Long-Reads Sequencing Strategy to Localize Variants in TTN Repeated Domains.
Journal
The Journal of molecular diagnostics : JMD
ISSN: 1943-7811
Titre abrégé: J Mol Diagn
Pays: United States
ID NLM: 100893612
Informations de publication
Date de publication:
07 2022
07 2022
Historique:
received:
17
02
2022
revised:
23
03
2022
accepted:
18
04
2022
pubmed:
18
5
2022
medline:
8
7
2022
entrez:
17
5
2022
Statut:
ppublish
Résumé
Titin protein is responsible for muscle elasticity. The TTN gene, composed of 364 exons, is subjected to extensive alternative splicing and leads to different isoforms expressed in skeletal and cardiac muscle. Variants in TTN are responsible for myopathies with a wide phenotypic spectrum and autosomal dominant or recessive transmission. The I-band coding domain, highly subject to alternative splicing, contains a three-zone block of repeated sequences with 99% homology. Sequencing and localization of variants in these areas are complex when using short-reads sequencing, a second-generation sequencing technique. We have implemented a protocol based on the third-generation sequencing technology (long-reads sequencing). This new method allows us to localize variants in these repeated areas to improve the diagnosis of TTN-related myopathies and offer the analysis of relatives in postnatal or in prenatal screening.
Identifiants
pubmed: 35580751
pii: S1525-1578(22)00131-3
doi: 10.1016/j.jmoldx.2022.04.006
pii:
doi:
Substances chimiques
Connectin
0
Protein Isoforms
0
TTN protein, human
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
719-726Informations de copyright
Copyright © 2022 Association for Molecular Pathology and American Society for Investigative Pathology. Published by Elsevier Inc. All rights reserved.