TSG101 promotes the proliferation,migration and invasion of hepatocellular carcinoma cells by regulating the PEG10

The tumour susceptibility gene 101 (TSG101) is reported to play important roles in the development and progression of several human cancers. However, its potential roles and underlined mechanisms in human hepatocellular carcinoma (HCC) are still needed to be further clarified. In the present study, we reported that knock down of TSG101 suppressed the proliferation, migration and invasion of HCC cells, while overexpression of TSG101 facilitated them. Molecularly, the results revealed that knock down of TSG101 significantly decreased the cell cycle related regulatory factor p53 and p21. In another point, knock down of TSG101 also obviously decreased the level of metallopeptidase inhibitor TIMP1 (Tissue inhibitors of metalloproteinases 1), which results in inhibition of MMP2, MMP7 and MMP9. In contrast, overexpression of TSG101 had opposite effects. The iTRAQ proteomics analysis identified that oncogenic protein PEG10 (Paternally expressed gene 10) might be a potential downstream target of TSG101. Further investigation showed that TSG101 interacted with PEG10 and protected it from proteasomal degradation thereby regulating the expression of p53, p21 and MMPs. Finally, we found that both TSG101 and PEG10 proteins are up‐regulated and presented a direct correlation in HCC patients. In conclusion, these results suggest that TSG101 is up‐regulated in human HCC patients, which may accelerate the proliferation, migration and invasion of HCC cells through regulating PEG10.     

Expression of baculovirus anti-apoptotic genes p35 and op-iap in cotton (Gossypium hirsutum L.) enhances tolerance to verticillium wilt

Background

Programmed cell death plays an important role in mediating plant adaptive responses to the environment such as the invasion of pathogens. Verticillium wilt, caused by the necrotrophic pathogen Verticillium dahliae, is a serious vascular disease responsible for great economic losses to cotton, but the molecular mechanisms of verticillium disease and effective, safe methods of resistance to verticillium wilt remain unexplored.

Methodology/Principal Findings

In this study, we introduced baculovirus apoptosis inhibitor genes p35 and op-iap into the genome of cotton via Agrobacterium-mediated transformation and analyzed the response of transgenic plants to verticillium wilt. Results showed that p35 and op-iap constructs were stably integrated into the cotton genome, expressed in the transgenic lines, and inherited through the T₃ generation. The transgenic lines had significantly increased tolerance to verticillium wilt throughout the developmental stages. The disease index of T₁–T₃ generation was lower than 19, significantly (P<0.05) better than the negative control line z99668. After treatment with 250 mg/L VD-toxins for 36 hours, DNA from negative control leaves was fragmented, whereas fragmentation in the transgenic leaf DNA did not occur. The percentage of cell death in transgenic lines increased by 7.11% after 60 mg/L VD-toxin treatment, which was less than that of the negative control lines''s 21.27%. This indicates that p35 and op-iap gene expression partially protects cells from VD-toxin induced programmed cell death (PCD).

Conclusion/Significance

Verticillium dahliae can trigger plant cells to die through induction of a PCD mechanism involved in pathogenesis. This paper provides a potential strategy for engineering broad-spectrum necrotrophic disease resistance in plants.     

An intramolecular disulfide bond is required for the thermostability of methyl parathion hydrolase, OPHC2

OPHC2, a methyl parathion hydrolase (MPH) from Pseudomonas pseudoalcaligenes C2-1 (CGMCC 1150), can degrade a wide range of organophosphate pesticides. Compared with other MPHs, OPHC2 exhibits high thermostability. Its thermostability mechanism, however, remains unknown. In the present study, sequence analysis demonstrated that two cysteines (Cys110 and Cys146) exist in OPHC2, but not in other MPHs. The three-dimensional structural model of OPHC2 performed by computer-assisted homology modelling revealed a potential stacking network with residues Cys110 and Cys146, which probably formed an intramolecular disulfide bond. Furthermore, both sodium dodecyl sulphate-polyacrylamide gel electrophoresis and thiol-titration analyses indicated that OPHC2 contains a disulfide bond. Substitution of the disulfide bond-forming cysteines with alanine, leucine or methionine residues substantially decreased the thermostability of OPHC2, suggesting that disulfide bond formation affects conformational stability. These results, combined with three-dimensional structural modelling, demonstrated that the formation of a C110-C146 disulfide bond may stabilise the conformation of OPHC2, contributing to its thermostability.     

