Abstract

BackgroundMutation breeding is an extraordinary tool in plant breeding to increase the genetic variability, where mutations in anthocyanin biosynthesis are targets to generate distinctive phenotypes in ornamental species. In poinsettia, ionizing radiation is routinely applied in breeding programs to obtaining a range of colours, with nearly all pink and white varieties being obtained after γ- or X-ray mutagenesis of red varieties. In the present study we performed a thorough characterization of a potential mutagenesis target gene as the main responsible for the ‘white paradox’ in poinsettia.ResultsWe identified a GST gene in poinsettia (Bract1) as an essential factor for the expression of anthocyanin-based red colouration of bracts, which presents a high phylogenetic similarity to known anthocyanin-related GSTs. Red poinsettia varieties and white mutants generated from these varieties by X-ray were analysed for polymorphisms related to the ‘white paradox’ in the species. A 4 bp mutation in a short repeat within the coding region of Bract1 is most likely responsible for the appearance of white phenotypes upon irradiation treatment. The polymorphism between wild-type and mutant alleles co-segregates with the phenotype in progeny from heterozygous red and white parents. Moreover, overexpression of Bract1 wild-type allele in Arabidopsis tt19 mutants restored the anthocyanin phenotype, while the Bract1 mutated allele showed to be non-functional.ConclusionsThe identified repeat seems to be highly unstable, since mutated plants can be easily detected among fewer than 200 shoots derived from 10 mutated plants. Our data indicate that particular short repeat sequences, similar to microsatellite sequences or so-called dynamic mutations, might be hot spots for genetic variability. Moreover, the identification of the Bract1 mutation fills a gap on the understanding on the molecular mechanism of colour formation in poinsettia.

Highlights

  • Mutation breeding is an extraordinary tool in plant breeding to increase the genetic variability, where mutations in anthocyanin biosynthesis are targets to generate distinctive phenotypes in ornamental species

  • Ionizing radiation is an important tool in mutation breeding for new colour variations in poinsettia, with most pink and white varieties being obtained after gamma or X-ray mutagenesis of shoots of red varieties

  • We show that a short repeat motif within the coding region of the gene is highly unstable upon mutation treatment, which leads to the high frequency of anthocyanin mutations observed in commercial mutation breeding

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Summary

Introduction

Mutation breeding is an extraordinary tool in plant breeding to increase the genetic variability, where mutations in anthocyanin biosynthesis are targets to generate distinctive phenotypes in ornamental species. In poinsettia, ionizing radiation is routinely applied in breeding programs to obtaining a range of colours, with most pink and white varieties being obtained after γ- or X-ray mutagenesis of red varieties. In the present study we performed a thorough characterization of a potential mutagenesis target gene as the main responsible for the ‘white paradox’ in poinsettia. Ionizing radiation is an important tool in mutation breeding for new colour variations in poinsettia, with most pink and white varieties being obtained after gamma or X-ray mutagenesis of shoots of red varieties. Several anthocyanin types have been identified in poinsettia bracts and are responsible for its colouration range [3, 55, 66]; molecular information is still limited for the species [28, 72]. Genes responsible for the biosynthesis of the anthocyanin pathway have been intensively characterized in a range of species, with its regulation being highly dependent on R2R3-MYB regulatory genes and MYB-bHLH-WD40 (MBW) regulatory complexes [16, 58, 76]

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