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1.
转基因生物与生物安全   总被引:7,自引:1,他引:6  
王加连 《生态学杂志》2006,25(3):314-317
20世纪70年代以来,以转基因技术为代表的现代生物技术在解决人类所面临的粮食短缺、环境污染等重大问题上发挥了巨大作用,并逐渐发展成为强大的现代生物技术产业。随着各类转基因生物的问世及其产品的不断上市,转基因生物的安全性问题已成为公众关心的焦点。本文分析了转基因生物可能对生物多样性、生态环境和人体健康等方面产生的负面影响,总结丁国内外有关转基因生物安全管理的现状,提出了加强转基因生物安全管理的策略。  相似文献   

2.
标记基因的产生方便了植物的转化,随着转基因植物的迅速发展及商品化,人类更关注抗性标记基因的安全性。目前解决的有效途径是发展正向选择系统,使用非抗性的生物安全标记基因,主要包括糖类代谢酶基因(pmi和xylA)、干扰氨基酸代谢酶基因(ak和dapA)、绿色荧光蛋白基因(gfp)、β-葡萄糖苷酸酶基因(gus)、核糖醇操纵子(rtl)和叶绿素生物合成基因(hemL)等。  相似文献   

3.
安全标记基因在转基因植物中的应用   总被引:5,自引:0,他引:5  
转基因植物的抗性标记一直是转基因生物安全性争论的焦点,是限制转基因植物应用的瓶颈之一。筛选安全标记基因替代抗生素标记基因已成为解决转基因植物安全性和促进转基因植物应用的重要策略。综述了生物安全标记基因的产生背景、系统分类、筛选原理及不同起源的标记基因在植物基因工程中的应用和存在问题。选用植物内源标记基因已成为转基因植物安全标记基因研究的重要方向。  相似文献   

4.
我国抗虫转基因杨树生态安全性研究进展   总被引:2,自引:0,他引:2  
转基因树木与农作物相比,人们更关注其长时间种植可能导致转基因扩散到周围野生近缘种.由于生长周期长,转基因树木会增加转基因不稳定性,对非靶标生物的影响,靶标害虫对转基因植物产生抗性,增加树木入侵性(杂草化),以及由于基因漂移或基因逃逸对环境产生的负面影响或新的环境风险.过去十几年,针对我国抗食叶害虫的两个商业化转Bt基测欧洲黑杨(Populus nigra)和转双抗虫基因741杨[B.alba×(P.davidiana+P.simonii)×p.tomentosa],已开展了有关生态安全性方面的多项研究.本文围绕抗虫转基因树木生态安全性研究进展进行了综述.抗虫转基因杨树对节肢动物种群和群落结构产生了一定影响,使昆虫的多样性提高,但对土壤微生物区系未见明显影响.转基因欧洲黑杨通过花粉和种子发生的基因漂移几率很低.转基因杨树通过内生菌发生的水平转移可能会对环境造成的潜在危险也进行了评价.文章最后指出对抗虫转基因杨树农林复合生态系统开展生物安全研究的必要性.  相似文献   

5.
卢宝荣  夏辉 《生命科学》2011,(2):186-194
转基因作物的商品化生产和大规模环境释放在带来巨大利益的同时,也引起了全球对其生物安全问题的广泛关注和争议,其中转基因通过花粉介导的基因漂移逃逸到非转基因作物及其野生近缘种,进而导致的潜在环境和生态风险就是备受争议的生物安全问题之一。转基因植物的环境生物安全涉及两方面关键问题:如何科学评价转基因植物商品化种植以后带来的环境和生态影响;如何利用环境生物安全的研究成果来制定科学有效的风险监测和管理措施。对转基因逃逸及其潜在生态风险的科学评价应包括三个重要环节:(1)检测转基因的逃逸的频率;(2)检测转基因逃逸后的表达和遗传规律;(3)确定逃逸后的转基因对野生近缘种群体适合度的影响及其进化潜力,本文将围绕对转基因逃逸及其潜在环境风险的科学评价,以转基因水稻为案例来对转基因逃逸带来生态影响的研究好评价的进展进行简要介绍,并对目前依据风险评价研究成果制定的各种管理策略进行了讨论。只有提高对转基因生物环境安全研究和评价的水平,并制定有效的风险监测和管理措施,才能为我国转基因技术的发展和转基因产品的商品化应用保驾护航。  相似文献   

