Full-genome RNAi profiling of early embryogenesis in Caenorhabditis elegans

A key challenge of functional genomics today is to generate well-annotated data sets that can be interpreted across different platforms and technologies. Large-scale functional genomics data often fail to connect to standard experimental approaches of gene characterization in individual laboratories. Furthermore, a lack of universal annotation standards for phenotypic data sets makes it difficult to compare different screening approaches. Here we address this problem in a screen designed to identify all genes required for the first two rounds of cell division in the Caenorhabditis elegans embryo. We used RNA-mediated interference to target 98% of all genes predicted in the C. elegans genome in combination with differential interference contrast time-lapse microscopy. Through systematic annotation of the resulting movies, we developed a phenotypic profiling system, which shows high correlation with cellular processes and biochemical pathways, thus enabling us to predict new functions for previously uncharacterized genes.     

A cooperative microRNA-tumor suppressor gene network in acute T-cell lymphoblastic leukemia (T-ALL)

The importance of individual microRNAs (miRNAs) has been established in specific cancers. However, a comprehensive analysis of the contribution of miRNAs to the pathogenesis of any specific cancer is lacking. Here we show that in T-cell acute lymphoblastic leukemia (T-ALL), a small set of miRNAs is responsible for the cooperative suppression of several tumor suppressor genes. Cross-comparison of miRNA expression profiles in human T-ALL with the results of an unbiased miRNA library screen allowed us to identify five miRNAs (miR-19b, miR-20a, miR-26a, miR-92 and miR-223) that are capable of promoting T-ALL development in a mouse model and which account for the majority of miRNA expression in human T-ALL. Moreover, these miRNAs produce overlapping and cooperative effects on tumor suppressor genes implicated in the pathogenesis of T-ALL, including IKAROS (also known as IKZF1), PTEN, BIM, PHF6, NF1 and FBXW7. Thus, a comprehensive and unbiased analysis of miRNA action in T-ALL reveals a striking pattern of miRNA-tumor suppressor gene interactions in this cancer.     

Seed germination characteristics of Chrysothamnus nauseosus ssp. viridulus (Astereae, Asteraceae)

Rubber rabbitbrush ( Chrysothamnus nauseosus [Pallas] Britt. ssp. viridulus ) may prove to be a source of high-quality cis-isoprene rubber, but its establishment is limited by a lack of information on seed germination. Consequently, seeds were germinated at alternating temperatures (5–15, 5–25, 15–25, and 20–30 C) in light and dark as well as constant temperatures (15–40 C with 5-C increments) to determine temperature response. Seeds were also germinated in solutions of polyethylene glycol 6000 (0 to –5 bar), salinity regimes (1, 17, 51, and 86 mM) at all the above-mentioned temperatures to determine salinity and temperature interaction. The hormones GA 3 (0, 2.9, 29.0, and 58.0 um) and kinetin (0, 4.7, 23.5, and 47.0 um) were used to study their effect on overcoming salt- and temperature-induced germination inhibition. Seeds of C. nauseosus ssp. viridulus were very sensitive to low temperature. Best germination was achieved at 25 and 30 C, but these seeds also germinated at a higher temperature (35 C). The seeds of rabbitbrush germinated at both constant and alternating temperatures. Light appears to play little or no role in controlling germination of the seeds of rubber rabbitbrush. However, seeds of rabbitbrush were sensitive to salinity, and seed germination was progressively inhibited by increase in salt concentration, although a few seeds still germinated at the highest saline level. Progressively higher concentrations of polyethylene glycol also progressively inhibited germination. Suppression of seed germination induced by high salt concentrations and high temperatures can be partially alleviated by the application of either GA 3 or kinetin.     

Mn0.8Zn0.2Fe2O4 nanoparticulates spinel ferrites:An approach to enhance the antenna field strength for improved magnitude versus offset（MVO）

Electromagnetic signals in deep reservoir are very weak so that it is difficult to predict about the presence of hydrocarbon in seabed logging(SBL) environment.In the present work,Mn0.8Zn0.2Fe2O4 nanoferrites were prepared by a sol–gel technique at different sintering temperatures of450 °C,650 °C and 850 °C to increase the strength of electromagnetic(EM) antenna.XRD,FESEM,Raman spectroscopy and HRTEM were used to analyze the phase,surface morphology and size of the nanoferrites.Magnetic properties of the nanoferrites were also measured using an impedance network analyzer.However,nanoferrites sintered at 850 °C with initial permeability of 200 and Q factor of 50 were used as magnetic feeders with the EM antenna.Lab scale experiments were performed to investigate the effect of magnetic field strength in scale tank.SPSS and MATLAB softwares were also used to confirm the oil presence in scale tank.It was observed that the magnitude of the EM waves for the antenna was increased up to 233%.Finally,the correlation values also show 208% increase in the magnetic field strength with the presence of the oil.Therefore,antenna with Mn0.8Zn0.2Fe2O4 nanoferrites based magnetic feeders can be used for deep water and deep target hydrocarbon exploration.     

