bioRxiv Science⌕ Search

bioRxiv · 10.1101/2025.04.05.647387

Predictive Ability of Enviromic Modeling in GxE Interactions for Upland Rice Site Recommendations

Abstract

Enviromics is an omics approach that investigates a phenomenon using all available environmental information. This study explores the use of enviromic covariates in studies of genotype x environment (GxE) interactions in upland rice in Brazil, utilizing a field trial dataset from 143 locations over 27 years, covering diverse environmental conditions. The platforms WorldClim, NASA POWER, and SoilGrids were used to extract data, resulting in 383 environmental covariates. The objective of this study was to evaluate the use of enviromic kernels to integrate GIS and genetic data for predicting upland rice productivity across Brazil and to determine the optimal number of environmental covariates required to ensure model accuracy and stability. The predictive abilities of the enviromic model peaked with around 81 covariates, stabilizing when all 383 were included, suggesting the importance of a comprehensive dataset for accurate predictions. Analysis reveals that environmental dissimilarities are more critical than geographical distance for genotypic variability, reinforcing the need to consider multiple covariates in predictive models. Heritability mapping revealed spatial variations, with regions of high heritability concentrated in southern Brazil, where genetic selection may be more efficient. The clustering of mega-environments was not efficient, highlighting the complexity of GxE interactions, and confirming that pixel-by-pixel enviromic models are a safer approach for recommending breeding actions for upland rice. This study suggests strategies to improve genotype selection for specific conditions, guiding the expansion of rice cultivation into new agricultural areas in Brazil. The findings also contribute to rice-growing regions worldwide, especially in countries cultivating upland rice under diverse conditions. Structured AbstractO_ST_ABSObjectiveC_ST_ABSThis study aimed to evaluate the predictive ability of enviromic models for site-specific recommendations in upland rice, focusing on genotype x environment (GxE) interactions by integrating environmental and phenotypic data. MethodsA total of 734 field trials conducted between 1995 and 2022 across 143 Brazilian locations were analyzed. Environmental data (383 covariates) were retrieved from WorldClim, NASA POWER, and SoilGrids using GIS-based procedures. Statistical analyses included mixed linear models and Random Forest to correct for design effects, estimate heritability, and perform spatial predictions. ResultsEnvironmental dissimilarity better explained genotypic ranking than geographic distance. Predictive ability plateaued after 81 covariates, but adding more covariates reduced variance and increased model stability, supporting the use of comprehensive environmental data. ConclusionsThe study reinforces the need for detailed environmental characterization and the use of comprehensive enviromic models. Pixel-based predictions are more reliable than broad clustering approaches, supporting the use of virtual trials to optimize breeding strategies and resource allocation.

Source connections

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Bahia, M. A. M., Marcatti, G. E., Breseghello, F., Melo, P. G. S., Dias, K. O. G., Xu, Y., Resende, R. T.. 2025-04-09. Predictive Ability of Enviromic Modeling in GxE Interactions for Upland Rice Site Recommendations. https://doi.org/10.1101/2025.04.05.647387

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Pangenome Discoveries from Clinical Long-Read Genomes in Underrepresented Populations with Neurodevelopmental Disorders

Genetic diagnoses remain elusive for many individuals with neurodevelopmental disorders (NDDs), and the gap is wider in populations poorly represented in genomic reference resources. To demonstrate the equitable advantage of long-read whole genome sequencing (LR-WGS) and pangenomes in terms of clinical utility, we analyzed 211 NDD cases and 107 unaffected relatives from 24 populations, integrating their assemblies, resulting in a total of 1204 haplotypes with the Human Pangenome Reference Consortium Release 2 (HPRC_r2) and the Arab Pangenome Reference (APR) datasets. Clinical interpretation of small variants and structural variants (SVs) revealed pathogenic or likely pathogenic findings in 38.9% of the cases (82/211), and our workflow further detected pathogenic repeat expansions in 3.8% of the cases and runs of homozygosity (ROHs) exceeding 300 Mb in 4.7% of the cases, revealing substantial autozygosity suggestive of strong inbreeding. Beyond these clinical assessments, pangenome analysis revealed 3.9 million population-level novel small variants, 39,782 SVs and an average of 2.17 Mb of novel sequence per individual absent from linear references and global pangenomes. We identified 85.9 kb of case-unique nonreference sequences in exonic segments overlapping with curated NDD gene sets. Graph-based tertiary analysis further identified rare exonic complex homozygous rearrangements in the NDD associated genes for 2.4% of the cases. Together, these findings emphasize how diverse genome assemblies extend variant discovery beyond established linear reference-based clinical interpretation.

genetics↗

Integrated exome-transcriptome analysis of a schizophrenia case with an exceptionally low polygenic risk score

Schizophrenia liability reflects both common polygenic variation and rarer variants of larger effect. We investigated a post-mortem schizophrenia case (SZ07) with a schizophrenia polygenic risk score below the first percentile among ancestry-matched cases, asking whether individual-level genomic and transcriptomic analyses could help identify potentially novel schizophrenia-relevant variants. We used exome analysis with multiple variant-prediction tools to generate a panel of variants and corresponding candidate genes potentially implicated in the pathological process in SZ07. The prioritised variants were then assessed using RNA sequencing of three cortical regions. Of these, only an IZUMO4 splice-acceptor variant showed direct RNA-level support. Beyond variant-specific analyses, we characterised broader transcriptomic abnormalities in the SZ07 brain. Pathway analysis of gene-level expression deviations implicated innate immune processes, calcium signalling, synaptic biology, and axon remodelling. Notably, compared with conventional single-sample biological pathway analysis, the analysis we used showed only a weak association with neuronal specificity, suggesting their reduced sensitivity to the main axis of variation related to cellular composition in bulk brain tissue gene expression data. Although the candidate genes showed no significant pathway-level convergence, the broader transcriptomic profile revealed coherent biological alterations largely compatible with the documented history of cerebrovascular disease in SZ07. These results demonstrate how the integration of exome and transcriptome data at the individual level enables the formulation and constraint of hypotheses regarding patient-specific genetic features and their molecular consequences, while highlighting important limitations related to tissue composition, comorbidity, and the choice of reference cohort.

genetics↗

A genetic screen to identify host factors required for commensal bacterial adherence to the gut epithelia

Bacterial adherence to gut epithelial cells likely involves host genetic components. We isolated a gut commensal bacterium, Lelliottia jeotgali, that can robustly colonize C. elegans through attachment to intestinal epithelial cells. Here, we developed a novel screen in C. elegans to identify host genes required for microbiome bacterial colonization. Using transgenic L. jeotgali strain expressing tdTomato, we conducted forward genetic screens in C. elegans to select for mutants that completely lost colonization. We identified multiple allelic mutations in five different C. elegans genes, termed knockout of Lelliottia adherence (kola) mutants, with a near complete loss of adherence. Each of kola-1-5 is uncharacterized and predicted to encode for a secreted or membrane-bound protein. We also identified gly-5, a GalNAc transferase that initiates O-linked glycosylation. Overall, we describe the first C. elegans screen to identify host factors that control microbiome bacterial colonization in the gut.

genetics↗