基于变权模型的舟山群岛生态安全预警

生态安全预警是生态安全研究的重要内容,对维护区域生态安全具有重要的指示意义.本文以浙江省舟山群岛为例,基于驱动力、压力、状态、影响、响应(DPSIR)框架模型构建了生态安全预警指标体系,使用变权模型对2000-2012年舟山市生态安全的预警等级进行测度,并使用马尔科夫预测方法对2013-2018年生态安全警情进行了预测.结果表明:变权模型能够有效地满足舟山群岛生态安全动态预警研究需要;2000-2012年,舟山群岛生态安全预警指数由0.286波动上升至0.484,警度等级从“重警”演变为“中警”,指示灯由“橙灯”演化为“黄灯”;2013-2018年,舟山群岛生态安全预警等级预测结果为“中警”,指示灯为“黄灯”.研究结果可为维护舟山群岛生态安全提供参考.     

运动性骨骼肌疲劳亚细胞机制的探讨

本实验采用持续性下坡跑运动,观察大鼠骨骼肌运动后不同时相线粒体形态、代谢、机能等指标的变化,结果表明：大鼠运动后即刻线粒体钙含量、细胞膜丙二醛（ＭＤＡ）值明显增加,ＡＴＰ含量和细胞膜Ｎａ＋,Ｋ＋－ＡＴＰ酶活性下降;运动后２４ｈ线粒体钙含量、ＭＤＡ值增加最明显,ＡＴＰ含量仍未恢复,细胞膜Ｎａ＋,Ｋ＋－ＡＴＰ酶活性基本恢复,线粒体体密度、平均体积比运动前明显增加,比表面缩小;运动后４８ｈＡＴＰ含量完全恢复,线粒体钙含量、ＭＤＡ值开始恢复。本研究结果提示,急性运动引起的细胞膜脂质过氧化加强、线粒体形态、代谢机能异常抑制线粒体氧化磷酸化过程、减少ＡＴＰ生成可能是运动性骨骼肌疲劳的亚细胞机制之一。耐力训练可以通过改善线粒体形态、代谢、机能提高机体的运动能力。     

保护性耕作条件下旱地农田麦-豆双序列轮作体系的水分动态及产量效应

保护性耕作(conservationtillage)能够减少水土流失、提高耕地产量,是一类具有生态保护意义的持续性农业耕作形式。2002年至2004年在定西旱地农业地区进行了保护性耕作条件下旱地农田春小麦豌豆双序列轮作土壤水分动态及产量效应的试验研究,结果表明:保护性耕作能够显著改善0～200cm土层土壤贮水量及含水量,随着降水量的增多土壤对降水的保蓄能力增强。在降水较少年份免耕秸秆覆盖的这种作用表现突出,而在降水充沛的年份免耕地膜覆盖则更具优势。耕层土壤水分因受降水等因素的影响而变化剧烈,耕层以下土壤水分变幅相对较小。播种期、五叶期及收获期土壤具有较高含水量,而开花期土壤含水量则较低。在两种轮作体系中,播种期春小麦和豌豆免耕秸秆覆盖处理0～50cm土层含水量分别较常规耕作增加28%、26%和11%、23%,降水生产效率较常规耕作提高了17.79%～26.81%。在春小麦豌豆轮作体系中免耕秸秆覆盖处理的作物产量(春小麦 豌豆)及水分利用效率分别为3420kghm2和8.11kg(hm2·mm),较常规耕作分别提高26.81%和25.39%。     

