Academic literature on the topic 'ADN viral – Synthèse'

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Journal articles on the topic "ADN viral – Synthèse"

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McIntosh, E. M., and R. H. Haynes. "dUTP pyrophosphatase as a potential target for chemotherapeutic drug development." Acta Biochimica Polonica 44, no. 2 (1997): 159–71. http://dx.doi.org/10.18388/abp.1997_4410.

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Aberrant dUTP metabolism plays a critical role in the molecular mechanism of cell killing induced by inhibitors of dihydrofolate reductase and thymidylate synthase. While considerable effort has been directed towards discovering new, more potent inhibitors of these two enzymes, little attention has been given dUTP pyrophosphatase (dUTPase)--the key modulator of cellular dUTP levels--as a potential target for chemotherapeutic drug development. Recent studies have provided evidence that dUTPase is vital for cellular and, in some cases, viral DNA replication. Furthermore, some retroviruses encode dUTPases--a fact which suggests that cellular dUTP metabolism may be more important than previously realized. Here, we briefly review current knowledge of cellular and viral dUTPases and discuss the potential of these enzymes as targets for cancer chemotherapeutic and anti-viral drug development.
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Duschene, Kaitlin S., and Joan B. Broderick. "Viperin: a radical response to viral infection." BioMolecular Concepts 3, no. 3 (2012): 255–66. http://dx.doi.org/10.1515/bmc-2011-0057.

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AbstractOne of the first lines of defense of the host immune response to infection is upregulation of interferons, which play a vital role in triggering the early nonspecific antiviral state of the host. Interferons prompt the generation of numerous downstream products, known as interferon-stimulated genes (ISGs). One such ISG found to be either directly induced by type I, II, and III interferons or indirectly through viral infection is the ‘virus inhibitory protein, endoplasmic reticulum-associated, interferon-inducible’ protein, or viperin. Not only is viperin capable of combating a wide array of viral infections but its upregulation is also observed in the presence of endotoxins, various bacterial infections, or even in response to other immune stimuli, such as atherosclerotic lesions. Recent advances in the understanding of possible mechanisms of action of viperin involve, but are perhaps not limited to, interaction with farnesyl pyrophosphate synthase and disruption of lipid raft domains to prevent viral bud release, inhibition of hepatitis C virus secretory proteins, and coordination to lipid droplets and inhibition of viral replication. Unexpectedly, new insight into the human cytomegalovirus induction of this antiviral protein demonstrates that mitochondrial viperin plays a necessary and beneficial role for viral propagation.
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Briolay, Anne, Jamel Bouzenzana, Michel Guichardant, et al. "Cell Wall Polysaccharide Synthases Are Located in Detergent-Resistant Membrane Microdomains in Oomycetes." Applied and Environmental Microbiology 75, no. 7 (2009): 1938–49. http://dx.doi.org/10.1128/aem.02728-08.

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ABSTRACT The pathways responsible for cell wall polysaccharide biosynthesis are vital in eukaryotic microorganisms. The corresponding synthases are potential targets of inhibitors such as fungicides. Despite their fundamental and economical importance, most polysaccharide synthases are not well characterized, and their molecular mechanisms are poorly understood. With the example of Saprolegnia monoica as a model organism, we show that chitin and (1→3)-β-d-glucan synthases are located in detergent-resistant membrane microdomains (DRMs) in oomycetes, a phylum that comprises some of the most devastating microorganisms in the agriculture and aquaculture industries. Interestingly, no cellulose synthase activity was detected in the DRMs. The purified DRMs exhibited similar biochemical features as lipid rafts from animal, plant, and yeast cells, although they contained some species-specific lipids. This report sheds light on the lipid environment of the (1→3)-β-d-glucan and chitin synthases, as well as on the sterol biosynthetic pathways in oomycetes. The results presented here are consistent with a function of lipid rafts in cell polarization and as platforms for sorting specific sets of proteins targeted to the plasma membrane, such as carbohydrate synthases. The involvement of DRMs in the biosynthesis of major cell wall polysaccharides in eukaryotic microorganisms suggests a function of lipid rafts in hyphal morphogenesis and tip growth.
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Glück, Brigitte, Ingrid Merkle, Gesche Dornberger, and Axel Stelzner. "Expression of Inducible Nitric Oxide Synthase in Experimental Viral Myocarditis." Herz 25, no. 3 (2000): 255–60. http://dx.doi.org/10.1007/s000590050016.

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Lidbury, Brett A., and Surendran Mahalingam. "Specific Ablation of Antiviral Gene Expression in Macrophages by Antibody-Dependent Enhancement of Ross River Virus Infection." Journal of Virology 74, no. 18 (2000): 8376–81. http://dx.doi.org/10.1128/jvi.74.18.8376-8381.2000.

