慎重对待转基因作物

转基因作物是当今世界各国现代生物技术产业研究的热点。本文介绍了我国转基因作物研发和应用的现状,对转基因作物存在的潜在危害及其对人类可持续性发展的负面影响进行了分析,并对我国转基因作物的安全管理提出了几点建议。     

转基因作物研究

随着转基因作物的研究不断发展,转基因作物的种植面积逐年扩大。转基因作物具有传统农作物无法比拟的优越性,对人类未来生活产生重要影响,但转基因作物对环境和人类健康等方面可能存在风险。本文介绍了转基因作物在国内外研究现状,转基因作物的特点,转基因作物对人类健康和生态环境存在的潜在的危害性。     

昆虫对转Bt基因作物的抗性及对策

本文主要总结了近年来害虫对表达苏云金芽胞杆菌( Bacillus thuringiensis, Bt)杀虫毒素的转基因作物在实验室和自然田野环境下产生抗性的现状,及研究表明害虫产生抗性可能的机理,简单地讨论了昆虫抗性遗传机制对转基因作物持续性应用可能造成的影响和目前延缓昆虫产生抗性的策略.最后探讨了未来新的转基因技术的发展前景和延缓昆虫抗性策略的发展方向.     

转Bt基因抗虫作物对鳞翅目非靶标昆虫生态影响的研究进展

任何转基因作物在进入商业化应用之前都必须经过严格的环境风险评价。评价转基因作物特别是抗虫作物对农田重要非靶标节肢动物的生态影响是其中一项重要内容。当前,全球种植的转基因抗虫作物大多表达对鳞翅目害虫具有活性的Cry1或Cry2类杀虫蛋白。由于非靶标鳞翅目昆虫如斑蝶、家蚕等与靶标害虫具有较近的亲缘关系,其幼虫可能同样对这类杀虫蛋白敏感。因此,这类转基因抗虫作物对非靶标鳞翅目害虫的潜在影响引起了研究者的广泛关注。在总结国内外相关研究数据的基础上,系统分析了转基因抗虫作物对非靶标蝶类和蚕类昆虫的潜在影响,获得以下结论：虽然蚕类和蝶类昆虫对Cry1或Cry2类杀虫蛋白敏感,但在自然条件下这类非靶标昆虫暴露于Cry杀虫蛋白的水平很低,抗鳞翅目害虫转基因作物的种植不可能显著影响田间蝶类昆虫的种群密度,也不会给我国的蚕丝产业带来负面影响。     

转基因作物潜在风险分析

转基因作物及其产品的发展非常快,它给人类带来巨大利益的同时,也可能产生一系列风险,着重分析转基因作物对生态环境和对人类健康两方面可能产生的潜在影响及其表现。     

转基因的逃逸及生态风险

转基因技术的发展为提高农作物产量和解决全球人口不断增长而引发的粮食问题带来了无限的机遇,但生物技术的应用和转基因作物的环境释放也带来了一系列生物安全问题．转基因产品是否会对植物、动物、人类健康、遗传资源和环境带来危害已成为公众关注的焦点．诸多生物安全问题中最引人注目的问题之一就是转基因的逃逸及其可能导致的生态风险．文中就转基因逃逸的可能性和逃逸的不同途径、转基因逃逸后可能导致的各种生态风险、转基因逃逸的不同控制方法以及转基因作物安全距离设立应该考虑的因素等问题进行了讨论,旨在了解转基因作物的环境释放和外源基因的逃逸可能导致的生物安全问题,以及如何控制和避免转基因逃逸．     

转基因低水平混杂问题——政策与内涵

转基因技术近年来在世界范围内快速发展,但由于不同国家在转基因审批上的不同步,以及各国设立严格的转基因低水平混杂阈值,导致正常的农产品贸易由于无意混入少量转基因成分而发生贸易摩擦,甚至导致贸易中断.从转基因低水平混杂(LLP)的含义出发分析其特殊性,分析了世界主要国家的LLP政策以及严格的LLP政策对贸易产生的负面影响.根据研究结果指出:在当前转基因作物采用率不断提高,以及转基因新品种研发加速背景下,转基因低水平混杂在技术上是不可避免的.因此,有必要在全球范围内建立转基因安全互信机制,各国需要尽量减少审批不同步时滞,设置合理的转基因低水平阈值,降低对正常贸易的负面影响.研究结果对中国转基因LLP政策和有关标准制定有一定借鉴意义.     

