The lack of negative association between TE load and subgenome dominance in synthesized Brassica allotetraploids.

Polyploidization is important to the evolution of plants. Subgenome dominance is a distinct phenomenon associated with most allopolyploids. A gene on the dominant subgenome tends to express to higher RNA levels in all organs as compared to the expression of its syntenic paralogue (homoeolog). The mechanism that underlies the formation of subgenome dominance remains unknown, but there is evidence for the involvement of transposon/DNA methylation density differences nearby the genes of parents as being causal. The subgenome with lower density of transposon and methylation near genes is positively associated with subgenome dominance. Here, we generated eight generations of allotetraploid progenies from the merging of parental genomes Brassica rapa and Brassica oleracea. We found that transposon/methylation density differ near genes between the parental (rapa:oleracea) existed in the wide hybrid, persisted in the neotetraploids (the synthetic Brassica napus), but these neotetraploids expressed no expected subgenome dominance. This absence of B. rapa vs. B. oleracea subgenome dominance is particularly significant because, while there is no negative relationship between transposon/methylation level and subgenome dominance in the neotetraploids, the more ancient parental subgenomes for all Brassica did show differences in transposon/methylation densities near genes and did express, in the same samples of cells, biased gene expression diagnostic of subgenome dominance. We conclude that subgenome differences in methylated transposon near genes are not sufficient to initiate the biased gene expressions defining subgenome dominance. Our result was unexpected, and we suggest a "nuclear chimera" model to explain our data.

Health poverty alleviation in China from the perspective of historical institutionalism: policy changes and driving factors.

Health poverty alleviation is an effective tool for improving the living quality and developmental conditions of impoverished populations. Since 1978, China has been actively implementing health poverty alleviation projects, resulting in a more robust rural healthcare service network and increased convenience for the local population to access medical treatment. However, it is crucial to acknowledge that China still faces a complex situation with the simultaneous existence of multiple disease threats and the interweaving of various health influencing factors. Ongoing risks of emerging infectious diseases persist, and some previously controlled or eliminated infectious diseases are at risk of resurgence. The incidence of chronic diseases is on the rise and exhibits a trend toward affecting younger populations. Therefore, examining the successful experiences of China's health poverty alleviation over the past 40 years becomes a critically important issue. The study focuses on China's health poverty alleviation policies, employing historical institutionalism as a theoretical perspective to analyze the historical changes and evolutionary logic of health poverty alleviation policies. A historical institutionalist analytical framework for health poverty alleviation policies is constructed. The research findings reveal that China's health poverty alleviation policy has undergone three distinct periods since 1978: the initial phase (1978-2000), the exploratory phase (2000-2012), and the stable development phase (2013-present). At the macro level, the political, economic, and social contexts of different periods have influenced the evolution of health poverty alleviation policies. On the meso level, coordination effects and adaptive expectations have had an impact on China's health poverty alleviation policy. At the micro level, various actors, including the central government, local governments at different levels, social forces, and impoverished communities, interact during the evolution of health poverty alleviation policies. This paper summarizes the theoretical aspects of China's health poverty alleviation policy experience. The research conclusions, viewed through the lens of historical institutionalism, offer practical insights into the evolution of government policies. This provides directional guidance for enhancing health poverty alleviation projects.

A novel dental infiltration resin based on isosorbide-derived dimethacrylate with high biocompatibility, hydrolysis resistance, and antibacterial effect.

Objectives: The available infiltration resin has raised biosafety and treatment stability concerns because of the cytotoxicity of the main component, TEGDMA, and its susceptibility to hydrolysis in the oral environment. This study aimed to develop a TEGDMA-free infiltration resin to overcome these drawbacks. Methods: Using the synthetic bioderived monomer bis(methacrylate) isosorbide (IBM) and the zwitterionic compound 2-methacryloyloxyethyl phosphorylcholine (MPC), a novel infiltrant IBMA was developed and preferentially selected. We investigated the performance of the IBMA resin regarding cytotoxicity, antibiofilm adhesion, and hydrolysis resistance and further verified its ability to restore the demineralized enamel and stability of the infiltrated area under artificial aging conditions. Results: Compared with the commercial TEGDMA-based infiltration resin ICON, IBMA not only demonstrated similar enamel morphologic and esthetic restorative effects in chalky lesions but also exhibited favorable cell viability, durable Streptococcus mutans UA159 biofilm-repellent performance, and higher enamel microhardness (204.0 ± 5.12 HV) of the infiltrated enamel. Specifically, because of the high crosslink density [(47.77 ± 5.76) ×103 mol/mm3] and low water sorption [12.79 ± 2.56 µg/mm3] of the polymer network, the IBMA resin was more resistant to hydrolysis than ICON, which prevents the disruption of the infiltrant's micropore-blocking effect after aging. Enamel lesions treated with IBMA demonstrated good color stability after the tea-staining challenge, which was significantly better than that in the ICON group. Conclusion: Based on these findings, the IBMA resin exhibits favorable cell viability, hydrolysis resistance, and biofilm-repellent properties, which alleviates the defects of traditional TEGDMA systems. Therefore, it is a better alternative for microinvasive treatment involving early caries and enamel whitish discoloration.

