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为构建斜纹夜蛾核型多角体病毒 (SpltMNPV)的重组病毒,以该病毒日本C3株基因组DNA为PCR扩增模板,根据GenBank SpltMNPV中国G2株基因序列,设计了两对引物分别扩增多角体蛋白基因的5′端侧翼序列(含启动子)和3′端侧翼序列(含终止子),将这两个片段依次克隆于pUC18质粒载体后,再将绿色荧光蛋白(GFP)基因亚克隆到上述载体的多角体蛋白基因启动子和终止子之间,获得转移载体pSplt-gfp。将pSplt-gfp与野生型SpltMNPV 基因组DNA共转染Spli细胞,通过同源重组和有限稀释法筛选,获得了以gfp基因替代多角体蛋白基因的重组病毒SpltMNPV-gfp。SpltMNPV-gfp感染Spli细胞和斜纹夜蛾幼虫,分别在感染24h和48h后可发现绿色荧光蛋白的表达。该重组病毒的获得,为建立斜纹夜蛾核型多角体病毒表达体系奠定了基础。  相似文献   

4.
The soluble enzyme phenoloxidase (tyrosinase) from the larval cuticle of Lymantria dispar has been partially purified using Ultrogel ACA 34, and the activity has been determined using phenolic substrates. The enzyme exhibited more activity toward O-diphenolic substrates and monophenolic substrates. The enzyme is inhibited by diethyl dithiocarbamate, phenylthiourea, and thiourea. The enzyme has been localized in the 7% slab and disc PAGE as an intense band. The enzyme is suggested to be involved in wound healing. © 1992 Wiley-Liss, Inc.  相似文献   

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The Vegetative insecticidal Vip3A proteins display a wide range of insecticidal spectrum against several agricultural insect pests. The fact that the expression of vip3 genes occurs only during the vegetative growth phase of Bacillus thuringiensis is a limiting factor in term of production level. Therefore, extending the synthesis of the Vip proteins to the sporulation phase is a good alternative to reach high levels of toxin synthesis. In this study, we have demonstrated that the maximal production of the secreted Vip3LB (also called Vip3Aa16) during the growth of the wild-type strain B. thuringiensis BUPM 95 is reached at the end of the vegetative growth phase, and that the protein remains relatively stable in the culture supernatant during the late sporulation stages. The vip3LB gene was cloned and expressed under the control of the sporulation dependant promoters BtI and BtII in B. thuringiensis BUPM 106 (Vip3(-)) and BUPM 95 (Vip3(+)) strains. The examination of the culture supernatants during the sporulation phase evidenced the synthesis of Vip3LB and its toxicity against the second-instars larvae of the Lepidopteron insect Spodoptera littoralis for the recombinant BUPM 106. Moreover, there was an increase of the Vip3LB synthesis level and an enhancement of the oral toxicity for the recombinant BUPM 95 resulting from the expression of the vip3LB gene during both the vegetative and sporulation phases and the relative stability of the Vip3LB protein.  相似文献   

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The gypsy moth (Lymantria dispar) is an insect folivore that feeds on a broad range of hosts, and undergoes intermittent outbreaks that cause extensive tree mortality. Like many other herbivorous insects, gypsy moth larvae consume a substrate that is low in nitrogen. Gypsy moth larvae have been known to cannibalize under crowded conditions in the laboratory. In this study, we assessed the influence of nitrogen and density on cannibalism behavior in gypsy moth larvae. Cannibalism rates increased with decreased nitrogen and increased density. There was no interaction between these two parameters. Developmental experiments confirmed that low dietary nitrogen is detrimental, in agreement with previous studies. In a second experiment, we assessed the influence of previous cannibalism experiences on subsequent cannibalism behavior. Gypsy moth larvae that had previously cannibalized other larvae subsequently exhibited higher cannibalism rates than those larvae that had not cannibalized. In conclusion, low nitrogen, high larval density, and previous cannibalism experience are important factors contributing to gypsy moth larval cannibalism. Future studies are needed to estimate benefits to larvae, and to more closely approximate field conditions.  相似文献   

