Fernández-Caballero Lidia, Blanco-Kelly Fiona, Swafiri Saoud Tahsin, Martín-Mérida María Inmaculada, Quinodoz Mathieu, Ullah Mukhtar, Carreño Ester, Martin-Gutierrez María Pilar, García-Sandoval Blanca, Minguez Pablo, Rivolta Carlo, Corton Marta, Ayuso Carmen
Department of Genetics & Genomics, Instituto de Investigación Sanitaria-Fundación Jiménez Díaz University Hospital, Universidad Autónoma de Madrid (IIS-FJD, UAM), Avda. Reyes Católicos, 2, 28040, Madrid, Spain.
Center for Biomedical Network Research on Rare Diseases (CIBERER), Instituto de Salud Carlos III, Madrid, Spain.
Sci Rep. 2025 Apr 28;15(1):14904. doi: 10.1038/s41598-025-97768-9.
THRB encodes thyroid hormone receptor β which produces two human isoforms (TRβ1 and TRβ2) by alternative splicing. The first THRB variant associated with autosomal dominant macular dystrophy (ADMD), NM_001354712.2:c.283 + 1G > A, was recently described. This study aims to refine the ophthalmologic phenotype, report a novel THRB variant, and investigate the impact of these splicing variants at the protein level. THRB variants were identified by re-analysis of next-generation sequencing data from the FJD database. Family segregation was performed using Sanger sequencing. Clinical data were collected from self-reported ophthalmic history questionnaires and ophthalmic exams. Functional splicing test was performed by in vitro minigene approach. We identified 12 patients with ADMD from 3 families carrying variants in THRB. Two families carried the variant NM_001354712.2:c.283 + 1G > A, and one the novel variant NM_001354712.2:c.283G > A. Patients exhibited common ophthalmologic findings with disruption of subfoveal ellipsoid layers, and variable onset of symptoms. Splicing assays showed complete exon 5 skipping or a 6 bp deletion in both variants. Our results support the association of THRB with ADMD. The high intra-familial variability could be influenced by phenotype modifiers. Aberrant TRβ1/TRβ2 proteins could lead to a gain-of-function mechanism. Including THRB in inherited retinal dystrophy genetic panels could enhance diagnoses and clinical patient management.
THRB基因编码甲状腺激素受体β,该受体通过可变剪接产生两种人类异构体(TRβ1和TRβ2)。最近描述了第一个与常染色体显性黄斑营养不良(ADMD)相关的THRB变异体,即NM_001354712.2:c.283 + 1G > A。本研究旨在细化眼科表型,报告一种新的THRB变异体,并在蛋白质水平上研究这些剪接变异体的影响。通过对FJD数据库中的二代测序数据进行重新分析来鉴定THRB变异体。使用桑格测序法进行家系分离分析。临床数据通过自我报告的眼科病史问卷和眼科检查收集。通过体外小基因方法进行功能剪接测试。我们从3个携带THRB变异体的家庭中鉴定出12例ADMD患者。两个家庭携带变异体NM_001354712.2:c.283 + 1G > A,另一个家庭携带新变异体NM_001354712.2:c.283G > A。患者表现出常见的眼科表现,包括黄斑下椭圆体层破坏,且症状发作时间不一。剪接分析显示,这两种变异体均出现外显子5完全跳跃或6 bp缺失。我们的结果支持THRB与ADMD之间的关联。家族内的高变异性可能受表型修饰因子的影响。异常的TRβ1/TRβ2蛋白可能导致功能获得机制。将THRB纳入遗传性视网膜营养不良基因检测面板可提高诊断水平并改善临床患者管理。