转基因作物与非转基因作物的共存立法动态研究——以美、日、欧应对基因污染事件为视角

随着基因工程技术的运用与发展,越来越多的转基因作物基因污染事件的发生也引起了世界各国对转基因作物与非转基因作物之间的和谐发展问题的高度重视。以美、日、欧为代表,世界各国对转基因作物与非转基因作物的共存问题都进行了积极地探索。借鉴美、日、欧转基因与非转基因作物共存法律制度,以期为我国转基因与非转基因作物共存法律制度的构建提供参考。     

复合性状转基因植物安全性评价的研究进展

随着转基因技术的不断发展,转基因作物实现了产业化。目前,单性状的转基因作物无法满足农业发展的需求,而复合性状转基因作物拓宽了转基因作物的功能,提高了资源的利用率,满足了农民多元化需求,具有广阔的应用前景,是转基因植物发展的新方向。由于转基因技术有一定的风险,因此对转基因作物的安全性监管较为重要,对于复合性状转基因作物,不同国家的安全性评价制度却不尽相同。综述了不同国家对复合性状转基因作物的安全性评价体制,旨为我国复合性状作物提供监管依据。     

转Bt基因植物对蜜蜂的安全性研究进展

蜜蜂是农业生态系统中重要的传粉昆虫,也是重要的经济昆虫.其可通过取食抗虫转基因作物花粉而摄取到外源转基因杀虫蛋白.因此,蜜蜂通常作为重要的指示物种用于转基因抗虫作物的环境安全评价工作中.本文在总结国内外相关研究数据的基础上,系统分析了抗虫转基因作物的种植对蜜蜂的安全性,获得以下结论:Bt杀虫蛋白具有较强的杀虫专一性,当前商业化应用的Bt杀虫蛋白对蜜蜂没有直接毒性,因此,转Bt基因作物的种植不会对蜜蜂种群及其发挥的重要生态功能产生显著的负面影响.而早期曾用于植物转基因的蛋白酶抑制剂和植物凝集素对蜜蜂的生长发育及行为具有显著的不利影响,因此,表达这类杀虫蛋白的转基因作物应该不会进入商业化应用.     

Expansion of the silkworm GMC oxidoreductase genes is associated with immunity

The glucose-methanol-choline (GMC) oxidoreductases constitute a large gene family in insects. Some of these enzymes play roles in developmental or physiological process, such as ecdysteroid metabolism. However, little is known about the functional diversity of the insect GMC family. Here, we identified 43 GMC genes in the silkworm genome, the largest number of GMC genes among all the insect genomes sequenced to date. Similar to the other insects, there is a highly conserved GMC cluster within the second intron of the silkworm flotillin-2 (flo-2) gene. However, the silkworm GMC genes outside of the conserved GMC cluster have experienced a large expansion. Phylogenetic analysis suggested that the silkworm GMCβ subfamily contained 22 copies and made a major contribution to expansion of the silkworm GMC genes. Eighteen of the 22 members of the silkworm GMCβ subfamily are located outside of the conserved GMC cluster, and are known as silkworm expansion genes (SEs). Relative-rate tests showed that SEs evolved significantly faster than the GMCβ genes inside the conserved GMC cluster. Accordingly, the third position GC content (GC3s) and codon bias of SEs are significantly different from those of the GMCβ genes in the conserved GMC cluster. The elevated evolutionary rate of the silkworm GMCβ genes outside of the conserved GMC cluster may reflect the evolution of function diversity. At least 24 of the 43 silkworm GMC genes were differently transcribed and expressed in a tissue- or stage-specific manner during the larval stage. Strikingly, microarray data revealed that four different pathogens upregulated most of the silkworm GMCβ genes. Furthermore, RNA interference of representative upregulated GMCβ genes reduced the survival rate of the silkworm when infected by pathogens. Taken together, the results suggested that expansion of the silkworm GMC oxidoreductase genes is associated with immunity.     

