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

Genes (Basel). 2022 Sep 5;13(9):1592. doi: 10.3390/genes13091592.

Abstract

Rheum officinale 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 R. officinale is still elusive. Here, we performed comparative transcriptome analyses to elucidate the differentially expressed genes (DEGs) in the root, stem, and leaf of R. officinale. 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 PKS III family in Polygonaceae indicated that probably only PL_741 PKSIII1, PL_11549 PKSIII5, and PL_101745 PKSIII6 encoded PKSIII in the polyketide pathway. These results will shed light on the molecular basis of the tissue-specific accumulation and regulation of secondary metabolites in R. officinale, and lay a foundation for the future genetic diversity, molecular assisted breeding, and germplasm resource improvement of this essential medicinal plant.

Keywords: Rheum officinale; SSR; anthraquinone; biosynthesis; differentially expressed genes; transcriptome.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anthraquinones
  • Catechin*
  • Gallic Acid
  • Gene Expression Profiling
  • Polyketides*
  • Rheum* / genetics

Substances

  • Anthraquinones
  • Polyketides
  • 9,10-anthraquinone
  • Gallic Acid
  • Catechin

Grants and funding

This research was co-supported by the National Natural Science Foundation of China, grant number 81903739 and 31770364, and the Natural Science Foundation of Shaanxi Province, grant number 2020JQ-024 and 2020JZ-05.