Ras-dependent apoptosis correlates with persistent activation of stress-activated protein kinases and induction of isoform(s) of Bcl-x

Ras proteins are signal transducers for many cellular responses. However, it is not well established whether Ras-signaling also contributes to apoptosis. We have constructed H-RasR12-transformed Rat1 fibroblasts using tetracycline operator/repressor (TetO/TetR)-based conditional vectors. Rat1/TetO-RasR12 (Rat1-Ras) cells produced high levels of H-RasR12 protein and exhibited oncogenic transformation. Treatment of Rat1-Ras cells with 0.1% serum triggered massive apoptosis. Rat1-Ras cells expressed increased basal activities of extracellular response kinase (ERK) and p46/p54 stress-activated protein kinase/c-Jun NH2-terminal kinase (SAPK/JNK). Interestingly, Ras-dependent apoptosis correlated with further persistent activation of both p46 and p54 SAPK/JNK and concurrent inhibition of ERK. Differential modulation of SAPK/JNK and ERK was not detected in tetracycline-treated cells that did not commit apoptosis. Furthermore, two Bcl-x related proteins of 15 kDa and 18 kDa were highly induced in apoptotic Rat1-Ras cells. Our results establish a direct role for Ras in apoptosis, and suggest a functional relationship between H-Ras, SAPK/JNK, ERK and Bcl-x in regulating apoptosis.     

蚂蚁筑巢对不同恢复阶段热带森林土壤易氧化有机碳时空动态的影响

为探明热带森林恢复过程中蚂蚁筑巢对土壤易氧化有机碳(readily oxidizable carbon, ROC)时空动态的影响及机制, 本研究以西双版纳白背桐(Mallotus paniculatus)群落、野芭蕉(Musa acuminata)群落和崖豆藤(Mellettia leptobotrya)群落3种恢复阶段热带森林为研究对象, 设置“蚂蚁筑巢地”与“非巢地”2种处理进行野外控制实验, 对比分析蚁巢和非蚁巢土壤ROC含量的时空变化特征, 并揭示这些变化与土壤微生物生物量碳及理化性质之间的相互关系。结果表明: (1)蚂蚁筑巢显著影响热带森林土壤ROC含量(P < 0.05), 蚁巢土壤ROC含量较非蚁巢提高了14.2%。不同恢复阶段蚁巢与非蚁巢土壤ROC含量大小顺序为: 野芭蕉群落 > 崖豆藤群落 > 白背桐群落。(2)不同恢复阶段热带森林蚁巢与非蚁巢土壤ROC含量均呈单峰型的时间变化趋势(P < 0.05), 最大值出现在6月, 且各月份蚁巢土壤ROC含量均高于非蚁巢。(3)不同恢复阶段热带森林蚁巢和非蚁巢土壤ROC含量均随土层深度增加呈显著递减的垂直变化趋势(P < 0.05), 且蚁巢土壤ROC含量均大于非蚁巢(P < 0.05)。(4)蚂蚁筑巢引起的土壤理化性质变化对土壤ROC含量产生了一定的影响。土壤ROC含量与土壤pH和容重呈显著负相关(P < 0.05), 与土壤有机碳、微生物生物量碳、全氮、铵态氮及硝态氮呈显著正相关(P < 0.05)。土壤微生物生物量碳与总有机碳是蚁巢土壤ROC时空变化的主要贡献者, 而铵态氮、全氮和总有机碳是非蚁巢ROC时空变化的主控因子。因此, 蚂蚁筑巢改变热带森林土壤微生物量(如微生物生物量碳)及土壤理化性质(如总有机碳、铵态氮与全氮等), 进而显著影响土壤ROC的时空动态。     

南海北部生态系统食物网结构、能量流动及系统特征

根据20072008年在南海北部(107°00'120°00'E、17°00'23°30'N)进行的海洋生态综合调查数据,应用Ecopath with Ecosim软件构建了南海北部生态系统的生态通道模型,并通过模型分析了南海北部海洋生态系统的食物网结构、能量流动和系统的总体特征,并简要总结过度捕捞生态系统的基本特征。结果表明,南海北部海洋生态系统以捕食食物链为主要能流通道,初级生产者是系统能量的主要来源。各功能群的营养级范围为13.99,哺乳动物占据了最高的营养层,平均渔获物营养级为2.93。利用生态网络分析,系统的能量流动主要有6级,来自初级生产者的能流效率为12.6%,来自碎屑的转换效率为10.4%,平均能量转换效率为11.5%。系统连接指数(Connectance Index,CI)和系统杂食指数(System Omnivory Index,SOI)分别为0.290和0.239;Finn’s循环指数(Finn’scy cling index,FCI)和系统平均路径长度(Finn’s mean path length,MPL)分别为4.380和2.476;总初级生产力/总呼吸为2.596,综合研究表明当前南海北部海洋生态系统处于不成熟阶段。     

Suppression of Grb2 expression improved hepatic steatosis, oxidative stress, and apoptosis induced by palmitic acid in vitro partly through insulin signaling alteration