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We previously identified a novel baculovirus-encoded apoptosis suppressor, Apsup, from the baculovirus Lymantria dispar multiple nucleopolyhedrovirus (LdMNPV). Apsup inhibits the apoptosis of L. dispar Ld652Y cells triggered by infection with p35-defective Autographa californica MNPV (vAcΔp35) and exposure to actinomycin D or UV light. Here, we examined the functional role of Apsup in apoptosis regulation in insect cells. Apsup prevented apoptosis and the proteolytic processing of L. dispar initiator caspase Dronc (Ld-Dronc) in Ld652Y cells triggered by overexpression of Ld-Dronc, LdMNPV inhibitor-of-apoptosis 3 (IAP3), or Hyphantria cunea MNPV IAP1. In vAcΔp35-infected apoptotic Ld652Y cells, Apsup restricted apoptosis induction and prevented processing of endogenous Ld-Dronc. Conversely, upon RNA interference (RNAi)-mediated silencing of apsup, LdMNPV-infected Ld652Y cells, which typically support high-titer virus replication, underwent apoptosis, accompanied by the processing of endogenous Ld-Dronc. Furthermore, endogenous Ld-Dronc coimmunoprecipitated with transiently expressed Apsup, indicating that Apsup physically interacts with Ld-Dronc. Apsup prevented the apoptosis of Sf9 cells triggered by vAcΔp35 infection but did not inhibit apoptosis or activation of caspase-3-like protease in vAcΔp35-infected Drosophila melanogaster S2 cells. Apsup also inhibited the proteolytic processing of L. dispar effector caspase Ld-caspase-1 in the transient expression assay but did not physically interact with Ld-caspase-1. These results demonstrate that Apsup inhibits apoptosis in Ld652Y cells by preventing the proteolytic processing of Ld-Dronc. Together with our previous findings showing that Apsup prevents the processing of both overexpressed Ld-Dronc and Bombyx mori Dronc, these results also demonstrate that Apsup functions as an effective apoptotic suppressor in various lepidopteran, but not dipteran, insect cells.  相似文献   

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Autophagy is an evolutionary ancient process based on the activity of genes conserved from yeast to metazoan taxa. Whereas its role as a mechanism to provide energy during cell starvation is commonly accepted, debate continues about the occurrence of autophagy as a means specifically activated to achieve cell death. The IPLB-LdFB insect cell line, derived from the larval fat body of the lepidoptera Lymantria dispar, represents a suitable model to address this question, as both autophagic and apoptotic cell death can be induced by various stimuli. Using morphological and functional approaches, we have observed that the culture medium conditioned by IPLB-LdFB cells committed to death by the ATPase inhibitor oligomycin A stimulates autophagic cell death in untreated IPLB-LdFB cells. Moreover, proteomic analysis of the conditioned media suggests that, in IPLB-LdFB cells, oligomycin A promotes a shift towards lipid metabolism, increases oxidative stress and specifically directs the cells towards autophagic activity. Electronic Supplementary Material  The online version of this article (doi:) contains supplementary material, which is available to authorized users. This work was supported by an F.A.R. grant from the University of Modena and Reggio Emilia (D.M. and E.O.) and by an “Experimental approaches to the study of evolution” grant from the Department of Animal Biology of the University of Modena and Reggio Emilia (D.M.).  相似文献   

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Peripheral injection of the endotoxin LPS in rats 3 weeks prior to a second injection of LPS derived from another bacterial strain results in elevated corticosterone and decreased pro-inflammatory cytokines in the blood. We further investigated this model by measuring cytokine expression in the hypothalamus and spleen. In LPS-pretreated rats, hypothalamic expression of a range of cytokines was attenuated in response to the second injection of LPS while splenic expression was elevated. This is the first demonstration that prior exposure to an endotoxin can differentially affect cytokine expression in the brain and peripheral tissues when a host is confronted with a second, acute, pro-inflammatory stimulus. Changes in hypothalamic cytokine expression in endotoxin pretreated rats may provide new evidence for the involvement of central cytokine pathways in modulating peripheral inflammation and mediating psychopathological alterations associated with inflammatory diseases.  相似文献   

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以O型口蹄疫病毒为研究对象,经过RTPCP扩增得到非结构蛋白3ABC基因,克隆到转移载体pFastbacHT,将其转入含穿梭载体Bacmid的DH10Bac,与Bacmid发生位点特异性转座作用,得到3ABC的重组穿梭载体Bacmid3ABC,再将其转染昆虫细胞HiFive。PCR鉴定证实3ABC基因正确地插入到病毒基因组的多角体蛋白基因启动子下游,经过SDSPAGE和Westernblot检测,3ABC基因在昆虫细胞中表达了大小约为50kDa的蛋白条带,3ABC基因在BactoBac系统中的成功表达为建立以基因工程产品为抗原、鉴别诊断自然感染和免疫动物的方法提供了技术条件。  相似文献   

