Back to Search Start Over

TCTEX1D1 is a genetic modifier of disease progression in Duchenne muscular dystrophy.

Authors :
Spitali P
Zaharieva I
Bohringer S
Hiller M
Chaouch A
Roos A
Scotton C
Claustres M
Bello L
McDonald CM
Hoffman EP
Koeks Z
Eka Suchiman H
Cirak S
Scoto M
Reza M
't Hoen PAC
Niks EH
Tuffery-Giraud S
Lochmüller H
Ferlini A
Muntoni F
Aartsma-Rus A
Source :
European journal of human genetics : EJHG [Eur J Hum Genet] 2020 Jun; Vol. 28 (6), pp. 815-825. Date of Electronic Publication: 2020 Jan 02.
Publication Year :
2020

Abstract

Duchenne muscular dystrophy (DMD) is caused by pathogenic variants in the DMD gene leading to the lack of dystrophin. Variability in the disease course suggests that other factors influence disease progression. With this study we aimed to identify genetic factors that may account for some of the variability in the clinical presentation. We compared whole-exome sequencing (WES) data in 27 DMD patients with extreme phenotypes to identify candidate variants that could affect disease progression. Validation of the candidate SNPs was performed in two independent cohorts including 301 (BIO-NMD cohort) and 109 (CINRG cohort of European ancestry) DMD patients, respectively. Variants in the Tctex1 domain containing 1 (TCTEX1D1) gene on chromosome 1 were associated with age of ambulation loss. The minor alleles of two independent variants, known to affect TCTEX1D1 coding sequence and induce skipping of its exon 4, were associated with earlier loss of ambulation. Our data show that disease progression of DMD is affected by a new locus on chromosome 1 and demonstrate the possibility to identify genetic modifiers in rare diseases by studying WES data in patients with extreme phenotypes followed by multiple layers of validation.

Details

Language :
English
ISSN :
1476-5438
Volume :
28
Issue :
6
Database :
MEDLINE
Journal :
European journal of human genetics : EJHG
Publication Type :
Academic Journal
Accession number :
31896777
Full Text :
https://doi.org/10.1038/s41431-019-0563-6