2,037 research outputs found
Bounds for eigenvalue ratios of the Laplacian
For a bounded domain with a piecewise smooth boundary in an
-dimensional Euclidean space , we study eigenvalues of the
Dirichlet eigenvalue problem of the Laplacian. First we give a general
inequality for eigenvalues of the Laplacian. As an application, we study lower
order eigenvalues of the Laplacian and derive the ratios of lower order
eigenvalues of the Laplacian.Comment: 14 page
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Comparative genomics suggests that an ancestral polyploidy event leads to enhanced root nodule symbiosis in the Papilionoideae
Root nodule symbiosis (RNS) is one of the most efficient biological systems for nitrogen fixation
and it occurs in 90% of genera in the Papilionoideae, the largest subfamily of legumes. Most
papilionoid species show evidence of a polyploidy event occurred approximately 58 million years
ago. Although polyploidy is considered to be an important evolutionary force in plants, the role of
this papilionoid polyploidy event, especially its association with RNS, is not understood. In this
study, we explored this role using an integrated comparative genomic approach and conducted
gene expression comparisons and gene ontology enrichment analyses. The results show the
following: (1) approximately a quarter of the papilionoid-polyploidy-derived duplicate genes are
retained; (2) there is a striking divergence in the level of expression of gene duplicate pairs derived
from the polyploidy event; and (3) the retained duplicates are frequently involved in the processes
crucial for RNS establishment, such as symbiotic signalling, nodule organogenesis, rhizobial
infection and nutrient exchange and transport. Thus, we conclude that the papilionoid polyploidy
event might have further refined RNS and induced a more robust and enhanced symbiotic system.
This conclusion partly explains the widespread occurrence of the Papilionoideae
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Reassessment of the evolution of wheat chromosomes 4A, 5A, and 7B.
Key messageComparison of genome sequences of wild emmer wheat and Aegilops tauschii suggests a novel scenario of the evolution of rearranged wheat chromosomes 4A, 5A, and 7B. Past research suggested that wheat chromosome 4A was subjected to a reciprocal translocation T(4AL;5AL)1 that occurred in the diploid progenitor of the wheat A subgenome and to three major rearrangements that occurred in polyploid wheat: pericentric inversion Inv(4AS;4AL)1, paracentric inversion Inv(4AL;4AL)1, and reciprocal translocation T(4AL;7BS)1. Gene collinearity along the pseudomolecules of tetraploid wild emmer wheat (Triticum turgidum ssp. dicoccoides, subgenomes AABB) and diploid Aegilops tauschii (genomes DD) was employed to confirm these rearrangements and to analyze the breakpoints. The exchange of distal regions of chromosome arms 4AS and 4AL due to pericentric inversion Inv(4AS;4AL)1 was detected, and breakpoints were validated with an optical Bionano genome map. Both breakpoints contained satellite DNA. The breakpoints of reciprocal translocation T(4AL;7BS)1 were also found. However, the breakpoints that generated paracentric inversion Inv(4AL;4AL)1 appeared to be collocated with the 4AL breakpoints that had produced Inv(4AS;4AL)1 and T(4AL;7BS)1. Inv(4AS;4AL)1, Inv(4AL;4AL)1, and T(4AL;7BS)1 either originated sequentially, and Inv(4AL;4AL)1 was produced by recurrent chromosome breaks at the same breakpoints that generated Inv(4AS;4AL)1 and T(4AL;7BS)1, or Inv(4AS;4AL)1, Inv(4AL;4AL)1, and T(4AL;7BS)1 originated simultaneously. We prefer the latter hypothesis since it makes fewer assumptions about the sequence of events that produced these chromosome rearrangements
Chansu inhibits the expression of cortactin in colon cancer cell lines in vitro and in vivo
Background: Chansu is a transitional Chinese medicine that has been used for centuries as therapy for inflammation, anaesthesia and arrhythmia in China and other Asian countries. Recently, it has also been used for anti-cancer purposes. We have previously shown that Chansu has a huge pro-apoptotic potential on colon cancer cells, but to date the detailed mechanism of this action is not well understood. Methods: One of the major components of Chansu, Cinobufagin (CBF) was used to treat cancer cells. The expressions of levels of cortactin, an important factor in tumour progression and cancer invasion, were assessed in in vitro and in vivo experiments. Additional analyses were performed in subcellular protein fractions and immune-fluorescent staining was used to define cortactin protein expression and the changes of location in CBF-treated cells. Results: CBF strongly inhibited the expression of cortactin in HCT116 cells. There were reductions of both mRNA transcription and protein synthesis, which were more significant in the absence of oxygen in vitro. In addition, nuclear translocation of cortactin was observed in HCT116 cells post CBF exposure but not in the negative control, indicating that CBF is likely to interrupt co-localisation of cortactin to cytoskeletal proteins. Most importantly, CBF could diminish the expression of cortactin in human HCT116 xenograft tumours in nude mouse in vivo. Conclusions: CBF inhibits cortactin expression and nuclear translocation in colon cancer cells in vitro and in mouse models bearing human colon tumour in vivo, suggesting it might disrupt actin-regulated cell movement. Thus, CBF or Chansu could be developed as an effective anti-cancer therapy to stop local invasion and metastasis
