Orphan crops serve as essential resources for both nutrition and income in
local communities and offer potential solutions to the challenges of food
security and climate vulnerability. Tef [Eragrostis tef (Zucc.)], a
small-grained allotetraploid, C4 cereal mainly cultivated in Ethiopia,
stands out for its adaptability to marginal conditions and high
nutritional value, which holds both local and global promise. Despite its
significance, tef is considered an orphan crop due to limited genetic
improvement efforts, reliance on subsistence farming, and its nutritional,
economic, and cultural importance. Although pre-Semitic inhabitants of
Ethiopia have cultivated tef for millennia (4000-1000 BCE), the genetic
and environmental drivers of local adaptation remain poorly understood. To
address this, we resequenced a diverse collection of traditional tef
varieties to investigate their genetic structure and identify genomic
regions under environmental selection using redundancy analysis (RDA),
complemented by single-site differentiation and LD-based methods. We
identified 145 loci associated with abiotic environmental factors, with
minimal geographic influence observed in the genetic structure of the
sample population. Overall, this work contributes to the broader
understanding of local adaptation and its genetic basis in tef, providing
insights that support efforts to develop elite germplasms with improved
environmental resilience. The Ethiopian Biodiversity Institute provided the genetic
materials for this study and granted access to passport information for
environmental data curation. Bioclimatic (bio1-bio19) and altitudinal data
were obtained using latitude and longitude coordinates from each site,
with WorldClim version 2.1 layers at 10-minute resolution based on
long-term averages for 1970-2000 (Fick & Hijmans, 2017).
Researchers at the Ethiopian Institute of Agricultural Research, including
Tadelech Bizuneh, Adanech Teshome, and Doni Hinsene, prepared DNA samples
from young leaf samples for each greenhouse-grown tef accession. DNA
concentration and quality were determined using a 1.5% agarose gel and a
NanoDrop Spectrophotometer. The extracted DNA was sent to the BioFrontiers
Sequencing Core at the University of Colorado Boulder for unique dual
indexing 10 bp library preparation. Genomic libraries of the Ethiopian tef
accessions were then sent to the Genomics and Microarray Core at the
University of Colorado Anschutz Medical Campus for paired-end whole genome
sequencing (2 × 150 bp at ~10× coverage) using an Illumina NovaSeq 6000
platform. Details regarding the variant calling pipeline and downstream
analyses are provided in the manuscript. # Data from: Genetic diversity and environmental adaptation in Ethiopian
tef
[
doi.org](
doi.org) ## Description of the data and file structure Additional_Files_SuppInfo.xlxs * S1.1: Detailed information on tef germplasm collection, DNA extraction, and plate coordinates referenced through the Illumina NovaSeq 6000 platform. - S1.2: Geographic and environmental (WorldClim version 2.1) data associated with each sample. - S1.3: Individual population genetic assignments for all samples, including axis loadings from discriminant analysis of principal components (LD1 - LD4), principal components analysis (PC1 and PC2), and K-means cluster assignments. - S1.4: Genetic distances estimated as pairwise FST, alongside geographical and environmental distance matrices, based on 39 individual samples from 16 distinct geographic locations and using 20 WorldClim environmental variables. Only sampling locations with two or more collected varieties were included. - S1.5: Redundancy analysis model output (without correction for population structure), including identified outlier loci and correlation coefficients to each environmental variable.. - S1.6: Redundancy analysis model output (with correction for population structure), including identified outlier loci and correlation coefficients to each environmental variable. - S1.7: Detailed genotype information and associated metadata for each non-synonymous site identified by the redundancy analysis. - S1.8: Genome-wide sliding window iHH12 scores calculated using Selscan v2.0.0 (Szpiech, 2021; Szpiech & Hernandez, 2014). - S1.9: Genome-wide sliding window FST values calculated using VCFtools version 0.1.16 (Danecek et al., 2011; Weir & Cockerham, 1984). - S1.10: GO enrichment analysis results, including GO terms and descriptions of biological processes, for *E. tef* v3 genes associated with outlier loci identified through redundancy analysis. - S1.11: GO enrichment analysis results, including GO terms and descriptions of biological processes, and their associated environmental variables from redundancy analysis. ## Sharing/Access information Links to other publicly accessible locations of the data and scripts: * [
github.com](
https) Genetic materials and passport information were derived from the following sources: * Ethiopian Biodiversity Institute through a collaborative project with the Ethiopian Institute of Agricultural Research.