Complexity of gene paralogues resolved in biosynthetic pathway of hepatoprotective iridoid glycosides in a medicinal herb, Picrorhiza kurroa through differential NGS transcriptomes
Autor: | Anjali Kharb, Rajinder Singh Chauhan |
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Rok vydání: | 2021 |
Předmět: |
0106 biological sciences
0301 basic medicine Iridoid Glycosides Picrorhiza kurroa Iridoid Glucosides Sequence Homology Computational biology Biology Genes Plant Plant Roots 01 natural sciences Transcriptome 03 medical and health sciences Gene Expression Regulation Plant Genetics Gene silencing Gene Regulatory Networks Molecular Biology Gene Picrorhiza Plants Medicinal Multiple sequence alignment Functional analysis Gene Expression Profiling General Medicine Human genetics Biosynthetic Pathways High-Throughput Screening Assays 030104 developmental biology Liver Cinnamates Cytoprotection Plant Shoots 010606 plant biology & botany |
Zdroj: | Molecular Genetics and Genomics. 296:863-876 |
ISSN: | 1617-4623 1617-4615 |
DOI: | 10.1007/s00438-021-01787-w |
Popis: | Picrorhiza kurroa is a medicinal herb with diverse pharmacological applications due to the presence of iridoid glycosides, picroside-I (P-I), and picroside-II (P-II), among others. Any genetic improvement in this medicinal herb can only be undertaken if the biosynthetic pathway genes are correctly identified. Our previous studies have deciphered biosynthetic pathways for P-I and P-II, however, the occurrence of multiple copies of genes has been a stumbling block in their usage. Therefore, a methodological strategy was designed to identify and prioritize paralogues of pathway genes associated with contents of P-I and P-II. We used differential transcriptomes varying for P-I and P-II contents in different tissues of P. kurroa. All transcripts for a particular pathway gene were identified, clustered based on multiple sequence alignment to notify as a representative of the same gene (≥ 99% sequence identity) or a paralogue of the same gene. Further, individual paralogues were tested for their expression level via qRT-PCR in tissue-specific manner. In total 44 paralogues in 14 key genes have been identified out of which 19 gene paralogues showed the highest expression pattern via qRT-PCR. Overall analysis shortlisted 6 gene paralogues, PKHMGR3, PKPAL2, PKDXPS1, PK4CL2, PKG10H2 and PKIS2 that might be playing role in the biosynthesis of P-I and P-II, however, their functional analysis need to be further validated either through gene silencing or over-expression. The usefulness of this approach can be expanded to other non-model plant species for which transcriptome resources have been generated. |
Databáze: | OpenAIRE |
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