In this study, we aimed to study the role of growth factor receptor-bound protein 2 (Grb2) in palmitic acid-induced steatosis and other “fatty liver” symptoms in vitro. HepG2 cells, with or without stably suppressed Grb2 expression, were incubated with palmitic acid for 24 h to induce typical clinical “fatty liver” features, including steatosis, impaired glucose metabolism, oxidative stress, and apoptosis. MTT and Oil Red O assays were applied to test cell viability and fat deposition, respectively. Glucose uptake assay was used to evaluate the glucose utilization of cells. Quantitative polymerase chain reaction and Western blot were used to measure expressional changes of key markers of insulin signaling, lipid/glucose metabolism, oxidative stress, and apoptosis. After 24-h palmitic acid induction, increased fat accumulation, reduced glucose uptake, impaired insulin signaling, enhanced oxidative stress, and increased apoptosis were observed in HepG2 cells. Suppression of Grb2 in HepG2 significantly reduced fat accumulation, improved glucose metabolism, ameliorated oxidative stress, and restored the activity of insulin receptor substrate-1/Akt and MEK/ERK pathways. In addition, Grb2 deficiency attenuated hepatic apoptosis shown by reduced activation of caspase-3 and fluorescent staining. Modulation of Bcl-2 and Bak1 also contributed to reduced apoptosis. In conclusion, suppression of Grb2 expression in HepG2 cells improved hepatic steatosis, glucose metabolism, oxidative stress, and apoptosis induced by palmitic acid incubation partly though modulating the insulin signaling pathway.     

TNF-alpha-induced cyclooxygenase-2 expression in human lung epithelial cells: involvement of the phospholipase C-gamma 2, protein kinase C-alpha, tyrosine kinase, NF-kappa B-inducing kinase, and I-kappa B kinase 1/2 pathway

TNF-alpha induced a dose- and time-dependent increase in cyclooxygenase-2 (COX-2) expression and PGE2 formation in human NCI-H292 epithelial cells. Immunofluorescence staining demonstrated that COX-2 was expressed in cytosol and nuclear envelope. Tyrosine kinase inhibitors (genistein or herbimycin) or phosphoinositide-specific phospholipase C inhibitor (U73122) blocked TNF-alpha-induced COX-2 expression. TNF-alpha also stimulated phosphatidylinositol hydrolysis and protein kinase C (PKC) activity, and both were abolished by genistein or U73122. The PKC inhibitor, staurosporine, also inhibited TNF-alpha-induced response. The 12-O-tetradecanoylphorbol 13-acetate (TPA), a PKC activator, also stimulated COX-2 expression, this effect being inhibited by genistein or herbimycin. NF-kappaB DNA-protein binding and COX-2 promoter activity were enhanced by TNF-alpha, and these effects were inhibited by genistein, U73122, staurosporine, or pyrolidine dithiocarbamate. TPA stimulated both NF-kappaB DNA-protein binding and COX-2 promoter activity, these effects being inhibited by genistein, herbimycin, or pyrolidine dithiocarbamate. The TNF-alpha-induced, but not the TPA-induced, COX-2 promoter activity was inhibited by phospholipase C-gamma2 mutants, and the COX-2 promoter activity induced by either agent was attenuated by dominant-negative mutants of PKC-alpha, NF-kappaB-inducing kinase, or I-kappaB (inhibitory protein that dissociates from NF-kappaB) kinase (IKK)1 or 2. IKK activity was stimulated by both TNF-alpha and TPA, and these effects were inhibited by staurosporine or herbimycin. These results suggest that, in NCI-H292 epithelial cells, TNF-alpha might activate phospholipase C-gamma2 via an upstream tyrosine kinase to induce activation of PKC-alpha and protein tyrosine kinase, resulting in the activation of NF-kappaB-inducing kinase and IKK1/2, and NF-kappaB in the COX-2 promoter, then initiation of COX-2 expression and PGE2 release.     

The primase active site is on the outside of the hexameric bacteriophage T7 gene 4 helicase-primase ring

Gene 4 of bacteriophage T7 encodes a protein (gp4) that can translocate along single-stranded DNA, couple the unwinding of duplex DNA with the hydrolysis of dTTP, and catalyze the synthesis of short RNA oligoribonucleotides for use as primers by T7 DNA polymerase. Electron microscopic studies have shown that gp4 forms hexameric rings, and X-ray crystal structures of the gp4 helicase domain and of the highly homologous RNA polymerase domain of Escherichia coli DnaG have been determined. Earlier biochemical studies have shown that when single-stranded DNA is bound to the hexameric ring, the primase domain remains accessible to free DNA. Given these results, a model was suggested in which the primase active site in the gp4 hexamer is located on the outside of the hexameric ring. We have used electron microscopy and single-particle image analysis to examine T7 gp4, and have determined that the primase active site is located on the outside of the hexameric ring, and therefore provide direct structural support for this model.     

Non-equilibrium allele frequency spectra via spectral methods

A major challenge in the analysis of population genomics data consists of isolating signatures of natural selection from background noise caused by random drift and gene flow. Analyses of massive amounts of data from many related populations require high-performance algorithms to determine the likelihood of different demographic scenarios that could have shaped the observed neutral single nucleotide polymorphism (SNP) allele frequency spectrum. In many areas of applied mathematics, Fourier Transforms and Spectral Methods are firmly established tools to analyze spectra of signals and model their dynamics as solutions of certain Partial Differential Equations (PDEs). When spectral methods are applicable, they have excellent error properties and are the fastest possible in high dimension; see Press et al. (2007). In this paper we present an explicit numerical solution, using spectral methods, to the forward Kolmogorov equations for a Wright–Fisher process with migration of K populations, influx of mutations, and multiple population splitting events.