生物工程技术讲座[八]

应用微细胞检测基因产物的方法由于质粒和噬菌体等的DAN分子能在细胞内进行自我复制,以及DNA重组技术的普及,质粒DNA做为异源性DNA分子的载体,在基因工程中目前已被广泛应用。在克隆或分析真核生物或原核生物的多种不同基因时,常用检测基因表达来确定其存在。把含有某一目的基因的DNA片段和载体质粒的DNA进行重组,再通过重组DNA在受体细胞中的转录、翻译、     

登革3型病毒prM-E基因重组质粒DNA的构建和真核表达

构建登革 3型病毒 prM E基因的真核表达重组质粒 ,并进行体外表达 ,为登革DNA疫苗的研究奠定基础。用RT -PCR法获得 prM -E基因片段 ,然后将其克隆到真核表达载体中。用电穿孔法将重组质粒DNA转入BHK细胞 ,通过免疫荧光法检测外源基因在真核细胞中的表达。结果 ,通过酶切和序列测定证实了构建的重组质粒DNA含序列正确的 prM- E基因。用免疫荧光法检测到转染了重组质粒DNA的BHK细胞的胞浆中有登革 3型病毒特异蛋白的表达。说明含有登革 3型病毒prM -E基因的真核表达重组质粒可以在BHK细胞中表达 ,该结果为观察该重组质粒的免疫原性奠定了基础。     

丙型肝炎病毒NS5A基因在昆虫细胞中的表达及其分布研究

应用PCR方法从含有丙肝病毒全部非结构蛋白基因的质粒pBAC25中扩增出全长的NS5A基因DNA片段(约1.34kb),PCR扩增NS5A基因片段克隆到转移载体pBlueBacHisA中.重组转移质粒pBlueBacHis5A DNA与野生型杆状病毒(AcNPV)DNA共转染SF-9昆虫细胞,通过空斑纯化获得带有NS5A基因的重组病AcNS5A.对重组病毒基因组DNA进行酶切和PCR鉴定,证实HCV NS5A基因已插入重组病毒基因组中.AcNS5A感染SF-9细胞后,在细胞中表达出一条64kD的蛋白,用Western-blot分析,结果表明这种蛋白与抗HCV HS5A特异性抗体发生强烈反应,说明NS5A基因已在细胞中得到表达,应用免疫荧光技术与免疫组化技术进一步研究NS5A蛋白在昆虫细胞中不同时间的表达情况及其分布,结果表明,NS5A蛋白在AcNS5A重组病毒感染细胞24h后主要分布在细胞质膜上,而在48h后则同时分布于细胞质膜和细胞核内,在72h则完全布满整个细胞,我们认为NS5A蛋白定位于质膜和细胞核中,暗示着在病毒复制过程中NS5A蛋白可能参与病毒RNA在质膜上复制和细胞基因表达的调控.     

DNA重组技术在水稻育种上的应用

七十年代相继发现的限制性内切酶、质粒、转形变异现象等已发展成为分子生物学研究的基础。微生物领域开发的DNA重组技术(基因操作),在高等植物上的应用正方兴未艾。 DNA重组技术是指用能识别、切断特定碱基序列的限制酶,切出担当遗传信息的DNA,用DNA连接酶与在寄主内自动增殖具有双连结构的DNA质粒接合,形成重组DNA,再将重组DNA返回寄主细胞所进行的操作。转移进来的外源DNA与质粒DNA在寄主内同时增殖,来发现目的性状。在水稻等多种高等植物上,即使能鉴定、分离出目的基因,但运载其基因的有效媒介体,还大部分未被开发出来。     

