accessions The importance of soil in driving adaptation in the system and elucidate the basis of evolutionary potential of M. truncatula to respond to global climate change and anthropogenic disruption of the nitrogen cycle Guerrero et al. (2018)
GLM Abiotic stress Zea mays 355,442 SNPs tmax, tmin, tavg, srad, vapr, ph5, and prec https://soilgrids.org http://worldclim.org/version2 1,143 accessions Combining large-scale genomic and ecological data in this diverse maize panel, this study supports a polygenic adaptation model of maize and offers a framework to enhance the understanding of maize adaptation Li et al. (2019)
SUPERFarmCPU, BLINK, GLM, and MLM Heat stress Phaseolus vulgaris 23,373 SNPs PCA from temperature biovariables, modified heat Thornthwaite index, and heat index http://worldclim.org/version2 78 accessions It is feasible to identify genome-wide environmental associations with modest sample sizes by using a combination of various carefully chosen environmental indices and last-generation GWAS algorithms López-Hernández and Cortés (2019)
Bayenv2 Drought and heat stress Betula nana 14,889 SNPs Biovariables http://worldclim.org/version2 130 accessions Significant correlation between the number of loci associated with each environmental variable in the GEA, and the importance of each variable in environmental niche modeling Borrell et al. (2019)
LFMMs Drought and heat stress Quercus aquifolioides 381 SNPs Isothermality, mean temperature of the driest quarter, precipitation during the dry season, and precipitation during the wet season http://worldclim.org/version2 60 accessions Genetic variation in Q. aquifolioides showed contrasted patterns of local adaptation in the two lineages Du et al. (2020)
CANCOR Drought stress Lolium perenne 189,968 SNPs Environment index http://etccdi.pacificclimate.org/index.shtml, soil data https://esdac.jrc.ec.europa.eu/, and biovariables http://worldclim.org/version2 469 natural populations CANCOR retrieved 633 outlier loci associated with two climatic gradients, characterized by cold–dry vs. mild–wet winter, and long rainy season vs. long summer, pointing out traits putatively conferring adaptation at the extremes of these gradients Blanco-Pastor et al. (2020)
BLINK Drought and heat stress Sorghum bicolor L. 72,190 SNPs Altitude, annual temperature, and precipitation of accessions’ passport data from Girma et al. (2020) 1,425 accessions Candidate loci identified with the GEA will have potential utilization for germplasm identification and sorghum breeding for stress Girma et al. (2020)
BAYESCENV Drought and heat stress Circaeaster agrestis 6,120 SNPs Isothermality, evapotranspiration, temperature seasonality, temperature annual range, annual precipitation, and seasonality precipitation www.chelsa-climate.org 139 accessions Genome-wide data provide new insights into the important role of environmental heterogeneity in accessing the footprints of local adaptation in an ancient relictual species Zhang et al. (2020)
LFMMs Abiotic stress Populus tremula 8,007,303 SNPs Abiotic index ENVIREM http://envirem.github.io, climatic variables based on the CCSM4.0 model http://www.cesm.ucar.edu/models/ccsm4.0/ccsm/, and biovariables http://worldclim.org/current 94 trees Climate adaptation in P. tremula under present and future scenarios Ingvarsson and Bernhardsson (2020)
BLINK Drought and heat stress Sorghum bicolor L. 54,080 SNPs Altitude, annual temperature, and precipitation http://worldclim.org/version2 940 accessions The current study aimed to better understand the GEA of a large collection of Ethiopian sorghum landraces, characterized with genome-wide SNP markers, to investigate key traits related to adaptation Menamo et al. (2021)
FarmCPU Cold stress Broussonetia papyrifera 2,936,477 SNPs Frost-free period and other climatic information http://data.cma.cn 134 accessions Significant selective regions and candidate genes were identified, and the potential molecular mechanism of local adaptation to low temperature in woody plants was discussed Hu et al. (2021)
MLM Drought stress Phaseolus acutifolius A. Gray † Genes Asr2, Dreb2B, ERECTA Drought index using Thornthwaite model and annual precipitation http://worldclim.org/version2 52 accessions The results suggested that tepary bean, specially wild accessions, could be sources of novel alleles for drought tolerance Buitrago-Bitar et al. (2021)
MLM Abiotic stress Phaseolus vulgaris L. † 28,823 SNPs Biovariables from http://worldclim.org/version2 110 accessions SNP markers and candidate genes associated with bio-climatic variables should be validated in segregating populations for water MAS Elias et al. (2021)
LFMMs Abiotic stress Medicago truncatula 14,160 SNPs Worldclim.org (WC), The Climatic Research Unit (University of East Anglia) (CRU), The Satellite Application Facility on Climate Monitoring, and The NASA Distributed Active Archive Centre for Biogeochemical Dynamics (DAAC) 675 accessions Authors identified a set of candidate genes for adaptation associated with environmental gradients along the distribution range Blanco-Pastor et al. (2021)
LFMMs Abiotic stress Medicago sativa 10,478 SNPs 202 accessions

