Storey, E and Fuller, HR (2022) Genotype-phenotype correlations in human diseases caused by mutations of LINC complex-associated genes: a systematic review and meta-summary. Cells. ISSN 2073-4409

[thumbnail of cells-2059552 08122022 final accepted version.docx] Text
cells-2059552 08122022 final accepted version.docx - Accepted Version

Download (2MB)
[thumbnail of cells-11-04065-v2.pdf]
Preview
Text
cells-11-04065-v2.pdf - Published Version

Download (2MB) | Preview

Abstract

Mutations in genes encoding proteins associated with the linker of nucleoskel-eton and cytoskeleton (LINC) complex within the nuclear envelope cause dif-ferent diseases with varying phenotypes including skeletal muscle, cardiac, metabolic, or nervous system pathologies. There is some understanding of the structure of LINC complex-associated proteins and how they interact, but it is unclear how mutations in genes encoding them can cause the same disease, and different diseases with different phenotypes. Here, published mutations in LINC complex-associated proteins were systematically reviewed and ana-lyzed to ascertain whether patterns exist between the genetic sequence vari-ants and clinical phenotypes. This revealed LMNA is the only LINC complex-associated gene in which mutations commonly cause distinct conditions, and there are no clear genotype-phenotype correlations. Clusters of LMNA vari-ants causing striated muscle disease are located in exons 1 and 6, and metabol-ic disease-associated LMNA variants are frequently found in the tail of lamin A/C. Additionally, exon 6 of the emerin gene, EMD, may be a mutation “hot-spot”, and diseases related to SYNE1, encoding nesprin-1, are most often caused by nonsense type mutations. These results provide insight into the di-verse roles of LINC-complex proteins in human disease and provide direction for future gene-targeted therapy development.

Item Type: Article
Additional Information: © 2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
Subjects: R Medicine > R Medicine (General)
R Medicine > RM Therapeutics. Pharmacology
R Medicine > RS Pharmacy and materia medica
Divisions: Faculty of Medicine and Health Sciences > School of Pharmacy and Bioengineering
Depositing User: Symplectic
Date Deposited: 14 Dec 2022 09:24
Last Modified: 09 Jan 2023 15:47
URI: https://eprints.keele.ac.uk/id/eprint/11793

Actions (login required)

View Item
View Item