Revisiting the Power Law Characteristics of the Plastic Shock Front under Shock Loading.

Under uniaxial shock compression, the steepness of the plastic shock front usually exhibits power law characteristics with the Hugoniot pressure, also known as the "Swegle-Grady law." In this Letter, we show that the Swegle-Grady law can be described better by a third power law rather than the classical fourth power law at the strain rate between 10^{5}-10^{7} s^{-1}. A simple dislocation-based continuum model is developed, which reproduced the third power law and revealed very good agreement with recent experiments of multiple types of metals quantitatively. New insights into this unusual macroscopic phenomenon are presented through quantifying the connection between the macroscopic mechanical response and the collective dynamics of dislocation assembles. It is found that the Swegle-Grady law results from the particular stress dependence of the plasticity behaviors, and that the difference between the third power scaling and the classical fourth power scaling results from different shock dissipative actions.

Mechanistic study of the formation of fiber-like micelles with a π-conjugated oligo(p-phenylenevinylene) core.

HYPOTHESIS: Crystallization-driven self-assembly (CDSA) of block copolymers (BCPs) with a crystallizable core-forming oligo(p-phenylenevinylene) (OPV) segment can be a powerful strategy for the preparation of uniform fiber-like nanostructures containing a π-conjugated core with controlled dimension and composition. However, the self-assembly landscape can be complex, and our understanding of the nucleation and growth processes in the CDSA of BCPs with a crystalline π-conjugated segment is limited. EXPERIMENTS: We used fluorescence spectroscopy and 1H NMR to follow the self-assembly of oligo(p-phenylenevinylene)-b-poly(N-isopropyl acrylamide) (OPV5-b-PNIPAM49), a typical π-conjugated-coil BCP, as solution of the BCP in ethanol is cooled from 80 °C to 23 °C and allowed to age, µDSC to monitor the crystallization exotherm, and DLS and TEM to follow micelle growth. We see a striking difference in the experiments that monitor unimer in solution comparing to those that monitor micelle growth. We see nearly complete disappearance of unimer within 30 min upon cooling. In contrast, the micelles continue to grow, increasing in length by a factor of ten over the next several hours. We are able to exclude growth by end-to-end coupling. FINDINGS: We propose a self-assembly mechanism in which short semi-crystalline rod-like micelles form upon cooling, accompanied by small amorphous aggregates. Unimers that dissociate from these aggregates subsequently deposit on the growing ends of the core-crystalline micelles. We also find that the length of the PNIPAM block affects the elongation kinetics of OPV5-b-PNIPAM.

Self-Assembled Helical and Twisted Nanostructures of a Preferred Handedness from Achiral π-Conjugated Oligo( p-phenylenevinylene) Derivatives.

The formation of chiral nanostructures from the self-assembly of achiral building blocks without external symmetry breaking inducing factors is believed to associate with the origin of chirality. Herein, we reported the synthesis and self-assembly of oligo( p-phenylenevinylene)- b-poly(ethylene glycol) (OPV3- b-PEG17, the subscripts represent the number of repeat unit of each block) in solution. We systematically examined the influence of solvent, heating temperature, and concentration of OPV3- b-PEG17 on the self-assembly of OPV3- b-PEG17 by UV/vis absorption and fluorescence spectrometry, circular dichroism technique, and transmission electron and atomic force microscopy. Interestingly, helical and twisted nanoribbons and nanotubes of a preferred handedness can be formed from achiral OPV3- b-PEG17 in the mixture of water/ethanol (v/v = 1/1) and the solution showed an obvious exciton-coupled bisignated signal, which indicated that symmetry breaking occurred during the formation of these nanostructures without external inducing factors. Our results showed that the occurrence of symmetry breaking is subtle to the experimental factors including solvent, heating temperature, and concentration of OPV3- b-PEG17. The directional π-π stacking along with steric repulsion between PEG domains should be the driving force for the formation of these chiral nanostructures. The occurrence of statistical fluctuations in the initial stage of self-assembly led to an accidental excess of helical or/and twisted structures, that is, symmetry breaking. Subsequently, the autocatalysis effect resulted in the formation of helical or/and twisted nanoribbons with a preferred handedness.

Size-Tuned Plastic Flow Localization in Irradiated Materials at the Submicron Scale.

Three-dimensional discrete dislocation dynamics (3D-DDD) simulations reveal that, with reduction of sample size in the submicron regime, the mechanism of plastic flow localization in irradiated materials transitions from irradiation-controlled to an intrinsic dislocation source controlled. Furthermore, the spatial correlation of plastic deformation decreases due to weaker dislocation interactions and less frequent cross slip as the system size decreases, thus manifesting itself in thinner dislocation channels. A simple model of discrete dislocation source activation coupled with cross slip channel widening is developed to reproduce and physically explain this transition. In order to quantify the phenomenon of plastic flow localization, we introduce a "deformation localization index," with implications to the design of radiation-resistant materials.

Monodisperse Fiber-like Micelles of Controlled Length and Composition with an Oligo(p-phenylenevinylene) Core via "Living" Crystallization-Driven Self-Assembly.