FarmCPU, fixed and random model circulating probability unification; BLINK, Bayesian-information and linkage-disequilibrium iteratively nested keyway; LFMMs, latent factor mixed models; CANCOR, canonical correlation analysis; SUPER, settlement of MLM under progressively exclusive relationship; MSOD-MSR, Moran spectral outlier detection/randomization; EMMA, mixed linear association model; MAS, marker-assisted selection.

Symbol † indicates studies in legume species.

Meanwhile, for model plants, GEA has also gained in popularity and has a somewhat longer history: Hancock et al. (2011) and Lasky et al. (2012) have explored natural adaptive genetic variation in Arabidopsis at a continental scale and for water use efficiency, Yoder et al. (2014) disclosed the genetic basis of adaptation to drought and heat stress in Medicago truncatula.

For orphan crops, rather than nondomesticated natural plant species, fewer GEA studies have been undertaken. Although still limited to the easier-to-grow annual grain species compared to perennial and root/tuber crops, GEA is starting to make important contributions to genetic analysis of landraces and WCR germplasm, often richly represented in the world’s major gene banks for crop species. The analytical pipeline for GEA studies is shown in Figure 1, with the input data, analytical models, and outputs found when inferring genome-wide signatures of environmental adaptation in crop wild relatives (CWR) and landraces that span heterogeneous environments. The reader is referred to pertinent examples of GEA in crop species or their CWR which include Lasky et al. (2015), who prospected natural tolerance to aluminum toxicity and drought in cultivated sorghum; Berthouly-Salazar et al. (2016), who captured genomic regions involved in adaptation on two climate gradients in pearl millet; Cortés and Blair (2018a), who evaluated drought-tolerance sources of common bean (Phaseolus vulgaris) WCR; or López-Hernández and Cortés (2019), who identified pervasive divergent adaptation to continental-level heat gradients in wild accessions of this same species.

FIGURE 1.

FIGURE 1

Analytical pipeline to infer genome-wide signatures of environmental adaptation in crop wild relatives (CWR) and landraces that span heterogeneous environments. The green shaded box refers to gene bank collections, while white, red and blue shaded boxes represent input data, analytical models and output inferences, respectively (Cortés et al., 2020a; Cortés et al., 2020b; Cortés and López-Hernández, 2021). Genomic prediction (GP) and genomic-estimated adaptation values (GEAVs) promise speeding up plant breeding goals.

Historically, based on the technological improvements in sequencing and SNP detection and as a means to improve GEA, the field has moved from the candidate gene approach (Cortés et al., 2012a; Cortés et al., 2012b; Blair et al., 2016; Buitrago-Bitar et al., 2021) into full genomic scans (Cortés and Blair, 2018a; López-Hernández and Cortés, 2022), which better account for linkage disequilibrium (LD) heterogeneity. In this movement, the targeting of discrete responses to abiotic pressures has aided GEA studies, by explicitly relying on the mechanistic ecophysiological models and traits (Cortés et al., 2013) for overall conditions such as drought (Cortés and Blair, 2018a) and heat stress (López-Hernández and Cortés, 2022).