11.
以O型口蹄疫病毒为研究对象,经过RT-PCP扩增得到非结构蛋白3ABC基因,克隆到转移载体pFastbacHT,将其转入含穿梭载体Bacmid的DH10Bac,与Bacmid发生位点特异性转座作用,得到3ABC的重组穿梭载体Bacmid-3ABC,再将其转染昆虫细胞Hi Five.PCR鉴定证实3ABC基因正确地插入到病毒基因组的多角体蛋白基因启动子下游,经过SDS-PAGE和Western blot检测,3ABC基因在昆虫细胞中表达了大小约为50kDa的蛋白条带,3ABC基因在Bac-to-Bac系统中的成功表达为建立以基因工程产品为抗原、鉴别诊断自然感染和免疫动物的方法提供了技术条件.  相似文献   

12.
Ovaries from Lymantria dispar females were transplanted into an environment lacking vitellogenin, the male milieu, in order to determine how the presence of vitellogenin in the hemolymph affects the process of protein uptake by gypsy moth oocytes. When undeveloped ovaries from newly ecdysed last instar females were transplanted into males of the same stage, follicles detached from the germarium and increased in size, but the growth of oocytes proceeded more slowly than those from female controls. Although chorion fromation was delayed in male-grown ovaries, scanning electron microscopy of chorionated eggs recovered from adult males showed that a chorion with normal surface architecture was formed by the adult stage. SDS-PAGE analysis of the male-grown ovaries and hemolymph from males receiving ovaries showed that vitellogenin production was not stimulated by the organ transplant and only male hemolymph proteins were internalized by the male-incubated ovaries. Thus, in the absence of vitellogenin, endocytosis of male hemolymph proteins occurred, but the rate of oocyte growth was slowed.  相似文献   

13.
乙烯利调控甘蔗生长前期基因表达初报   总被引:1,自引:0,他引:1  
在甘蔗(Saccharum of ficinarum L.)生长前期分别叶面喷施200mg L-1乙烯利和清水,利用cDNA-AFLP技术分析甘蔗经不同处理后体内基因表达的差异情况,以期通过对差异表达基因进行序列分析和功能分析,探讨乙烯利调控甘蔗生长的分子机理。结果表明:经乙烯利处理后的甘蔗叶片,cDNA-AFLP的扩增产物多态性丰富,基因表达差异显著;部分差异片断序列与抗病、抗逆及促进光合作用等相关基因具有较高的同源性。  相似文献   

14.
利用Bac-to-Bac系统表达棉蚜的乙酰胆碱酯酶   总被引:1,自引:0,他引:1  
Bac-to-Bac昆虫杆状病毒表达系统是一种高效真核表达系统。采用重组DNA技术构建棉蚜乙酰胆碱酯酶1(AChE1)表达质粒,应用该系统在昆虫Sf9细胞系中成功表达了棉蚜的AChE1。表达的AChE以可溶性形式释放于细胞培养液中,对其自然底物类似物ATChI的Km值为(144·5±28·6)μm;对抗蚜威、唑蚜威、氧化乐果和灭赐松等4种杀虫剂的敏感性指数(Ki值)分别为513、1883、5和23(mM·min)-1,与文献报道的测定结果基本一致。昆虫细胞被重组病毒感染后第2~3天所得产物的活性最高;该产物在-20℃保存90d后活性没有明显下降,4℃保存60d后下降40%,室温(22℃)保存7d后即下降70%。  相似文献   

15.
Lotus (Nelumbo Adans) is an aquatic perennial plant that flourished during the middle Albian stage. In this study, we characterized the digital gene expression signatures for China Antique lotus under conditions of heat shock stress. Using RNA-seq technology, we sequenced four libraries, specifically, two biological replicates for control plant samples and two for heat stress samples. As a result, 6,528,866 to 8,771,183 clean reads were mapped to the reference genome, accounting for 92–96% total clean reads. A total of 396 significantly altered genes were detected across the genome, among which 315 were upregulated and 81 were downregulated by heat shock stress. Gene ontology (GO) enrichment of differentially expressed genes revealed protein folding, cell morphogenesis and cellular component morphogenesis as the top three functional terms under heat shock stress. Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis led to the identification of protein processing in endoplasmic reticulum, plant-pathogen interactions, spliceosome, endocytosis, and protein export as significantly enriched pathways. Among the upregulated genes, small heat shock proteins (sHsps) and genes related to cell morphogenesis were particularly abundant under heat stress. Data from the current study provide valuable clues that may help elucidate the molecular events underlying heat stress response in China Antique lotus.  相似文献   