丙型肝炎病毒NS5A基因在昆虫细胞中的表达及其分布研究

应用PCR方法从含有丙肝病毒全部非结构蛋白基因的质粒pBAC25中扩增出全长的NS5A基因DNA片段（约1.34kb),PCR扩增NS5A基因片段克隆到转移载体plueBacHisA中。重组转移质粒pBlueBacHis5ADNA与野生型杆状病（AcNPV)DNA共转染SF-9昆虫细胞,通过空斑纯化获得带有NS5A基因的重组病AcNS5A,对重组病毒基因组DNA进行酶切和PCR鉴定,证实HCV NS5A基因已插入重组病毒基因组中,AcNS5A感染SF-9细胞后,在细胞中表达出一条64kD的蛋白,用Western-blot分析,结果表明这种蛋白与抗HVCHS5A特异性抗体发生强烈反应,说明NS5A基因已在细胞中得到表达,应用免疫荧光技术与免疫组化技术进一步研究NS5A蛋白在昆虫细胞中不同时间的表达情况及其分布,结果表明,NS5A蛋白在AcNS5A重组病毒感染细胞24h后主要分布在细胞质膜上,而在48h后则同时分布于细胞质膜和细胞核内,在72h则完全布满整个细胞,我们认为NS5A蛋白定位于质膜和细胞核中,暗示着在病毒复制过程中NS5A蛋白可能参与病毒RNA在质膜上复制和细胞基因表达的调控。     

遗传工程的成就和展望

遗传工程一般是指将外源基因与DNA载体结合,形成重组DNA,然后引入到受体细胞,使外源基因复制并产生相应基因产物的技术,亦称为基因工程或重组DNA技术。也有人把细胞融合和染色体工程包括在遗传工程的范畴之内。 五十年代和六十年代分子遗传学的蓬勃发展,使人们搞清了基因的本质以及遗传信息复制和传递的机制,再加上七十年代初限制性内切酶的发现,基因分离技术的进展和细胞转化方法的建立,使遗传工程这门定向改造生物的新技术应运而生。1973年,Cohen等使大肠杆菌的抗四环素质粒和抗链霉素质粒在试管中重组,并在大肠杆菌中表达,进行了第一项遗传工程实验。     

分子生物学在昆虫中的研究与应用

<正> 遗传学和分子生物学的结合对于昆虫学者是一个较新的课题,然而,这一领域在过去几年里已经有了变化。昆虫对于DNA重组(rec-DNA)技术等分子生物学的研究起了重要作用,反过来分子生物学的发展又为昆虫学的许多基础领域,如发生生物学、行为生物学、进化生物学、分类和生态学,以及应用昆虫学的研究展示了新的前景。     

利用Red重组系统敲除鲍曼不动杆菌asa A基因

目的利用Red重组系统敲除鲍曼不动杆菌ATCC 17978的asaA。方法设计上下游引物中包含asaA的同源序列,并以pKD4质粒为模板,扩增含有卡那霉素抗性基因的DNA片段。将该片段转化于表达重组酶的17978感受态细胞中,在卡那霉素筛选压力下,得到经两次同源双交换的具有卡那霉素基因标记的突变菌株。随后,在重组酶的作用下将抗性基因去除,最终得到无抗性基因标记的突变菌株ΔasaA。结果通过该重组系统,首先将卡那霉素抗性基因的DNA片段替换了基因组中asaA的DNA片段,然后将卡那霉素抗性基因的DNA片段消除,最终获得了asaA缺失的突变体。结论通过Red重组系统为鲍曼不动杆菌中其他基因的缺失突变提供方法与思路。     

基因工程:重组体DNA研究

重组体脱氧核糖核酸(DNA)研究是人为地将一小段DNA(基因)嵌入另一种DNA分子中,成为DNA杂交分子。然后使含有此杂交分子的宿主进行繁殖。这段外来的基因随着杂交分子的复制而增加其模板本。所以称此过程为分子繁殖。这种技术在基因的结构和功能的研究中有非常重要的作用,而在应用方面(医学、农业、工业、环境卫生等)都有广阔的发展前景,因而又有基因工程之称。本文介绍了重组体DNA研究的技术概要,它在基础理论研究中的价值和发展,以及它在医学卫生、工农业等方面的实用可能。最后介绍了关于这项研究所引起的安全问题的争论。     

