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51.
The genome of influenza A viruses (IAV) is split into eight viral RNAs (vRNAs) that are encapsidated as viral ribonucleoproteins. The existence of a segment-specific packaging mechanism is well established, but the molecular basis of this mechanism remains to be deciphered. Selective packaging could be mediated by direct interaction between the vRNA packaging regions, but such interactions have never been demonstrated in virions. Recently, we showed that the eight vRNAs of a human H3N2 IAV form a single interaction network in vitro that involves regions of the vRNAs known to contain packaging signals in the case of H1N1 IAV strains. Here, we show that the eight vRNAs of an avian H5N2 IAV also form a single network of interactions in vitro, but, interestingly, the interactions and the regions of the vRNAs they involve differ from those described for the human H3N2 virus. We identified the vRNA sequences involved in five of these interactions at the nucleotide level, and in two cases, we validated the existence of the interaction using compensatory mutations in the interacting sequences. Electron tomography also revealed significant differences in the interactions taking place between viral ribonucleoproteins in H5N2 and H3N2 virions, despite their canonical ‘7 + 1’ arrangement.  相似文献   
52.
Lipopeptides secreted by bacteria attract interest because of their uses in biomedicine, biotechnology and food technology; however, harnessing their megasynthases (non-ribosomal peptide synthetases, NRPSs) has met with some difficulties in heterologous expression and crystallization. Here, we used similarity and phylogenetic analysis of NRPS sequences, including the fengycin and iturin family synthetases from Bacillus spp., and have developed a novel approach for delineating the length and boundaries of NRPS domains from Bacillus amyloliquefaciens strain Q-426. The sequences were further characterized (including specific residues and conserved motifs) that gave insight into the basis of the substrate specificity. Data from the prediction of the NRPS domains, obtained by the self-optimized prediction method with Alignment program, showed they are all structurally unstable, making it difficult to determine their crystal structures.  相似文献   
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This study aims to investigate the influence of high temperature on cadmium (Cd) toxicity in Aphanius fasciatus (Pisces: Cyprinodontidae). For this reason, Cd, mineral, and organic content in the vertebral column as well as the histological structure of gills and bone were compared in fishes exposed for 30 days to Cd (2 mg/L CdCl2) and/or high temperature (26 °C). Cd exposure caused a negative correlation between Cd and Ca concentrations (r?=?0.98, p?<?0.05), as well as a significant decrease in inorganic components (p?<?0.05) and ash weight/dry weight ratio (p?<?0.05) in the vertebral column. These changes were accompanied by an increased frequency of histological alterations in gills and bone. Concomitant treatment with Cd and high temperature increases Cd accumulation and Ca depletion in the skeletal tissue and increases the frequency and the severity of histological alterations. These results confirm that temperature increases Cd toxicity and needs to be taken into account for the accurate prediction and assessment of Cd-induced spinal deformities in fish.  相似文献   
54.
We previously demonstrated that sphingosine kinase 1 (Sphk1) expression and activity are up-regulated by exogenous palmitate (PAL) in a skeletal muscle model system and in diet-induced obesity in mice; however, potential functions and in vivo relevance of this have not been addressed. Here, we aimed to determine the mechanism by which PAL regulates SphK1 in muscle, and to determine potential roles for its product, sphingosine-1-phosphate (S1P), in muscle biology in the context of obesity. Cloning and analysis of the mouse Sphk1 promoter revealed a peroxisome proliferator-activated receptor (PPAR) α cis-element that mediated activation of a reporter under control of the Sphk1 promoter; direct interaction of PPARα was demonstrated by chromatin immunoprecipitation. PAL treatment induced the proinflammatory cytokine interleukin (IL)-6 in a manner dependent on SphK1, and this was attenuated by inhibition of the sphingosine-1-phosphate receptor 3 (S1PR3). Diet-induced obesity in mice demonstrated that IL-6 expression in muscle, but not adipose tissue, increased in obesity, but this was attenuated in Sphk1−/− mice. Moreover, plasma IL-6 levels were significantly decreased in obese Sphk1−/− mice relative to obese wild type mice, and muscle, but not adipose tissue IL-6 signaling was activated. These data indicate that PPARα regulates Sphk1 expression in the context of fatty acid oversupply and links PAL to muscle IL-6 production. Moreover, this function of SphK1 in diet-induced obesity suggests a potential role for SphK1 in obesity-associated pathological outcomes.  相似文献   
55.