A hybrid brain-computer interface combining the EEG and NIRS
Compared to the conventional brain-computer interface (BCI) system, the hybrid BCI provides a more efficient way for the communication between the brain and the external device. The Electroencephalography (EEG) signal and the change of oxygenation in the brain are two prevailing approaches used in the BCI. However, single physiological signal couldn't provide enough information for a satisfied BCI. This paper proposes a hybrid BCI system based on the combination of the EEG signal and the cerebral blood oxygen changes measured by the near-infrared spectroscopy system (NIRS) to detect the state of motor imagery (MI). The result shows that the average recognition rate can achieve above 75.04% and the highest rate 91.11%, which are higher than when only using EEG or NIRS. It suggests that the proposed hybrid BCI system has a good performance in the combination of these two different signals. Further investigation may help develop better BCIs with high accuracy and significant efficiency. © 2012 IEEE.published_or_final_versio
Analysis of the value of information used in inventory control of an inventory-production system
This paper studies the value of information in an inventory-production system consisting of a warehouse and a workshop. The focal point is the use of information about the production status of the workshop in inventory control in the warehouse. Systems with various information levels are analyzed to determine what information is most valuable. Examples are presented to demonstrate how to identify the most important information about production status
A high-throughput FRET-based assay for determination of Atg4 activity
Atg4 is required for cleaving Atg8, allowing it to be conjugated to phosphatidylethanolamine on phagophore membranes, a key step in autophagosome biogenesis. Deconjugation of Atg8 from autophagosomal membranes could be also a regulatory step in controlling autophagy. Therefore, the activity of Atg4 is important for autophagy and could be a target for therapeutic intervention. In this study, a sensitive and specific method to measure the activity of two Atg4 homologs in mammalian cells, Atg4A and Atg4B, was developed using a fluorescence resonance energy transfer (FRET)-based approach. Thus LC3B and GATE-16, two substrates that could be differentially cleaved by Atg4A and Atg4B, were fused with CFP and YFP at the N- and C-terminus, respectively, allowing FRET to occur. The FRET signals decreased in proportion to the Atg4-mediated cleavage, which separated the two fluorescent proteins. This method is highly efficient for measuring the enzymatic activity and kinetics of Atg4A and Atg4B under in vitro conditions. Applications of the assay indicated that the activity of Atg4B was dependent on its catalytic cysteine and expression level, but showed little changes under several common autophagy conditions. In addition, the assays displayed excellent performance in high throughput format and are suitable for screening and analysis of potential modulators. In summary, the FRET-based assay is simple and easy to use, is sensitive and specific, and is suitable for both routine measurement of Atg4 activity and high-throughput screening
Exploring the active mechanism of berberine against HCC by systematic pharmacology and experimental validation
This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.Berberine (BBR) is the main component of Coptidis rhizoma, the dried rhizome of Coptis chinensis and is a potential plant alkaloid used for the treatment of cancer due to its high antitumor activity. The present study examined the therapeutic potential and molecular mechanism of action of BBR against HCC, using systematic pharmacology combined with a molecular docking approach and experimental validation in vitro. Through systematic pharmacological analysis, it was found that BBR serves a significant role in inhibiting HCC by affecting multiple pathways, especially the PI3K/AKT signaling pathway. Furthermore, the docking approach indicated that the binding of BBR to AKT could lead to the suppression of AKT activity. The present study examined the inhibitory effect of BBR on the PI3K/AKT pathway in HCC and identified that BBR downregulated the expressions of phosphorylated AKT and PI3K in MHCC97‑H and HepG2 cells, inhibiting their growth, cell migration and invasion in a dose‑dependent manner. In addition, inhibition of the AKT pathway by BBR also contributed to cell apoptosis in MHCC97‑H and HepG2 cells. Taken together, the results of the present study suggested that BBR may be a promising antitumor drug for HCC that acts by inhibiting the PI3K/AKT pathway
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