We report the preparation of a series of fiber-like micelles of narrow length distribution with an oligo(p-phenylenevinylene) (OPV)-core and a poly(N-isopropylacrylamide) (PNIPAM) corona via two different crystallization-driven self-assembly (CDSA) strategies. The average length Ln of these micelles can be varied up to 870 nm by varying the temperature in self-seeding experiments. In addition, seeded growth was employed not only to prepare uniform micelles of controlled length, but also to form fiber-like A-B-A triblock comicelles with an OPV-core.

Controlling Strain Bursts and Avalanches at the Nano- to Micrometer Scale.

We demonstrate, through three-dimensional discrete dislocation dynamics simulations, that the complex dynamical response of nano- and microcrystals to external constraints can be tuned. Under load rate control, strain bursts are shown to exhibit scale-free avalanche statistics, similar to critical phenomena in many physical systems. For the other extreme of displacement rate control, strain burst response transitions to quasiperiodic oscillations, similar to stick-slip earthquakes. External load mode control is shown to enable a qualitative transition in the complex collective dynamics of dislocations from self-organized criticality to quasiperiodic oscillations.

Cyclic deformation leads to defect healing and strengthening of small-volume metal crystals.

When microscopic and macroscopic specimens of metals are subjected to cyclic loading, the creation, interaction, and accumulation of defects lead to damage, cracking, and failure. Here we demonstrate that when aluminum single crystals of submicrometer dimensions are subjected to low-amplitude cyclic deformation at room temperature, the density of preexisting dislocation lines and loops can be dramatically reduced with virtually no change of the overall sample geometry and essentially no permanent plastic strain. This "cyclic healing" of the metal crystal leads to significant strengthening through dramatic reductions in dislocation density, in distinct contrast to conventional cyclic strain hardening mechanisms arising from increases in dislocation density and interactions among defects in microcrystalline and macrocrystalline metals and alloys. Our real-time, in situ transmission electron microscopy observations of tensile tests reveal that pinned dislocation lines undergo shakedown during cyclic straining, with the extent of dislocation unpinning dependent on the amplitude, sequence, and number of strain cycles. Those unpinned mobile dislocations moving close enough to the free surface of the thin specimens as a result of such repeated straining are then further attracted to the surface by image forces that facilitate their egress from the crystal. These results point to a versatile pathway for controlled mechanical annealing and defect engineering in submicrometer-sized metal crystals, thereby obviating the need for thermal annealing or significant plastic deformation that could cause change in shape and/or dimensions of the specimen.

Characterization and antimicrobial activity of a pharmaceutical microemulsion.

The characterization of a pharmaceutical microemulsion system with glycerol monolaurate as oil, ethanol as cosurfactant, Tween 40 as surfactant, sodium diacetate and water, and the antimicrobial activities against Escherichia coli, Staphylococcus aureus, Bacillus subtilis, Candida albicans, Aspergillus niger and Penicillium expansum have been studied. The influence of ethanol and sodium diacetate on oil solubilization capability was clearly reflected in the phase behavior of these systems. One microemulsion formulation was obtained and remained stable by physical stability studies. The antimicrobial assay using solid medium diffusion method showed that the prepared microemulsion was comparable to the commonly used antimicrobials as positive controls. The kinetics of killing experiments demonstrated that the microemulsion caused a complete loss of viability of bacterial cells (E. coli, S. aureus and B. subtilis) in 1 min, killed over 99% A. niger and P. expansum spores and 99.9% C. albicans cells rapidly within 2 min and resulted in a complete loss of fungal viability in 5 min. The fast killing kinetics of the microemulsion was in good agreement with the transmission electron microscopy observations, indicating the antimembrane activity of the microemulsion on bacterial and fungal cells due to the disruption and dysfunction of biological membranes and cell walls.

Antibacterial interactions of monolaurin with commonly used antimicrobials and food components.

Monolaurin is a nontraditional antimicrobial agent that possesses better antimicrobial activities but causes no health problems to consumers, but the use of monolaurin in the food industry as a preservative is still limited. Using a microtiter plate assay, the minimum inhibitory concentrations for monolaurin were 25 microg/mL against Escherichia coli, 12.5 microg/mL against Staphylococcus aureus, and 30 microg/mL against Bacillus subtilis. The interaction with commonly used antimicrobials revealed that monolaurin and nisin acted synergistically against the test microorganisms, monolaurin in combination with sodium dehydroacetate or ethylenediaminetetraacetic acid was synergistic against E. coli and B. subtilis but not S. aureus, and monolaurin combined with calcium propionate or sodium lactate showed no synergistic effects against any test microorganism. The interaction with food components revealed that the antibacterial effectiveness of monolaurin was reduced by fat or starch while the monolaurin activity remained unchanged in the presence of protein. This study contributes to a better understanding on the use of monolaurin as a nontraditional preservative in food products. Results from this study suggest the potential use of monolaurin as a nontraditional preservative in combination with commonly used antimicrobials, such as nisin, sodium dehydroacetate, or ethylenediaminetetraacetic acid, and suggest that the antibacterial effectiveness of monolaurin may be reduced significantly in high-fat or low-starch food products.