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长读测序策略定位 TTN 重复结构域中的变异。

Long-Reads Sequencing Strategy to Localize Variants in TTN Repeated Domains.

机构信息

Molecular Diagnostic Laboratory, Montpellier University Hospital, Montpellier, France; PhyMedExp, University of Montpellier, INSERM, CNRS, Montpellier, France.

Molecular Diagnostic Laboratory, Montpellier University Hospital, Montpellier, France.

出版信息

J Mol Diagn. 2022 Jul;24(7):719-726. doi: 10.1016/j.jmoldx.2022.04.006. Epub 2022 May 14.

Abstract

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.

摘要

肌联蛋白蛋白负责肌肉弹性。TTN 基因由 364 个外显子组成,它广泛存在可变剪接,导致在骨骼肌和心肌中表达不同的异构体。TTN 中的变异导致具有广泛表型谱的肌病,呈常染色体显性或隐性遗传。高度可变剪接的 I 带编码结构域包含一个三区域重复序列块,同源性为 99%。使用第二代测序技术(短读测序)时,这些区域中的变异的测序和定位非常复杂。我们已经实施了基于第三代测序技术(长读测序)的方案。这种新方法使我们能够定位这些重复区域中的变异,从而改善 TTN 相关肌病的诊断,并为产后或产前筛查中的亲属提供分析。

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