Abstract

TILLING (Targeting Induced Local Lesions IN Genomes) is a strategy used for functional analysis of genes that combines the classical mutagenesis and a rapid, high-throughput identification of mutations within a gene of interest. TILLING has been initially developed as a discovery platform for functional genomics, but soon it has become a valuable tool in development of desired alleles for crop breeding, alternative to transgenic approach. Here we present the HorTILLUS (Hordeum—TILLING—University of Silesia) population created for spring barley cultivar “Sebastian” after double-treatment of seeds with two chemical mutagens: sodium azide (NaN3) and N-methyl-N-nitrosourea (MNU). The population comprises more than 9,600 M2 plants from which DNA was isolated, seeds harvested, vacuum-packed, and deposited in seed bank. M3 progeny of 3,481 M2 individuals was grown in the field and phenotyped. The screening for mutations was performed for 32 genes related to different aspects of plant growth and development. For each gene fragment, 3,072–6,912 M2 plants were used for mutation identification using LI-COR sequencer. In total, 382 mutations were found in 182.2 Mb screened. The average mutation density in the HorTILLUS, estimated as 1 mutation per 477 kb, is among the highest mutation densities reported for barley. The majority of mutations were G/C to A/T transitions, however about 8% transversions were also detected. Sixty-one percent of mutations found in coding regions were missense, 37.5% silent and 1.1% nonsense. In each gene, the missense mutations with a potential effect on protein function were identified. The HorTILLUS platform is the largest of the TILLING populations reported for barley and best characterized. The population proved to be a useful tool, both in functional genomic studies and in forward selection of barley mutants with required phenotypic changes. We are constantly renewing the HorTILLUS population, which makes it a permanent source of new mutations. We offer the usage of this valuable resource to the interested barley researchers on cooperative basis.

Highlights

  • IntroductionThere are many techniques, available today, of creating mutants that can be used to study gene function

  • Mutants are essential for functional analysis of genes

  • In the other barley TILLING populations created till after chemical mutagenesis, this value ranges from 1 mutation/2,500 kb to 1 mutation/374 kb (Caldwell et al, 2004; Talamè et al, 2008, 2009; Gottwald et al, 2009; Lababidi et al, 2009; Kurowska et al, 2012; Supplementary Table 4)

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Summary

Introduction

There are many techniques, available today, of creating mutants that can be used to study gene function Among these techniques there are standard chemical or physical mutagenic treatments causing mutations that are spread throughout the genome, as well as modern techniques of gene editing, such as CRISPR/Cas9based system that can be used for creation of mutations within a specific target gene (Cong et al, 2013). In the case of barley, such protocols are well established only for one variety “Golden Promise” (a Scottish cultivar developed in 1967; Lawrenson et al, 2015), while transformation efficiency of modern barley cultivars is still insufficient for a routine use The methods, such as TILLING (Targeting Induced Local Lesions IN Genomes), are still relevant for functional analysis of genes in many species, including barley

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