Abstract

BackgroundUnderstanding the determinants of free asparagine concentration in wheat grain is necessary to reduce levels of the processing contaminant acrylamide in baked and toasted wheat products. Although crop management strategies can help reduce asparagine concentrations, breeders have limited options to select for genetic variation underlying this trait. Asparagine synthetase enzymes catalyse a critical step in asparagine biosynthesis in plants and, in wheat, are encoded by five homeologous gene triads that exhibit distinct expression profiles. Within this family, TaASN2 genes are highly expressed during grain development but TaASN-B2 is absent in some varieties.ResultsNatural genetic diversity in the asparagine synthetase gene family was assessed in different wheat varieties revealing instances of presence/absence variation and other polymorphisms, including some predicted to affect the function of the encoded protein. The presence and absence of TaASN-B2 was determined across a range of UK and global common wheat varieties and related species, showing that the deletion encompassing this gene was already present in some wild emmer wheat genotypes. Expression profiling confirmed that TaASN2 transcripts were only detectable in the grain, while TaASN3.1 genes were highly expressed during the early stages of grain development. TaASN-A2 was the most highly expressed TaASN2 homeologue in most assayed wheat varieties. TaASN-B2 and TaASN-D2 were expressed at similar, lower levels in varieties possessing TaASN-B2. Expression of TaASN-A2 and TaASN-D2 did not increase to compensate for the absence of TaASN-B2, so total TaASN2 expression was lower in varieties lacking TaASN-B2. Consequently, free asparagine concentrations in field-produced grain were, on average, lower in varieties lacking TaASN-B2, although the effect was lost when free asparagine accumulated to very high concentrations as a result of sulphur deficiency.ConclusionsSelecting wheat genotypes lacking the TaASN-B2 gene may be a simple and rapid way for breeders to reduce free asparagine concentrations in commercial wheat grain.

Highlights

  • Understanding the determinants of free asparagine concentration in wheat grain is necessary to reduce levels of the processing contaminant acrylamide in baked and toasted wheat products

  • For each orthologous gene, Sorting Intolerant From Tolerant (SIFT) analysis was performed on the translated protein to predict whether the variation in amino acid sequences was likely to disrupt protein function or to be tolerated

  • TaASN-B1 was deleted in SY Mattis, while eight other varieties carried an allelic variant with a 16 bp deletion in exon seven, introducing a frame shift and bringing a premature stop codon into frame

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Summary

Introduction

Understanding the determinants of free asparagine concentration in wheat grain is necessary to reduce levels of the processing contaminant acrylamide in baked and toasted wheat products. Asparagine synthetase enzymes catalyse a critical step in asparagine biosynthesis in plants and, in wheat, are encoded by five homeologous gene triads that exhibit distinct expression profiles Within this family, TaASN2 genes are highly expressed during grain development but TaASN-B2 is absent in some varieties. Asparagine in its free (soluble, non-protein) form is an important nitrogen transport and storage molecule in plants (see [1] for review). The current EU regulation on acrylamide in food (Commission Regulation (EU) 2017/2158 [5]) states that acrylamide in food ‘potentially increases the risk of developing cancer for consumers in all age groups’ It sets Benchmark Levels for acrylamide in different food types, and carries an explicit threat to set Maximum Levels (i.e. levels above which it would be illegal to sell a product) in the future

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