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Vicinal oxygen chelate (VOC) proteins are members of an enzyme superfamily with dioxygenase or non‐dioxygenase activities. However, the biological functions of VOC proteins in plants are poorly understood. Here, we show that a VOC in Nicotiana benthamiana (NbVOC1) facilitates viral infection. NbVOC1 was significantly induced by infection by beet necrotic yellow vein virus (BNYVV). Transient overexpression of NbVOC1 or its homolog from Beta vulgaris (BvVOC1) enhanced BNYVV infection in N. benthamiana, which required the nuclear localization of VOC1. Consistent with this result, overexpressing NbVOC1 facilitated BNYVV infection, whereas, knockdown and knockout of NbVOC1 inhibited BNYVV infection in transgenic N. benthamiana plants. NbVOC1 interacts with the basic leucine zipper transcription factors bZIP17/28, which enhances their self‐interaction and DNA binding to the promoters of unfolded protein response (UPR)‐related genes. We propose that bZIP17/28 directly binds to the NbVOC1 promoter and induces its transcription, forming a positive feedback loop to induce the UPR and facilitating BNYVV infection. Collectively, our results demonstrate that NbVOC1 positively regulates the UPR that enhances viral infection in plants. [ABSTRACT FROM AUTHOR]

Electrochemical water splitting offers an advancing approach to producing highly pure hydrogen and oxygen, motivated by the prevalence of a low‐carbon economy and the goal of a sustainable future. The customized modulation of electronic structures enables the electrocatalyst to directionally promote hydrogen evolution reaction (HER) and oxygen evolution reaction (OER), which is a promising shortcut to overall water splitting (OWS). Herein, 3D homologous WSeS/CoSeS heterojunction nanoarrays (WSeS/CoSeS NAs) and W‐doped CoSeS nanoarrays (W‐CoSeS NAs) are investigated. Abundant heterointerfaces within WSeS/CoSeS NAs facilitate HER kinetics, boosting mass diffusivity, and increasing carrier separation and transfer process. High‐valence W6+ doping into CoSeS prevents phase separation and stabilizes Co sites by charge offset effect, leading to enhanced OER. Consequently, the WSeS/CoSeS NAs and W‐CoSeS NAs reach 10 mA cm−2 at an overpotential of 43.8 and 233.3 mV in 1.0 m KOH electrolyte for HER and OER, respectively. Moreover, when asymmetrically engaged as an electrolyzer, this configuration exhibits extraordinary electrocatalytic performances (cell voltage of 1.51 V at 10 mA cm−2) with satisfying stability and mechanical robustness (over 1000 h at 1000 mA cm−2). The modulation and manufacture of reaction‐property‐oriented materials are experimentally and theoretically validated potential, illuminating the light of inspiration for multiple applications. [ABSTRACT FROM AUTHOR]

A non‐precious metal‐based catalyst for water electrolysis provides great promise for cost‐effective and highly efficient sustainable hydrogen production. It herein rationally synthesizes uniform superminiature CoNi nanoparticles (2.6 nm) embedded in 3D N‐doped randomly oriented and erected porous carbon nanosheets (CoNi@N‐PCNS). Taking advantage of the large specific surface area, expedited intermediate transport, and effectively exposed active sites of the hierarchical architecture, located CoNi nanoparticles yield a high atom utilization efficiency. Density functional theory calculations indicate that synergetic and cooperative interactions inside CoNi alloy modulate the d‐band center, leading to a moderate adsorption and desorption energy of reaction intermediates, further accelerating both hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) kinetics. Accordingly, the as‐synthesized CoNi@N‐PCNS catalyst establishes superb catalytic activities for HER and OER, revealing overpotentials of 71.2 and 263.8 mV at 10 mA cm−2, respectively. Remarkably, when assembled as a two‐electrode electrolyzer, a satisfying cell voltage of 1.59 V at 10 mA cm−2, and superior stability are demonstrated, highlighting great promise toward water electrolysis. [ABSTRACT FROM AUTHOR]

Liquid nitrogen (LN2) fracturing is a potential stimulation method in unconventional hydrocarbon recovery, showing its merits in being water free, creating low formation damage and being environmentally friendly. The microstructure evolution of rocks subjected to LN2 cooling is a fundamental concern for the engineering application of LN2 fracturing. In this paper, pore-scale imaging and characterization were performed on two rocks, i.e., tight sandstone and coal specimens subjected to LN2 cooling using computed tomography scanning. The digital core technique was employed to reconstruct the microstructures of rocks and give a quantitative analysis of the pore structure evolution of both dry and water-saturated rocks. The results indicate that LN2 cooling has a great effect on the pores' morphology and their spatial distribution, leading to a great improvement in pore diameter and aspect ratio. When compared to the sandstone, coal is more sensitive to LN2 cooling and thermal stresses, having a more noticeable growth in pore–throat size. The porosity growth of coal is 291% higher than that of sandstone. There is a growing trend in the irregularity and complexity of pore structures. After LN2 cooling, the fractal dimensions of the pores of sandstone and coal grow by 11.7% and 0.87%, respectively, and the proportion of pores with a shape factor > 100 increases. More bundle-like and strip-shape pores with multiple branches are generated, which causes a significant growth in the throat size and the proportion of connected pores with a coordination number ≥ 1, enhancing the complexity and connectivity of pore structures dramatically. Additionally, pore water plays an important role in aggravating rock damage during LN2 cooling, enhancing the pore space and connectivity. The porosities of the saturated sandstone and coal samples grow by 22.6% and 490.4%, respectively, after LN2 cooling, which are 5.6% and 186.6% higher than dry samples. The generation of macropores ≥ 70 μm is the primary contributor to porosity growth during LN2 cooling, although such pores account for only a small proportion of the total. These findings contribute to our understanding of the microscopic mechanism of LN2 cooling on rock damage and may provide some guidance for the engineering application of LN2 fracturing. [ABSTRACT FROM AUTHOR]

