Current insights into LMNA cardiomyopathies: Existing models and missing LINCs.

Brayson, D. and Shanahan, C.M. 2017. Current insights into LMNA cardiomyopathies: Existing models and missing LINCs. Nucleus. 8 (1), pp. 17-33. https://doi.org/10.1080/19491034.2016.1260798

TitleCurrent insights into LMNA cardiomyopathies: Existing models and missing LINCs.
TypeJournal article
AuthorsBrayson, D. and Shanahan, C.M.
Abstract

The nuclear lamina is a critical structural domain for the maintenance of genomic stability and whole-cell mechanics. Mutations in the LMNA gene, which encodes nuclear A-type lamins lead to the disruption of these key cellular functions, resulting in a number of devastating diseases known as laminopathies. Cardiomyopathy is a common laminopathy and is highly penetrant with poor prognosis. To date, cell mechanical instability and dysregulation of gene expression have been proposed as the main mechanisms driving cardiac dysfunction, and indeed discoveries in these areas have provided some promising leads in terms of therapeutics. However, important questions remain unanswered regarding the role of lamin A dysfunction in the heart, including a potential role for the toxicity of lamin A precursors in LMNA cardiomyopathy, which has yet to be rigorously investigated.

JournalNucleus
Journal citation8 (1), pp. 17-33
ISSN1949-1034
1949-1042
Year2017
PublisherTaylor & Francis
Publisher's version
License
CC BY-NC-ND 4.0
Digital Object Identifier (DOI)https://doi.org/10.1080/19491034.2016.1260798
PubMed ID28125396
Web address (URL)http://europepmc.org/abstract/med/28125396
Publication dates
PublishedJan 2017

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