16.
用Bac-to-Bac杆状病毒系统表达人生长激素   总被引:6,自引:0,他引:6  
利用Bac to Bac杆状病毒载体表达系统将人生长激素 (humangrowthhormone ,hGH)基因cDNA克隆至转移载体pFastBac1中 ,得到pFastBac hGH ,再将其转化进入含穿梭载体Bacmid的受体菌DH10Bac中 ,发生转座作用 ,得到含hGH基因的重组穿梭载体rBacmid hGH .纯化DNA ,直接转染培养的昆虫细胞Sf9,得到重组病毒rAcV Bac hGH .经酶切PCR及Southern杂交鉴定 ,hGH基因正确地插入病毒基因组的多角体蛋白基因启动子下 ,SDS PAGE测得产物蛋白分子量为 2 2kD左右 .用免疫化学发光法测得转染上清中hGH表达水平可达 18μg ml ,与用传统的BEVS表达hGH相比 ,转染上清中hGH表达水平提高 4 0 0倍以上  相似文献   

17.
通过对猪生长激素(pGH)基因的cDNA进行测序,得到pGHcDNA的全序列,并与Seeburg等报道的序列进行了比较和讨论。然后利用具人工合成启动子和多角体蛋白XIV启动子的转移载体质粒pSXIVVI^+X3/4构建出含pGH基因的重组质粒pX3/4-pGH。将pX3/4-pGH与致死缺失型线性化AcMNPV-OCC^-DNA共转染Sf9细胞,构建出既能形成多角体又能表达pGH基因的苜蓿丫纹夜蛾  相似文献   

18.
猪生长激素基因在杆状病毒载体系统中的表达   总被引:8,自引:0,他引:8  
通过对猪生长激素(pGH)基因的cDNA进行测序,得到pGH cDNA的全序列,并与Seeburg等报道的序列进行了比较和讨论.然后利用具人工合成启动子和多角体蛋白XIV启动子的转移载体质粒pSXIVVI+X3/4构建出含pGH基因的重组质粒pX3/4-pGH.将pX3/4-pGH与致死缺失型线性化AcMNPV-OCC- DNA共转染Sf9细胞,构建出既能形成多角体又能表达pGH基因的苜蓿丫纹夜蛾核多角体重组病毒AcMNPV-pX3/4-pGH-OCC+.感染重组毒株的Hi 5细胞可溶蛋白及其培养上清的SDS-PAGE和Western blot的分析结果表明,感染细胞的蛋白电泳带的20.7 kDa处有一条猪生长激素特异带,但培养上清中没有.凝胶黑度扫描估测结果显示pGH蛋白占细胞可溶蛋白的4.48%.  相似文献   

19.
The mechanisms of nucleopolyhedrovirus (NPV)transmission through gypsy moth (Lymantriadispar L., Lepidoptera: Lymantriidae)populations in Western Siberia wereinvestigated. Field and laboratory studies werecarried out during 1992–1998 in a gypsy mothoutbreak in the Novosibirsk Area (WesternSiberia), Russia. The damaged trees were primarilytwo species of birch, Betula pendula Roth. and B. pubescensEhrh. Investigations were performed at threestages of the outbreak: population increase(1992–1993), population peak (1994–1995) andpopulation decline (1996–1998). Experiments onactivation of occult virus by different stressfactors were carried out in order to clarifythe mechanism of transgenerational transmissionof NPV. In both laboratory and fieldexperiments NPV-caused mortality levels werelow; most insects did not acquire a lethal doseof virus. Occult virus can provide an importantroute of transgenerational NPV transmission,particularly in Western Siberia where gypsymoths migrate by female flight and can moveaway from trees contaminated by virus fromprevious larval infections.  相似文献   

20.
用灵敏度较高的RT—PCR检测培养4周的大豆幼苗的5个不同组织:嫩叶、老叶、茎、离层和根,测得脱落纤维素酶基因的表达量互不相同,离层中表达量最高,茎中表达量最低。选取表达量最高的离层作为逆境处理材料,分别用高温(46C)、干旱、盐(200mmol/L NaCl)处理不同时间后,检测脱落纤维素酶基因的时间表达模式。结果表明:3种逆境条件下,脱落纤维素酶基因的时间表达模式各不相同,但总的来说,高温能抑制脱落纤维素酶基因的表达,干旱和盐都能促进脱落纤维素酶基因的表达。  相似文献   

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