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小麦高分子量麦谷蛋白亚基的缺失显著降低了面团强度和面包烘焙品质。

Deletion of high-molecular-weight glutenin subunits in wheat significantly reduced dough strength and bread-baking quality.

机构信息

Institute of Cereal and Oil Crops, Hebei Academy of Agriculture and Forestry Sciences, 162 Hengshan Street, Shijiazhuang, 050035, China.

Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, 1 Beichenxi Road, Beijing, 100101, China.

出版信息

BMC Plant Biol. 2018 Dec 3;18(1):319. doi: 10.1186/s12870-018-1530-z.

Abstract

BACKGROUND

High-molecular-weight glutenin subunits (HMW-GS) play important roles in the elasticity of dough made from wheat. The HMW-GS null line is useful for studying the contribution of HMW-GS to the end-use quality of wheat.

METHODS

In a previous work, we cloned the Glu-1Ex gene from Thinopyrum bessarabicum and introduced it into the wheat cultivar, Bobwhite. In addition to lines expressing the Glu-1Ex gene, we also obtained a transgenic line (LH-11) with all the HMW-GS genes silenced. The HMW-GS deletion was stably inherited as a dominant and conformed to Mendel's laws. Expression levels of HMW-GS were determined by RT-PCR and epigenetic changes in methylation patterns and small RNAs were analyzed. Glutenins and gliadins were separated and quantitated by reversed-phase ultra-performance liquid chromatography. Measurement of glutenin macropolymer, and analysis of agronomic traits and end-use quality were also performed.

RESULTS

DNA methylation and the presence of small double-stranded RNA may be the causes of post-transcriptional gene silencing in LH-11. The accumulation rate and final content of glutenin macropolymer (GMP) in LH-11 were significantly lower than in wild-type (WT) Bobwhite. The total protein content was not significantly affected as the total gliadin content increased in LH-11 compared to WT. Deletion of HMW-GS also changed the content of different gliadin fractions. The ratio of ω-gliadin increased, whereas α/β- and γ-gliadins declined in LH-11. The wet gluten content, sedimentation value, development time and stability time of LH-11 were remarkably lower than that of Bobwhite. Bread cannot be made using the flour of LH-11.

CONCLUSIONS

Post-transcriptional gene silencing through epigenetic changes and RNA inhibition appear to be the causes for the gene expression deficiency in the transgenic line LH-11. The silencing of HMW-GW in LH-11 significantly reduced the dough properties, GMP content, wet gluten content, sedimentation value, development time and stability time of flour made from this wheat cultivar. The HMW-GS null line may provide a potential material for biscuit-making because of its low dough strength.

摘要

背景

高分子量谷蛋白亚基(HMW-GS)在小麦面团弹性中发挥重要作用。HMW-GS 缺失系可用于研究 HMW-GS 对小麦食用品质的贡献。

方法

在之前的工作中,我们从中间偃麦草中克隆了 Glu-1Ex 基因,并将其导入小麦品种 Bobwhite。除了表达 Glu-1Ex 基因的系外,我们还获得了一个 HMW-GS 基因全部沉默的转基因系(LH-11)。HMW-GS 缺失作为显性性状稳定遗传,并符合孟德尔定律。通过 RT-PCR 测定 HMW-GS 的表达水平,并分析甲基化模式和小 RNA 的表观遗传变化。通过反相超高效液相色谱法分离和定量谷蛋白和醇溶蛋白。还进行了谷蛋白大聚合体(GMP)的测量,以及农艺性状和食用品质的分析。

结果

DNA 甲基化和小双链 RNA 的存在可能是 LH-11 中转录后基因沉默的原因。LH-11 中谷蛋白大聚合体(GMP)的积累率和最终含量明显低于野生型(WT)Bobwhite。与 WT 相比,LH-11 中总醇溶蛋白含量增加,但总蛋白含量没有明显受到影响。HMW-GS 的缺失也改变了不同醇溶蛋白馏分的含量。ω-醇溶蛋白的比例增加,而 LH-11 中的α/β-和γ-醇溶蛋白减少。LH-11 的湿面筋含量、沉淀值、形成时间和稳定时间明显低于 Bobwhite。不能用 LH-11 的面粉制作面包。

结论

通过表观遗传变化和 RNA 抑制的转录后基因沉默似乎是 LH-11 中转基因系基因表达缺陷的原因。LH-11 中 HMW-GW 的沉默显著降低了这种小麦品种面粉的面团特性、GMP 含量、湿面筋含量、沉淀值、形成时间和稳定时间。由于其面团强度低,HMW-GS 缺失系可能为制作饼干提供了潜在的材料。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55c6/6276161/c972a12bce23/12870_2018_1530_Fig1_HTML.jpg

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