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Grain size is a key constituent of grain weight and appearance in rice. However, insufficient attention has been paid to the small-effect quantitative trait loci (QTLs) on the grain size. In the present study, residual heterozygous populations were developed for mapping two genetically linked small-effect QTLs for grain size. After the genotyping and the phenotyping of five successive generations, qGS7.1 was dissected into three QTLs and two were selected for further analysis. The qTGW7.2a was finally mapped into a 21.10 kb interval containing four annotated candidate genes. Transcript levels assay showed that the expression of the candidates LOC_Os07g39490 and the LOC_Os07g39500 were significantly reduced in the NIL-qTGW7.2aBG1. The cytological observation indicated that qTGW7.2a regulated the grain width through controlling the cell expansion. Using the same strategy, qTGW7.2b was fine-mapped into a 52.71 kb interval containing eight annotated candidate genes, showing a significant effect on the grain length and width with opposite allelic directions, but little on the grain weight. Our study provides new genetic resources for yield improvement and for fine-tuning of grain size in rice.

BackgroundGuanXinNing tablet (GXNT), a traditional Chinese patent medicine, has been found to have remarkable antithrombotic effects and can effectively inhibit pro-thrombotic factors in previous studies. However, the mechanism of its antithrombotic effects remains little known.MethodsIn this study, we first determined and identified the sources of each main compound in GXNT using liquid chromatography-mass spectrometry (LC-MS). Through the approach of network pharmacology, we predicted the action targets of the active components, mapped the target genes related to thrombus, and obtained potential antithrombotic targets for active ingredients. We then performed gene ontology (GO) enrichment analyses and KEGG signaling pathway analyses for the action targets, and constructed networks of active component–target and active component–target–pathway for GXNT. Additionally, we evaluated the pharmacodynamic effects of GXNT on thrombus using the rat thrombus model induced by FeCl3, observed the effects of antiplatelet aggregation via platelet assay, and further verified the results predicted by network pharmacology via Western blot.ResultsIn total, 14 active ingredients were identified in GXNT, and 83 action targets were predicted, 17 of which are antithrombotic targets that potentially participate in processes including response to oxidative stress and positive regulation of blood vessel endothelial cell migration. KEGG pathway analyses revealed that the predicted action targets were involved in multiple signal pathways, such as MAPK, IL-17, and platelet activation. Pharmacodynamics study found that GXNT could significantly reduce the thrombus length and weight, lower platelet aggregation function, and decrease the levels of Fbg and PAI-1. In addition, GXNT could significantly increase 6-keto-PGF1α content and regulate the ratio of TXB2/6-keto-PGF1α, while not having dramatic effects on TXB2. GXNT was also observed to visibly inhibit maximum platelet aggregation. Herein, we further studied the thrombus-related MAPKs signaling pathway and found that GXNT could significantly reduce the phosphorylation levels of p38MAPK, ERK, and JNK proteins in platelet.ConclusionsThis study revealed the pharmacodynamic material basis of GXNT and its potential multicomponent–multitarget–multipath pharmacological effects, confirmed the antithrombotic effects of GXNT, and showed that its mechanism may be related to inhibiting phosphorylation of p38, ERK, and JNK proteins in MAPKs signaling pathway, partially verifying the results from network pharmacology. The results from this study could provide a theoretical basis for the development and clinical application of GXNT.

Rough structure microspheres developed using electrospinning show many superior properties, such as increased specific surface area and enhanced wettability, yielding numerous benefits to the applications in adsorption, separation, and others. In this study, biomimetic rough microspheres on string of polymethyl methacrylate nanofiber with hierarchical structure of micron-scale microsphere, and nanoscale Y-shape edges on the microsphere were innovatively and successfully developed by electrospinning. The resulting microsphere exhibited a steering-wheel-like Y shape, and the formation process was physically explained by the geometric potential theory. In the spinning process, irregular hexahedron-like droplet was firstly formed. Then, the hexahedron-like droplet changed to tetrahedron-like after the bottom contacted the collector. The tetrahedron-like droplet evolved into Y-shaped microsphere due to the geometric potential and the collapse of the center part owing to the solvent evaporation. Furthermore, similar to the natural lotus leaf, the hierarchical steering-wheel structure strengthened the nanofiber membrane roughness and endowed the membrane with superhydrophobicity, indicating the potential application in water treatment (oil-water separation, and dye and heavy metal ion adsorption), functional surface materials (self-cleaning fabrics), energy generation and other salient areas. [ABSTRACT FROM AUTHOR]

Herein, polyvinyl alcohol nanofibrous membrane was fabricated firstly by the high-curvature solid-needle electrospinning. The influence of electrode curvature (needle angle), spinning voltage, solution concentration and collector distance on nanofiber morphology was systematically investigated numerically and experimentally. Numerical simulation shows that the electrical field increases with the increase of spinning voltage, while decreases with the increase of needle angle and collector distance. The experimental results are consistent with the numerical results. Furthermore, the solution concentration can be used to adjust the diameter of polyvinyl alcohol nanofibers. The possible applications of the nanofiber membrane to energy generation, water treatment, and separation are also discussed. [ABSTRACT FROM AUTHOR]