Abstract

Key messageThe Taguchi method and metAFLP analysis were used to optimise barley regenerants towards maximum andminimum levels of tissue culture-induced variation. The subtle effects of symmetric and asymmetric methylationchanges in regenerants were identified.Plant tissue cultures (PTCs) provide researchers with unique materials that accelerate the development of new breeding cultivars and facilitate studies on off-type regenerants. The emerging variability of regenerants derived from PTCs may have both genetic and epigenetic origins, and may be desirable or degrade the value of regenerated plants. Thus, it is crucial to determine how the PTC variation level can be controlled. The easiest way to manipulate total tissue culture-induced variation (TTCIV) is to utilise appropriate stress factors and suitable medium components. This study describes the optimisation of in vitro tissue culture-induced variation in plant regenerants derived from barley anther culture, and maximizes and minimizes regenerant variation compared with the source explants. The approach relied on methylation amplified fragment length polymorphism (metAFLP)-derived TTCIV characteristics, which were evaluated in regenerants derived under distinct tissue culture conditions and analysed via Taguchi statistics. The factors that may trigger TTCIV included CuSO4, AgNO3 and the total time spent on the induction medium. The donor plants prepared for regeneration purposes had 5.75% and 2.01% polymorphic metAFLP loci with methylation and sequence changes, respectively. The level of TTCIV (as the sum of all metAFLP characteristics analyzed) identified in optimisation and verification experiments reached 7.51 and 10.46%, respectively. In the trial designed to produce a minimum number of differences between donor and regenerant plants, CuSO4 and AgNO3 were more crucial than time, which was not a significant factor. In the trial designed to produce a maximum number of differences between donor and regenerant plants, all factors had comparable impact on variation. The Taguchi method reduced the time required for experimental trials compared with a grid method and suggested that medium modifications were required to control regenerant variation. Finally, the effects of symmetric and asymmetric methylation changes on regenerants were identified using novel aspects of the metAFLP method developed for this analysis.

Highlights

  • Plants regenerated via tissue culture methods of androgenesis or somatic embryogenesis are not completely uniform at morphological (Al Hattab et al 2017), geneticElectronic supplementary material The online version of this article contains supplementary material, which is available to authorized users.(Hazubska-Przybył and Dering 2017) and epigenetic (Han et al 2018) levels

  • The direction ofmutations depended on the species; in triticale, genetic changes prevailed over methylation alterations (Machczyńska et al 2014a), whereas the opposite was observed in barley (Bednarek et al 2007)

  • From the prepared pool of donor plants, one plant was chosen for Experiment 1, and six plants were chosen for Experiment 2

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Summary

Introduction

In vitro plant regeneration from anthers or isolated microspores in barley (Bednarek et al 2007), triticale (Machczyńska et al 2015) and many other species (Fiuk et al 2010) induce numerous changes that affect genome sequences and DNA methylation patterns. These genetic changes occur with varying frequency, from complete absence (Palombi and Damiano 2002; Tiwari et al 2015) to 50% (Thomas et al 2006) or 72% (Bairu et al 2006). This knowledge will be crucial to continue exploiting tissue culture-based plant regeneration approaches

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