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The electrochemically activated persulfate (PDS) system was constructed with boron-doped diamond (BDD) anode and Ti cathode to study the transformation of bromide in the presence of humic acid (HA). The mechanism of the electroactive system and the generation path of brominated by-products were analyzed through scanning cyclic voltammetry and free radical quenching experiments. The effects of initial PDS dosage, current density, and initial pH on the formation of brominated by-products in the electroactive PDS system were investigated. The results show that bromate and brominated organic by-products (Br-DBPs) were detected in the system when HA concentration in the reaction solution was 3.0 mg/L (in TOC), bromine ion concentration was 1.0 mg/L, PDS concentration was 5.0 mmol/L, current density was 20 mA/cm2, and pH was 7.0 in the reaction solution, and the highest concentration was 4.11 and 1.02 μmol/L, respectively, within 120 min. The transformation of bromine was mainly caused by the complex radical oxidants (OH· and SO4·-) produced in the system. With the increase of PDS dosage and activation current density, the production of active substances in the solution was increased within a certain range, and the oxidizability of the electrical activation system was improved. Thus, the reaction process of Br-DBPs generation and synchronous mineralization was accelerated. The optimmum pH range for controlling the total production of brominated byproducts was acidic; however, Br-DBPs (especially bromoacetic acid) also showed a higher generation trend in acidic reaction environment. Therefore, in actual use, the operating conditions should be reasonably determined by considering the factors such as degradation efficiency, operating cost, and health risks of produced water.

Tea plants that have a large leaf area mainly suffer from heavy metal accumulation in the above-ground parts through foliar uptake. With the world rapid industrialization, this pollution in tea is considered a crucial challenge due to its potential health risks. The present study proposes an innovative approach based on visible and near-infrared (Vis-NIR) spectroscopy coupled with chemometrics for the characterization of tea chemical indicators under airborne lead stress, which can be performed fast and in situ. The effects of lead stress on chemical indicators and accumulation in leaves of the two tea varieties at different time intervals and levels of treatment were investigated. In addition, changes in cell structure and leaf stomata were monitored during foliar uptake of aerosol particles by transmission electron microscopy (TEM) and scanning electron microscopy (SEM). The spectral variation was able to classify the tea samples into the Pb treatment groups through the linear discriminant analysis (LDA) model. Two machine learning techniques, namely, partial least squares (PLS) and radial basis function neural network (RBFNN), were evaluated and compared for building the quantitative determination models. The RBFNN models combined with correlation-based feature selection (CFS) and PLS data compression methods were used to optimize the prediction performance. The results demonstrated that the PLS–RBFNN as a non-linear model outperformed the PLS model and provided the R-value of 0.944, 0.952, 0.881, 0.937, and 0.930 for prediction of MDA, starch, sucrose, fructose, glucose, respectively. It can be concluded that the proposed approach has strong application potential in monitoring the quality and safety of plants under airborne heavy metal stress.

Metabolic engineering of cyanobacteria has received much attention as a sustainable strategy to convert CO2 to various longer carbon chain fuels. Pinene has become increasingly attractive since pinene dimers contain high volumetric energy and have been proposed to act as potential aircraft fuels. However, cyanobacteria cannot directly convert geranyl pyrophosphate into pinene due to the lack of endogenous pinene synthase. Herein, we integrated the gene encoding Abies grandis pinene synthase into the model cyanobacterium Synechococcus sp. PCC 7002 through homologous recombination. The genetically modified cyanobacteria achieved a pinene titer of 1.525 ± 0.l45 mg L−1 in the lab-scale tube photobioreactor with CO2 aeration. Specifically, the results showed a mixture of α- and β-pinene (∼33:67 ratio). The ratio of β-pinene in the product was significantly increased compared with that previously reported in the engineered Escherichia coli. Furthermore, we investigated the photoautotrophic growth performances of Synechococcus overlaid with different concentrations of dodecane. The work demonstrates that the engineered Synechococcus is a suitable potential platform for β-pinene production.

