Yang Bingxian, Guan Qijie, Tian Jingkui, Komatsu Setsuko
College of Biomedical Engineering & Instrument Science, Zhejiang University, Hangzhou 310027, China; National Institute of Crop Science, National Agriculture and Food Research Organization, Tsukuba 305-8518, Japan.
College of Biomedical Engineering & Instrument Science, Zhejiang University, Hangzhou 310027, China.
J Proteomics. 2017 Jan 6;150:323-340. doi: 10.1016/j.jprot.2016.10.001. Epub 2016 Oct 17.
High level of UV-B irradiation followed by dark treatment (HUV-B+D) causes accumulation of secondary metabolites in Clematis terniflora DC. To investigate the response mechanism under HUV-B+D, transcriptomic and proteomic analyses were performed in leaves of C. terniflora. The number of genes related to tetrapyrrole synthesis, amino acid metabolism, tricarboxylic acid cycle, and mitochondrial electron transport chains was hierarchically changed in leaves of C. terniflora under HUV-B+D. Data from RNA-sequencing transcriptomics and gel-free/label-free proteomics were integrated. The genes related to biosynthesis of lignins and flavonoids/isoflavonoids were significantly upregulated. Luteolin 7-O-β-D-glucosiduronic acid, rutin, and kaempferol 3-O-rutinose were accumulated. The number of differentially expressed genes (DEGs) and differentially abundant proteins (DAPs) related to protein metabolism were largely changed in posttranslational modification, ubiquitin proteasome, and ribosomal protein. The expression of NADP-dependent malic enzyme and the abundance of NADP-malate dehydrogenase were upregulated and increased, respectively. The activities of these two enzymes were also enhanced. These results suggest that the secondary metabolism pathway and tricarboxylic acid cycle might be activated in leaves of C. terniflora in response to HUV-B+D.
This study reported response mechanism in leaves of Clematis terniflora DC. under high level of UV-B irradiation followed by dark treatment using transcriptomic and proteomic techniques. Transcriptomic analysis revealed that the number of genes related to secondary metabolism was increased by >2 times. Phenylalanine ammonia-lyase, 4-Coumarate: CoA ligase, chalcone synthase, isoflavone reductase homolog, and cinnamoyl-CoA reductase were significantly upregulated, which suggests that the secondary metabolism pathway related to lignins and flavonoids/isoflavonoids might be activated. Genes and proteins related to protein metabolism were largely changed in postranslational modification, ubiquitin proteasome, and ribosomal protein. NADP-dependent malic enzyme and NADP-malate dehydrogenase were activated in tricarboxylic acid cycle, which suggests that tricarboxylic acid cycle might be enhanced in leaf of C. terniflora in response to HUV-B+D.
高强度UV-B照射后进行暗处理(HUV-B+D)会导致三叶铁线莲中次生代谢产物的积累。为了研究HUV-B+D处理下的响应机制,对三叶铁线莲的叶片进行了转录组学和蛋白质组学分析。在HUV-B+D处理下,三叶铁线莲叶片中与四吡咯合成、氨基酸代谢、三羧酸循环和线粒体电子传递链相关的基因数量发生了分层变化。整合了RNA测序转录组学和无凝胶/无标记蛋白质组学的数据。与木质素和黄酮类/异黄酮类生物合成相关的基因显著上调。木犀草素7-O-β-D-葡萄糖醛酸、芦丁和山奈酚3-O-芸香糖积累。与蛋白质代谢相关的差异表达基因(DEG)和差异丰度蛋白质(DAP)的数量在翻译后修饰、泛素蛋白酶体和核糖体蛋白方面发生了很大变化。NADP依赖性苹果酸酶的表达和NADP-苹果酸脱氢酶的丰度分别上调和增加。这两种酶的活性也增强了。这些结果表明,三叶铁线莲叶片中的次生代谢途径和三羧酸循环可能在响应HUV-B+D时被激活。
本研究报道了三叶铁线莲叶片在高强度UV-B照射后进行暗处理时的响应机制,采用了转录组学和蛋白质组学技术。转录组分析表明,与次生代谢相关的基因数量增加了2倍以上。苯丙氨酸解氨酶、4-香豆酸:辅酶A连接酶、查尔酮合酶、异黄酮还原酶同源物和肉桂酰辅酶A还原酶显著上调,这表明与木质素和黄酮类/异黄酮类相关的次生代谢途径可能被激活。与蛋白质代谢相关的基因和蛋白质在翻译后修饰、泛素蛋白酶体和核糖体蛋白方面发生了很大变化。NADP依赖性苹果酸酶和NADP-苹果酸脱氢酶在三羧酸循环中被激活,这表明三叶铁线莲叶片中的三羧酸循环可能在响应HUV-B+D时增强。