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Contrasting gene expression patterns in grain of high and low asparagine wheat genotypes in response to sulphur supply

  • Curtis, Tanya Y.1, 2
  • Raffan, Sarah1
  • Wan, Yongfang1
  • King, Robert3
  • Gonzalez-Uriarte, Asier3, 4
  • Halford, Nigel G.1
  • 1 Rothamsted Research, Plant Sciences Department, Harpenden, Hertfordshire, AL5 2JQ, UK , Harpenden (United Kingdom)
  • 2 Present Address: Curtis Analytics Ltd, Daniel Hall Building, Rothamsted RoCRE, Harpenden, AL5 2JQ, UK , Harpenden (United Kingdom)
  • 3 Rothamsted Research, Computational and Analytical Sciences Department, Harpenden, Hertfordshire, AL5 2JQ, UK , Harpenden (United Kingdom)
  • 4 Present Address: The European Bioinformatics Institute (EMBL-EBI), Wellcome Genome Campus, Hinxton, Cambridgeshire, CB10 1SD, UK , Cambridgeshire (United Kingdom)
Published Article
BMC Genomics
Springer (Biomed Central Ltd.)
Publication Date
Aug 01, 2019
DOI: 10.1186/s12864-019-5991-8
Springer Nature


BackgroundFree asparagine is the precursor for acrylamide formation during cooking and processing of grains, tubers, beans and other crop products. In wheat grain, free asparagine, free glutamine and total free amino acids accumulate to high levels in response to sulphur deficiency. In this study, RNA-seq data were acquired for the embryo and endosperm of two genotypes of bread wheat, Spark and SR3, growing under conditions of sulphur sufficiency and deficiency, and sampled at 14 and 21 days post anthesis (dpa). The aim was to provide new knowledge and understanding of the genetic control of asparagine accumulation and breakdown in wheat grain.ResultsThere were clear differences in gene expression patterns between the genotypes. Sulphur responses were greater at 21 dpa than 14 dpa, and more evident in SR3 than Spark. TaASN2 was the most highly expressed asparagine synthetase gene in the grain, with expression in the embryo much higher than in the endosperm, and higher in Spark than SR3 during early development. There was a trend for genes encoding enzymes of nitrogen assimilation to be more highly expressed in Spark than SR3 when sulphur was supplied. TaASN2 expression in the embryo of SR3 increased in response to sulphur deficiency at 21 dpa, although this was not observed in Spark. This increase in TaASN2 expression was accompanied by an increase in glutamine synthetase gene expression and a decrease in asparaginase gene expression. Asparagine synthetase and asparaginase gene expression in the endosperm responded in the opposite way. Genes encoding regulatory protein kinases, SnRK1 and GCN2, both implicated in regulating asparagine synthetase gene expression, also responded to sulphur deficiency. Genes encoding bZIP transcription factors, including Opaque2/bZIP9, SPA/bZIP25 and BLZ1/OHP1/bZIP63, all of which contain SnRK1 target sites, were also expressed. Homeologues of many genes showed differential expression patterns and responses, including TaASN2.ConclusionsData on the genetic control of free asparagine accumulation in wheat grain and its response to sulphur supply showed grain asparagine levels to be determined in the embryo, and identified genes encoding signalling and metabolic proteins involved in asparagine metabolism that respond to sulphur availability.

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