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dc.contributor.authorGulyurtlu, Selma
dc.contributor.authorMagon, Monika S.
dc.contributor.authorGuest, Patrick Neville
dc.contributor.authorPapavasiliou, Panagiotis P.
dc.contributor.authorMorrison, Kim
dc.contributor.authorPrescott, Alan
dc.contributor.authorSleeman, Judith E.
dc.date.accessioned2022-08-12T09:30:02Z
dc.date.available2022-08-12T09:30:02Z
dc.date.issued2022-08-02
dc.identifier279713062
dc.identifier91871891-9c8b-4234-9536-abc9c0aac821
dc.identifier85135502031
dc.identifier000862448500003
dc.identifier.citationGulyurtlu , S , Magon , M S , Guest , P N , Papavasiliou , P P , Morrison , K , Prescott , A & Sleeman , J E 2022 , ' Condensation properties of stress granules and processing bodies are compromised in myotonic dystrophy type 1 ' , Disease Models & Mechanisms , vol. 15 , no. 7 , dmm049294 . https://doi.org/10.1242/dmm.049294en
dc.identifier.issn1754-8403
dc.identifier.otherORCID: /0000-0003-0345-6508/work/117211382
dc.identifier.urihttps://hdl.handle.net/10023/25830
dc.descriptionThis work was supported by Muscular Dystrophy UK (project grant number 16GRO-PG360065 to JES), BBSRC (EASTBIO DTP studentship award to SG) and the Wellcome Trust (ISSF award 105621/Z/14/Z to JES and PG).en
dc.description.abstractRNA regulation in mammalian cells requires complex physical compartmentalisation using structures thought to be formed by liquid-liquid phase separation. Disruption of these structures is implicated in numerous degenerative diseases. Myotonic Dystrophy Type 1 (DM1) is a multi-systemic trinucleotide repeat disorder resulting from a CTG expansion in the DM1 protein kinase gene (DMPK). The cellular hall-mark of DM1 is the formation of nuclear foci containing expanded DMPK RNA (CUGexp). We report here the deregulation of stress granules (SGs) and processing bodies (P-bodies), two cytoplasmic structures key for mRNA regulation, in cell culture models of DM1. Alterations to the rates of formation and dispersal of SGs suggest an altered ability of cells to respond to stress associated with DM1, while changes to the structure and dynamics of SGs and P-bodies suggest that a widespread alteration to the biophysical properties of cellular structures may be a consequence of the presence of CUGexp RNA.
dc.format.extent14430576
dc.language.isoeng
dc.relation.ispartofDisease Models & Mechanismsen
dc.subjectLLPSen
dc.subjectMyotonic Dystrophy Type-1en
dc.subjectP-bodiesen
dc.subjectStress granulesen
dc.subjectTrinucleotide repeatsen
dc.subjectQH301 Biologyen
dc.subjectNDASen
dc.subject.lccQH301en
dc.titleCondensation properties of stress granules and processing bodies are compromised in myotonic dystrophy type 1en
dc.typeJournal articleen
dc.contributor.sponsorMuscular Dystrophy UKen
dc.contributor.sponsorThe Wellcome Trusten
dc.contributor.institutionUniversity of St Andrews. School of Biologyen
dc.contributor.institutionUniversity of St Andrews. Centre for Biophotonicsen
dc.contributor.institutionUniversity of St Andrews. Institute of Behavioural and Neural Sciencesen
dc.contributor.institutionUniversity of St Andrews. Biomedical Sciences Research Complexen
dc.identifier.doi10.1242/dmm.049294
dc.description.statusPeer revieweden
dc.identifier.grantnumber16RGO-PG36-65en
dc.identifier.grantnumber105621/Z/14/Zen


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