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利用大豆转录组和蛋白质组分析鉴定与耐淹相关的基因/蛋白质。

Identification of Genes/Proteins Related to Submergence Tolerance by Transcriptome and Proteome Analyses in Soybean.

机构信息

Crop Research Institute, Shandong Academy of Agricultural Sciences, Jinan, China.

Institute of Food Crops, Hainan Academy of Agricultural Sciences, Haikou, China.

出版信息

Sci Rep. 2019 Oct 11;9(1):14688. doi: 10.1038/s41598-019-50757-1.

Abstract

Flooding can lead to yield reduction of soybean. Therefore, identification of flooding tolerance genes has great significance in production practice. In this study, Qihuang 34, a highly-resistant variety to flooding stress, was selected for submergence treatments. Transcriptome and proteome analyses were conducted, by which twenty-two up-regulated differentially expressed genes (DEGs)/differentially expressed proteins (DEPs) associated with five KEGG pathways were isolated. The number of the DEGs/DEPs enriched in glycolysis/gluconeogenesis was the highest. Four of these genes were confirmed by RT-qPCR, suggesting that glycolysis/gluconeogenesis may be activated to generate energy for plant survival under anaerobic conditions. Thirty-eight down-regulated DEGs/DEPs associated with six KEGG pathways were identified under submergence stress. Eight DEGs/DEPs enriched in phenylpropanoid biosynthesis were assigned to peroxidase, which catalyzes the conversion of coumaryl alcohol to hydroxy-phenyl lignin in the final step of lignin biosynthesis. Three of these genes were confirmed by RT-qPCR. The decreased expression of these genes led to the inhibition of lignin biosynthesis, which may be the cause of plant softening under submergence stress for a long period of time. This study revealed a number of up-/down-regulated pathways and the corresponding DEGs/DEPs, by which, a better understanding of the mechanisms of submergence tolerance in soybean may be achieved.

摘要

flooding 可能导致大豆减产。因此,鉴定耐淹基因在生产实践中具有重要意义。本研究以耐淹性强的品种齐黄 34 为材料进行淹水处理,对其进行转录组和蛋白质组分析,共分离到与 5 条 KEGG 途径相关的 22 个上调差异表达基因(DEGs)/差异表达蛋白(DEPs)。其中,富集到糖酵解/糖异生途径的 DEGs/DEPs 数量最多。通过 RT-qPCR 验证了其中的 4 个基因,表明在缺氧条件下,糖酵解/糖异生途径可能被激活以产生能量供植物存活。此外,还鉴定到 38 个受淹处理下调的 DEGs/DEPs,与 6 条 KEGG 途径相关。在受淹胁迫下,有 8 个 DEGs/DEPs 富集到苯丙烷生物合成途径,被分配到过氧化物酶中,过氧化物酶在木质素生物合成的最后一步中催化肉桂醇转化为羟基苯基木质素。通过 RT-qPCR 验证了其中的 3 个基因。这些基因的表达下调导致木质素生物合成受到抑制,这可能是植物在长时间受淹胁迫下软化的原因。本研究揭示了大量上调/下调的途径及其相应的 DEGs/DEPs,这有助于更好地理解大豆耐淹机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f9c/6789146/83f7b2f7a3e5/41598_2019_50757_Fig1_HTML.jpg

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