De novo transcriptome analysis unravels tissue-specific expression of candidate genes involved in major secondary metabolite biosynthetic pathways of Plumbago zeylanica: implication for pharmacological potential
Authors
Balachandran Sundari
Central Research Facility, Sri Ramachandra Institute of Higher Education and Research, Chennai, 600116 India
Roli Budhwar
Bionivid Technology [P] Limited, Kasturi Nagar, Bangalore, 560043 India
Bilikere Dwarakanath
Central Research Facility, Sri Ramachandra Institute of Higher Education and Research, Chennai, 600116 India
S Thyagarajan
Central Research Facility, Sri Ramachandra Institute of Higher Education and Research, Chennai, 600116 India
Key message
The present study provides comparative transcriptome analysis, besides identifying functional secondary metabolite genes of Plumbago zeylanica with pharmacological potential for future functional genomics, and metabolomic engineering of secondary metabolites from this plant towards diversified biomedical applications.
Plumbago zeylanica is a widely used medicinal plant of the traditional Indian system of medicine with wide pharmacological potential to treat several disorders. The present study aimed to carry out comparative transcriptome analysis in leaf and root tissue of P. zeylanica using Illumina paired end sequencing to identify tissue-specific functional genes involved in the biosynthesis of secondary metabolites, contributing to its therapeutic efficacy. De novo sequencing assembly resulted in the identification of 62,321 “Unigenes” transcripts with an average size of 1325 bp. Functional annotation using BLAST2GO resulted in the identification of 50,301 annotated transcripts (80.71%) and GO assigned to 18,814 transcripts. KEGG pathway annotation of the “Unigenes” revealed that 2465 transcripts could be assigned to 242 KEGG pathway maps wherein the number of transcripts involved in secondary metabolism was distinct in root and leaf transcriptome. Among the secondary metabolite biosynthesis pathways, the cluster of “Unigenes” encoding enzymes of ‘Phenylpropanoid biosynthesis pathway’ represents the largest group (84 transcripts) followed by ‘Terpenoid Backbone biosynthesis’ (48 transcripts). The transcript levels of the candidate unigenes encoding key enzymes of phenylpropanoid (PAL, TAL) and flavanoid biosynthesis (CHS, ANS, FLS) pathways were up-regulated in root, while the expression levels of candidate “Unigenes” transcript for monoterpenoid (DXS, ISPF), diterpenoid biosynthesis (SPS, SDS) and indole alkaloid pathways (STR) were significantly higher in leaf of P. zeylanica. Interestingly, validation of differential gene expression profile by qRT-PCR also confirmed that candidate “Unigenes” enzymes of phenylpropanoid and flavonoid biosynthesis were highly expressed in the root, while the key regulatory enzymes of terpenoid and indole alkaloid compounds were up-regulated in the leaf, suggesting that (differences in) the levels of these functional genes could be attributed to the (differential) pharmacological activity (between root and leaf) in tissues of P. zeylanica.
Electronic supplementary material
The online version of this article (10.1007/s13205-020-02263-9) contains supplementary material, which is available to authorized users.
Keywords: Plumbago zeylanica, Secondary metabolites, Candidate unigenes, Transcriptome, Tissue-specific expression, Pharmacological potential
Author Biography
Bilikere Dwarakanath, Central Research Facility, Sri Ramachandra Institute of Higher Education and Research, Chennai, 600116 India
Shanghai Proton and Heavy Ion Center, Pudong, 201321 Shanghai China
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