Gao Cong, Zhu Xiuru, Lu Shuai, Xu Jingbiao, Zhou Rong, Lv Jianying, Chen Yaoyu, Cao Yunying
School of Life Sciences, Nantong University, Nantong, China.
Front Plant Sci. 2022 Jan 25;12:808312. doi: 10.3389/fpls.2021.808312. eCollection 2021.
We used mutant and Nipponbare in field experiments to analyze agronomic traits, photosynthetic parameters, transcriptome, and gene expression. The results demonstrated cytoplasmic localization of , while GUS allogeneic () tissue-staining and quantitative analysis showed the gene was expressed in many organs, including flower buds; furthermore, it was involved in root, stem, and leaf growth. Compared to Nipponbare plants, grain filling rate and final grain weight decreased in plants of the knockout mutant owing to a delay in attainment of maximum grain filling rate. Photosystem II (PSII) efficiency was also reduced. Enrichment analysis showed that the functions of differentially expressed genes (DEGs) focused on nucleoside-, nucleotide-, and lipid-binding, as well as hydrolase, transferase, and phosphorylase activities. Signaling pathways mainly included starch and sucrose metabolism, as well as photosynthesis. Additionally, some DEGs were verified by fluorescence analysis. The results showed that knockout of affected photosynthesis and starch-, sucrose-, and amino acid metabolism-related gene expression; furthermore, the mutation reduced PSII utilization efficiency, it blocked the synthesis and metabolism of starch and sucrose, and affected the formation and transport of assimilates, thereby reducing final grain weight.
我们在田间试验中使用突变体和日本晴来分析农艺性状、光合参数、转录组和基因表达。结果表明[具体基因名称]定位于细胞质中,而GUS异源([具体基因名称])组织染色和定量分析表明该基因在包括花芽在内的许多器官中表达;此外,它还参与根、茎和叶的生长。与日本晴植株相比,敲除突变体植株的灌浆速率和最终粒重因最大灌浆速率达到延迟而降低。光系统II(PSII)效率也降低。富集分析表明,差异表达基因(DEGs)的功能集中在核苷、核苷酸和脂质结合以及水解酶、转移酶和磷酸化酶活性上。信号通路主要包括淀粉和蔗糖代谢以及光合作用。此外,一些DEGs通过荧光分析得到验证。结果表明,[具体基因名称]的敲除影响了光合作用以及与淀粉、蔗糖和氨基酸代谢相关的基因表达;此外,该突变降低了PSII的利用效率,阻断了淀粉和蔗糖的合成与代谢,并影响了同化物的形成和运输,从而降低了最终粒重。