32 research outputs found

    Gestion électronique des documents et la réédition de documents informatisés (La)

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    Gestion électronique des documents et la réédition de documents informatisés (La)

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    Gestion électronique des documents et la réédition de documents informatisés (La)

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    Étude d\u27opportunité préalable à la mise en place d\u27un système de GEIDE COLD

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    Computer design of obligate heterodimer meganucleases allows efficient cutting of custom DNA sequences

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    Meganucleases cut long (>12 bp) unique sequences in genomes and can be used to induce targeted genome engineering by homologous recombination in the vicinity of their cleavage site. However, the use of natural meganucleases is limited by the repertoire of their target sequences, and considerable efforts have been made to engineer redesigned meganucleases cleaving chosen targets. Homodimeric meganucleases such as I-CreI have provided a scaffold, but can only be modified to recognize new quasi-palindromic DNA sequences, limiting their general applicability. Other groups have used dimer-interface redesign and peptide linkage to control heterodimerization between related meganucleases such as I-DmoI and I-CreI, but until now there has been no application of this aimed specifically at the scaffolds from existing combinatorial libraries of I-CreI. Here, we show that engineering meganucleases to form obligate heterodimers results in functional endonucleases that cut non-palindromic sequences. The protein design algorithm (FoldX v2.7) was used to design specific heterodimer interfaces between two meganuclease monomers, which were themselves engineered to recognize different DNA sequences. The new monomers favour functional heterodimer formation and prevent homodimer site recognition. This design massively increases the potential repertoire of DNA sequences that can be specifically targeted by designed I-CreI meganucleases and opens the way to safer targeted genome engineering

    A combinatorial approach to create artificial homing endonucleases cleaving chosen sequences

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    Meganucleases, or homing endonucleases (HEs) are sequence-specific endonucleases with large (>14 bp) cleavage sites that can be used to induce efficient homologous gene targeting in cultured cells and plants. These findings have opened novel perspectives for genome engineering in a wide range of fields, including gene therapy. However, the number of identified HEs does not match the diversity of genomic sequences, and the probability of finding a homing site in a chosen gene is extremely low. Therefore, the design of artificial endonucleases with chosen specificities is under intense investigation. In this report, we describe the first artificial HEs whose specificity has been entirely redesigned to cleave a naturally occurring sequence. First, hundreds of novel endonucleases with locally altered substrate specificity were derived from I-CreI, a Chlamydomonas reinhardti protein belonging to the LAGLIDADG family of HEs. Second, distinct DNA-binding subdomains were identified within the protein. Third, we used these findings to assemble four sets of mutations into heterodimeric endonucleases cleaving a model target or a sequence from the human RAG1 gene. These results demonstrate that the plasticity of LAGLIDADG endonucleases allows extensive engineering, and provide a general method to create novel endonucleases with tailored specificities

    The C-terminal loop of the homing endonuclease I-CreI is essential for site recognition, DNA binding and cleavage

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    Meganucleases are sequence-specific endonucleases with large cleavage sites that can be used to induce efficient homologous gene targeting in cultured cells and plants. These enzymes open novel perspectives for genome engineering in a wide range of fields, including gene therapy. A new crystal structure of the I-CreI dimer without DNA has allowed the comparison with the DNA-bound protein. The C-terminal loop displays a different conformation, which suggests its implication in DNA binding. A site-directed mutagenesis study in this region demonstrates that whereas the C-terminal helix is negligible for DNA binding, the final C-terminal loop is essential in DNA binding and cleavage. We have identified two regions that comprise the Ser138–Lys139 and Lys142–Thr143 pairs whose double mutation affect DNA binding in vitro and abolish cleavage in vivo. However, the mutation of only one residue in these sites allows DNA binding in vitro and cleavage in vivo. These findings demonstrate that the C-terminal loop of I-CreI endonuclease plays a fundamental role in its catalytic mechanism and suggest this novel site as a region to take into account for engineering new endonucleases with tailored specificity

    Horizon 2019 : bibliothèques en prospective

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    Colloque organisé du 19 au 21 novembre 2009 à l\u27enssib avec pour but d\u27imaginer l\u27avenir proche des bibliothèques dans le monde occidental. Le colloque s\u27organise en trois temps : "Enjeux et défis", "Quelles missions pour les bibliothèques" et "Hypothèses et scénarios"

    Large expert-curated database for benchmarking document similarity detection in biomedical literature search

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    Document recommendation systems for locating relevant literature have mostly relied on methods developed a decade ago. This is largely due to the lack of a large offline gold-standard benchmark of relevant documents that cover a variety of research fields such that newly developed literature search techniques can be compared, improved and translated into practice. To overcome this bottleneck, we have established the RElevant LIterature SearcH consortium consisting of more than 1500 scientists from 84 countries, who have collectively annotated the relevance of over 180 000 PubMed-listed articles with regard to their respective seed (input) article/s. The majority of annotations were contributed by highly experienced, original authors of the seed articles. The collected data cover 76% of all unique PubMed Medical Subject Headings descriptors. No systematic biases were observed across different experience levels, research fields or time spent on annotations. More importantly, annotations of the same document pairs contributed by different scientists were highly concordant. We further show that the three representative baseline methods used to generate recommended articles for evaluation (Okapi Best Matching 25, Term Frequency-Inverse Document Frequency and PubMed Related Articles) had similar overall performances. Additionally, we found that these methods each tend to produce distinct collections of recommended articles, suggesting that a hybrid method may be required to completely capture all relevant articles. The established database server located at https://relishdb.ict.griffith.edu.au is freely available for the downloading of annotation data and the blind testing of new methods. We expect that this benchmark will be useful for stimulating the development of new powerful techniques for title and title/abstract-based search engines for relevant articles in biomedical research.Peer reviewe

    La Covid-19 et l’organisation des études universitaires : injonctions et adaptations

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    In the context of the health crisis, educational institutionsin France have generally adapted in a sequentialand sometimes erratic manner. Universitieswere quickly able to organize themselves and proposeprotocols that limited the number of face-to-facesessions while attempting to guarantee the essentialelements of learning, thanks in particular to digitaltechnology. This contribution proposes a analysisof the official decisions, announced by the Presidentof the Republic and applied to the higher educationinstitutions by way of ministerial circulars, with thedecisions and adaptations implemented within auniversity, from a consideration of the feelings andopinions of the students.Dans le contexte de la crise sanitaire, les institutions d'enseignement ont globalement, en France, fait preuve d'adaptation, de manière séquentielle et parfois erratique. Les universités ont rapidement pu s'organiser et proposer des protocoles limitant le présentiel tout en tentant de garantir l'essentiel des apprentissages grâce notamment au digital. Cette contribution propose une mise en en perspective des décisions officielles, annoncées par le Président de la République et appliquées aux établissements d'enseignement supérieur par voie de circulaires, avec les décisions et adaptations mise en oeuvre au sein d'une université, à partir d'une prise en compte des ressentis et avis des étudiants
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