More Powerful Next-Generation GEA Models Meet Evolutionary Ecology

As discussed previously, GEA is becoming a key tool to prospect for new genes among crop wild accessions and landraces as an alternative to traditional phenotyping and GWAS analyses (Cortés et al., 2022). However, there is still room for innovation. For example, we envision dual GEA models that combine inferences at various spatial and temporal scales, following Cortés et al. (2020a), by 1) predicting regional- and microhabitat-wise evolutionary adaptation with in situ ecological georeferencing of accessions, and by 2) revealing the genomic architecture of adaptation via cutting-edge predictive models (Rellstab et al., 2015; Forester et al., 2016).

Concerning the first point, standardized climate data for GEA studies are as important as high-quality genotyping to guarantee analytical power (Waldvogel et al., 2020). Climate-based inferences may target extreme regions, like those where drought is coupled with extreme temperatures (Lei et al., 2019). The high-resolution climate data can be gathered from worldwide repositories (such as WorldClim, https://www.worldclim.org/) using georeferencing and statistical downscaling (Zellweger et al., 2019) in order to build explicit heat–stress physiological indices (Cortés et al., 2013; López-Hernández and Cortés, 2019) at regional and local scales, respectively. The use of explicit indices, instead of raw environmental variables, helps describing physiological processes more accurately, especially those that confer tolerance to abiotic stress. For instance, the same environmental dataset can be inputted into an evapotranspiration model to infer drought stress (Cortés et al., 2013) and its genetic bases (Cortés et al., 2012a; Cortés et al., 2012b; Blair et al., 2016; Cortés and Blair, 2018a), or to assess heat tolerance (López-Hernández and Cortés, 2019). It is equally paramount to collect the spatial high-resolution climate data to improve predictions not only at regional scales (Pluess et al., 2016), but also at microhabitat levels (Cortés et al., 2015; Frachon et al., 2018), where adaptive variation to cope with abiotic pressures is overlooked but is sufficient (Cortés and Wheeler, 2018). Remote sensing (Zellweger et al., 2019) also promises better capture of environmental heterogeneity (Ratcliffe et al., 2019).

Concerning the second opportunity for improvement, characterizing genome-wide signatures of environmental adaptation to habitat-inferred stress in CWR and landraces that span heterogeneous climates will benefit from inputting habitat-based abiotic stress indices into the last-generation mixed linear models (MLMs) and machine learning (ML) (Schrider and Kern, 2018; Cortés et al., 2020b), capable of handling spurious effects (Barton et al., 2019) in multidimensional data, while detecting predictive genomic regions that correlate with habitat/environmental heterogeneity, as an indication of the genomic imprint by climate gradients (Hancock et al., 2011).

Overcoming Polygenic Adaptation

Overall, CWR and landraces undeniably harbor unique adaptations to abiotic stresses, rarely present in the cultivated and improved genepools (Tester and Langridge, 2010). However, unlocking and utilizing this potential (Tanksley and McCouch, 1997; Langridge and Robbie, 2019) has remained challenging partly due to phenotyping bottlenecks in the wild, and the complex inheritance (Morran et al., 2011) of trait variation for abiotic stress tolerance, typically involving many loci with low effects (López-Hernández and Cortés, 2019). To bridge this gap, we propose extending genomic prediction (GP) models and genomic estimated breeding values (GEBVs) to account for the habitat-based dimensions by coining the analogous parameter genomic estimated adaptation values—GEAVs (Capblancq et al., 2020; Arenas et al., 2021), equivalent to the polygenic risk score (PRS) within a preimplantation genetic diagnosis framework. To compute GEAVs, the GP models used must be calibrated (trained and tested) to predict the environmental indices and polygenic adaptability (liability) thresholds.

GP works either on the basis of shared relatedness (typically measured as relationships due to recent coancestry) or on the basis of linkage disequilibrium (LD) between the SNP marker loci and the genetic variants that underlie phenotypic variation (Thistlethwaite et al., 2020). The relationships between the training and testing datasets are critically important and therefore must be optimized as part of any GP effort. As a general suggestion, the more diverse the training dataset is, the more robust the prediction will be. Hence, coupling cross-validation calibration curves under various training/testing ratios with simple measures of diversity, such as heterozygosity and runs of homozygosity (ROH), is appropriate. However, in the absence of demonstrated relationships or LD, there is no apparent basis for GP’s predictive accuracy, raising the possibility of statistical artifacts. To overcome this issue, pairwise LD among SNP markers helps to interpret GWAS-type GEA associations (Morton, 2005), and this a prerequisite for any GP initiative.

