Search Results - "WEIL, Dominique"
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P-Bodies: Cytosolic Droplets for Coordinated mRNA Storage
Published in Trends in genetics (01-08-2018)“…P-bodies (PBs) are cytosolic RNP granules that are conserved among eukaryotic organisms. In the past few years, major progress has been made in understanding…”
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P-Body Purification Reveals the Condensation of Repressed mRNA Regulons
Published in Molecular cell (05-10-2017)“…Within cells, soluble RNPs can switch states to coassemble and condense into liquid or solid bodies. Although these phase transitions have been reconstituted…”
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RNA is a critical element for the sizing and the composition of phase-separated RNA–protein condensates
Published in Nature communications (19-07-2019)“…Liquid–liquid phase separation is thought to be a key organizing principle in eukaryotic cells to generate highly concentrated dynamic assemblies, such as the…”
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P-body assembly requires DDX6 repression complexes rather than decay or Ataxin2/2L complexes
Published in Molecular biology of the cell (15-07-2015)“…P-bodies are cytoplasmic ribonucleoprotein granules involved in posttranscriptional regulation. DDX6 is a key component of their assembly in human cells. This…”
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Translationally repressed mRNA transiently cycles through stress granules during stress
Published in Molecular biology of the cell (01-10-2008)“…In mammals, repression of translation during stress is associated with the assembly of stress granules in the cytoplasm, which contain a fraction of arrested…”
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The DDX6-4E-T interaction mediates translational repression and P-body assembly
Published in Nucleic acids research (27-07-2016)“…4E-Transporter binds eIF4E via its consensus sequence YXXXXLΦ, shared with eIF4G, and is a nucleocytoplasmic shuttling protein found enriched in P-(rocessing)…”
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GC content shapes mRNA storage and decay in human cells
Published in eLife (19-12-2019)“…mRNA translation and decay appear often intimately linked although the rules of this interplay are poorly understood. In this study, we combined our recent…”
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Rare De Novo Missense Variants in RNA Helicase DDX6 Cause Intellectual Disability and Dysmorphic Features and Lead to P-Body Defects and RNA Dysregulation
Published in American journal of human genetics (05-09-2019)“…The human RNA helicase DDX6 is an essential component of membrane-less organelles called processing bodies (PBs). PBs are involved in mRNA metabolic processes…”
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CPEB Interacts with an Ovary-specific eIF4E and 4E-T in Early Xenopus Oocytes
Published in The Journal of biological chemistry (28-12-2007)“…CPEB (cytoplasmic polyadenylation element-binding protein) is an important regulator of translation in oocytes and neurons. Although previous studies of CPEB…”
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10
Localization of Usher 1 proteins to the photoreceptor calyceal processes, which are absent from mice
Published in The Journal of cell biology (15-10-2012)“…The mechanisms underlying retinal dystrophy in Usher syndrome type I (USH1) remain unknown because mutant mice lacking any of the USH1 proteins-myosin VIIa,…”
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Multiple binding of repressed mRNAs by the P-body protein Rck/p54
Published in RNA (Cambridge) (01-09-2012)“…Translational repression is achieved by protein complexes that typically bind 3' UTR mRNA motifs and interfere with the formation of the cap-dependent…”
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Role of p54 RNA helicase activity and its C-terminal domain in translational repression, P-body localization and assembly
Published in Molecular biology of the cell (01-05-2009)“…The RNA helicase p54 (DDX6, Dhh1, Me31B, Cgh-1, RCK) is a prototypic component of P-(rocessing) bodies in cells ranging from yeast to human. Previously, we…”
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Cytoplasmic organelles on the road to mRNA decay
Published in Biochimica et biophysica acta (01-06-2013)“…Localization of both mRNAs and mRNA decay factors to internal membranes of eukaryotic cells provides a means of coordinately regulating mRNAs with common…”
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Defect in the gene encoding the EAR/EPTP domain-containing protein TSPEAR causes DFNB98 profound deafness
Published in Human molecular genetics (01-09-2012)“…We report a consanguineous Iranian family affected by congenital profound sensorineural deafness segregating in an autosomal recessive mode. Auditory tests…”
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RNA-related nuclear functions of human Pat1b, the P-body mRNA decay factor
Published in Molecular biology of the cell (01-01-2012)“…The evolutionarily conserved Pat1 proteins are P-body components recently shown to play important roles in cytoplasmic gene expression control. Using human…”
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A core cochlear phenotype in USH1 mouse mutants implicates fibrous links of the hair bundle in its cohesion, orientation and differential growth
Published in Development (Cambridge) (15-04-2008)“…The planar polarity and staircase-like pattern of the hair bundle are essential to the mechanoelectrical transduction function of inner ear sensory cells…”
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Stereocilin connects outer hair cell stereocilia to one another and to the tectorial membrane
Published in Journal of comparative neurology (1911) (01-02-2011)“…Stereocilin is defective in a recessive form of deafness, DFNB16. We studied the distribution of stereocilin in the developing and mature mouse inner ear and…”
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Dual RNA Processing Roles of Pat1b via Cytoplasmic Lsm1-7 and Nuclear Lsm2-8 Complexes
Published in Cell reports (Cambridge) (01-08-2017)“…Pat1 RNA-binding proteins, enriched in processing bodies (P bodies), are key players in cytoplasmic 5′ to 3′ mRNA decay, activating decapping of mRNA in…”
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Usher type 1G protein sans is a critical component of the tip-link complex, a structure controlling actin polymerization in stereocilia
Published in Proceedings of the National Academy of Sciences - PNAS (05-04-2011)“…The mechanotransducer channels of auditory hair cells are gated by tip-links, oblique filaments that interconnect the stereocilia of the hair bundle. Tip-links…”
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Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy
Published in Nature genetics (01-07-2006)“…Auditory neuropathy is a particular type of hearing impairment in which neural transmission of the auditory signal is impaired, while cochlear outer hair cells…”
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