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The polymorphism level determined

The polymorphism level determined

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Using allozyme analysis, genetic and genotypic variation of rare relict species, a member of one of ancient angiosperm families, Araliaceae, the clonal plant Oplopanax elatus (Nakai) Nakai, was evaluated. Electrophoretic separation of the enzymes is described, and genetic interpretation of the enzymes variation patterns is presented. The values of...

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... these reasons, evoluu tionary history of the species and the associated gene drift can be considered as the main factors responsible for the low level of species variation observed. Interestingly, the index of observed heterozygosity in O. elatus is the highest among the Araliaceae species investigated (Table 4). Low levels of heterozygosity in the populations of members of Araliaceae are to a great degree associated with their mating system, mostly represented by selffpollination, and in some species, by cleistogamy [29]. ...

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... The level within the inter-population genetic variability is substantially higher, compared to the values reported for species with vegetative reproduction. These results suggest a certain contribution of seed propagation in species formation (Reunova et al., 2010;Kholina et al., 2010;Kholina et al., 2012). ...
... This is likely the result of the long-term isolation of populations and the subsequent low gene flow among them, the short dispersal distances causing inbreeding, and the genetic bottlenecks derived from consecutive habitat changes experienced during Pleistocene glaciations and interglacials (Segarra-Moragues et al., 2007;Segarra-Moragues & Catal an, 2008). Clonality is another common explanation for the low genetic diversity levels observed in alpine plants (Hamrick & Godt, 1996;Nybom, 2004;Kholina et al., 2010). However, vegetative propagation has not been documented in B. pyrenaica (Garc ıa & Antor, 1995b;Segarra-Moragues & Catal an, 2002) and, thus, clonality is discarded as a possible explanation for the low levels of genetic diversity in this species. ...
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... Ho = 0.131, He = 0.113; Kholina et al., 2010). Allozyme analysis has shown a slight excess of heterozygotes in this population. ...
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Plant growth environment plays an important role in shaping soil microbial communities. To understand the response of soil rhizosphere microbial communities in Oplopanax elatus Nakai plant to a changed growth conditions from natural habitation to cultivation after transplant. Here, a comparative study of soil chemical properties and microbial community using high-throughput sequencing was conducted under cultivated conditions (CT) and natural conditions (WT), in Changbai Mountain, Northeast of China. The results showed that rhizosphere soil in CT had higher pH and lower content of soil organic matter (SOM) and available nitrogen compared to WT. These changes influenced rhizosphere soil microbial communities, resulting in higher soil bacterial and fungi richness and diversity in CT soil, and increased the relative abundance of bacterial phyla Acidobacteria, Chloroflexi, Gemmatimonadetes, Firmicutes and Patescibacteria, and the fungi phyla Mortierellomycota and Zoopagomycota, while decreased bacterial phyla Actinobacteria, WPS-2, Gemmatimonadetes, and Verrucomicrobia, and the fungi phyla Ascomycota, and Basidiomycota. Redundancy analysis analysis indicated soil pH and SOM were the primarily environmental drivers in shaping the rhizosphere soil microbial community in O. elatus under varied growth conditions. Therefore, more attention on soil nutrition management especially organic fertilizer inputs should be paid in O. elatus cultivation.
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Bioreactor-cultured adventitious roots (ARs) of the endangered medicinal plant Oplopanax elatus Nakai is a novel alternative plant material. To utilize ARs in the product production, the present study investigated the anti-inflammatory effect of O. elatus ARs. In the in vivo experiment, lipopolysaccharide (LPS)-induced acute lung injury disease model was established and several inflammatory indexes were determined. For the LPS-stimulated mice, after pretreatment of AR crude extract (200 mg/kg), cell infiltration in lungs was decreased, the production of proinflammatory mediators, including nitric oxide (NO), tumor necrosis factor (TNF)-α, and interleukin (IL)-6, and 1β in the bronchoalveolar lavage fluid was evidently reduced, which indicated that O. elatus ARs had an anti-inflammatory effect. In the in vitro experiment, ethyl acetate (EtOAc) fractions (12.5, 25, and 50 μg/mL) were used to treat LPS-induced peritoneal macrophages (PMs) of mice. The production of NO, prostaglandin E2, TNF-α, IL-6, and IL-1β in LPS-stimulated PMs was obviously inhibited (p < 0.05) after pretreatment with EtOAc fractions, and the expression of the inducible nitric oxide synthase and cyclooxygenase were also suppressed. To clarify the anti-inflammatory mechanism, effects of EtOAc fraction on changes of proteins related to the pathways of mitogen-activated protein kinases (MAPKs) and nuclear factor-kappa B (NF-κB) were investigated. The phosphorylation of extracellular regulated protein kinases, c-jun n-terminal kinase, and p38 MAPK in LPS-induced PMs was inhibited after pretreatment of EtOAc fractions. In addition, EtOAc fractions enhanced inhibitor of nuclear factor-kappa B-α expression and decreased nuclear translocation of p65 NF-κB. Thus, EtOAc from O. elatus ARs is involved in regulating MAKP and NF-κB signaling pathways to inhibit LPS-induced inflammation.
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