4 research outputs found

    Etude des rƩpƩtitions 2.0 : KINOAI, logiciel web

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    International audienceNous deĢcrivons une seĢrie dā€™expeĢrimentations meneĢes avec le logiciel KinoAI pour lā€™eĢtude des reĢpeĢtitions de theĢaĢ‚tre. KinoAI permet de rendre accessibles les reĢpeĢtitions en utilisant un outil inteĢgreĢ depuis longtemps aĢ€ la pratique theĢaĢ‚trale - la videĢo. Lors des reĢpeĢtitions, lā€™accumulation des prises de vues meĢ€ne souvent aĢ€ une surproduction de donneĢes qui sont remiseĢes sur un quelconque disque dur, et plus jamais utiliseĢes, ni regardeĢes. KinoAI offre des nouvelles fonctions dā€™analyse, de cadrage et de montage qui permettent dā€™affronter ces difficulteĢs en post-production. Ces innovations sont de nature aĢ€ renouveler lā€™eĢtude des reĢpeĢtitions, en offrant aux chercheurs et aux artistes une meĢmoire numeĢrique commune, doteĢe dā€™un zoom temporel et spatial qui facilite le traitement des donneĢes recueillies, tout en preĢservant l'inventiviteĢ de ses acteurs

    Etude des rƩpƩtitions 2.0 : KINOAI, logiciel web

    Get PDF
    International audienceNous deĢcrivons une seĢrie dā€™expeĢrimentations meneĢes avec le logiciel KinoAI pour lā€™eĢtude des reĢpeĢtitions de theĢaĢ‚tre. KinoAI permet de rendre accessibles les reĢpeĢtitions en utilisant un outil inteĢgreĢ depuis longtemps aĢ€ la pratique theĢaĢ‚trale - la videĢo. Lors des reĢpeĢtitions, lā€™accumulation des prises de vues meĢ€ne souvent aĢ€ une surproduction de donneĢes qui sont remiseĢes sur un quelconque disque dur, et plus jamais utiliseĢes, ni regardeĢes. KinoAI offre des nouvelles fonctions dā€™analyse, de cadrage et de montage qui permettent dā€™affronter ces difficulteĢs en post-production. Ces innovations sont de nature aĢ€ renouveler lā€™eĢtude des reĢpeĢtitions, en offrant aux chercheurs et aux artistes une meĢmoire numeĢrique commune, doteĢe dā€™un zoom temporel et spatial qui facilite le traitement des donneĢes recueillies, tout en preĢservant l'inventiviteĢ de ses acteurs

    The isolation of proteins on nascent DNA (iPOND) reveals a role for RIF1 in the organization of replication factories

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    Eukaryotic genomes are duplicated from thousands of replication origins that fire sequentially forming a defined spatiotemporal pattern of replication clusters. The importance of the organization of replisomes into functional clusters, called replication factories, is still poorly understood. Here we show that the isolation of Proteins On Nascent DNA (iPOND) method is strongly dependent on the organization level of replication factories. We find that RIF1 is a component of replication factories. The purification of replication-associated proteins from RIF1-depleted cells using iPOND reveals a major defect in the clustering of replication factors upon mild replicative stress. The loss of organization caused by RIF1 depletion leads to defects in replication forks dynamic and yields DNA lesions. We propose a model whereby RIF1 encases replication factories to prevent the formation of DNA lesions in response to replicative stress. The data highlight the importance of the organization of replication factories for the maintenance of genome integrity

    GNL3 regulates replication origin firing and protects stalled replication forks

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    DNA replication by the replisome requires specific proteins that protect replication forks and so prevent the formation of DNA lesions that may damage the genome. Here, we show that human GNL3/nucleostemin, a GTP-binding protein localized in the nucleolus and the nucleoplasm, is a new component of the replisome. Depletion of GNL3 reduces fork speed but increases replication origin firing. When subjected to replication stress, the nascent DNA of GNL3-depleted cells undergoes nuclease-dependent resection, a source of DNA lesions. Inhibition of origin firing decreases this resection, indicating that the increased replication origin firing seen upon GNL3 depletion mainly accounts for the observed DNA resection. We show that GNL3 and DNA replication initiation factor ORC2 interact in the nucleolus, and that GNL3 regulates ORC2 subnuclear localization. The accumulation of GNL3 in the nucleolus is thus required to limit DNA resection in response to replicative stress, potentially through the regulation of ORC2 functions
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