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ABSTRACT Ross River virus (RRV) is an indigenous Australian arthropod-borne alphavirus responsible for epidemic polyarthritis (EPA), myalgia, and lethargy in humans. Macrophages and monocytes have been associated with human RRV disease, and previous studies have shown that RRV is capable of infecting macrophages via both a natural virus receptor and by Fc receptor-mediated antibody-dependent enhancement (ADE). Similar to other viruses, such as human immunodeficiency virus and dengue virus, ADE infection results in dramatic RRV growth increases for in vitro macrophage cultures. This study demonstrates that RRV could resist lipopolysaccharide (LPS)-induced antiviral activity in macrophage cultures when infection was via the ADE pathway. Investigation of this infection pathway found that RRV was able to suppress the transcription and translation of key antiviral genes (tumor necrosis factor and inducible nitric oxide synthase) in LPS-stimulated macrophages by disrupting the transcription into mRNA of the genes coding for the associated transcription factors IRF-1 and NF-κB. The transcription of non-antiviral control genes was not perturbed by RRV-ADE infection, and de novo protein synthesis also was not significantly affected in RRV-ADE infected cells. The ADE pathway of infection allowed RRV to specifically target antiviral genes in macrophages, resulting in unrestricted virus replication. As ADE has been observed for several virus families and associated with disease and adverse vaccination outcomes, these findings may have broad relevance to viral disease formation and antiviral vaccination strategies.
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Date, Taro, Seibu Mochizuki, Adam J. Belanger та ін. "Expression of constitutively stable hybrid hypoxia-inducible factor-1α protects cultured rat cardiomyocytes against simulated ischemia-reperfusion injury". American Journal of Physiology-Cell Physiology 288, № 2 (2005): C314—C320. http://dx.doi.org/10.1152/ajpcell.00374.2004.

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Preconditioning in cultured cardiomyocytes elevates the expression of several protective genes including Glut-4 and heat shock protein (HSP)70. Hypoxia-inducible factor-1 (HIF-1) is known to mediate the transcriptional activation of hypoxia-responsive genes. In this study, we examined the effect of adenovirus-mediated expression of constitutively stable hybrid forms of HIF-1α on cardiomyocyte viability and gene expression. Cultured neonatal rat cardiomyocytes were subjected to simulated ischemia-reperfusion with or without preinfection with recombinant adenoviral vectors [Ad2/HIF-1α/herpes simplex virus protein VP16 and Ad2/HIF-1α/nuclear factor-κB (NF-κB)]. Cellular viability and mRNA levels of several cardioprotective genes were measured. We demonstrated that infection with Ad2/HIF-1α/VP16 and Ad2/HIF-1α/NF-κB mimicked the upregulation of the mRNA levels of vascular endothelial growth factor (VEGF), Glut-1, Glut-4, HSP70, and inducible NO synthase (iNOS) and the protection of cultured neonatal rat cardiomyocytes by late-phase preconditioning against simulated ischemia-reperfusion. The same dose of a control viral vector expressing no transgene had no effect. Preconditioning also elevated HIF-1α protein levels. These results suggest that adenovirus-mediated expression of HIF-1α/VP16 or HIF-1α/NF-κB, a constitutively stable hybrid transcriptional factor, protected cultured neonatal cardiomyocytes against simulated ischemia-reperfusion injury by inducing multiple protective genes.
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Malisan, Florence, Luigi Franchi, Barbara Tomassini, et al. "Acetylation Suppresses the Proapoptotic Activity of GD3 Ganglioside." Journal of Experimental Medicine 196, no. 12 (2002): 1535–41. http://dx.doi.org/10.1084/jem.20020960.

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GD3 synthase is rapidly activated in different cell types after specific apoptotic stimuli. De novo synthesized GD3 accumulates and contributes to the apoptotic program by relocating to mitochondrial membranes and inducing the release of apoptogenic factors. We found that sialic acid acetylation suppresses the proapoptotic activity of GD3. In fact, unlike GD3, 9-O-acetyl-GD3 is completely ineffective in inducing cytochrome c release and caspase-9 activation on isolated mitochondria and fails to induce the collapse of mitochondrial transmembrane potential and cellular apoptosis. Moreover, cells which are resistant to the overexpression of the GD3 synthase, actively convert de novo synthesized GD3 to 9-O-acetyl-GD3. The coexpression of GD3 synthase with a viral 9-O-acetyl esterase, which prevents 9-O-acetyl-GD3 accumulation, reconstitutes GD3 responsiveness and apoptosis. Finally, the expression of the 9-O-acetyl esterase is sufficient to induce apoptosis of glioblastomas which express high levels of 9-O-acetyl-GD3. Thus, sialic acid acetylation critically controls the proapoptotic activity of GD3.
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Karupiah, Gunasegaran, Jian-He Chen, Surendran Mahalingam, Carl F. Nathan та John D. MacMicking. "Rapid Interferon γ–dependent Clearance of Influenza A Virus and Protection from Consolidating Pneumonitis in Nitric Oxide Synthase 2–deficient Mice". Journal of Experimental Medicine 188, № 8 (1998): 1541–46. http://dx.doi.org/10.1084/jem.188.8.1541.

