Fragile X Mental Retardation Protein Regulates Proliferation and Differentiation of Adult Neural Stem/Progenitor Cells

Fragile X syndrome (FXS), the most common form of inherited mental retardation, is caused by the loss of functional fragile X mental retardation protein (FMRP). FMRP is an RNA–binding protein that can regulate the translation of specific mRNAs. Adult neurogenesis, a process considered important for neuroplasticity and memory, is regulated at multiple molecular levels. In this study, we investigated whether Fmrp deficiency affects adult neurogenesis. We show that in a mouse model of fragile X syndrome, adult neurogenesis is indeed altered. The loss of Fmrp increases the proliferation and alters the fate specification of adult neural progenitor/stem cells (aNPCs). We demonstrate that Fmrp regulates the protein expression of several components critical for aNPC function, including CDK4 and GSK3β. Dysregulation of GSK3β led to reduced Wnt signaling pathway activity, which altered the expression of neurogenin1 and the fate specification of aNPCs. These data unveil a novel regulatory role for Fmrp and translational regulation in adult neurogenesis

The Helmholtz equation on Lipschitz domains

We use the method of layer potentials to study interior and exterior Dirichlet and Neumann problems for the Helmholtz equation ( + k2)u = 0 on a Lipschitz domain for all wave number k 2C with Imk 0. Following the approach for the case of smooth boundary [3], we pursue as solution a single layer potential for Neumann problem or a double layer potential for Dirichlet problem. The lack of smoothness of a Lipschitz boundary brought some additional di culties. These are overcome through the use of harmonic analysis techniques together with a careful study of the properties of layer potentials near the boundary and the spectra of the traces of the layer potentials

Recent Advances in Rapid Synthesis of Non-proteinogenic Amino Acids from Proteinogenic Amino Acids Derivatives via Direct Photo-Mediated C–H Functionalization

Non-proteinogenic amino acids have attracted tremendous interest for their essential applications in the realm of biology and chemistry. Recently, rising C–H functionalization has been considered an alternative powerful method for the direct synthesis of non-proteinogenic amino acids. Meanwhile, photochemistry has become popular for its predominant advantages of mild conditions and conservation of energy. Therefore, C–H functionalization and photochemistry have been merged to synthesize diverse non-proteinogenic amino acids in a mild and environmentally friendly way. In this review, the recent developments in the photo-mediated C–H functionalization of proteinogenic amino acids derivatives for the rapid synthesis of versatile non-proteinogenic amino acids are presented. Moreover, postulated mechanisms are also described wherever needed

Data from: Optimization and kinetic study of methyl laurate synthesis using ionic liquid [Hnmp]HSO4 as a catalyst

Methyl laurate was synthesized from lauric acid (LA) and methanol via an esterification reaction using ionic liquids (ILs) as catalysts. The efficiencies of three different catalysts, 1-methylimidazole hydrogen sulfate ([Hmim]HSO4), 1-methyl-2-pyrrolidonium hydrogen sulfate ([Hnmp]HSO4) and H2SO4, were compared. The effect of the methanol/LA molar ratio, reaction temperature, reaction time and catalyst dosage on the esterification rate of LA was investigated by single-factor experiments. Based on the single-factor experiments, the esterification of LA and methanol was optimized using response surface methodology. The results showed that the most effective catalyst was the IL [Hnmp]HSO4. The optimal conditions were as follows: [Hnmp]HSO4 dosage of 5.23%, methanol/LA molar ratio of 7.68 : 1, reaction time of 2.27 h and reaction temperature of 70°C. Under these conditions, the LA conversion of the esterification reached 98.58%. A kinetic study indicated that the esterification was a second-order reaction with an activation energy and a frequency factor of 68.45 kJ mol−1 and 1.9189 × 109 min−1, respectively. The catalytic activity of [Hnmp]HSO4 remained high after five cycles

Interactive Effects of Drought–Flood Abrupt Alternation on Morpho-Agronomic and Nutrient Use Traits in Rice

The frequent occurrence of drought–flood abrupt alternation (DFAA) in Huaibei Plain has shown a great impact on local rice production. Pot experiments were performed in 2016–2018 to investigate the effects of co-occurring drought and flooding stresses on dry weight (DW), grain yield, nitrogen (N), phosphorus (P) and potassium (K) uptake and use efficiencies (NUE, PUE and KUE) in rice. The results showed that DFAA changed the accumulation of biomass and nutrients among different organs in rice. Compared with control, DFAA significantly reduced the grain yield (−29.8%) and root DW (−30.0%), but increased the DW in stem and leaf (10.2% and 9.7%). The root/shoot ratio and morphological size of the root system in DFAA-treated plants was smaller than those of drought alone and flooding alone. Under DFAA stresses, the specific absorption rate of N, P and K increased significantly (47.9%, 31.8% and 32.8%, respectively), while NUE, PUE and KUE decreased significantly (−27.9%, −10.8% and −19.7%, respectively). The decrease of nutrient use efficiencies was mainly due to the redundant growth of branches and leaves, and the key factor limiting grain yield under DFAA conditions was the effective utilization of N. Compared with the earlier drought, the subsequent flooding might have more influence on rice growth, nutrient utilization and yield formation, but the interaction of the two weakened the cumulative effect of drought and flooding. These findings provide a scientific basis for establishing a nutrient and water management system of rice cultivation under transient soil moisture conditions

The Arabidopsis Gene zinc finger protein 3(ZFP3) Is Involved in Salt Stress and Osmotic Stress Response.

Plants are continuously challenged by various abiotic and biotic stresses. To tide over these adversities, plants evolved intricate regulatory networks to adapt these unfavorable environments. So far, many researchers have clarified the molecular and genetic pathways involved in regulation of stress responses. However, the mechanism through which these regulatory networks operate is largely unknown. In this study, we cloned a C2H2-type zinc finger protein gene ZFP3 from Arabidopsis thaliana and investigated its function in salt and osmotic stress response. Our results showed that the expression level of ZFP3 was highly suppressed by NaCl, mannitol and sucrose. Constitutive expression of ZFP3 enhanced tolerance of plants to salt and osmotic stress while the zfp3 mutant plants displays reduced tolerance in Arabidopsis. Gain- and Loss-of-function studies of ZFP3 showed that ZFP3 significantly changes proline accumulation and chlorophyll content. Furthermore, over-expression of ZFP3 induced the expressions of stress-related gene KIN1, RD22, RD29B and AtP5CS1. These results suggest that ZFP3 is involved in salt and osmotic stress response