6.
卡那霉素抗性(Kan^r)基因是转基因植物中广泛使用的一类标记基因,其生物安全性受到普遍关注,本文详细讲座了转基因植物中Kan^r基因的漂流及其对自然生态环境的影响,并对Kan^r基因及编码蛋白APH(3′)-Ⅱ的人畜食用安全性进行了综述分析。  相似文献   

7.
我国转基因水稻商品化应用的潜在环境生物安全问题   总被引:4,自引:1,他引:3  
转基因水稻的研发和商品化应用将为提高我国水稻的生产力提供新的机遇,并缓解我国的粮食安全问题.转基凶水稻的人规模环境释放和商品化生产可能会带来一定的环境生物安全问题,处理不好会影响转基因水稻的进一步研究和发展.通常所指的环境生物安全问题主要包括以下几个方面:(1)抗生物胁迫转基因对非靶标生物的影响及效应;(2)外源基因向非转基因作物和野生近缘种逃逸及其可能带来的生态后果;(3)转基因作物对农业生态系统、土壤微生物以及生物多样性的潜在影响;(4)抗生物胁迫转基因的长期使用导致靶标生物对转基因产生抗性等.为了安全有效和持续利用转基因生物技术及其产品,有必要对转基因水稻的环境生物安全性进行科学评价.基于风险评价的原则,本文对转基因水稻在我国商品化生产和大规模种植可能带来的环境生物安全问题进行了理性分析,希望为我国转基因水稻商品化应用的决策和生物安全评价提供科学依据.  相似文献   

8.
Plantibody——在转基因植物中生产的抗体关键词Plantibody转基因植物抗体抗体与抗原结合作用已广泛应用于生物学和医学领域,许多不能天然产生抗体的宿主生物(包括植物)正在发展用来生产抗体。植物现在能产生多种重组抗体(又称植物抗体),包括具...  相似文献   

9.
随着转基因动物在新品种培育、异种器官移植、生物反应器和疾病模型等方面的研究与发展,转基因动物的生物安全性引起了人们的广泛关注。目前,各国政府与机构已制定了相应的法律法规来规范转基因动物的研究与应用。文中介绍了转基因动物生物安全研究的内容、评价原则、评价政策与程序、上市或有望上市的转基因动物产品。最后,对转基因动物及其产品的研究与应用进行了展望。  相似文献   

10.
基因工程植物的安全性问题   总被引:9,自引:1,他引:8  
转基因植物的研究进展很迅速,但基因工程植物是否安全—直争论不休,主要表现在转基因食品的安全性及生态安全性问题上。转基因食品的安全性涉及这些食品的过敏性、毒性以及抗生素标记基因的安全性几个方面。转基因植物的生态安全性包括基因漂流、是否能诱发昆虫产生Bt抗性和对生物多样性的影响等。本文针对这些问题,对转基因植物潜在危害以及国际上现有的评价作简要综述。  相似文献   

11.
用绿色荧光蛋白监测转基因植物中选择标记基因的消除   总被引:1,自引:1,他引:0  
绿色荧光蛋白(GFP)可直接进行活体观察,它的这个优点可被用于监测转基因植物中选择标记基因的消除。为此,构建了植物表达载体pGNG,将绿色荧光蛋白基因(gfp)和卡那霉素抗性基因表达盒(NosP-nptll-NosT)一起克隆在两个同向的lox位点间,在第一个lox位点上游置有CaMV 35S启动子以驱动GFP表达,第二个lox位点下游置有不含启动子的大肠杆菌β-葡萄糖醛酸酶(GUS)基因。首先在含卡那霉素(Kan)的培养基上筛选出转pGNG的烟草,借助绿色荧光可容易地检出表达GFP的转化体。然后用另一转化载体pCambia1300Cre二次转化表达GFP的转基因植物,利用另一选择标记基因潮霉素抗性基因(hpt)进行筛选,在获得的再生植株中,Cre重组酶的表达消除了转化体中两lox位点间的gfpnptll。实验结果表明可借助GFP荧光的消失,快速选出nptII被消除的二次转化体,同时GUS(作为目的蛋白) 在CaMV 35S启动子驱动下获得表达。最后利用后代的分离将hptcre除去。  相似文献   