登革2型病毒PrM基因的重组甲病毒RNA介导的抗病毒作用的研究

将扩增的登革 2型病毒株PrM基因导入pSFV载体的SP6启动子下游 ,筛选出含该基因正、反向插入的重组质粒DNA。用SpeI酶分别将重组的和辅助的质粒DNA线性化 ,并将其体外转录成 5′末端含帽子结构的RNA。再将这两种RNA共转染BHK细胞。然后将转染的宿主细胞用登革 2型病毒株攻击 ,并分别观察含正、反义PrM基因的重组甲病毒RNA介导的抗病毒效果。通过碱基序列测定 ,筛选出含PrM基因正、反向插入的pSFV PrM重组质粒。并获得了经重组RNA与辅助RNA共转染细胞而产生的重组病毒颗粒。含有反义PrM基因的重组病毒RNA ,在宿主细胞中具有抗登革 2型病毒复制的作用 ,而且强于含正义PrM基因的重组病毒RNA。     

昆虫种群遗传控制技术中启动子的研究

利用昆虫遗传转化技术对害虫进行遗传控制是害虫防治研究的新方向,该技术具有物种特异、防效高且对环境友好的特点。启动子是基因表达调控的重要元件,选择合适的启动子是外源基因高效、准确表达的关键,对获得高效、稳定的遗传修饰昆虫品系至关重要。本文简要介绍了昆虫基因启动子的结构特征,重点描述了昆虫种群遗传防治中组成型启动子、性别和组织特异型启动子、特定发育时期启动子和诱导型启动子的研究和应用概况,并对这几类启动子在害虫遗传控制中的应用前景进行了展望。     

Current status of the management of fall webworm,Hyphantria cunea: Towards the integrated pest management development

The fall‐webworm (FWW), Hyphantria cunea, is a highly polyphagous insect pest that is native to North America and distributed in different countries around the world. To manage this insect pest, various control methods have been independently evaluated in the invaded areas. Some of the control methods have been limited to the laboratory and need further study to verify their effectiveness in the field. On the other hand, currently, integrated pest management (IPM) has become a promising ecofriendly insect pest management option to reduce the adverse effect of insecticides on the environment. The development of an IPM for an insect pest must combine different management options in a compatible and applicable manner. In the native areas of the insect pests, there are some recommended management options. However, to date, there is no IPM for the management of the FWW in the newly invaded areas. Therefore, to develop an IPM for this insect pest, compilation of effective management option information is the first step. Thus, believing in the contribution of an IPM to the established management strategies, the chemical, biological, natural enemy, sex pheromone, and molecular studies regarding this insect were reviewed and potential future research areas were delineated in this review study. Therefore, using the currently existing management options, IPM development for this insect pest should be the subject of future research in the newly invaded areas.     

Strategies to improve the insecticidal activity of Cry toxins from Bacillus thuringiensis

Bacillus thuringiensis Cry toxins have been widely used in the control of insect pests either as spray products or expressed in transgenic crops. These proteins are pore-forming toxins with a complex mechanism of action that involves the sequential interaction with several toxin-receptors. Cry toxins are specific against susceptible larvae and although they are often highly effective, some insect pests are not affected by them or show low susceptibility. In addition, the development of resistance threatens their effectiveness, so strategies to cope with all these problems are necessary. In this review we will discuss and compare the different strategies that have been used to improve insecticidal activity of Cry toxins. The activity of Cry toxins can be enhanced by using additional proteins in the bioassay like serine protease inhibitors, chitinases, Cyt toxins, or a fragment of cadherin receptor containing a toxin-binding site. On the other hand, different modifications performed in the toxin gene such as site-directed mutagenesis, introduction of cleavage sites in specific regions of the protein, and deletion of small fragments from the amino-terminal region lead to improved toxicity or overcome resistance, representing interesting alternatives for insect pest control.     