GAP43, MARCKS, and CAP23 modulate PI(4,5)P(2) at plasmalemmal rafts, and regulate cell cortex actin dynamics through a common mechanism

The dynamic properties of the cell cortex and its actin cytoskeleton determine important aspects of cell behavior and are a major target of cell regulation. GAP43, myristoylated alanine-rich C kinase substrate (MARCKS), and CAP23 (GMC) are locally abundant, plasmalemma-associated PKC substrates that affect actin cytoskeleton. Their expression correlates with morphogenic processes and cell motility, but their role in cortex regulation has been difficult to define mechanistically. We now show that the three proteins accumulate at rafts, where they codistribute with PI(4,5)P(2), and promote its retention and clustering. Binding and modulation of PI(4, 5)P(2) depended on the basic effector domain (ED) of these proteins, and constructs lacking the ED functioned as dominant inhibitors of plasmalemmal PI(4,5)P(2) modulation. In the neuron-like cell line, PC12, NGF- and substrate-induced peripheral actin structures, and neurite outgrowth were greatly augmented by any of the three proteins, and suppressed by DeltaED mutants. Agents that globally mask PI(4,5)P(2) mimicked the effects of GMC on peripheral actin recruitment and cell spreading, but interfered with polarization and process formation. Dominant negative GAP43(DeltaED) also interfered with peripheral nerve regeneration, stimulus-induced nerve sprouting and control of anatomical plasticity at the neuromuscular junction of transgenic mice. These results suggest that GMC are functionally and mechanistically related PI(4,5)P(2) modulating proteins, upstream of actin and cell cortex dynamics regulation.     

Arctigenin protects against neuronal hearing loss by promoting neural stem cell survival and differentiation

Neuronal hearing loss has become a prevalent health problem. This study focused on the function of arctigenin (ARC) in promoting survival and neuronal differentiation of mouse cochlear neural stem cells (NSCs), and its protection against gentamicin (GMC) induced neuronal hearing loss. Mouse cochlea was used to isolate NSCs, which were subsequently cultured in vitro. The effects of ARC on NSC survival, neurosphere formation, differentiation of NSCs, neurite outgrowth, and neural excitability in neuronal network in vitro were examined. Mechanotransduction ability demonstrated by intact cochlea, auditory brainstem response (ABR), and distortion product optoacoustic emissions (DPOAE) amplitude in mice were measured to evaluate effects of ARC on GMC‐induced neuronal hearing loss. ARC increased survival, neurosphere formation, neuron differentiation of NSCs in mouse cochlear in vitro. ARC also promoted the outgrowth of neurites, as well as neural excitability of the NSC‐differentiated neuron culture. Additionally, ARC rescued mechanotransduction capacity, restored the threshold shifts of ABR and DPOAE in our GMC ototoxicity murine model. This study supports the potential therapeutic role of ARC in promoting both NSCs proliferation and differentiation in vitro to functional neurons, thus supporting its protective function in the therapeutic treatment of neuropathic hearing loss in vivo.     

Cytokine regulation of localized inflammation. Induction of activated B cells and IL-6-mediated polyclonal IgG and IgA synthesis in inflamed human gingiva

It is well established that increased numbers of plasma cells occur in the localized tissues of chronic inflammatory diseases such as adult periodontitis, and enzymatic isolation has shown that most B lineage cells produce IgG-subclass with some IgA-subclass responses. It would be of importance to determine if excess production of cytokines in the localized lesion account for these responses and in the present study we have assessed gingival mononuclear cell (GMC) supernatants for cytokines that activate B cells including IL-6R expression and for levels of IL-6 present. Inasmuch as limited numbers (approximately 1 to 3 x 10(6) cells) of GMC were obtained from surgically removed tissues (approximately 400 mg), we have focused on the analysis of IL-6 production by GMC in this study. Further, initial evidence of additional cytokines that are produced by GMC and induce expression of IL-6R on resting B cells has been obtained. The GMC and PBMC from individual patients were cultured in the presence (or absence) of Con A. Higher levels of IL-6 were produced spontaneously by GMC when compared with Con A-stimulated PBMC. When PBMC cultures were supplemented with GMC supernatants obtained from the same patient, high numbers of spot-forming cells (SFC), mainly of IgG followed by IgA isotype, were seen. The induction of SFC by GMC supernatants was inhibited by incubation with a goat anti-human IL-6 antibody. When the effect of GMC supernatants on subclasses of PBMC SFC was determined, the response was IgG1 greater than IgG2 greater than IgG3 = IgG4 and IgA1 greater than IgA2, a pattern remarkably similar to the distribution of plasma cells in the GMC itself. To assess for cytokines in GMC supernatants that mediated B cell activation, supernatants containing anti-IL-6 were cultured with PBMC or purified B cells for 72 h. This treatment induced small proliferative B cell responses and elevated expression of IL-6R on B cells, but did not induce SFC responses. Further, incubation of B cells with GMC supernatants induced resting B cells (G0/G1) to enter the cell cycle (S and G2/M). Addition of human rIL-6 to these cultures on day 3 restored IgG- and IgA-subclass SFC responses by day 7. Cytokine-induced IL-6R expression also occurred in vivo because freshly isolated GMC expressed high levels of this receptor.(ABSTRACT TRUNCATED AT 400 WORDS)     