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Viral infection often activates the interferon (IFN)-γ–inducible gene, nitric oxide synthase 2 (NOS2). Expression of NOS2 can limit viral growth but may also suppress the immune system and damage tissue. This study assessed each of these effects in genetically deficient NOS2−/− mice after infection with influenza A, a virus against which IFN-γ has no known activity. At inocula sufficient to cause consolidating pneumonitis and death in wild-type control mice, NOS2−/− hosts survived with little histopathologic evidence of pneumonitis. Moreover, they cleared influenza A virus from their lungs by an IFN-γ–dependent mechanism that was not evident in wild-type mice. Even when the IFN-γ–mediated antiviral activity was blocked in NOS2−/− mice with anti–IFN-γ mAb, such mice failed to succumb to disease. Further evidence that this protection was independent of viral load was provided by treating NOS2+/+ mice with the NOS inhibitor, Nω-methyl-l-arginine (l-NMA). l-NMA prevented mortality without affecting viral growth. Thus, host NOS2 seems to contribute more significantly to the development of influenza pneumonitis in mice than the cytopathic effects of viral replication. Although NOS2 mediates some antiviral effects of IFN-γ, during influenza infection it can suppress another IFN-γ–dependent antiviral mechanism. This mechanism was observed only in the complete absence of NOS2 activity and appeared sufficient to control influenza A virus growth in the absence of changes in cytotoxic T lymphocyte activity.
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Komatsu, Takashi, Zhengbiao Bi та Carol S. Reiss. "Interferon-γ induced type I nitric oxide synthase activity inhibits viral replication in neurons". Journal of Neuroimmunology 68, № 1-2 (1996): 101–8. http://dx.doi.org/10.1016/0165-5728(96)00083-5.

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Arvizu-Flores, Aldo A., Emmanuel Aispuro-Hernandez, Karina D. Garcia-Orozco, et al. "Functional identity of the active sites of crustacean and viral thymidylate synthases." Comparative Biochemistry and Physiology Part C: Toxicology & Pharmacology 150, no. 3 (2009): 406–13. http://dx.doi.org/10.1016/j.cbpc.2009.06.008.

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Dissertations / Theses on the topic "ADN viral – Synthèse"

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Bataille, Dominique. "Analyses de la structure des intermédiaires de la réplication de l'ADN du virus Herpes simplex de type 1." Lyon 1, 1997. http://www.theses.fr/1997LYO10146.

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Le theme de cette these est l'etude des intermediaires de la replication du virus herpes simplex de type 1 (hsv-1), dans le but de mieux caracteriser le mecanisme par lequel ce virus synthetise son adn. Lors de l'initiation de ce travail, il etait admis que hsv-1 repliquait son adn selon le modele du cercle roulant, generant de longs concatemeres lineaires. Cependant, ce modele n'avait pas ete demontre directement en raison de la grande taille du genome hsv-1. La technique d'electrophorese en champs pulses m'a permis de separer l'adn des unites genomiques de celui constituant les intermediaires de replication, afin d'analyser ces derniers. Les resultats obtenus confirment que les structures replicatives sont sous forme de concatemeres. Cependant des inversions de composantes l adjacentes sont retrouvees en proportion equimolaire au sein des concatemeres. L'etude de souches hsv-1 mutantes montre que ces inversions se produisent tot dans le cycle viral et sont responsables du phenomene d'isomerisation genomique. De plus, les analyses en pfge revelent que la majeure partie des intermediaires de replication se trouve sous la forme d'une structure complexe, non lineaire, probablement constituee d'adn branche. L'ensemble de ces observations concernant la structure des intermediaires de replication ne peut etre explique par le mecanisme du cercle roulant classique, qui doit donc etre revu, et implique probablement que des phenomenes de recombinaison soient constitutivement lies a la synthese de l'adn viral. Le role dans le cycle viral des topoisomerases de type i et ii cellulaires a aussi ete evalue. Ces enzymes apparaissent necessaires a la production de particules infectieuses, probablement en intervenant sur differentes etapes de la maturation de l'adn. Cependant, aucune d'entre elles ne semble strictement requise ni pour la formation des inversions genomiques, ni pour la resolution des structures complexes.
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Book chapters on the topic "ADN viral – Synthèse"

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Samano, Ninos, and Domingos Souza. "No-touch saphenous vein grafts in coronary artery bypass surgery." In State of the Art Surgical Coronary Revascularization, edited by Tristan D. Yan, Ki-Bong Kim, Paul G. Bannon, and Mario Gaudino. Oxford University Press, 2021. http://dx.doi.org/10.1093/med/9780198758785.003.0041.