The predictive ability of GP models may be further biased depending on whether the entire SNP set is used, or the most predictive SNP data are chosen after the GWAS-type analysis (Wray et al., 2013), the latter being a common practice in modern GP studies. The polygenic infinitesimal model that makes GP so unique may be jeopardized by subsampling the SNP markers because relying only on GEA-derived SNP markers would disregard SNPs with low effects that are usually missed, but that may still account for the overall missing heritability.

Better approaches to be implemented and reported include 1) weighted GP models using de novo GWAS-based GEA estimates gathered from other (or even the same) panels (Spindel et al., 2016) and 2) optimization of the marker set by computing the saturating curves of the predictive ability, given various sets of markers ranked by their beta effects from the exact same GP model and not from any parallel GWAS-derived GEA models (Resende et al., 2012; Tan et al., 2017). GP can also be improved in efficiency by validating the GEAV scores across diverse populations, allowing better G × E predictions within the nascent field of enviromics (Resende et al., 2021; Cooper and Messina, 2021; Costa-Neto et al., 2021). GEAVs can boost incorporation of landraces and CWR as parents in marker-assisted backcrossing (MAB). Marker set optimization for environmental GP (Jarquín et al., 2013; Lopez-Cruz et al., 2015) would benefit crop prebreeding initiatives for abiotic tolerance MAB, mergeable with the speed-breeding strategies (Migicovsky and Myles, 2017; Watson et al., 2018), high-throughput screening (Cuppen, 2007), and ML-updated best linear unbiased prediction (BLUP) models (Wenlong et al., 2018; Crossa et al., 2019; Abdollahi-Arpanahi et al., 2020; Cortés et al., 2020b; Wang et al., 2020; Zingaretti et al., 2020; Montesinos-López et al., 2021).

Perspectives to Better Harness Genome Functionality in the Wild

Next-generation GEA models and GEAVs will allow the use of “exotic” parents for targeted predictive prebreeding in crop species. They offer feasible methodologies to trace the sources of abiotic stress adaptation and tolerance targeting crop resources in low-income countries, which are also the most vulnerable to climate change. Here, we have discussed strategies to implement the latest-generation predictive (e.g., Cortés et al., 2013) and genomic (Cortés and Blair, 2018a; López-Hernández and Cortés, 2019) approaches to study adaptation in CWR and landraces (Cortés and Blair, 2018b; Cortés et al., 2020a), but similar work could be done for any orphan crop.

Modern GEA approaches will allow further studies of evolutionary conservatism, parallelism, and convergence in the genetic architecture of adaptation to various types of abiotic stresses across a wide range of environments, landraces, and wild accessions (Cortés and López-Hernández, 2021). Approaches such as these are needed to discern among drivers (Ellegren and Galtier, 2016) of the adaptive landscape of genomic divergence (Feder et al., 2012; Gompert et al., 2014; Cortés et al., 2018b), such as ecological diversity, population structure, ancestral polymorphisms, mutation/recombination rates (Feder et al., 2012; Ellegren and Wolf, 2017; Ravinet et al., 2017; Cortés and Blair, 2018b), and nested levels of divergence (Nosil and Feder, 2011; Wolf and Ellegren, 2017; Cortés et al., 2018a).

How genetic diversity and genomic divergence arise and are shaped based on ecological pressures is one of the main questions in molecular evolution (Tiffin and Ross-Ibarra, 2014) and has been implicit even in the pregenetics-era studies of ecological transects by famous botanists such as von Humboldt. GEA studies can contribute valuable insights into the field of molecular evolution due to their ability to detect convergent or nonconvergent adaptations (Schmutz et al., 2014). Ecologically associated SNPs are likely to exhibit hitchhiking effects (Feder and Nosil, 2010) due to the low recombination rate and extensive LD (Kelleher et al., 2012; Blair et al., 2018).