车辆悬架系统的自适应模糊控制(英文)

悬架是用来支持车身的系统,通过隔离道路干扰使得乘客感觉舒适、并确保车辆稳定.为此研究了全车模型悬架系统在下列几种控制方式下的性能:被动控制、半主动控制、自适应标准可加性模型(SAM)下的主动控制.全车模型可以为车辆悬架系统提供一些必要的性能参数,如车身偏移、车轮偏移和悬架偏斜.乘坐的舒适性和车辆的操控性决定了所需悬架系统的性能.乘坐的舒适性取决于车身偏移和乘客座位的偏移,而车辆的稳定由其他自由度(如俯仰和滚转)决定.半主动和主动悬架控制的设计通过MATLAB/SIMULINK加以实现,充分考虑了不规则的路面,并以此验证半主动控制和SAM主动控制的性能.实验结果表明,SAM主动控制能够改善乘坐的舒适性和车辆的操控性.     

Two types of muscarinic acetylcholine receptors in Drosophila and other arthropods

Muscarinic acetylcholine receptors (mAChRs) play a central role in the mammalian nervous system. These receptors are G protein-coupled receptors (GPCRs), which are activated by the agonists acetylcholine and muscarine, and blocked by a variety of antagonists. Mammals have five mAChRs (m1–m5). In this study, we cloned two structurally related GPCRs from the fruit fly Drosophila melanogaster, which, after expression in Chinese hamster ovary cells, proved to be muscarinic acetylcholine receptors. One mAChR (the A-type; encoded by gene CG4356) is activated by acetylcholine (EC₅₀, 5 × 10^?8 M) and muscarine (EC₅₀, 6 × 10^?8 M) and blocked by the classical mAChR antagonists atropine, scopolamine, and 3-quinuclidinyl-benzilate (QNB), while the other (the B-type; encoded by gene CG7918) is also activated by acetylcholine, but has a 1,000-fold lower sensitivity to muscarine, and is not blocked by the antagonists. A- and B-type mAChRs were also cloned and functionally characterized from the red flour beetle Tribolium castaneum. Recently, Haga et al. (Nature 2012, 482: 547–551) published the crystal structure of the human m2 mAChR, revealing 14 amino acid residues forming the binding pocket for QNB. These residues are identical between the human m2 and the D. melanogaster and T. castaneum A-type mAChRs, while many of them are different between the human m2 and the B-type receptors. Using bioinformatics, one orthologue of the A-type and one of the B-type mAChRs could also be found in all other arthropods with a sequenced genome. Protostomes, such as arthropods, and deuterostomes, such as mammals and other vertebrates, belong to two evolutionarily distinct lineages of animal evolution that split about 700 million years ago. We found that animals that originated before this split, such as cnidarians (Hydra), had two A-type mAChRs. From these data we propose a model for the evolution of mAChRs.     

藏东地区发现罕见的恐龙足迹群和古大象足迹群

西藏昌都市卡若区发现罕见的蜥脚类、兽脚类、鸟脚类频密共生的恐龙足迹化石群,产于中侏罗世达布卡组滨湖相沉积中;昌都市江达县雪集拉山发现古近纪大象足迹化石群,产于贡觉组湖相、三角洲相地层中.这两个化石群是青藏高原中新生代地质演化的重要历史见证,对研究青藏高原隆升和恐龙、古大象的迁徙、演化、古生态有着极其重要的意义.     

硫酸中香蕉皮还原低品位锰矿的浸出行为及动力学模型

Manganese was leached from a low-grade manganese ore (LGMO) using banana peel as the reductant in a dilute sulfuric acid medium. The effects of banana peel amount, H₂SO₄ concentration, reaction temperature, and time on Mn leaching from the complex LGMO were studied. A leaching efficiency of ~98% was achieved at a leaching time of 2 h, banana peel amount of 4 g, leaching temperature of 120°C, manganese ore amount of 5 g, and sulfuric acid concentration of 15vol%. The phase, microstructural, and chemical analyses of LGMO samples before and after the leaching process confirmed the successful leaching of manganese. Furthermore, the leaching process followed the shrinking core model and the leaching rate was controlled by a surface chemical reaction (1 ? (1 ? x)1/3 = kt) mechanism with an apparent activation energy of 40.19 kJ·mol?1.