4.7 Article

Transcriptome-Wide Identification and Quantification of Caffeoylquinic Acid Biosynthesis Pathway and Prediction of Its Putative BAHDs Gene Complex in A. spathulifolius

Journal

Publisher

MDPI
DOI: 10.3390/ijms22126333

Keywords

phenylpropanoid pathway (PPP); 5-Caffeoylquinic acid (5-CQA or CQA); BAHD acyltransferases (BAHDs); hydroxycinnamoyl-coenzyme A; quinate hydroxycinnamoyl transferase (HQT); hydroxycinnamoyl-coenzyme A; shikimate; quinate hydroxycinnamoyl transferase (HCT); hydroxycinnamic acids (HCs); Aster spathulifolius; differentially expressed genes (DEGs)

Funding

  1. Yeungnam University Grant 2021 commission, Korea [221A380124]

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The phenylpropanoid pathway plays a crucial role in producing byproducts that promote human health, with caffeoylquinic acid being a common soluble phenolic compound in angiosperms. The study identified candidate genes for the biosynthesis of caffeoylquinic acid from the phenylpropanoid pathway in A. spathulifolius flowers and leaves through transcriptome analysis. Differential expression of genes related to PPP and CQA biosynthesis was observed between the flowers and leaves, indicating a potential tissue-specific regulation of these pathways.
The phenylpropanoid pathway is a major secondary metabolite pathway that helps plants overcome biotic and abiotic stress and produces various byproducts that promote human health. Its byproduct caffeoylquinic acid is a soluble phenolic compound present in many angiosperms. Hydroxycinnamate-CoA shikimate/quinate transferase is a significant enzyme that plays a role in accumulating CQA biosynthesis. This study analyzed transcriptome-wide identification of the phenylpropanoid to caffeoylquinic acid biosynthesis candidate genes in A. spathulifolius flowers and leaves. Transcriptomic analyses of the flowers and leaves showed a differential expression of the PPP and CQA biosynthesis regulated unigenes. An analysis of PPP-captive unigenes revealed a major duplication in the following genes: PAL, 120 unigenes in leaves and 76 in flowers; C3 ' H, 169 unigenes in leaves and 140 in flowers; 4CL, 41 unigenes in leaves and 27 in flowers; and C4H, 12 unigenes in leaves and 4 in flowers. The phylogenetic analysis revealed 82 BAHDs superfamily members in leaves and 72 in flowers, among which five unigenes encode for HQT and three for HCT. The three HQT are common to both leaves and flowers, whereas the two HQT were specialized for leaves. The pattern of HQT synthesis was upregulated in flowers, whereas HCT was expressed strongly in the leaves of A. spathulifolius. Overall, 4CL, C4H, and HQT are expressed strongly in flowers and CAA and HCT show more expression in leaves. As a result, the quantification of HQT and HCT indicates that CQA biosynthesis is more abundant in the flowers and synthesis of caffeic acid in the leaves of A. spathulifolius.

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