ABSTRACT Objective: As the most prevalent type of thyroid malignancy, papillary thyroid carcinoma (PTC) accounts for over 80% of all thyroid cancers. Circular RNAs (circRNAs) have been found to regulate multiple cancers, including PTC. Materials and methods: Quantitative real-time polymerase chain reaction (qRT-PCR) and western blotting were used to analyse RNA and protein levels. Fluorescence in situ hybridization (FISH) was used to detect the distribution of the target genes. Functional experiments and animal experiments were implemented to analyse the biological functions of target genes in vitro and in vivo. Luciferase reporter, RNA pulldown, RNA binding protein immunoprecipitation (RIP) and mRNA stability assays were used to probe the underlying mechanisms. Results: CircSEMA6Awas found to be upregulated in PTC tissues and cells, and its circular structure was verified. CircSEMA6A promotes PTC cell migration and invasion. Moreover, circSEMA6A functions as a competing endogenous RNA (ceRNA) to upregulate proline rich and Gla domain 4 (PRRG4) expression by sponging microRNA-520h (miR-520h). CircSEMA6A recruits ELAV1 to stabilize PRRG4 mRNA and drives PTC progression via PRRG4. Conclusion: CircSEMA6A upregulates PRRG4 by targeting miR-520h and recruiting ELAVL1 to affect the invasion and migration of PTC cells, offering insight into the molecular mechanisms of PTC. Objective malignancy (PTC 80 cancers circRNAs (circRNAs methods realtime real time qRTPCR qRT PCR (qRT-PCR levels FISH (FISH vivo reporter pulldown RIP (RIP Results CircSEMAAwas CircSEMA Awas cells verified CircSEMAA A Moreover circSEMAA circSEMA ceRNA (ceRNA PRRG (PRRG4 microRNA520h microRNAh microRNA 520h h miR520h. miR520h miRh miR . (miR-520h) ELAV Conclusion ELAVL 8 (PRRG (miR-520h

Abstract Background Transferring herbicide resistance genes to plant cultivars is one of the most effective methods for managing weed growth in agricultural land. The RePAT gene, previously isolated from the marine bacterium Rhodococcus sp . strain YM12, was found to provide glufosinate resistance to plants. Objective In this study, we further investigated the protein structure and function of RePAT isolated from the marine. Methods The physicochemical properties, two-dimensional structure, three-dimensional structure, and functional domains of the RePAT protein were analyzed and predicted using bioinformatics tools, and RePAT was optimized according to codon bias present in Arabidopsis thaliana . Site-directed mutagenesis of RePAT was performed, and the wild-type ( RePAT ) and mutant ( RePAT V120I ) genes were successfully transferred into A. thaliana . Results Our results showed that RePAT was an unstable hydrophilic protein, and six phosphorylation sites and two N-glycosylation sites were predicted. In addition, conserved domains containing the NAT_SF super family and coenzyme A-binding pocket were predicted in RePAT. Transgenic experiments and glufosinate resistance assays showed that the glufosinate resistance of A. thaliana containing the mutant gene ( RePAT V120I ) was lower than that of plants containing the wild-type gene, indicating that the missense mutation in RePAT V120I had a significant effect on its glufosinate resistance. Conclusions Our study provided improvement result for knowing the transferring herbicide resistance gene RePAT .

ABSTRACT To seek a simple, rapid and sensitive Coprinus cinereus Peroxidase (CIP) activity assay, a convenient one-factor-at-a-time (OFAT) method and a response surface methodology (RSM) were used. The recombinant CIP expressed in Pichia pastoris was purified with the Ni-NTA spin column. Based on the results of catalytic efficiency (kcat/Km) analysis, 2,2'-azinobis (ethylbenzthiazoline -6-sulfonate) (ABTS) was selected as the optimal enzyme substrate. Results of the OFAT method showed that enzymatic reaction performed in 0.1 mol/L sodium acetate (pH 5.0) buffer in a 200-µl reaction mixture containing 0.5 mmol/L ABTS, 10 mmol/L hydrogen peroxide (H2O2), 49.7 ng CIP at 25°C gave an average CIP activity of 88 U/mL. The ABTS and H2O2 concentrations were then further optimized to improve the sensitivity of the assay. To do that, RSM was conducted through central composite design, and a reduced quadratic model with good fit regression equation was generated. ANOVA analysis of this model indicated that the concentrations of ABTS and H2O2 and their interaction had significant impact on the assay sensitivity. The optimal reaction mixture was determined to include an initial ABTS concentration of 0.82 mmol/L 49.7 ng CIP and 16.36 mmol/L H2O2, and the activity under this condition was determined to be 138.89 U/mL.

Three new biphenyls were isolated from Garcinia multiflora. The structures of these biphenyls were elucidated by spectroscopic methods, and their rotavirus activity was evaluated.

New butyrolactones aspernolides C and D, along with two known butyrolactones (A and B) were isolated from the culture of the endophytic fungus Aspergillus versicolor. Their structures were elucidated on the basis of extensive spectroscopic analysis, including 1D and 2D nuclear magnetic ressonance techniques, and electronic circular dichroism. The butyrolactones aspernolides C and D were tested for their anti-tobacco mosaic virus activity. The results showed that butyrolactones aspernolides C and D exhibited moderate anti-tobacco mosaic virus activity with IC50 values of 64.2 and 88.6 μM, respectively.