17 research outputs found

    Data from: Carbon dynamics and environmental controls of a hilly tea plantation in Southeast China

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    Tea plantations are widely distributed and continuously expanding across subtropical China in recent years. However, carbon flux exchanges from tea plantation ecosystems are poorly understood at the ecosystem level. In this study, we use the eddy covariance technique to quantify the magnitude and temporal variations of the net ecosystem exchange (NEE) in tea plantation in Southeast China over four years (2014-2017). The result showed that the tea plantation was a net carbon sink, with an annual NEE that ranged from -182.40 g C m-2 to -301.51 g C m-2, which was a much lower carbon sequestration potential than other ecosystems in subtropical China. Photosynthetic photon flux density (PPFD) explained the highest proportion of the variation in NEE and gross primary productivity (GPP) (for NEE: F=389.89, P < 0.01; for GPP: F=1018.04, P < 0.01), and air temperature (Ta) explained the highest proportion of the variation in ecosystem respiration (RE) (F=13141.81, P < 0.01). The strong pruning activity in April not only reduced the carbon absorption capacity but also provided many plant residues for respiration, which switched the tea plantation to a carbon source from April to June. Suppression of NEE at higher air temperatures was due to the decrease in GPP more than the decrease in RE, which indicated that future global warming may transform this subtropical tea plantation from a carbon sink to carbon source

    Hypoxia-induced RBBP7 promotes esophagus cancer progression by inducing CDK4 expression

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    Hypoxia-induced epigenetic regulation calls for more effective therapeutic targets for esophageal cancer. We used GEPIA and UALCAN databases to screen survival-related and cancer stage-associated genes. Eca109 and KYSE450 esophageal cancer cell lines were cultured under normoxia, hypoxia, or CoCl2-induced hypoxia conditions, which were further transfected with plasmids expressing RB binding protein 7 (RBBP7), hypoxia-inducible factor 1 (HIF1)-α, or RBBP7 shRNA. Colony formation and MTT assays were used to detect cell proliferation. Tumor sphere formation and stemness marker detection were applied to assess cell stemness. RT-PCR and western blot analysis were used to detect the relative mRNA level and protein expression, respectively. Luciferase assay was utilized to detect the direct interaction between HIF1α and RBBP7. Up-regulated RBBP7 was identified as one of the most prominent survival-related genes, which is negatively correlated with the overall survival (OS), disease recurrence-free survival (DFS), and tumor stages. Hypoxia-induced HIF1α up-regulates RBBP7 expression, which promotes esophagus cancer cell viability, proliferation, and stemness with increased cyclin-dependent kinase 4 (CDK4) expression. Luciferase reporter assay verified that HIF1α transcriptionally regulates the expression of RBBP7. We conclude that hypoxia induces high expression of RBBP7 which is at least partially mediated by HIF1α, up-regulates the expression of downstream CDK4, and thereby promotes tumor progression in esophageal cancer cells
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