FTY720 induces cell cycle arrest and apoptosis of rat glomerular mesangial cells

The present study aimed to examine the effect of FTY720, a new immunosuppressive agent, on the proliferation and apoptosis of glomerular mesangial cells (GMC), and investigate the underlying mechanisms. Cultured rat GMC were treated by FTY720, and the cell viability, apoptosis and cell cycle progression were examined. Furthermore, cell cycle related gene expression profile was analyzed by cDNA microarray, and the protein expression of cell cycle related genes as well as Bax and Bcl-2 were examined by Western blot. The results showed that FTY720 inhibited GMC proliferation and induced apoptosis of GMC in a dose- and time-dependent manner, and induced G(1) phase cell cycle arrest in GMC in a dose-dependent manner as well. cDNA microarray analysis revealed that FTY720 regulated the expression of cell cycle-related gene. Western blot analysis showed that FTY720 induced the downregulation of cyclin D1, cyclin E, CDK2, CDK4, Bcl-2 and E2F1 and the upregulation of Kip1/p27, Cip1/p21, Bax and Rb in GMC in a dose-dependent manner. These results demonstrated that FTY720 could inhibit the proliferation of GMC through inducing cell cycle arrest and apoptosis, probably via the regulation of the expression of cell cycle-related genes and Bax/Bcl-2.     

Pyranose oxidase identified as a member of the GMC oxidoreductase family

Fungal pyranose oxidase is a flavoenzyme whose preferred substrate among several monosaccharides is D-glucose. After a comprehensive analysis of conserved features in a structure-based multiple sequence alignment of homologous proteins, we could classify this enzyme into the GMC oxidoreductase family. The identified homology also suggests a three-dimensional protein structure similar to the functionally related glucose oxidase.     

Sublytic C5b-9 complexes induce apoptosis of glomerular mesangial cells in rats with Thy-1 nephritis through role of interferon regulatory factor-1-dependent caspase 8 activation

The apoptosis of glomerular mesangial cells (GMC) in rat Thy-1 nephritis (Thy-1N), a model of human mesangioproliferative glomerulonephritis, is accompanied by sublytic C5b-9 deposition, but the mechanism of sublytic C5b-9-mediated GMC apoptosis has not been elucidated. In the present study, the gene expression profiles both in the GMC stimulated by sublytic C5b-9 and the rat renal tissue of Thy-1N were detected using microarrays. Among the co-up-regulated genes, the up-regulation of interferon regulatory factor-1 (IRF-1) was further confirmed. Increased caspase 8 and caspase 3 expression and caspase 8 promoter activity in the GMC were also identified. Meanwhile, overexpression or knockdown of IRF-1 not only enhanced or inhibited GMC apoptosis and caspase 8 and 3 induction but also increased or decreased caspase 8 promoter activity, respectively. The element of IRF-1 binding to the caspase 8 promoter was first revealed. Furthermore, silencing IRF-1 or repressing the activation of caspases 8 and 3 significantly reduced GMC apoptosis, including other pathologic changes of Thy-1N. These novel findings indicate that GMC apoptosis of Thy-1N is associated with the IRF-1-activated caspase 8 pathway.