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961.
962.
Sophie Casteret Najat Chbab Jeanne Cambefort Corinne Augé-Gouillou Yves Bigot Florence Rouleux-Bonnin 《Molecular genetics and genomics : MGG》2009,282(5):531-546
Previous studies have shown that the transposase and the inverted terminal repeat (ITR) of the Mos1
mariner elements are suboptimal for transposition; and that hyperactive transposases and transposon with more efficient ITR configurations
can be obtained by rational molecular engineering. In an attempt to determine the extent to which this element is suboptimal
for transposition, we investigate here the impact of the three main DNA components on its transposition efficiency in bacteria
and in vitro. We found that combinations of natural and synthetic ITRs obtained by systematic evolution of ligands by exponential
enrichment did increase the transposition rate. We observed that when untranslated terminal regions were associated with their
respective natural ITRs, they acted as transposition enhancers, probably via the early transposition steps. Finally, we demonstrated
that the integrity of the Mos1 inner region was essential for transposition. These findings allowed us to propose prototypes of optimized Mos1 vectors, and to define the best sequence features of their associated marker cassettes. These vector prototypes were assayed
in HeLa cells, in which Mos1 vectors had so far been found to be inactive. The results obtained revealed that using these prototypes does not circumvent
this problem. However, such vectors can be expected to provide new tools for the use in genome engineering in systems such
as Caenorhabditis elegans in which Mos1 is very active. 相似文献
963.
Aurélia Boulaflous Claude Saint-Jore-Dupas Marie-Carmen Herranz-Gordo Sophie Pagny-Salehabadi Carole Plasson Frédéric Garidou Marie-Christine Kiefer-Meyer Christophe Ritzenthaler Lo?c Faye Véronique Gomord 《BMC plant biology》2009,9(1):144
Background
In eukaryotic cells, the membrane compartments that constitute the exocytic pathway are traversed by a constant flow of lipids and proteins. This is particularly true for the endoplasmic reticulum (ER), the main "gateway of the secretory pathway", where biosynthesis of sterols, lipids, membrane-bound and soluble proteins, and glycoproteins occurs. Maintenance of the resident proteins in this compartment implies they have to be distinguished from the secretory cargo. To this end, they must possess specific ER localization determinants to prevent their exit from the ER, and/or to interact with receptors responsible for their retrieval from the Golgi apparatus. Very few information is available about the signal(s) involved in the retention of membrane type II protein in the ER but it is generally accepted that sorting of ER type II cargo membrane proteins depends on motifs mainly located in their cytosolic tails. 相似文献964.
Frank Delvigne Mathieu Boxus Sophie Ingels Philippe Thonart 《Microbial cell factories》2009,8(1):15-17
Background
Extensive studies have shown that up-scaling of bioprocesses has a significant impact on the physiology of the microorganisms. Among the factors associated with the fluid dynamics of the bioreactor, concentration gradients induced by loss of the global mixing efficiency associated with the increasing scale is the main phenomena leading to strong physiological modifications at the level of the microbial population. These changes are not fully understood since they involve complex physiological mechanisms. In this work, we intend to investigate, at the single cell level, the expression of the rpoS gene associated with the stress response of E. coli. The cultures of the reporter strain have been performed in a small scale reactor as well as in a series of scaled-down bioreactors able to induce extracellular perturbations with increasing level of magnitude. 相似文献965.
966.
Sophie Reuse Miriam Calao Kabamba Kabeya Allan Guiguen Jean-Stéphane Gatot Vincent Quivy Caroline Vanhulle Aurélia Lamine Dolores Vaira Dominique Demonte Valérie Martinelli Emmanuelle Veithen Thomas Cherrier Véronique Avettand Solène Poutrel Jacques Piette Yvan de Launoit Michel Moutschen Arsène Burny Christine Rouzioux Stéphane De Wit Georges Herbein Olivier Rohr Yves Collette Olivier Lambotte Nathan Clumeck Carine Van Lint 《PloS one》2009,4(6)
967.
Tomasz Jaworski Ilse Dewachter Benoit Lechat Sophie Croes Annelies Termont David Demedts Peter Borghgraef Herman Devijver Robert K. Filipkowski Leszek Kaczmarek Sebastian Kügler Fred Van Leuven 《PloS one》2009,4(10)
In Alzheimer''s disease tauopathy is considered secondary to amyloid, and the duality obscures their relation and the definition of their respective contributions.Transgenic mouse models do not resolve this problem conclusively, i.e. the relative hierarchy of amyloid and tau pathology depends on the actual model and the genes expressed or inactivated. Here, we approached the problem in non-transgenic models by intracerebral injection of adeno-associated viral vectors to express protein tau or amyloid precursor protein in the hippocampus in vivo. AAV-APP mutant caused neuronal accumulation of amyloid peptides, and eventually amyloid plaques at 6 months post-injection, but with only marginal hippocampal cell-death. In contrast, AAV-Tau, either wild-type or mutant P301L, provoked dramatic degeneration of pyramidal neurons in CA1/2 and cortex within weeks. Tau-mediated neurodegeneration proceeded without formation of large fibrillar tau-aggregates or tangles, but with increased expression of cell-cycle markers.We present novel AAV-based models, which demonstrate that protein tau mediates pyramidal neurodegeneration in vivo. The data firmly support the unifying hypothesis that post-mitotic neurons are forced to re-enter the cell-cycle in primary and secondary tauopathies, including Alzheimer''s disease. 相似文献
968.
Myriam Ermonval Anne Baudry Florence Baychelier Elodie Pradines Mathéa Pietri Kimimitsu Oda Beno?t Schneider Sophie Mouillet-Richard Jean-Marie Launay Odile Kellermann 《PloS one》2009,4(8)
Background
The cellular prion protein, PrPC, is GPI anchored and abundant in lipid rafts. The absolute requirement of PrPC in neurodegeneration associated to prion diseases is well established. However, the function of this ubiquitous protein is still puzzling. Our previous work using the 1C11 neuronal model, provided evidence that PrPC acts as a cell surface receptor. Besides a ubiquitous signaling function of PrPC, we have described a neuronal specificity pointing to a role of PrPC in neuronal homeostasis. 1C11 cells, upon appropriate induction, engage into neuronal differentiation programs, giving rise either to serotonergic (1C115-HT) or noradrenergic (1C11NE) derivatives.Methodology/Principal Findings
The neuronal specificity of PrPC signaling prompted us to search for PrPC partners in 1C11-derived bioaminergic neuronal cells. We show here by immunoprecipitation an association of PrPC with an 80 kDa protein identified by mass spectrometry as the tissue non-specific alkaline phosphatase (TNAP). This interaction occurs in lipid rafts and is restricted to 1C11-derived neuronal progenies. Our data indicate that TNAP is implemented during the differentiation programs of 1C115-HT and 1C11NE cells and is active at their cell surface. Noteworthy, TNAP may contribute to the regulation of serotonin or catecholamine synthesis in 1C115-HT and 1C11NE bioaminergic cells by controlling pyridoxal phosphate levels. Finally, TNAP activity is shown to modulate the phosphorylation status of laminin and thereby its interaction with PrP.Conclusion/Significance
The identification of a novel PrPC partner in lipid rafts of neuronal cells favors the idea of a role of PrP in multiple functions. Because PrPC and laminin functionally interact to support neuronal differentiation and memory consolidation, our findings introduce TNAP as a functional protagonist in the PrPC-laminin interplay. The partnership between TNAP and PrPC in neuronal cells may provide new clues as to the neurospecificity of PrPC function. 相似文献969.