Comparative Transcriptome Analyses of Different <i>Rheum officinale</i> Tissues Reveal Differentially Expressed Genes Associated with Anthraquinone, Catechin, and Gallic Acid Biosynthesis

<i>Rheum officinale</i> Baill. is an important traditional Chinese medicinal herb, its dried roots and rhizomes being widely utilized to cure diverse diseases. However, previous studies mainly focused on the active compounds and their pharmacological effects, and the molecular mechanism...

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Bibliographic Details
Main Authors: Lipan Zhou, Jiangyan Sun, Tianyi Zhang, Yadi Tang, Jie Liu, Chenxi Gao, Yunyan Zhai, Yanbing Guo, Li Feng, Xinxin Zhang, Tao Zhou, Xumei Wang
Format: Article
Language:English
Published: MDPI AG 2022-09-01
Series:Genes
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Online Access:https://www.mdpi.com/2073-4425/13/9/1592
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Summary:<i>Rheum officinale</i> Baill. is an important traditional Chinese medicinal herb, its dried roots and rhizomes being widely utilized to cure diverse diseases. However, previous studies mainly focused on the active compounds and their pharmacological effects, and the molecular mechanism underlying the biosynthesis of these ingredients in <i>R. officinale</i> is still elusive. Here, we performed comparative transcriptome analyses to elucidate the differentially expressed genes (DEGs) in the root, stem, and leaf of <i>R. officinale</i>. A total of 236,031 unigenes with N50 of 769 bp was generated, 136,329 (57.76%) of which were annotated. A total of 5884 DEGs was identified after the comparative analyses of different tissues; 175 and 126 key enzyme genes with tissue-specific expression were found in the anthraquinone, catechin/gallic acid biosynthetic pathway, respectively, and some of these key enzyme genes were verified by qRT-PCR. The phylogeny of the <i>PKS III</i> family in Polygonaceae indicated that probably only <i>PL_741 PKSIII1</i>, <i>PL_11549 PKSIII5</i>, and <i>PL_101745 PKSIII6</i> encoded <i>PKSIII</i> in the polyketide pathway. These results will shed light on the molecular basis of the tissue-specific accumulation and regulation of secondary metabolites in <i>R. officinale</i>, and lay a foundation for the future genetic diversity, molecular assisted breeding, and germplasm resource improvement of this essential medicinal plant.
ISSN:2073-4425