Long non-coding RNAs (lncRNAs) regulate gene expression in a variety of ways at epigenetic, chromatin remodeling, transcriptional, and translational levels. Accumulating evidence suggests that lncRNA X-inactive specific transcript (lncRNA Xist) serves as an important regulator of cell growth and development. Despites its original roles in X-chromosome dosage compensation, lncRNA Xist also participates in the development of tumor and other human diseases by functioning as a competing endogenous RNA (ceRNA). In this review, we comprehensively summarized recent progress in understanding the cellular functions of lncRNA Xist in mammalian cells and discussed current knowledge regarding the ceRNA network of lncRNA Xist in various diseases. Long non-coding RNAs (lncRNAs) are transcripts that are more than 200 nt in length and without an apparent protein-coding capacity (Furlan and Rougeulle, 2016; Maduro et al., 2016). These RNAs are believed to be transcribed by the approximately 98–99% non-coding regions of the human genome (Derrien et al., 2012; Fu, 2014; Montalbano et al., 2017; Slack and Chinnaiyan, 2019), as well as a large variety of genomic regions, such as exonic, tronic, and intergenic regions. Hence, lncRNAs are also divided into eight categories: Intergenic lncRNAs, Intronic lncRNAs, Enhancer lncRNAs, Promoter lncRNAs, Natural antisense/sense lncRNAs, Small nucleolar RNA-ended lncRNAs (sno-lncRNAs), Bidirectional lncRNAs, and non-poly(A) lncRNAs (Ma et al., 2013; Devaux et al., 2015; St Laurent et al., 2015; Chen, 2016; Quinn and Chang, 2016; Richard and Eichhorn, 2018; Connerty et al., 2020). A range of evidence has suggested that lncRNAs function as key regulators in crucial cellular functions, including proliferation, differentiation, apoptosis, migration, and invasion, by regulating the expression level of target genes via epigenomic, transcriptional, or post-transcriptional approaches (Cao et al., 2018). Moreover, lncRNAs detected in body fluids were also believed to serve as potential biomarkers for the diagnosis, prognosis, and monitoring of disease progression, and act as novel and potential drug targets for therapeutic exploitation in human disease (Jiang W. et al., 2018; Zhou et al., 2019a). Long non-coding RNA X-inactive specific transcript (lncRNA Xist) are a set of 15,000–20,000 nt sequences localized in the X chromosome inactivation center (XIC) of chromosome Xq13.2 (Brown et al., 1992; Debrand et al., 1998; Kay, 1998; Lee et al., 2013; da Rocha and Heard, 2017; Yang Z. et al., 2018; Brockdorff, 2019). Previous studies have indicated that lncRNA Xist regulate X chromosome inactivation (XCI), resulting in the inheritable silencing of one of the X-chromosomes during female cell development. Also, it serves a vital regulatory function in the whole spectrum of human disease (notably cancer) and can be used as a novel diagnostic and prognostic biomarker and as a potential therapeutic target for human disease in the clinic (Liu et al., 2018b; Deng et al., 2019; Dinescu et al., 2019; Mutzel and Schulz, 2020; Patrat et al., 2020; Wang et al., 2020a). In particular, lncRNA Xist have been demonstrated to be involved in the development of multiple types of tumors including brain tumor, Leukemia, lung cancer, breast cancer, and liver cancer, with the prominent examples outlined in Table 1. It was also believed that lncRNA Xist (Chaligne and Heard, 2014; Yang Z. et al., 2018) contributed to other diseases, such as pulmonary fibrosis, inflammation, neuropathic pain, cardiomyocyte hypertrophy, and osteoarthritis chondrocytes, and more specific details can be found in Table 2. This review summarizes the current knowledge on the regulatory mechanisms of lncRNA Xist on both chromosome dosage compensation and pathogenesis (especially cancer) processes, with a focus on the regulatory network of lncRNA Xist in human disease.

A novel graphene oxide (GO)-based carrier was fabricated for the controlled release of Benazepril (BENA). Freeze dried samples of GO–BENA carrier were prepared for controlled drug release at different pHs (pH = 2, 7, and 10) and release kinetics indicate BENA desorption from GO is by Fickian diffusion. The BENA yield from the carrier amounted to ~55% of the adsorbed material in a strongly acidic medium after 50 h. Binding fractions of BENA to 10 mg/L GO was determined for different solution concentrations of the drug. In vitro assays of cell proliferation (WST-1 kit), cell structural integrity (LDH kit) and flow cytometric indicators of necrosis in three different cell lines (CACO-2, SGC-7901, and primary mouse hepatic fibroblast) all demonstrated that the GO carrier had a good biocompatibility. The pH-dependent release sensitivity of the GO-based carrier suggests that it is a potential candidate for use in the controlled release of drugs in the acidic environment of the stomach.

