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Soil fungi are important components of belowground biodiversity and play important roles in soil carbon and nutrient cycling. We investigated fungal communities in the top soil (0-10 cm) of 22 Pinus massoniana forests in the Three Gorges Reservoir Region using high-throughput sequencing technique. We found that Ascomycota and Basidiomycota were the dominant fungi phyla, and Eurotiales, Russulales, and Tremellales were the most abundant fungi orders. The dominant functional groups in P. massoniana forests were saprophytic fungi, ectomycorrhizal fungi, and ericoid mycorrhizal fungi. Results of redundancy analysis showed that environmental variables but not spatial variables were the main drivers of soil fungal community structure across the 22 P. massoniana forests, which suggested that habitat filtering rather than dispersal limitation shaped soil fungal community structure. Aboveground biomass, soil conductivity, available phosphorus, soil bulk density, carbon to nitrogen ratio, nitrate concentration, and proportion of slit were the main factors explaining the variation in soil fungal community structure. It should be noted that the key factors influencing different fungal functional groups differed across forests. [ABSTRACT FROM AUTHOR]

Difunctionalizations of alkenes represent one of the most straightforward protocols to build molecular complexity due to the simultaneous construction of two vicinal bonds cross π-bond of alkenes. It is extremely attractive yet challenging to control the stereochemistry outcome of this event. Over the past years, visible-light and Ni-catalyzed asymmetric difunctionalizations of alkenes provide an environmental benign and promising solution for the construction of saturated carbon centers with the control of regio- and enantioselectivity. In this Concept, the initiative and progress of regio- and enantioselective difunctionalizations of alkenes enabled by visible-light and nickel catalysis has been summarized. Moreover, further efforts and directions for the development of visible-light mediated Ni-catalyzed asymmetric difunctionalizations of alkenes has been discussed., (© 2024 Wiley‐VCH GmbH.)

Catalytic methods allowing for the reliable prediction and control of diverse regioselectivity along with the control of enantioselectivity to access different regio- and enantiomers by switching the least reaction parameters are one of the most attractive ways in organic synthesis, which provide access to diverse enantioenriched architectures from identical starting materials. Herein, a Co-catalyzed regiodivergent and enantioselective reductive hydroalkylation of 1,3-dienes with aldehydes has been achieved, furnishing different enantioenriched homoallylic alcohol architectures in good levels of enantioselectivity. The reaction features the switch of regioselectivity tuned by the selection of proton source. The use of an acid as proton source provided asymmetric 1,2-hydroalkylation products under reductive conditions, yet asymmetric 4,3-hydroalkylation products were obtained with silane as hydride source. This catalytic protocol allows for the access of homoallylic alcohols with two continuous saturated carbon centers in good levels of regio-, diastereo-, and enantioselectivity., (© 2024 Wiley-VCH GmbH.)

Functionalizing specific positions on a saturated alkyl molecule is a key challenge in synthetic chemistry. Herein, a ligand-controlled regiodivergent alkylations of alkyl bromides at different positions by Ni-catalyzed alkyl-alkyl cross-electrophile coupling with the second alkyl bromides has been developed. The reaction undergoes site-selective isomerization on one alkyl bromides in a controlled manner, providing switchable access to diverse alkylated structures at different sites of alkyl bromides. The reaction occurs at three similar positions with excellent chemo- and regioselectivity, representing a remarkable ligand tuned reactivity between alkyl-alkyl cross-coupling and nickel migration along the hydrocarbon side chain. This reaction offers a catalytic platform to diverse saturated architectures by alkyl-alkyl bond-formation from identical starting materials., (© 2022 Wiley-VCH GmbH.)

Soil fungi are important components of belowground biodiversity and play important roles in soil carbon and nutrient cycling. We investigated fungal communities in the top soil (0-10 cm) of 22 Pinus massoniana forests in the Three Gorges Reservoir Region using high-throughput sequencing technique. We found that Ascomycota and Basidiomycota were the dominant fungi phyla, and Eurotiales, Russulales, and Tremellales were the most abundant fungi orders. The dominant functional groups in P. massoniana forests were saprophytic fungi, ectomycorrhizal fungi, and ericoid mycorrhizal fungi. Results of redundancy analysis showed that environmental variables but not spatial variables were the main drivers of soil fungal community structure across the 22 P. massoniana forests, which suggested that habitat filtering rather than dispersal limitation shaped soil fungal community structure. Aboveground biomass, soil conductivity, available phosphorus, soil bulk density, carbon to nitrogen ratio, nitrate concentration, and proportion of slit were the main factors explaining the variation in soil fungal community structure. It should be noted that the key factors influencing different fungal functional groups differed across forests.

Objective: To investigate whether the genetic polymorphism, upstream variable number of tandem repeats (uVNTR), in the monoamine oxidase A (MAOA) gene, is associated with major depressive disorder (MDD) in adolescents and to test whether there is gene-environment interaction between MAOA-uVNTR polymorphism and stressful life events (SLEs)., Methods: A total of 394 Chinese Han subjects, including 187 adolescent patients with MDD and 207 normal students as a control group, were included in the study. Genotyping was performed by SNaP-shot assay. SLEs in the previous 12 months were evaluated. The groups were compared in terms of the frequency distributions of MAOA-uVNTR genotypes and alleles using statistical software. The binary logistic regression model of gene-environment interaction was established to analyze the association of the gene-environment interaction between MAOA-u VNTR genotypes and SLEs with adolescent MDD., Results: The distribution profiles of MAOA-u VNTR genotypes and alleles were not related to the onset of MDD, severity of depression, comorbid anxiety and suicidal ideation/behavior/attempt in adolescents. The gene-environment interaction between MAOA-u VNTR genotypes and SLEs was not associated with MDD in male or female adolescents., Conclusions: It is not proven that MAOA-u VNTR polymorphism is associated with adolescent MDD. There is also no gene-environment interaction between MAOA-u VNTR polymorphism and SLEs that is associated with adolescent MDD.

Resveratrol functions as an agonist for estrogen receptor (ER)-mediated transcription. However, other researchers have reported that resveratrol decreases proliferation of breast cancer cells that are either ER-positive or ER-negative, which suggests that the interaction of resveratrol with the ER may not fully explain its inhibitory effect on proliferation. Similar to those effects associated with caloric restriction (CR), resveratrol has multiple beneficial activities, such as increased life span and delay in the onset of diseases associated with aging. One key enzyme thought to be activated during CR is the AMP-activated kinase (AMPK), a sensor of cellular energy levels. The suppression of nonessential energy expenditure by activated AMPK along with the CR mimetic and antiproliferative properties of resveratrol has led us to hypothesize that resveratrol activity might have an important role in the activation of AMPK. Here, we show that resveratrol activated AMPK in both ER-positive and ER-negative breast cancer cells. Once activated, AMPK inhibited 4E-BP1 signaling and mRNA translation via mammalian target of rapamycin (mTOR). Moreover, we also found that AMPK activity mediated by resveratrol in cancer cells was due to inducing the expression of Sirtuin type 1 (SIRT1) via elevation in the cellular NAD(+)/NADH in ER-positive cells. To our knowledge, we demonstrate here for the first time that resveratrol induces the expression of SIRT1 protein in human cancer cells. These observations raise the possibility that SIRT1 functions as a novel upstream regulator for AMPK signaling and may additionally modulate tumor cell proliferation. Targeting SIRT1/AMPK signaling by resveratrol may have potential therapeutic implications for cancer and age-related diseases.