Therefore, GEA efforts can be enhanced by exploring SNP density and statistics of site frequency spectra (e.g., nucleotide diversity and Tajima’s D) in associated vs. nonassociated regions (Cortés and Blair, 2018a). Figure 2 shows an example of these principles used in common bean to identify and harness natural signatures of environmental adaptation across diverse genepools, with the genome-wide patterns of genetic divergence, as measured by the FST statistic (A). Once the potential confounding demographic patterns have been accounted for, it is then feasible to disentangle genuine signatures of environmental adaptation (B) from spurious concurring genetic drift due to genomic constraining features. Finally, these combined summary statistics (i.e., ecophysiological indices, population stratification, and LD) can ultimately redound in prebreeding efforts aiming to introgress exotic adaptive variation into elite lines (C), for instance, via backcrossing (BC) schemes for abiotic and biotic stresses.

FIGURE 2.

FIGURE 2

An integrated case study inspired in common bean (Phaseolus vulgaris L.) accessions exemplifies how to identify and harness natural signatures of environmental adaptation across diverse genepools. First, (A) genome-wide patterns of genetic divergence, as measured by the F ST and delta divergence (Roesti et al., 2014) statistics, inform underlying confounding demographic processes across wild accessions (Blair et al., 2012) and landraces (Blair et al., 2009). Even though highly polymorphic markers have traditionally been preferred for demographic inferences (Blair et al., 2009; Kwak and Gepts, 2009), modern SNP genotyping technologies also enable reconstructing the genomic landscape of divergence at a higher resolution (Cortés et al., 2011; Wu et al., 2020). Once potential confounding demographic patterns have been accounted for, (B) it is then feasible to disentangle genuine (in red) signatures of environmental adaptation (Cortés et al., 2018b) from spurious concurring genetic drift due to genomic constraining features such as low recombining regions, reduced effective population size, and translocations (Blair et al., 2018). In order to improve genome–environment associations (GEA), the field has moved from the candidate gene approach (Cortés et al., 2012a; Cortés et al., 2012b; Blair et al., 2016; Buitrago-Bitar et al., 2021) into full genomic scans (Cortés and Blair, 2018a; López-Hernández and Cortés, 2022), which better account for linkage disequilibrium (LD) heterogeneity. It is also advisable to target discrete abiotic pressures by explicitly relying on the mechanistic ecophysiological models (Cortés et al., 2013) such as drought (Cortés and Blair, 2018a) and heat stress (López-Hernández and Cortés, 2022). Finally, (C) these combined summary statistics (i.e., ecophysiological indices, population stratification, and LD) can ultimately redound in prebreeding efforts aiming to introgress exotic adaptive variation into elite lines, for instance, via backcrossing (BC) schemes for abiotic (Muñoz et al., 2003; Blair et al., 2006; Blair and Izquierdo, 2012; Burbano-Erazo et al., 2021) and biotic (Garzon et al., 2008) stresses, all guided with indirect (Miklas et al., 2006) genomic selection tools such as marker-assisted selection (MAS) and genomic selection, GS (Cortés et al., 2020a; Cortés et al., 2020b; Cortés and López-Hernández, 2021) within a moder enviromics approach (Cooper et al., 2021). Different line colors stand for hypothetical distinct chromosomes. Dashed horizontal lines mark significance thresholds.

All drivers must be considered as ad hoc multiple hypotheses (Chamberlin, 1897) since extensive LD and hitchhiking may not only be due to physical linkage and low recombination/effective population size (Slatkin, 2008), but also to population stratification, sample’s co-ancestry (Price et al., 2010; Blair et al., 2012), within-pathway gene-gene and G × E interactions (Ortiz et al., 2022), and context-dependent effects of epistasis, even if assumed to be minimal in diploid model crop species.