Neural stem cells (NSCs) have the ability to differentiate into neurons, astrocytes and oligodendrocytes. They are self-renewing and sufficient to provide large amounts of brain tissue cells. NSCs have promising application prospects for the treatment of central nervous system diseases. Spider toxins are important tools for use in neurobiology and neuropharmacology. In this study, a Cell Counting Kit (CCK-8), immunofluorescence staining, real-time quantitative polymerase chain reaction (RT-qPCR) and Western blotting were used to qualitatively and quantitatively analyse the effects of different concentrations (1, 10 and 20 μg/mL) of Chilobrachys jingzhao crude venom on the proliferation and differentiation of C17.2 cells in vitro. At low concentrations, C. jingzhao crude venom did not significantly inhibit the proliferation of NSCs; however, the highest concentration of 20 μg/mL partially inhibited the NSC proliferation. In the differentiation medium, addition of C. jingzhao crude venom effectively promoted the differentiation of NSCs towards neuronal cells, with a final concentration of 10 μg/mL having the most obvious effect. These results suggest that C. jingzhao crude venom exerts a regulatory effect on the proliferation and differentiation of C17.2 cells. Therefore, spider venom can be used as an ‘ammunition library’ to find factors that regulate the proliferation and differentiation of NSCs, laying the groundwork for the application of NSCs in the treatment of central nervous system diseases.

Beijing is severely affected by land subsidence, and rapid urbanisation and building construction might accelerate the land subsidence process. Based on 39 Envisat Advanced Synthetic Aperture Radar (ASAR) images acquired between 2003–2010, 55 TerraSAR-X images acquired between 2010–2016, and urban building information, we analysed the relationship between land subsidence and buildings at the regional, block, and building scales. The results show that the surface displacement rate in the Beijing urban area ranged from −109 mm/year to +13 mm/year between 2003–2010, and from −151 mm/year to +19 mm/year between 2010–2016; two subsidence bowls were mainly distributed in the eastern part of the Chaoyang District. The displacement rate agreed well with the levelling measurements, with an average bias of less than six mm/year. At the regional scale, the spatial pattern of land subsidence was mainly controlled by groundwater extraction, compressible layer thickness, and geological faults. Subsidence centres were located in the area around ground water funnels with a compressible layer depth of 50–70 m. The block-scale analysis demonstrated a clear correlation between the block construction age and the spatial unevenness of subsidence. The blocks constructed between 1998–2005 and after 2005 showed considerably more subsidence unevenness and temporal instability than the blocks constructed before 1998 during both time periods. The examination of the new blocks showed that the spatial unevenness increased with building volume variability. For the 16 blocks with a high building volume, variability, and subsidence unevenness, the building-scale analysis showed a positive relationship between building volume and settlement in most blocks, although the R2 was lower than 0.5. The results indicate that intense building construction in urban areas could cause differential settlement at the block scale in Beijing, while the settlement of single buildings could be influenced by the integrated effects of building volume, foundation structures, and the hydrogeological background.

Background: Let-7 miRNAs are reported to play an inhibitory role in carcinogenesis, tumor progression, recurrence, and pluripotency of cancer. However, few studies have reported the relationship between let-7 and drug sensitivity, especially for let-7a (a subtype of let-7). This study aimed to investigate the function of let-7a in regulating the sensitivity of hepatocellular carcinoma (HCC) cell lines to cetuximab. Methods: The cytotoxicity of cetuximab on HCC cell lines (Huh7, Hep3B, HepG2, SNU449, and SNU387) was evaluated using a cell viability assay (the Cell Counting Kit-8 assay) and a cell proliferation assay (the Click-iT EdU Imaging Kit) in the presence of a control, a let-7a mimic, and a let-7a inhibitor. Small interfering RNA to knockdown the expression of signal transducer and activator of transcription 3 (STAT3) were employed. Protein and mRNA expression levels were determined using quantitative polymerase chain reaction and Western blot analysis. Results: It was found that let-7a enhances the sensitivity of HCC cells with an epithelial phenotype (Huh7, Hep3B, and HepG2) to cetuximab, but has no effect on cells with the mesenchymal phenotype (SNU449 and SNU387). It was determined that STAT3 was a target mRNA of let-7a using TargetScan. Expression of STAT3 and let-7a mRNA were negatively correlated in HCC cell lines. Moreover, let-7a altered the protein and mRNA expression of STAT3. Furthermore, STAT3 knockdown enhanced the function of cetuximab on HCC cell lines with epithelial phenotypes, but not on HCC cell lines with mesenchymal phenotypes. Finally, a rescue experiment confirmed that let-7a affected the sensitivity of HCC cell lines to cetuximab by interacting with STAT3. Conclusions: There is a functional link between let-7a and STAT3 in enhancing the sensitivity of HCC cells with an epithelial phenotype to cetuximab. Our results provide novel insight into new methodologies for combating HCC drug resistance. [ABSTRACT FROM AUTHOR]

Presents a study which investigated the role of bozozok (boz) gene in establishing dorsoventral polarity of zebrafish at the molecular level. Materials and methods used; Role of boz during zebrafish organizer formation; Regulation of bmp2b gene expression by boz; Effect of boz on bmp2b regulatory region; Model for the role of boz during initiation of the organizer.