4.7 Article

Gene Expression and Isoform Identification of PacBio Full-Length cDNA Sequences for Berberine Biosynthesis in Berberis koreana

Journal

PLANTS-BASEL
Volume 10, Issue 7, Pages -

Publisher

MDPI
DOI: 10.3390/plants10071314

Keywords

Berberis koreana; benzylisoquinoline alkaloids (BIAs); berberine; isoforms; PacBio Iso-Seq

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Funding

  1. National Institute of Biological Resources [NIBR202021101, NIBR202124101]

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Berberis koreana is a medicinal plant that produces berberine, a bioactive compound widely used for its health benefits in the food and drug industry. Gene expression analysis and full-length cDNA sequencing were used to investigate the berberine biosynthesis pathway, revealing multiple gene isoforms and gene duplication contributing to the specificity of alkaloid synthesis. The study also showed how B. koreana streamlines berberine biosynthesis by blocking pathways leading to other benzylisoquinoline alkaloids, emphasizing the presence of specific enzymes only for berberine synthesis.
Berberis koreana is a medicinal plant containing berberine, which is a bioactive compound of the benzylisoquinoline alkaloid (BIA) class. BIA is widely used in the food and drug industry for its health benefits. To investigate the berberine biosynthesis pathway, gene expression analysis was performed in leaves, flowers, and fruits at different stages of growth. This was followed by full-length cDNA sequencing analysis using the PacBio sequencer platform to determine the number of isoforms of those expressed genes. We identified 23,246 full-length unigenes, among which 8479 had more than one isoform. The number of isoforms ranged between two to thirty-one among all genes. Complete isoform analysis was carried out on the unigenes encoding BIA synthesis. Thirteen of the sixteen genes encoding enzymes for berberine synthesis were present in more than one copy. This demonstrates that gene duplication and translation into isoforms may contribute to the functional specificity of the duplicated genes and isoforms in plant alkaloid synthesis. Our study also demonstrated the streamlining of berberine biosynthesis via the absence of genes for enzymes of other BIAs, but the presence of all the genes for berberine biosynthesize in B. koreana. In addition to genes encoding enzymes for the berberine biosynthesis pathway, the genes encoding enzymes for other BIAs were not present in our dataset except for those encoding corytuberine synthase (CTS) and berbamunine synthase (BS). Therefore, this explains how B. koreana produces berberine by blocking the pathways leading to other BIAs, effectively only allowing the pathway to lead to berberine synthesis.

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