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151.
Nucleocapsid-glycoprotein interactions required for assembly of alphaviruses. 总被引:30,自引:19,他引:11 下载免费PDF全文
We have studied interactions between nucleocapsids and glycoproteins required for budding of alphaviruses, using Ross River virus-Sindbis virus chimeras in which the nucleocapsid protein is derived from one virus and the envelope glycoproteins are derived from the second virus. A virus containing the Ross River virus genome in which the capsid protein had been replaced with that from Sindbis virus was almost nonviable. Nucleocapsids formed in normal numbers in the infected cell, but very little virus was released from the cell. There are 11 amino acid differences between Ross River virus and Sindbis virus in their 33-residue E2 cytoplasmic domains. Site-specific mutagenesis was used to change 9 of these 11 amino acids in the chimera from the Ross River virus to the Sindbis virus sequence in an attempt to adapt the E2 of the chimera to the nucleocapsid. The resulting mutant chimera grew 4 orders of magnitude better than the parental chimeric virus. This finding provides direct evidence for a sequence-specific interaction between the nucleocapsid and the E2 cytoplasmic domain during virus budding. The mutated chimeric virus readily gave rise to large-plaque variants that grew almost as well as Ross River virus, suggesting that additional single amino acid substitutions in the structural proteins can further enhance the interactions between the disparate capsid and the glycoproteins. Unexpectedly, change of E2 residue 394 from lysine (Ross River virus) to glutamic acid (Sindbis virus) was deleterious for the chimera, suggesting that in addition to its role in nucleocapsid-E2 interactions, the N-terminal part of the E2 cytoplasmic domain may be involved in glycoprotein-glycoprotein interactions required to assemble the glycoprotein spikes. The reciprocal chimera, Sindbis virus containing the Ross River virus capsid, also grew poorly. Suppressor mutations arose readily in this chimera, producing a virus that grew moderately well and that formed larger plaques. 相似文献
152.
Joanie McKeon Eric Slade Donald A. R. Sinclair Niansheng Cheng Mitchell Couling Hugh W. Brock 《Molecular & general genetics : MGG》1994,244(5):474-483
Mutations in severalPolycomb (Pc) group genes cause maternal-effect or zygotic segmentation defects, suggesting thatPc group genes may regulate the segmentation genes ofDrosophila. We show that individuals doubly heterozygous for mutations inpolyhomeotic and six otherPc group genes show gap, pair rule, and segment polarity segmentation defects. We examined double heterozygous combinations ofPc group and segmentation mutations for enhancement of adult and embryonic segmentation defects.Posterior
sex combs andpolyhomeotic interact withKrüppel
2 and enhance embryonic phenotypes ofhunchback andknirps, andpolyhomeotic enhanceseven-skipped. Surprisingly, flies carrying duplications ofextra sex combs (esc), that were heterozygous for mutations ofeven-skipped (eve), were extremely subvital. Embryos and surviving adults of this genotype showed strong segmentation defects in even-numbered segments. Antibody studies confirm that expression ofeve is suppressed by duplications ofesc. However,esc duplications have no effect on other gap or pair rule genes tested. To our knowledge, this is only the second triplo-abnormal phenotype associated withPc group genes. Duplications of nine otherPc group genes have no detectable effect oneve. Expression ofengrailed (en) was abnormal in the central nervous systems of mostPc group mutants. These results support a role forPc genes in regulation of some segmentation genes, and suggest thatesc may act differently from otherPc group genes. 相似文献
153.
154.
155.
In our previous experiments, evidence of free radical formation has been demonstrated in gerbil brain after kainic acid (KA) administration. In the present study, the mechanisms involved in KA-induced free radical formation and subsequent cell degeneration were investigated using high density cortical neuron cultures. A free radical trapping agent,a-phenyl-N-tert-butyl-nitrone (PBN), as well as the combined action of superoxide dismutase and catalase attenuated KA neurotoxic effect. Calpain-induced xanthine oxidase (XO) activation may play an important role in KA excitotoxicity since calpain inhibitor I as well as allopurinol, a selective XO inhibitor, significantly protected the cortical neurons from KA-induced cell death. However, XO activation may not be the only source producing free radicals, other free radical generating systems such as nitric oxide synphase may also play a role in KA insult. 相似文献
156.
