Department of Plant Sciences, Rothamsted Research, Harpenden, UK.
Department of Computational and Analytical Sciences, Rothamsted Research, Harpenden, UK.
Plant Biotechnol J. 2021 Aug;19(8):1602-1613. doi: 10.1111/pbi.13573. Epub 2021 Mar 28.
Free asparagine is the precursor for acrylamide, which forms during the baking, toasting and high-temperature processing of foods made from wheat. In this study, CRISPR/Cas9 was used to knock out the asparagine synthetase gene, TaASN2, of wheat (Triticum aestivum) cv. Cadenza. A 4-gRNA polycistronic gene was introduced into wheat embryos by particle bombardment and plants were regenerated. T1 plants derived from 11 of 14 T0 plants were shown to carry edits. Most edits were deletions (up to 173 base pairs), but there were also some single base pair insertions and substitutions. Editing continued beyond the T1 generation. Free asparagine concentrations in the grain of plants carrying edits in all six TaASN2 alleles (both alleles in each genome) were substantially reduced compared with wildtype, with one plant showing a more than 90 % reduction in the T2 seeds. A plant containing edits only in the A genome alleles showed a smaller reduction in free asparagine concentration in the grain, but the concentration was still lower than in wildtype. Free asparagine concentration in the edited plants was also reduced as a proportion of the free amino acid pool. Free asparagine concentration in the T3 seeds remained substantially lower in the edited lines than wildtype, although it was higher than in the T2 seeds, possibly due to stress. In contrast, the concentrations of free glutamine, glutamate and aspartate were all higher in the edited lines than wildtype. Low asparagine seeds showed poor germination but this could be overcome by exogenous application of asparagine.
游离天冬酰胺是丙烯酰胺的前体,它在小麦制成的烘焙、烘烤和高温加工食品中形成。在这项研究中,使用 CRISPR/Cas9 敲除了小麦(Triticum aestivum) cv. Cadenza 的天冬酰胺合成酶基因 TaASN2。通过粒子轰击将一个 4-gRNA 多顺反子基因导入小麦胚胎并再生植物。从 14 个 T0 植物中的 11 个中获得的 T1 植物被证明携带编辑。大多数编辑是缺失(多达 173 个碱基对),但也有一些单碱基插入和替换。编辑在 T1 代后仍在继续。与野生型相比,携带所有六个 TaASN2 等位基因(每个基因组中的两个等位基因)编辑的植物的籽粒中天冬酰胺游离浓度显著降低,其中一个植物的 T2 种子中降低了 90%以上。一个只在 A 基因组等位基因中携带编辑的植物的籽粒中游离天冬酰胺浓度降低幅度较小,但仍低于野生型。编辑植物中游离天冬酰胺的浓度也作为游离氨基酸库的一部分降低。编辑植物的 T3 种子中的游离天冬酰胺浓度仍然明显低于野生型,尽管它高于 T2 种子,可能是由于应激。相比之下,编辑系中游离谷氨酰胺、谷氨酸和天冬氨酸的浓度均高于野生型。低天冬酰胺种子发芽不良,但通过外源添加天冬酰胺可以克服。