Tissue factor pathway inhibitor-2 (Tfpi-2) is an important serine protease inhibitor in the extracellular matrix (ECM), but its precise physiological significance remains unknown. This work is part of a series of studies intended to investigate functional roles of Tfpi-2 and explore the underlying molecular mechanisms. First, we cloned and identified zebrafish Tfpi-2 (zTfpi-2) as an evolutionarily conserved protein essential for zebrafish development. We also demonstrated that ztfpi-2 is mainly expressed in the central nervous system (CNS) of zebrafish, and embryonic depletion of ztfpi-2 caused severe CNS defects. In addition, changes of neural markers, including pax2a, egr2b, huC, ngn1, gfap and olig2, confirmed the presence of developmental abnormalities in the relevant regions of ztfpi-2 morphants. Using microarray analysis, we found that members of the Notch pathway, especially her4 and mib, which mediate lateral inhibition in CNS development, were also downregulated. Intriguingly, both her4 and mib were able to partially rescue the ztfpi-2 morphant phenotype. Furthermore, Morpholino knockdown of ztfpi-2 resulted in upregulation of neuronal markers while downregulation of glial markers, providing evidence that the Notch pathway is probably involved in ztfpi-2-mediated CNS development.  相似文献   
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【目的】研究水稻土淹水培养过程中Fe-氢酶微生物的多样性,对于揭示Fe-氢酶微生物的群落演替规律和产氢微生物的生化代谢机理具有重要的意义。【方法】采用PCR-变性梯度凝胶电泳和实时定量PCR技术进行基于梭菌属Fe-氢酶基因的多样性和丰度的分析。【结果】水稻土淹水培养过程中Fe-氢酶基因的变性梯度凝胶电泳图谱显示,培养1-5 d时Fe-氢酶基因条带数增加,10 d时Fe-氢酶基因条带数减少,20-40 d时Fe-氢酶基因条带数再次增加并保持稳定,对应的含Fe-氢酶微生物的群落结构随着培养过程的进行发生了显著变化。主成分分析表明,1 d与20 d、5 d与10 d、30 d与40 d的含Fe-氢酶微生物群落结构相似性较高,随着培养时间的增长含Fe-氢酶微生物群落结构趋于稳定。α多样性指数分析显示,1 d和10 d的丰富度指数(R)、Shannon-Weaver指数(H’)、Simpson指数(DS)与其他时间点相比较小,说明这2个时间点的Fe-氢酶多样性低,对应的含Fe-氢酶微生物群落结构较为简单,表明淹水培养过程中微生物的群落结构发生了演替变化。变性梯度凝胶电泳指纹图谱15个Fe-氢酶的优势条带测序后构建的系统发育树表明,培养前期的优势条带与梭菌属的Fe-氢酶关系较近,培养后期出现了非梭菌属的Fe-氢酶。淹水培养过程中Fe-氢酶基因的拷贝数在106/g干土的水平,占细菌的相对比例为1‰–2‰。【结论】水稻土淹水培养过程中发现了4种梭菌属Fe-氢酶和3种非梭菌属Fe-氢酶基因,对应的含Fe-氢酶微生物在培养前期群落结构发生显著演替变化,培养后期趋于稳定。  相似文献   
59.
刘伟  门丽娜  刘新民 《生态学报》2013,33(15):4724-4736
2006年5-9月,诱捕法采集粪金龟子,以农田为对照,选择内蒙古武川县不同农田退耕管理方式为研究样地,分析了农田退耕后采取不同管理方式对粪金龟子群落的影响,以为农田退耕还草管理措施生态效应的评价和完善提供依据.共捕获粪金龟子21671头,隶属于3科5属25种.优势种为直蜉金龟(Aphodius rectus)和蜉金龟属(Aphodius sp.7),占总捕获量的比例分别为59.34%和11.71%.几种退耕管理方式都导致粪金龟子群落物种丰富度、生物量和多度提高,且具有显著的季节特征.Pearson相关分析表明,粪金龟子群落的物种丰富度、生物量和种数以及不同功能群和主要种的个体数与退耕年限、平均草高和植物群落盖度的变化存在显著正相关关系(P<0.01或P<0.05).由于长期农业耕作以及缺少大型食草动物和较大面积放牧草地,研究地区的粪金龟子群落组成以功能群Ⅱ和Ⅲ为主,功能群Ⅰ的多度和物种丰度较低.可以认为,在研究地区以农田景观为主要基质的区域,采取多样化的农田退耕管理方式,提高了生境的空间异质性,在减少人为耕作活动对粪金龟子影响的基础上,对粪金龟子物种丰度和多度的维持起到了促进作用.农田退耕、保留适当面积放牧草地或适当数量大型放牧家畜将有利于功能群Ⅰ物种丰度和多度的提高,有益于粪金龟子群落物种多样性和整体生态功能的维持.  相似文献   
60.
Autophagy is activated to maintain cellular energy homeostasis in response to nutrient starvation. However, autophagy is not persistently activated, which is poorly understood at a mechanistic level. Here, we report that turnover of FoxO1 is involved in the dynamic autophagic process caused by glutamine starvation. X-box-binding protein-1u (XBP-1u) has a critical role in FoxO1 degradation by recruiting FoxO1 to the 20S proteasome. In addition, the phosphorylation of XBP-1u by extracellular regulated protein kinases1/2 (ERK1/2) on Ser61 and Ser176 was found to be critical for the increased interaction between XBP-1u and FoxO1 upon glutamine starvation. Furthermore, knockdown of XBP-1u caused the sustained level of FoxO1 and the persistent activation of autophagy, leading to a significant decrease in cell viability. Finally, the inverse correlation between XBP-1u and FoxO1 expression agrees well with the expression profiles observed in many human cancer tissues. Thus, our findings link the dynamic process of autophagy to XBP-1u-induced FoxO1 degradation.  相似文献   
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