Strawberry ( Fragaria x ananassa ) is an allopolyploid species with diverse and complex transcripts. The regulatory mechanisms of fruit development and maturation have been extensively studied; however, little is known about the signaling mechanisms that direct this process in octoploid strawberry ( Fragaria x ananassa ). Here, we used long-read sequencing (LRS) technology and RNA-seq analysis to investigate the diversity and complexity of the polyploid transcriptome and differentially expressed transcripts along four successive fruit developmental stages of cultivated strawberry. We obtained a reference transcriptome with 119,897 unique full-length isoforms, including 2017 new isoforms and 2510 long noncoding RNAs. Based on the genome of the plausible progenitor ( Fragaria vesca ), 20,229 alternative splicing (AS) events were identified. Using this transcriptome, we found 17,485 differentially expressed transcripts during strawberry fruit development, including 527 transcription factors (TFs) belonging to 41 families. The expression profiles of all members of the auxin, ABA pathway, and anthocyanin biosynthesis gene families were also examined, and many of them were highly expressed at the ripe fruit stage, strongly indicating that the role of those genes is in the regulation of fruit ripening. We produce a high-quality reference transcriptome for octoploid strawberry, including much of the full-length transcript diversity, to help understand the regulatory mechanisms of fruit development and maturation of polyploid species, particularly via elucidation of the biochemical pathways involved in auxin, ABA, and anthocyanin biosynthesis.
Light-emitting diodes (LEDs) have been widely used in plant factories and agricultural facilities. Different LEDs can be designed in accordance with the light quality and intensity requirements of different plants, allowing the regulation of plant growth and development, as well as metabolic processes. Blue and red lights have significant effects on anthocyanin metabolism in strawberry fruit, but their effects on other metabolites are unknown. Here, we studied the effects of blue and red lights on the metabolism and gene expression of strawberry using metabolomics combined with transcriptomics. A total of 33 differentially expressed metabolites (DEMs) and 501 differentially expressed genes (DEGs) were isolated and identified. Among these DEMs, chlorogenic acid synthesis was upregulated by the blue light compared with the red light. Co-expression network analysis of DEMs and DEGs revealed that the expression of hydroxycinnamoyl-CoA:shikimate hydroxycinnamoyltransferase (FvHCT), the main gene in the chlorogenic acid synthetic pathway, was induced by blue light. Using multi-omics-based approach, our results suggest that different LED lights have multiple effects on strawberry fruit, with blue light able to co-upregulate chlorogenic acid synthesis and FvHCT gene expression.
Novel representatives of the important group of biologically-active, dehydroabietic acid-bearing oxazolidinone moiety were synthesized to explore more efficacious and less toxic antitumor agents. Structures of all the newly target molecules were confirmed by IR, 1H-NMR, 13C-NMR, and HR-MS. The inhibitory activities of these compounds against different human cancer cell lines (MGC-803, CNE-2, SK-OV-3, NCI-H460) and human normal liver cell line LO2 were evaluated and compared with the commercial anticancer drug cisplatin, using standard MTT (methyl thiazolytetrazolium) assay in vitro. The pharmacological screening results revealed that most of the hybrids showed significantly improved antiproliferative activities over dehydroabietic acid and that some displayed better inhibitory activities compared to cisplatin. In particular, compound 4j exhibited promising cytotoxicity with IC50 values ranging from 3.82 to 17.76 µM against all the test cell lines and displayed very weak cytotoxicity (IC50 > 100 µM) on normal cells, showing good selectivity between normal and malignant cells. Furthermore, the action mechanism of the representative compound 4j was preliminarily investigated by Annexin-V/PI dual staining, Hoechst 33258 staining, which indicated that the compound can induce cell apoptosis in MGC-803 cells in a dose-dependent manner and arrest the cell cycle in G1 phase. Therefore, 4j may be further exploited as a novel pharmacophore model for the development of anticancer agents.
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