我国农业害虫综合防治研究现状与展望

害虫综合防治作为农业生产的一项重要策略,在农业可持续发展中具有举足轻重的作用。近年来,针对我国害虫防治所存在的技术需求,科技部等部门先后通过973计划、863计划、科技支撑计划和农业行业专项等对重要害虫防治研究立项支持。通过这些项目的实施,我国建成了一支由国家和省级科研单位和大学组成的专业科研队伍和研究平台,对害虫监测预警技术、基于生物多样性保护利用的生态调控技术、害虫生物防治技术、化学防治技术、抗虫转基因作物利用技术等方面的研究取得了一系列的重要进展,研究建立了棉花、水稻、玉米、小麦和蔬菜等作物重要害虫的综合防治技术体系,并在农业生产中发挥了重要作用。以基因工程和信息技术为代表的第二次农业技术革命的到来,推动了害虫综合防治的理论发展,为害虫综合防治技术的广泛应用提供了新的机遇。地理信息系统、全球定位系统等信息技术和计算机网络技术的应用,提高了对害虫种群监测和预警的能力和水平,转基因抗虫作物的商业化种植等技术的应用显著增强了对害虫种群的区域性调控效率。针对产业结构调整和全球气候变化所带来的害虫新问题,进一步发展IPM新理论与新技术将成为我国农业昆虫学研究的重要方向之一。     

Genetic variation and phylogeographic structure of Laodelphax striatellus in China based on microsatellite markers

The small brown planthopper (SBPH), Laodelphax striatellus (Fallén) (Hemiptera: Delphacidae), is an important agricultural pest that has caused serious economic losses in the major rice-producing areas of China. To effectively manage this insect pest, we analysed its genetic variation, genetic structure and population demographic history. We used nine nuclear microsatellite loci to investigate the genetic diversity and population genetic structure of SBPH at 43 sampling sites in China. High levels of genetic diversity and genetic differentiation among most populations were detected. Overall, neighbour-joining dendrograms, STRUCTURE and principal coordinate analysis (PCoA) revealed no genetically distinct groups and exhibited an admixed phylogeographic structure in China. Isolation by distance (IBD) and spatial autocorrelation analyses demonstrated no correlation between genetic distance and geographic distance. On the other hand, bottleneck analysis indicated that SBPH populations had not undergone severe bottleneck effects in these regions. This study provides useful data for resolving the genetic relationships and migration patterns of SBPH and thus contributes to developing effective management strategies for this pest.     

The utility of microsatellite DNA markers for the evaluation of area-wide integrated pest management using SIT for the fruit fly, Bactrocera dorsalis (Hendel), control programs in Thailand

The oriental fruit fly, Bactrocera dorsalis (Hendel), is a key pest that causes reduction of the crop yield within the international fruit market. Fruit flies have been suppressed by two Area-Wide Integrated Pest Management programs in Thailand using Sterile Insect Technique (AW-IPM-SIT) since the late 1980s and the early 2000s. The projects’ planning and evaluation usually rely on information from pest status, distribution, and fruit infestation. However, the collected data sometimes does not provide enough detail to answer management queries and public concerns, such as the long term sterilization efficacy of the released fruit fly, skepticism about insect migration or gene flow across the buffer zone, and the re-colonisation possibility of the fruit fly population within the core area. Established microsatellite DNA markers were used to generate population genetic data for the analysis of the fruit fly sampling from several control areas, and non-target areas, as well as the mass-rearing facility. The results suggested limited gene flow (m < 0.100) across the buffer zones between the flies in the control areas and flies captured outside. In addition, no genetic admixture was revealed from the mass-reared colony flies from the flies within the control area, which supports the effectiveness of SIT. The control pests were suppressed to low density and showed weak bottleneck footprints although they still acquired a high degree of genetic variation. Potential pest resurgence from fragmented micro-habitats in mixed fruit orchards rather than pest incursion across the buffer zone has been proposed. Therefore, a suitable pest control effort, such as the SIT program, should concentrate on the hidden refuges within the target area.     

