Yin Dong-Jie, Ye Shi-Jie, Sun Xiao-Yan, Chen Qin-Yi, Min Ting, Wang Hong-Xun, Wang Li-Mei
College of Life Science and Technology, Wuhan Polytechnic University, Wuhan, China.
College of Food Science and Engineering, Wuhan Polytechnic University, Wuhan, China.
Front Plant Sci. 2022 Jul 7;13:913265. doi: 10.3389/fpls.2022.913265. eCollection 2022.
Roxb. is grown worldwide as an important aquatic cash crop. Current research on primarily focuses on the separation and identification of active ingredients, as well as the inhibitory effect on tumors; however, research on the molecular mechanism of secondary metabolite accumulation is rather limited. Consequently, an integrative analysis of transcriptome and metabolome is required to identify the key metabolic pathways, and key genes, and to explain the molecular mechanism of .
The biosynthesis pathways of phenolics in were examined through transcriptome and metabolome analyses. Transcriptome analysis yielded 42.76 million clean reads representing 81,417 unigenes with an average length of 1,752 bp. KEGG pathway analysis revealed that 1,623 unigenes, including 88 candidate unigenes related to phenolics biosynthesis, were up-regulated in shell (FR) when compared to leaves (LF), root (RT), and stem (ST). The FR vs. LF group had the highest number of specific genes involved in phenylpropanoid, flavonoid, flavone, and flavonol biosynthesis pathways compared to all other comparison groups. In addition, RNA sequencing revealed 18,709 SSRs spanning 14,820 unigenes and 4,387 unigenes encoding transcription factors. Metabolome analysis identified 793 metabolites, including 136 flavonoids and 31 phenylpropane compounds. In the FR group compared to the LF group, there were 202 differentially accumulated metabolites (DAMs). The combined transcriptome and metabolome analyses indicated a significant correlation between 1,050 differentially expressed genes (DEGs) and 62 DAMs. This view proposes a schematic of flavonoid biosynthesis in the FR vs. LF group, providing evidence for the differences in genes and metabolites between FR and LF.
In this study, through transcriptome assembly and metabolome analysis, several DEGs and DAMs were identified, which were subsequently used to build flavonoid biosynthesis pathways and a correlation network. The findings pave the way for future research into the molecular mechanisms and functional characterization of candidate genes for phenolics biosynthesis.
[植物名称]作为一种重要的水生经济作物在全球范围内种植。目前对[该植物]的研究主要集中在活性成分的分离鉴定以及对肿瘤的抑制作用;然而,关于次生代谢产物积累的分子机制研究相当有限。因此,需要对转录组和代谢组进行综合分析,以确定关键代谢途径和关键基因,并解释[该植物次生代谢产物积累]的分子机制。
通过转录组和代谢组分析研究了[该植物]中酚类物质的生物合成途径。转录组分析产生了4276万个clean reads,代表81417个单基因,平均长度为1752 bp。KEGG通路分析表明,与叶片(LF)、根(RT)和茎(ST)相比,[该植物]壳(FR)中有1623个单基因上调,其中包括88个与酚类物质生物合成相关的候选单基因。与所有其他比较组相比,FR与LF组中参与苯丙烷类、黄酮类、黄酮和黄酮醇生物合成途径的特定基因数量最多。此外,RNA测序揭示了跨越14820个单基因的18709个SSR和4387个编码转录因子的单基因。代谢组分析鉴定出793种代谢物,包括136种黄酮类化合物和31种苯丙烷类化合物。与LF组相比,FR组中有202种差异积累代谢物(DAMs)。转录组和代谢组联合分析表明,1050个差异表达基因(DEGs)与62个DAMs之间存在显著相关性。该观点提出了FR与LF组中黄酮类生物合成的示意图,为FR和LF之间基因和代谢物的差异提供了证据。
在本研究中,通过[该植物]转录组组装和代谢组分析,鉴定了多个DEGs和DAMs,随后用于构建黄酮类生物合成途径和相关网络。这些发现为未来研究[该植物]酚类物质生物合成候选基因的分子机制和功能表征铺平了道路。