2019
DOI: 10.1186/s12870-019-1645-x
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Transcriptome analyses provide insights into the expression pattern and sequence similarity of several taxol biosynthesis-related genes in three Taxus species

Abstract: BackgroundTaxol is an efficient anticancer drug; however, the accumulation of taxoids can vary hugely among Taxus species. The mechanism underlying differential accumulation of taxoids is largely unknown. Thus, comparative analysis of the transcriptomes in three Taxus species, including T. media, T. mairei and T. cuspidata, was performed.ResultsKEGG enrichment analysis revealed that the diterpenoid biosynthesis and cytochrome P450 pathways were significantly enriched in different comparisons. Differential expr… Show more

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Cited by 46 publications
(33 citation statements)
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“…Transcriptome analysis is currently the most widely used and cost effective way to screen target gene(s) rapidly in functional genomic studies (Ali et al, 2018;Ma et al, 2019;Zhou et al, 2019). In this study, a total of 100,218 unigenes were generated by transtomic sequencing of three chemotypes of C. burmannii.…”
Section: Validation Of Degs Using Quantitative Real-time Pcr (Qrt-pcr)mentioning
confidence: 99%
“…Transcriptome analysis is currently the most widely used and cost effective way to screen target gene(s) rapidly in functional genomic studies (Ali et al, 2018;Ma et al, 2019;Zhou et al, 2019). In this study, a total of 100,218 unigenes were generated by transtomic sequencing of three chemotypes of C. burmannii.…”
Section: Validation Of Degs Using Quantitative Real-time Pcr (Qrt-pcr)mentioning
confidence: 99%
“…We previously performed metabolite analyses as part of a capacity building project for medicinal plants, which also included samples from T. media cell suspension cultures (16). Since these cultures were available to us as a source for candidate genes, we downloaded publicly available whole transcriptome shotgun sequencing (RNA-Seq) data sets acquired with this species (National Center for Biotechnology Information (NCBI) Bioproject numbers PRNJA169654, PRJNA341288, and PRNJA497542) (17,18), with an emphasis on suspension cells treated with the elicitor methyl jasmonate, which is commonly used to upregulate the formation of taxoids (19). We then searched in these publicly available data sets for gene sequences with homology to previously characterized AAEs of varying specificity (for details see Experimental procedures).…”
Section: Cloning and Categorization Of Candidate Aaesmentioning
confidence: 99%
“…First-strand cDNA was prepared from RNA with the SuperScript III First Strand Synthesis kit (Invitrogen, Carlsbad, CA, USA) with random hexamer oligonucleotides. Open reading frames for CoA ligases were amplified using gene-specific primers (Table S3) designed based on AAE sequences identified in publicly available T. media transcriptome data sets (NCBI Bioproject numbers PRNJA169654, PRJNA341288, and PRNJA497542) (17,18). Amplicons were ligated into the pET-32b vector featuring an encoded 6 x histidine tag (EMD Millipore, Burlington, MA, USA) and, following sequence confirmation, transformed into E. coli BL21(DE3) cells (New England Biolabs, Ipswich, MA, USA).…”
Section: Cloning and Heterologous Expression Of Candidate Aae Genesmentioning
confidence: 99%
“…In addition, DEGs were mapped to the KEGG database in order to elucidate their biological functions (Liang et al 2019;Miao et al 2019;Zhou et al 2019). The top 20 most enriched pathways are shown in Figure 5B and Table A7.…”
Section: Functional Annotation Of Degsmentioning
confidence: 99%