Show simple item record

Files in this item

Thumbnail

Item metadata

dc.contributor.authorŠoltić, Darija
dc.contributor.authorShorrock, Hannah K
dc.contributor.authorAllardyce, Hazel
dc.contributor.authorWilson, Emma L
dc.contributor.authorHolt, Ian
dc.contributor.authorSynowsky, Silvia Anna
dc.contributor.authorShirran, Sally Lorna
dc.contributor.authorParson, Simon
dc.contributor.authorGillingwater, Thomas
dc.contributor.authorFuller, Heidi
dc.date.accessioned2020-08-08T23:37:17Z
dc.date.available2020-08-08T23:37:17Z
dc.date.issued2019-08-09
dc.identifier.citationŠoltić , D , Shorrock , H K , Allardyce , H , Wilson , E L , Holt , I , Synowsky , S A , Shirran , S L , Parson , S , Gillingwater , T & Fuller , H 2019 , ' Lamin A/C dysregulation contributes to cardiac pathology in a mouse model of severe spinal muscular atrophy" ' , Human Molecular Genetics , vol. Advance Article . https://doi.org/10.1093/hmg/ddz195en
dc.identifier.issn0964-6906
dc.identifier.otherPURE: 261104044
dc.identifier.otherPURE UUID: 4ff9258f-98e4-4bb7-a64e-0796a166e53e
dc.identifier.otherORCID: /0000-0003-3516-3507/work/61622007
dc.identifier.otherScopus: 85077225252
dc.identifier.otherWOS: 000509912900001
dc.identifier.urihttp://hdl.handle.net/10023/20431
dc.descriptionFunding: Wellcome Trust [094476/Z/10/Z] (SLS).en
dc.description.abstractCardiac pathology is emerging as a prominent systemic feature of spinal muscular atrophy (SMA), but little is known about the underlying molecular pathways. Using quantitative proteomics analysis, we demonstrate widespread molecular defects in heart tissue from the Taiwanese mouse model of severe SMA. We identify increased levels of lamin A/C as a robust molecular phenotype in the heart of SMA mice, and show that lamin A/C dysregulation is also apparent in SMA patient fibroblast cells and other tissues from SMA mice. Lamin A/C expression was regulated in-vitro by knockdown of the E1 ubiquitination factor UBA1, a key downstream mediator of SMN-dependent disease pathways, converging on β-catenin signalling. Increased levels of lamin A are known to increase the rigidity of nuclei, inevitably disrupting contractile activity in cardiomyocytes. The increased lamin A/C levels in the hearts of SMA mice therefore provide a likely mechanism explaining morphological and functional cardiac defects, leading to blood pooling. Therapeutic strategies directed at lamin A/C may therefore offer a new approach to target cardiac pathology in SMA.
dc.language.isoeng
dc.relation.ispartofHuman Molecular Geneticsen
dc.rightsCopyright © The Author(s) 2019. Published by Oxford University Press. All rights reserved. This work has been made available online in accordance with publisher policies or with permission. Permission for further reuse of this content should be sought from the publisher or the rights holder. This is the author created accepted manuscript following peer review and may differ slightly from the final published version. The final published version of this work is available at https://doi.org/10.1093/hmg/ddz195en
dc.subjectQH301 Biologyen
dc.subjectQH426 Geneticsen
dc.subjectDASen
dc.subject.lccQH301en
dc.subject.lccQH426en
dc.titleLamin A/C dysregulation contributes to cardiac pathology in a mouse model of severe spinal muscular atrophy"en
dc.typeJournal articleen
dc.description.versionPostprinten
dc.contributor.institutionUniversity of St Andrews.School of Biologyen
dc.contributor.institutionUniversity of St Andrews.Biomedical Sciences Research Complexen
dc.contributor.institutionUniversity of St Andrews.School of Chemistryen
dc.identifier.doihttps://doi.org/10.1093/hmg/ddz195
dc.description.statusPeer revieweden
dc.date.embargoedUntil2020-08-09
dc.identifier.urlhttps://academic.oup.com/hmg/advance-article/doi/10.1093/hmg/ddz195/5545490#supplementary-dataen


This item appears in the following Collection(s)

Show simple item record