Abstract

Next-generation sequencing technologies (NGST) are being used to discover causal mutations in ethyl methanesulfonate (EMS)-mutagenized plant populations. However, the published protocols often deliver too many candidate sites and sometimes fail to find the mutant gene of interest. Accurate identification of the causal mutation from massive background polymorphisms and sequencing deficiencies remains challenging. Here we describe a NGST-based method, named SIMM, that can simultaneously identify the causal mutations in multiple independent mutants. Multiple rice mutants derived from the same parental line were back-crossed, and for each mutant, the derived F2 individuals of the recessive mutant phenotype were pooled and sequenced. The resulting sequences were aligned to the Nipponbare reference genome, and single nucleotide polymorphisms (SNPs) were subsequently compared among the mutants. Allele index (AI) and Euclidean distance (ED) were incorporated into the analysis to reduce noises caused by background polymorphisms and re-sequencing errors. Corrections of sequence bias against GC- and AT-rich sequences in the candidate region were conducted when necessary. Using this method, we successfully identified seven new mutant alleles from Huanghuazhan (HHZ), an elite indica rice cultivar in China. All mutant alleles were validated by phenotype association assay. A pipeline based on Perl scripts for SIMM is publicly available at https://sourceforge.net/projects/simm/.

Highlights

  • Forward genetics based on ethyl methanesulfonate (EMS) mutagenesis and cloning of mutant genes are of fundamental importance to the understanding of plant gene functions

  • Simultaneous identification of multiple mutations was primarily designed to identify casual mutations generated by EMS mutagenesis by simultaneous analysis of multiple mutants derived from the same parental plant, without requiring a wildtype parental genome sequence as reference (Figure 1)

  • Uniquely mapped reads were retained for single nucleotide polymorphism (SNP) calling using

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Summary

Introduction

Forward genetics based on EMS mutagenesis and cloning of mutant genes are of fundamental importance to the understanding of plant gene functions. Traditional map-based cloning approach has been widely used for cloning of mutant plant genes. It involves construction of mapping population(s) by crossing the mutant plant with wild-type plant of extensive genomic polymorphisms (Lukowitz et al, 2000). By identifying markers that are tightly associated with the mutant phenotype, chromosomal region harboring. The mutant gene is further defined by sequencing the chromosomal region and functional complementation (Lukowitz et al, 2000; Jander et al, 2002). It is not suitable for cloning of mutant genes with ambiguous phenotypes in the mapping population

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