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Keywords = Hosta plantaginea (Lam.) Aschers

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19 pages, 4364 KB  
Article
Combining Physiology and Transcriptome to Reveal Mechanisms of Hosta ‘Golden Cadet’ in Response to Alkali Stress
by Xiaogang Sun, Chunyao Zhu, Baizhou Li, Wei Ning and Jiahui Yin
Plants 2025, 14(4), 593; https://doi.org/10.3390/plants14040593 - 15 Feb 2025
Cited by 5 | Viewed by 1766
Abstract
As an ornamentally and medicinally worthy plant, Hosta plantaginea (Lam.) Aschers. has the adapted capacity to survive cold temperate monsoon climates in Northeastern China. However, its use is limited by the soil alkalization of urban gardens. Our pre-experiment found that Hosta ‘Golden Cadet’ [...] Read more.
As an ornamentally and medicinally worthy plant, Hosta plantaginea (Lam.) Aschers. has the adapted capacity to survive cold temperate monsoon climates in Northeastern China. However, its use is limited by the soil alkalization of urban gardens. Our pre-experiment found that Hosta ‘Golden Cadet’ has the potential to be alkali-tolerant. Hence, tissue-cultured seedlings of Hosta ‘Golden Cadet’ were used as experimental material. Its related growth, physiology, and transcripts were examined to reveal the molecular mechanism of Hosta plantaginea in response to alkali stress. The results show that the development of Hosta ‘Golden Cadet’ was affected by alkali stress. In comparison with the control, malondialdehyde (MDA) content increased by 4.28-fold at the 24th hour, superoxide dismutase (SOD) activity increased by 49% at the 6th hour, and peroxidase (POD) activity and soluble sugar (SS) content increased by 67% and 30% at the 12th hour, respectively. The RNA-seq analysis revealed that Hosta ‘Golden Cadet’ gene expressions at 0 h, 6 h, 12 h, 21 h and 48 h differed after 200 mmol/L NaHCO3 treatment. During 48 h under alkali stress, 2366 differentially expressed genes were found. The transcription factors MYB, AP2/ERF, and WRKY were activated in differentially expressed genes. The KEGG analysis found that phytohormone signaling pathways, starch and sucrose metabolism, and phenylpropane production were activated in Hosta ‘Golden Cadet’ in response to alkali stress. In summary, Hosta ‘Golden Cadet’ can reduce membrane damage by improving osmoregulation and antioxidant capacity, increase sucrose and starch metabolism, and regulate phenylpropane biosynthesis by activating transcription factors and inducing related phytohormone signaling, mitigating the effects of alkali toxicity. These findings guide an investigation into the mechanism of alkali tolerance in Hosta plants, screening alkali tolerance genes, and selecting and breeding novel alkali-tolerant Hosta plantaginea cultivars. Full article
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13 pages, 41215 KB  
Article
Transcriptome-Wide Analysis Reveals Key DEGs in Flower Color Regulation of Hosta plantaginea (Lam.) Aschers
by Jingying Zhang, Changhai Sui, Yanli Wang, Shuying Liu, Huimin Liu, Zhengren Zhang and Hongzhang Liu
Genes 2020, 11(1), 31; https://doi.org/10.3390/genes11010031 - 26 Dec 2019
Cited by 31 | Viewed by 4630
Abstract
Background: Hosta plantaginea (Lam.) Aschers (HPA), a species in the family Liliaceae, is an important landscaping plant and herbaceous ornamental flower. However, because the flower has only two colors, white and purple, color matching applications are extremely limited. To date, the mechanism underlying [...] Read more.
Background: Hosta plantaginea (Lam.) Aschers (HPA), a species in the family Liliaceae, is an important landscaping plant and herbaceous ornamental flower. However, because the flower has only two colors, white and purple, color matching applications are extremely limited. To date, the mechanism underlying flower color regulation remains unclear. Methods: In this study, the transcriptomes of three cultivars—H. plantaginea (HP, white flower), H. Cathayana (HC, purple flower), and H. plantaginea ‘Summer Fragrance’ (HS, purple flower)—at three flowering stages (bud stage, initial stage, and late flowering stage) were sequenced with the Illumina HiSeq 2000 (San Diego, CA, USA). The RNA-Seq results were validated by qRT-PCR of eight differentially expressed genes (DEGs). Then, we further analyzed the relationship between anthocyanidin synthase (ANS), chalcone synthase (CHS), and P450 and the flower color regulation by Gene Ontology (GO), Kyoto Encyclopedia of Genes and Genomes (KEGG), and Eukaryotic Orthologous Groups (KOG) network and pathway enrichment analyses. The overexpression of CHS and ANS in transgenic tobacco petals was verified using qRT-PCR, and the petal colors associated with the overexpression lines were confirmed using absorbance values. Results: Over 434,349 transcripts were isolated, and 302,832 unigenes were identified. Additionally, through transcriptome comparisons, 2098, 722, and 606 DEGs between the different stages were found for HP, HC, and HS, respectively. Furthermore, GO and KEGG pathway analyses showed that 84 color-related DEGs were enriched in 22 pathways. In particular, the flavonoid biosynthetic pathway, regulated by CHS, ANS, and the cytochrome P450-type monooxygenase gene, was upregulated in both purple flower varieties in the late flowering stage. In contrast, this gene was hardly expressed in the white flower variety, which was verified in the CHS and ANS overexpression transgenic tobacco petals. Conclusions: The results suggest that CHS, ANS, and the cytochrome P450s-regulated flavonoid biosynthetic pathway might play key roles in the regulation of flower color in HPA. These insights into the mechanism of flower color regulation could be used to guide artificial breeding of polychrome varieties of ornamental flowers. Full article
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