Deletion of high-molecular-weight glutenin subunits in wheat significantly reduced dough strength and bread-baking quality
文献类型: 外文期刊
作者: Zhang, Yingjun 1 ; Hu, Mengyun 1 ; Liu, Qian 1 ; Sun, Lijing 1 ; Chen, Xiyong 1 ; Lv, Liangjie 1 ; Liu, Yuping 1 ; Jia, X 1 ;
作者机构: 1.Hebei Acad Agr & Forestry Sci, Inst Cereal & Oil Crops, 162 Hengshan St, Shijiazhuang 050035, Hebei, Peoples R China
2.Chinese Acad Sci, Inst Genet & Dev Biol, 1 Beichenxi Rd, Beijing 100101, Peoples
关键词: Common wheat; High-molecular-weight glutenin subunits; Post-transcriptional gene silencing; Glutenin macropolymer; Gliadin content; Dough quality
期刊名称:BMC PLANT BIOLOGY ( 影响因子:4.215; 五年影响因子:4.96 )
ISSN: 1471-2229
年卷期: 2018 年 18 卷
页码:
收录情况: SCI
摘要: BackgroundHigh-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.MethodsIn a previous work, we cloned the Glu-1E(b)x gene from Thinopyrum bessarabicum and introduced it into the wheat cultivar, Bobwhite. In addition to lines expressing the Glu-1E(b)x 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.ResultsDNA 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 -gliadin increased, whereas /- and -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.ConclusionsPost-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.
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