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After almost 30 years since the first harvesting of the saphenous vein graft with a pedicle of surrounding tissue (no-touch technique), there is no doubt that this method is superior to the conventional technique in which a denuded vein is harvested. In summary, the no-touch harvesting technique decreases risk of graft spasm and the requirement for manual dilatation, limiting endothelial cell loss and long-term damage. The preservation of the vasa vasorum allows retrograde blood flow from the graft lumen, thereby decreasing transmural ischaemic damage. This also preserves endothelial nitric oxide synthase, known to decrease intimal hyperplasia, atherosclerosis, and long-term graft failure. Furthermore, the perivascular tissue acts as a natural external stent reducing the neointimal and medial thickening of the vein graft and preventing it from kinking, which is especially vital for sequential grafts. Finally, target vessel size, quality, and degree of stenosis have little effect on the patency rates of no-touch saphenous vein grafts, in contrast to arterial grafts.
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Bradley, Richard, Colin Haselgrove, Marc Vander Linden, and Leo Webley. "The Research in Retrospect." In The Later Prehistory of North-West Europe. Oxford University Press, 2015. http://dx.doi.org/10.1093/oso/9780199659777.003.0013.

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In some respects this project was the successor to the research published in 2007 as The Prehistory of Britain and Ireland, but there are significant contrasts between the books. The results of development-led archaeology have played a central role in both, but they have influenced their contents in different ways. When the earlier book was published it was among the first to draw extensively on fieldwork undertaken as part of the planning process. To some extent the course of that research was unpredictable, for it was not clear how far the results of the new excavations and surveys would diverge from what was already known. All that was certain from the outset was that a large amount of new information had been collected and that very little of it had entered the public domain. There was a disparity between the conventional archaeological literature—journal articles, monographs, and regional syntheses—and the great majority of reports, which were prepared for planning authorities and commercial clients. Those documents were difficult to trace and sometimes difficult to access. What the project showed was that such sources were vital to any understanding of the past. It also demonstrated that at least some of the orthodoxies on which public policy depended were inconsistent with the results of work that had already taken place. The same problem affected teaching and research, for they rarely took account of the new sources of information. In retrospect, the earlier project may have influenced later research in a way that had not been foreseen. It did not, and could not, offer a completely new version of British and Irish prehistory, as it was written at a time when many excavations were still in progress—the fieldwork associated with road-building in Ireland is a good example. In any case the dissemination of information in the archaeology of these islands was so inefficient that particularly in England it was difficult to find out what had been done. Tracing the results was an even harder task, and it was not completely successful.
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Morrow, Gary W. "Organic Synthesis in the Laboratory." In Bioorganic Synthesis. Oxford University Press, 2016. http://dx.doi.org/10.1093/oso/9780199860531.003.0011.

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The German chemist Friedrich Wöhler is generally credited with the first laboratory synthesis of a known organic compound (urea) from inorganic materials. He accomplished this by the simple heating of an inorganic salt, ammonium cyanate (NH4OCN). “I must tell you,” he wrote to his mentor Jöns Jakob Berzelius in 1828, “that I can prepare urea without requiring a kidney of an animal, either man or dog.” While this report may seem relatively minor given the structural simplicity of urea, its impact was revolutionary. For the first time, the preparation and isolation of an organic compound had been achieved in the absence of the elemental “vital force” of living systems previously believed to be required for the construction of all such compounds. This milestone of 19th century organic chemistry was later followed by many others, including Kolbe’s synthesis of acetic acid in 1847 and Fischer’s synthesis of glucose in 1890. With the support of evolving methods for compound separation, purification, and spectroscopic analysis, rapid advances in the sophistication of organic synthesis followed throughout the 20th century, developing in tandem with an ever-deepening understanding of the underlying organic processes associated with living systems. While it is certainly true that syntheses of many structurally complex unnatural compounds of theoretical interest are also among the most remarkable achievements in synthetic strategy, tactical execution, and perseverance, the realm of natural products remains the dominant source for the most challenging and potentially beneficial targets available for such synthetic efforts. Figure 8.1 shows a small selection of some natural (and unnatural) products which have been produced via synthesis over the years, from Wöhler’s time to the present. Note the increasing levels of structural sophistication and stereochemical complexity that have eventually been mastered by practitioners of organic synthesis. In our own time, the traditional boundaries between organic and biological chemistry are disappearing in ways that are likely to transform the design and synthesis of organic molecules, from the construction of synthetic biologicals designed to act as biomarkers, biosensors, or drug delivery agents, to the development of molecular motors, self-replicating macromolecular systems, and even synthetic life forms.
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