Anthracnose of poplar caused by Colletotrichum gloeosporioides is a leaf disease that seriously affects poplar growth. The pathogen invades the host in the form of adherent cells, which generate turgor pressure through the metabolism of intracellular substances prior to penetrating the epidermis of poplar leaves. In this study, the expansion-related pressure of the mature appressorium of the wild-type C. gloeosporioides was approximately 13.02 ± 1.54 MPa at 12 h, whereas it was 7.34 ± 1.23 MPa and 9.34 ± 2.22 MPa in the melanin synthesis-related gene knockout mutants ΔCgCmr1 and ΔCgPks1, respectively. The CgCmr1 and CgPks1 genes were highly expressed at 12 h in the wild-type control, implying that the DHN melanin biosynthesis pathway may play an important role in the mature appressorium stage. The transcriptome sequencing analysis indicated that the upregulated melanin biosynthesis genes in C. gloeosporioides, such as CgScd1, CgAyg1, CgThr1, CgThr2, and CgLac1, are involved in specific KEGG pathways (i.e., fatty acid biosynthesis, fatty acid metabolism, and biotin metabolism). Therefore, we speculate that the melanin synthesis-related genes and fatty acid metabolism pathway genes contribute to the regulation of the turgor pressure in the mature C. gloeosporioides appressorium, ultimately leading to the formation of infection pegs that enter plant tissues. These observations may reflect the co-evolution of C. gloeosporioides and its host. [ABSTRACT FROM AUTHOR]

Parkinson's disease (PD) is characterized by dopaminergic neurodegeneration and an abnormal accumulation of α-synuclein aggregates. A number of genetic factors have been shown to increase the risk of PD. Exploring the underlying molecular mechanisms that mediate PD's transcriptomic diversity can help us understand neurodegenerative pathogenesis. In this study, we identified 9897 A-to-I RNA editing events associated with 6286 genes across 372 PD patients. Of them, 72 RNA editing events altered miRNA binding sites and this may directly affect miRNA regulations of their host genes. However, RNA editing effects on the miRNA regulation of genes are more complex. They can (1) abolish existing miRNA binding sites, which allows miRNAs to regulate other genes; (2) create new miRNA binding sites that may sequester miRNAs from regulating other genes; or (3) occur in the miRNA seed regions and change their targets. The first two processes are also referred to as miRNA competitive binding. In our study, we found 8 RNA editing events that may alter the expression of 1146 other genes via miRNA competition. We also found one RNA editing event that modified a miRNA seed region, which was predicted to disturb the regulation of four genes. Considering the PD-related functions of the affected genes, 25 A-to-I RNA editing biomarkers for PD are proposed, including the 3 editing events in the EIF2AK2, APOL6, and miR-4477b seed regions. These biomarkers may alter the miRNA regulation of 133 PD-related genes. All these analyses reveal the potential mechanisms and regulations of RNA editing in PD pathogenesis. [ABSTRACT FROM AUTHOR]

Purpose: Immunotherapy for gastrointestinal stromal tumors (GISTs) remains a clinical challenge. The present study aimed to explore the clinical and prognostic significance of immune cell infiltration and PD-L1 expression in GISTs. Methods: A total of 507 clinical tissue specimens of primary GISTs were collected for immunohistochemical analysis of immune cell infiltration and PD-L1 expression. Influencing factors of survival were evaluated by Kaplan–Meier analysis. Univariate and multivariate analyses were performed using the Cox regression model. Results: There were significant differences in sex, tumor location, size, mitotic index, NIH risk grade, and cell morphology between different gene mutation types of GISTs. Immune cell infiltration in GISTs mainly involved macrophages and T cells. PD-1 was expressed in 48.5% of the tissue specimens, and PD-L1 expression was detected in 46.0% of the samples. PD-L1 expression was negatively correlated with the tumor size and mitotic index but positively correlated with the number of CD8+ T cells. There were significant differences in the number of CD8+ T cells between different gene mutation types. Wild type-mutant GISTs were enriched with CD8+ T cells as compared with KIT- and PDGFRA-mutant GISTs. The number of CD8+ T cells was higher in non-gastric GISTs. PD-L1 and CD8+ T cells were independent predictors for better relapse-free survival of GISTs. Conclusions: PD-L1 expression is a predictive biomarker for better prognosis of GISTs. Non-gastric GIST patients with wild-type mutations may be the beneficiaries of PD-1/PD-L1 inhibitors. [ABSTRACT FROM AUTHOR]