文献类型： 外文期刊

作者： Zhang, Wenlin ¹ ; Yang, Yang ³ ; Zhu, Xuedong ⁴ ; Yang, Suyu ³ ; Liao, Ximei ³ ; Li, Honglei ¹ ; Li, Zhexin ¹ ; Liao, Qinhong ¹ ; Tang, Jianmin ¹ ; Zhao, Guohua ² ; Wu, Lin ³ ;

作者机构： 1.Chongqing Univ Arts & Sci, Inst Special Plants, Coll Landscape Architecture & Life Sci, Chongqing Key Lab Econ Plant Biotechnol, Yongchuan 402160, Peoples R China

2.Southwest Univ, Coll Food Sci, Beibei 400715, Peoples R China

3.Southwest Univ, Coll Agron & Biotechnol, Chongqing Key Lab Biol & Genet Breeding Tuber & Ro, Beibei 400715, Peoples R China

4.Southeast Chongqing Acad Agr Sci, Fuling 408000, Peoples R China

关键词： Ginger; Metabolomics; Transcriptomics; Long non-coding RNAs; Gingerol biosynthesis

期刊名称：BMC GENOMICS （ 影响因子：4.4； 五年影响因子：4.7 ）

ISSN： 1471-2164

年卷期： 2023 年 24 卷 1 期

页码：

收录情况： SCI

摘要： Background As the characteristic functional component in ginger, gingerols possess several health-promoting properties. Long non-coding RNAs (lncRNAs) act as crucial regulators of diverse biological processes. However, lncRNAs in ginger are not yet identified so far, and their potential roles in gingerol biosynthesis are still unknown. In this study, metabolomic and transcriptomic analyses were performed in three main ginger cultivars (leshanhuangjiang, tonglingbaijiang, and yujiang 1 hao) in China to understand the potential roles of the specific lncRNAs in gingerol accumulation.Results A total of 744 metabolites were monitored by metabolomics analysis, which were divided into eleven categories. Among them, the largest group phenolic acid category contained 143 metabolites, including 21 gingerol derivatives. Of which, three gingerol analogs, [8]-shogaol, [10]-gingerol, and [12]-shogaol, accumulated significantly. Moreover, 16,346 lncRNAs, including 2,513, 1,225, and 2,884 differentially expressed (DE) lncRNA genes (DELs), were identified in all three comparisons by transcriptomic analysis. Gene ontology enrichment (GO) analysis showed that the DELs mainly enriched in the secondary metabolite biosynthetic process, response to plant hormones, and phenol-containing compound metabolic process. Correlation analysis revealed that the expression levels of 11 DE gingerol biosynthesis enzyme genes (GBEGs) and 190 transcription factor genes (TF genes), such as MYB1, ERF100, WRKY40, etc. were strongly correlation coefficient with the contents of the three gingerol analogs. Furthermore, 7 and 111 upstream cis-acting lncRNAs, 1,200 and 2,225 upstream trans-acting lncRNAs corresponding to the GBEGs and TF genes were identified, respectively. Interestingly, 1,184 DELs might function as common upstream regulators to these GBEGs and TFs genes, such as LNC_008452, LNC_006109, LNC_004340, etc. Furthermore, protein-protein interaction networks (PPI) analysis indicated that three TF proteins, MYB4, MYB43, and WRKY70 might interact with four GBEG proteins (PAL1, PAL2, PAL3, and 4CL-4).Conclusion Based on these findings, we for the first time worldwide proposed a putative regulatory cascade of lncRNAs, TFs genes, and GBEGs involved in controlling of gingerol biosynthesis. These results not only provide novel insights into the lncRNAs involved in gingerol metabolism, but also lay a foundation for future in-depth studies of the related molecular mechanism.