12.
13.
Public concerns about the issue of the environmental safety of genetically modified plants have led to a demand for technologies allowing the production of transgenic plants without selectable (antibiotic resistance) markers. We describe the development of an effective transformation system for generating such marker-free transgenic plants, without the need for repeated transformation or sexual crossing. This system combines an inducible site-specific recombinase for the precise elimination of undesired, introduced DNA sequences with a bifunctional selectable marker gene used for the initial positive selection of transgenic tissue and subsequent negative selection for fully marker-free plants. The described system can be generally applied to existing transformation protocols, and was tested in strawberry using a model vector in which site-specific recombination leads to a functional combination of a cauliflower mosaic virus 35S promoter and a GUS encoding sequence, thereby enabling the histochemical monitoring of recombination events. Fully marker-free transgenic strawberry plants were obtained following two different selection/regeneration strategies.  相似文献   

14.
一种新的用于删除选择标记基因的Cre/lox系统   总被引:11,自引:0,他引:11  
设计了一种新的诱导型Cre/lox系统,并在转基因烟草(NicotianatabacumL.)中进行了验证。在诱导剂的作用下,位于同向lox位点之间的选择标记基因(hpt)和重组酶基因(Cre)在烟草愈伤组织中被删除。在该系统中,Cre基因在玉米乙酰苯胺类化合物诱导启动子(In5-2)的控制下表达。对转基因后代的分子检测结果表明,不论是否加入了诱导剂,目的基因(gus)均被整合到烟草基因组中;在诱导剂处理的48株转基因烟草T0代中,45株的hpt基因被删除了。该系统只使用一个载体,克服了二次转化系统带来的问题。  相似文献   

15.
Yoo SY  Bomblies K  Yoo SK  Yang JW  Choi MS  Lee JS  Weigel D  Ahn JH 《Planta》2005,221(4):523-530
Positive selection of transgenic plants is essential during plant transformation. Thus, strong promoters are often used in selectable marker genes to ensure successful selection. Many plant transformation vectors, including pPZP family vectors, use the 35S promoter as a regulatory sequence for their selectable marker genes. We found that the 35S promoter used in a selectable marker gene affected the expression pattern of a transgene, possibly leading to a misinterpretation of the result obtained from transgenic plants. It is likely that the 35S enhancer sequence in the 35S promoter is responsible for the interference, as in the activation tagging screen. This affected expression mostly disappeared in transgenic plants generated using vectors without the 35S sequences within their T-DNA region. Therefore, we suggest that caution should be used in selecting a plant transformation vector and in the interpretation of the results obtained from transgenic approaches using vectors carrying the 35S promoter sequences within their T-DNA regions.  相似文献   

16.
Herzog K  Flachowsky H  Deising HB  Hanke MV 《Gene》2012,498(1):41-49
Production of marker-free genetically modified (GM) plants is one of the major challenges of molecular fruit breeding. Employing clean vector technologies, allowing the removal of undesired DNA sequences from GM plants, this goal can be achieved. The present study describes the establishment of a clean vector system in apple Malus×domestica Borkh., which is based on the use of the neomycin phosphotransferase II gene (nptII) as selectable marker gene and kanamycin/paramomycin as selective agent. The nptII gene can be removed after selection of GM shoots via site-specific excision mediated by heat-shock-inducible expression of the budding yeast FLP recombinase driven by the soybean Gmhsp17.5-E promoter. We created a monitoring vector containing the nptII and the flp gene as a box flanked by two direct repeats of the flp recognition target (FRT) sites. The FRT-flanked box separates the gusA reporter gene from the Cauliflower Mosaic Virus 35S (CaMV 35S) promoter. Consequently, GUS expression does only occur after elimination of the FRT-flanked box. Transformation experiments using the monitoring vector resulted in a total of nine transgenic lines. These lines were investigated for transgenicity by PCR, RT-PCR and Southern hybridization. Among different temperature regimes tested, exposure to 42 °C for 3.5 to 4h led to efficient induction of FLP-mediated recombination and removal of the nptII marker gene. A second round of shoot regeneration from leaf explants led to GM apple plants completely free of the nptII gene.  相似文献   