小鼠心脏发育中组蛋白乙酰化酶GCN5和PCAF的时空表达特征

目的研究组蛋白乙酰化酶氨合成通用控制蛋白5（general control nonderepressible-5 GCN5）和p300/CREB结合蛋白相关因子（p300/CREB binding protein-associated factor PCAF）在小鼠心脏发育过程中的时空表达规律。方法选取胎龄7.5-18d、出生1d和3月成年昆明小鼠正常心脏,利用免疫组织化学法和RT-PCR或Western blot技术半定量检测GCN5和PCAF在小鼠心脏发育过程中的时空表达变化。结果1.GCN5在E7.5-E9.5心脏原基中不表达;E10.5后心内膜垫及室间隔膜部和房室瓣相对强表达,心肌组织弱表达。GCN5 mRNA在E10.5-E11.5出现高峰表达,E12.5-E15.5表达水平下降,E16.5至成年鼠期表达极低。2.PCAF在E7.5-E9.5心脏原基中广泛弱表达;E10.5后心肌膜较强表达,心内膜、房室瓣和小梁网较弱表达,室间隔肌部弱表达,室间隔膜部极弱表达;PCAF蛋白在E10.5已有相对高表达,E11.5达到表达高峰,此后表达逐渐降低,在E13.5-E15.5和E16.5-生后1d仔鼠期出现两个表达平台期,成年鼠期心脏中表达最低。结论GCN5和PCAF在发育心脏中存在不同表达分布和变化规律,表明二者均参与了心脏的发生发育过程,且二者可能与心脏的特定结构发育密切相关。     

[反]-β-法尼烯合成酶基因在植物抗蚜分子育种中的应用

蚜虫是重要的农业害虫,每年造成数以亿计的经济损失。[反]-β-法尼烯[(E)-β-farnesene,EβF]是绝大多数蚜虫报警信息素的主要成分,可使蚜虫产生骚动、从植株上脱落,并吸引蚜虫天敌,有效控制蚜虫危害。EβF合成酶是催化合成EβF的关键酶,目前该基因已从薄荷、香橙、花旗松、黄花蒿、洋甘菊等植物中得到分离鉴定。植物中表达EβF合成酶基因以催化法呢基焦磷酸(Farnesyl diphosphate,FPP)合成EβF是控制蚜虫危害的重要策略。文中概括了当前植物抗蚜转基因研究现状,综述了植物EβF合成酶基因及其在植物抗蚜分子育种中的应用。针对当前转基因植物的EβF生成量较低等问题,展望了EβF合成酶基因在植物抗蚜分子育种中的应用前景和研究策略。     

鸭肝脂肪酸合成酶的NADPH底物抑制及作用动力学

己知动物脂肪酸合成酶的底物乙酰辅酶Ａ和丙二酰辅酶Ａ具有竞争性双底物抑制的乒乓机制。实验发现鸭肝脂肪酸合成酶的第三个底物ＮＡＤＰＨ也具有底物抑制,并研究了它的规律及与ＮＡＤＰＨ有关的稳态动力学。发现对于该酶的全反应,增加丙二酰辅酶Ａ浓度,降低环境盐浓度,均使ＮＡＤＰＨ底物抑制减少。但以ＮＡＤＰＨ作底物的酮酰还原和烯酰还原二步单独反应以及包含四步单独反应的乙酰乙酰辅酶Ａ还原反应都无ＮＡＤＰＨ底物抑制现象。ＮＡＤＰＨ底物抑制对丙二酰辅酶Ａ为竞争性,丙二酰辅酶Ａ底物抑制对ＮＡＤＰＨ为非竞争性。在全反应中ＮＡＤＰＨ和丙二酰辅酶Ａ之间发现为乒乓机制,在乙酰乙酰辅酶Ａ还原反应中,两个底物ＮＡＤＰＨ和乙酰乙酰辅酶Ａ之间则表现为序列反应机制。降低环境盐浓度使ＮＡＤＰＨ和丙二酰辅酶Ａ之间的乒乓机制向序列机制转化。在全反应中,ＮＡＤＰ产物抑制相对ＮＡＤＰ为竞争性,对丙二酰辅酶Ａ为非竞争性。     

双叉犀金龟表皮蛋白TdCPR12611与TdCPR7854的表达纯化及特性分析

[目的]探析双叉犀金龟Trypoxylus dichotomus表皮蛋白的序列特征及生化性质.[方法]利用RT-PCR克隆双叉犀金龟表皮蛋白基因,利用生物信息学方法分析表皮蛋白的结构特征及系统发育;采用大肠杆菌Escherichia coli表达系统对双叉犀金龟表皮蛋白进行重组表达,并通过金属离子鳌合层析的方法对重组蛋...