遗传不育技术在蚊媒疾病防控中的应用

疟疾、登革热等重大传染性蚊媒疾病严重危害人类健康,且目前缺乏有效的药物和疫苗,防治埃及伊蚊、冈比亚按蚊等媒介昆虫是控制和消除这些疾病的有效手段。化学杀虫剂的大规模使用在一定程度上控制了疾病的传播,但其抗药性和环境污染等问题也随之而来。分子生物学的飞速发展为昆虫不育技术(SIT)的更新及害虫防治提供了新的策略,由此发展起来的以释放携带显性致死基因昆虫(RIDL)为代表的一系列遗传不育技术为蚊虫种群防控提供了更加有效的选择。本文概述了遗传技术在蚊虫防控中的应用进展,包括蚊虫遗传防治的历史和策略,阐述了RIDL技术体系的原理,同时介绍了相关遗传控制品系和已经开展的田间释放研究,展示了遗传修饰不育技术在蚊媒疾病防治中的巨大潜力。     

Developing CRISPR-based sex-ratio distorters for the genetic control of fruit fly pests: A how to manual

Agricultural pest control using genetic-based methods provides a species-specific and environmentally harmless way for population suppression of fruit flies. One way to improve the efficiency of such methods is through self-limiting, female-eliminating approaches that can alter an insect populations' sex ratio toward males. In this microreview, we summarize recent advances in synthetic sex ratio distorters based on X-chromosome shredding that can induce male-biased progeny. We outline the basic principles to guide the efficient design of an X-shredding system in an XY heterogametic fruit fly species of interest using CRISPR/Cas gene editing, newly developed computational tools, and insect genetic engineering. We also discuss technical aspects and challenges associated with the efficient transferability of this technology in fruit fly pest populations, toward the potential use of this new class of genetic control approaches for pest management purposes.     

Regulatory impact on insect biotechnology and pest management

The application of insect biotechnology is promising for the development of environmentally compatible pest management solutions. As we have refined and enhanced genetic engineering techniques in several insect species that cause significant economic loss and public health injury, it has become clear that insect biotechnology will move forward as one of the key tools of pest management in agriculture and in the human environment. Well characterized genetic elements can be manipulated toward specific aims and maintain a viable insect, albeit one with diminished capacity to exchange genetic material, vector a virus or bacterium, or complete its life cycle. Despite this degree of knowledge and precision, there remain unanswered questions regarding environmental fate, release and public acceptance of this technology. The uncertainty surrounding any novel technology inevitably increases the level of regulatory scrutiny associated with its use. Although the term “insect biotechnology” has many connotations, it certainly includes the genetic modification of symbiotic or commensally associated microbes as a means of delivering a trait (e.g. a toxin) to manage plant and human diseases and insect pests. The distinction between this paratransgenic approach and direct genetic modification of insect pests is an important one biologically as well as from a regulatory standpoint. The regulatory framework for microbial applications to agriculture is in many instances in place; however, we must strive to forge the development of guidelines and regulations that will foster deployment of insect biotechnologies.     

The biology of insecticidal activity and resistance

Identifying insecticide resistance mechanisms is paramount for pest insect control, as the understandings that underpin insect control strategies must provide ways of detecting and managing resistance. Insecticide resistance studies rely heavily on detailed biochemical and genetic analyses. Although there have been many successes, there are also many examples of resistance that still challenge us. As a precursor to rational pest insect control, the biology of the insect, within the contexts of insecticide modes of action and insecticide metabolism, must be well understood. It makes sense to initiate this research in the best model insect system, Drosophila melanogaster, and translate these findings and methodologies to other insects. Here we explore the usefulness of the D. melanogaster model in studying metabolic-based insecticide resistances, target-site mediated resistances and identifying novel insecticide targets, whilst highlighting the importance of having a more complete understanding of insect biology for insecticide studies.