17.
在常用的植物组成型表达载体pBI121的选择标记基因NPTII两侧插入同向的lox位点并用多克隆位点(MCS)取代了GUS基因序列,构建了NPTII基因可被去除的和可插入目的基因的通用植物表达载体pBI121-lox-MCS。替换pBI121-lox-MCS中驱动目的基因表达的35S启动子,可构建成一系列具有其他表达特性的植物表达载体,如本文描述的韧皮部特异表达载体pBdENP-lox-MCS。为方便地筛选去除选择标记基因的转基因植物,还构建了绿色荧光蛋白(GFP)表达框与NPTII表达框连锁的pBI121-gfp-lox-MCS载体。上述植物表达载体可广泛应用于培育选择标记可去除的转基因植物。  相似文献   

18.
We present here a vector system to obtain homozygous marker-free transgenic plants without the need of extra handling and within the same time frame as compared to transformation methods in which the marker is not removed. By introducing a germline-specific auto-excision vector containing a cre recombinase gene under the control of a germline-specific promoter, transgenic plants become genetically programmed to lose the marker when its presence is no longer required (i.e. after the initial selection of primary transformants). Using promoters with different germline functionality, two modules of this genetic program were developed. In the first module, the promoter, placed upstream of the cre gene, confers CRE functionality in both the male and the female germline or in the common germline (e.g. floral meristem cells). In the second module, a promoter conferring single germline-specific CRE functionality was introduced upstream of the cre gene. Promoter sequences used in this work are derived from the APETALA1 and SOLO DANCERS genes from Arabidopsis (Arabidopsis thaliana) Columbia-0 conferring common germline and single germline functionality, respectively. Introduction of the genetic program did not reduce transformation efficiency. Marker-free homozygous progeny plants were efficiently obtained, regardless of which promoter was used. In addition, simplification of complex transgene loci was observed.  相似文献   

19.
The elimination of marker genes after selection is recommended for the commercial use of genetically modified plants. We compared the applicability of the two site-specific recombination systems Cre/lox and Flp/FRT for marker gene elimination in maize plants. The selection marker gene pat surrounded by two identically directed lox or FRT sites was introduced into maize. Sexual crossing with plants harboring the corresponding constitutively expressed recombinase led to the precise and complete excision of the lox-flanked marker gene in the F1 progeny, whereas Flp-mediated recombination of FRT sequences occurred rarely. Further examination of site-specific integration was done by biolistic bombardment of immature embryos harboring only one lox site with a lox.uidA sequence with results indicating directed integration.  相似文献   

20.
Luo K  Sun M  Deng W  Xu S 《Biotechnology letters》2008,30(7):1295-1302
To excise a selectable marker gene from transgenic plants, a new binary expression vector based on the 'genetically modified (GM)-gene-deletor' system was constructed. In this vector, the gene coding for FLP site-specific recombinase under the control of a heat shock-inducible promoter HSP18.2 from Arabidopsis thaliana and isopentenyltransferase gene (ipt), as a selectable marker gene under the control of the cauliflower mosaic virus 35S (CaMV 35S) promoter, were flanked by two loxP/FRT fusion sequences as recombination sites in direct orientation. Histochemical staining for GUS activity showed that, upon induction by heat shock, all exogenous DNA, including the selectable marker gene ipt, beta-glucuronidase (gusA) gene and the FLP recombinase gene, between two loxP/FRT sites was eliminated efficiently from primary transgenic tobacco plants. Molecular analysis further confirmed that excision of the marker gene (ipt) was heritable and stable. Our approach provides a reliable strategy for auto-excising a selectable marker gene from calli, shoots or other tissues of transgenic plants after transformation and producing marker-free transgenic plants.  相似文献   

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