Abstract

Nowadays, genetic diversity more than ever represents a key driver of adaptation to climate challenges like drought, heat, and salinity. Therefore, there is a need to replenish the limited elite gene pools with favorable exotic alleles from the wild progenitors of our crops. Nested association mapping (NAM) populations represent one step toward exotic allele evaluation and enrichment of the elite gene pool. We investigated an adaptive selection strategy in the wild barley NAM population HEB-25 based on temporal genomic data by studying the fate of 214,979 SNP loci initially heterozygous in individual BC1S3 lines after five cycles of selfing and field propagation. We identified several loci exposed to adaptive selection in HEB-25. In total, 48.7% (104,725 SNPs) of initially heterozygous SNP calls in HEB-25 were fixed in BC1S3:8 generation, either toward the wild allele (19.9%) or the cultivated allele (28.8%). Most fixed SNP loci turned out to represent gene loci involved in domestication and flowering time as well as plant height, for example, btr1/btr2, thresh-1, Ppd-H1, and sdw1. Interestingly, also unknown loci were found where the exotic allele was fixed, hinting at potentially useful exotic alleles for plant breeding.

Highlights

  • Around 10,000 years ago, domestication of crops enabled mankind to settle and to commence agriculture

  • We investigated an adaptive selection strategy in the wild barley Nested association mapping (NAM) population HEB-25 based on temporal genomic data by studying the fate of 214,979 SNP loci initially heterozygous in individual BC1S3 lines after five cycles of selfing and field propagation

  • 214,979 (6,02%) heterozygous SNP calls were obtained from 3,573,466 polymorphic SNP assays in generation BC1S3 of population HEB-25 (Supplementary Table S1), which is close to the expected frequency of 6.25%

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Summary

Introduction

Around 10,000 years ago, domestication of crops enabled mankind to settle and to commence agriculture. To cope with future agricultural challenges, there is a need to replenish the limited elite gene pools with favorable exotic alleles from the wild progenitors of our crops (Zamir, 2008; McCouch et al, 2013; Zhang et al, 2017). NAM populations can be developed to investigate a multitude of exotic allele effects in an adapted background. They are created by crossing a diverse set of wild progenitors with one recurrent elite cultivar. This way high allele richness and statistical power are combined to evaluate complex traits through genome-wide association studies (GWAS)

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