In-depth GEA studies on the molecular mechanisms of evolutionary divergence involving the genomics and functional genetic dissection of adaptive loci enable addressing long-term transdisciplinary questions such as 1) how genomic features (i.e., meiotic crossover hot- vs. cold-spots, as pericentromeric regions and inversions) impact the rate of adaptation and modulate adaptive evolution to new environments (Huang et al., 2020; Huang and Rieseberg, 2020; Todesco et al., 2020), 2) how old adaptive haplotypes (standing variation) and more recent recruitment of novel mutations balance during the rapid events of changing climate (Jones et al., 2012a; Jones et al., 2012b), 3) what effects the noncoding cis-regulatory mutations contribute to the genomic basis of adaptation, and 4) to which scale epigenomic marks [i.e., chromatin accessibility, histone profiling, transposable elements, and sRNA (Kaasik and Chi Lee, 2004; Slotkin and Martienssen, 2007)] regulate plastic gene expression within the same genotype (Bossdorf et al., 2008), and may be transferred via transgenerational epigenetic inheritance (Heard and Martienssen, 2014; Boskovic and Rando, 2018; Hu et al., 2018; Lacal and Ventura, 2018), eventually impacting divergent adaptation in natural populations (Chinnusamy and Zhu, 2009).

Ultimately, GEA is empowering the understanding on how plant genomes interact with their environment while shaping adaptive phenotypes. Such mechanistic insights of the genome functionality in the wild promise leveraging the characterization of landraces and CWR to assist prebreeding efforts through multi-dimensional adaptive scores (e.g. GEAVs), as well as the identification of underlying factors that may facilitate or constrain future adaptive responses to changing climate.

Lastly, GEA studies offer new possibilities to efficiently unlock crop diversity for climate adaptation (Tanksley and McCouch, 1997). Unexplored variation already contained in genebanks (Smale and Jamora, 2020) may speed up resilience to extreme temperatures, and more frequent drought and flooding events (Dwivedi et al., 2016). The modern genome–environment framework, coupled with explicit ecophysiological indices and last-generation association models, promises a scalable strategy to assist with the identification and deployment of exotic variation capable of maturing earlier and harvesting acceptably in erratic climatic conditions. Levering reverse genomic and ecological resources for CWR and landraces will improve available pipelines such as focused identification of germplasm strategy, FIGS (Stenberg and Ortiz, 2021). Such efforts to prebreed resilient crop genotypes with greater accuracy may ultimately enable small-scale farmers’ adaptation to changing climate (Razzaq et al., 2021).

Acknowledgments

Discussions with D. Ambachew, A. Asfaw, E. Burbano, C. Cordero, C.H. Galeano, G. Hyman, R. León, C.I. Medina, M. Mercado, F. Monserrate, D. Peláez, A. Tofiño, and M. Urban inspired some of the perspectives of GEA using climatic variables and crop utilization in hot and dry climatic zones discussed in this review. Recognition is also given to M.J. Torres for assistance during the preparation of this review. Reviewers and topic editors are thanked for envisioning and enabling an insightful Special Issue on “Genetics of Domestication and Diversification Towards Evolution of Crop Plants.”

Data Availability Statement

The original contributions presented in the study are included in the article. Further inquiries can be directed to the corresponding author.

Author Contributions

AJC and MWB conceived this work. FL-H collected literature and prepared tables. AJC prepared diagrams and wrote a first draft, later edited by MWB and FL-H.

Funding

Vetenskapsrådet and Kungliga Vetenskapsakademien are credited for funding AJC during the conception of this work through grants 4.1-2016-00418 and BS20170036. AGROSAVIA’s Department for Research Capacity Building is acknowledged for sponsoring FL-H’s internship in 2018 to carry out GEA studies for abiotic stresses. United States Department of Agriculture Evans Allen fund (TENX-07) is acknowledged for funding MWB. The Graduate Research School in Genomic Ecology (GENECO) from Lund University is appreciated for the mobility funding that assisted the synergistic kickoff meeting between AJC and MWB in the spring of 2015 at Nashville, TN, United States. Fulbright U.S. Specialist Program is thanked for supporting MWB’s visit to AJC and FL-H in Rionegro (Antioquia, Colombia) in the summer of 2019, during which the foundations of this review were discussed. The British Council is deeply appreciated for the Newton Fund, Grant ID 527023146, awarded to AJC as PI in Colombia, which enabled additional discussions among authors around the GEA paradigm.

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s Note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors, and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

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Data Availability Statement

The original contributions presented in the study are included in the article. Further inquiries can be directed to the corresponding author.


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