红毛五加叶的三萜皂甙 总被引:2,自引:0,他引:2
红毛五加(AcanthopanaxgiraldiiHarms)系五加科五加属植物,分布于河北、河南、四川、陕西、甘肃等省,有祛风湿、通关节、强筋骨、治痿痹等功效[1]。其化学成分未见报道。本文报道红毛五加叶的5个三萜皂甙(甙Ⅰ、Ⅱ、Ⅲ、Ⅳ和Ⅴ)的分离鉴定。它们均首次从该属植物发现,其结构如下: R1 R2 Ⅰ rham-(1→2)-ara H Ⅱ H rham-(1→4)-glc-(1→6)-glc … 相似文献
157.
河西走廊不同生态型芦苇核酸代谢季节动态研究 总被引:4,自引:0,他引:4
分布在甘肃河西走廊的4 种生态型芦苇(Phragm itescom m unisTrin.)的核酸代谢季节变化有差异。盐化草甸芦苇RNA 含量持续增加,DNA 含量相对稳定,其它3 种生态型芦苇的RNA 和DNA 含量以5月份为最高。过渡带芦苇的RNA 含量、沼泽芦苇及沙丘芦苇的DNA含量9 月份略有增高。盐化草甸芦苇与过渡带芦苇的DNase和RNase的活性7 月份最高,沼泽芦苇与沙丘芦苇的DNase和RNase活性5—9 月份呈增高趋势。盐化草甸芦苇的DNA 和RNA 合成活性不断升高,过渡带芦苇和沼泽芦苇的DNA 和RNA 合成活性及沙丘芦苇的RNA 合成活性5—9月份均降低,仅沙丘芦苇的DNA合成活性增强。RNA 聚丙烯酰胺梯度凝胶电泳分析结果表明,4 种生态型芦苇均含有25S、23S、18S、16S大分子量rRNA 和小分子量5.8S、5S、4.5SrRNA 及4StRNA。大分子量RNA 的含量高于小分子量RNA 含量。不同生态型及同一生态型芦苇的不同发育时期,相同的RNA 组分含量各不相同。且发育过程中23S、18S、16SrRNA 在不同月份发生不同程度的降解。由此,我们认为,核酸代谢的差异性是4 种生态型由生长转入衰 相似文献
158.
三褶脉紫菀中的新二萜甙 总被引:1,自引:0,他引:1
三褶脉紫菀(AsterageratoidesTurcz.)系菊科多年生草本植物,遍布全国,是民间常用的中药,有清热解毒、祛痰镇咳的功效[1,2]。化学工作者们曾从其同属植物紫菀(AstertararicusL.f.)中分离到紫菀酮(shionone)、槲皮素(quercetin)、无羁萜(friedelin)、表无羁萜(epifriedelinel)、毛叶醇(lachnophyllol)、乙酸毛叶酯(lachnophyllolacetate)、茴香醚(anethole)以及紫菀三萜皂甙[2—4]… 相似文献
159.
人脑髓鞘碱性蛋白cDNA体外扩增、克隆和鉴定 总被引:3,自引:0,他引:3
采用聚合酶链反应(PCR)从人脑cDNA文库中扩增出600bp的髓鞘碱性蛋白(MBP)cDNA片段,与载体pGEM-3Zf(+)平端连接.重组质粒DNA转化宿主菌JM109,在含X-gal和IPTG的平板上直接筛选阳性克隆.限制性内切酶分析和成套引物扩增鉴定证明,该克隆含有7个外显子的21.5kD人脑MBP全长编码序列. 相似文献
160.
不同性别黄鳝六种组织中LDH同工酶电泳谱的初步研究 总被引:3,自引:0,他引:3
本文报告了运用聚丙烯酰胺凝胶圆盘电泳研究不同性别黄鳝的血清、心肌、骨骼肌、肝、肾和生殖腺等六种组织器官中LDH同工酶。结果表明六种不同组织中LDH同工酶谱各不相同,具有明显的组织特异性。在不同性别中某些同一种组织的LDH同工酶谱也发生变化,这说明决定黄鳝LDH同工酶表达的因素在不同性别中有差异。 相似文献