Atypical phenotypes in titinopathies explained by second titin mutations.

Abstract

OBJECTIVE:

Several patients with previously reported titin gene (TTN) mutations causing tibial muscular dystrophy (TMD) have more complex, severe, or unusual phenotypes. This study aimed to clarify the molecular cause of the variant phenotypes in 8 patients of 7 European families.

METHODS:

Clinical, histopathological, and muscle imaging data of patients and family members were reanalyzed. The titin protein was analyzed by Western blotting and TTN gene by reverse transcription polymerase chain reaction (RT-PCR) and Sanger sequencing.

RESULTS:

Western blotting showed more pronounced C-terminal titin abnormality than expected for heterozygous probands, suggesting the existence of additional TTN mutations. RT-PCR indicated unequal mRNA expression of the TTN alleles in biopsies of 6 patients, 3 with an limb-girdle muscular dystrophy type 2J (LGMD2J) phenotype. Novel frameshift mutations were identified in 5 patients. A novel A-band titin mutation, c.92167C>T (p.P30723S), was found in 1 patient, and 1 Portuguese patient with a severe TMD phenotype proved to be homozygous for the previously reported Iberian TMD mutation.

INTERPRETATION:

The unequal expression levels of TTN transcripts in 5 probands suggested severely reduced expression of the frameshift mutated allele, probably through nonsense-mediated decay, explaining the more severe phenotypes. The Iberian TMD mutation may cause a more severe TMD rather than LGMD2J when homozygous. The Finnish patient compound heterozygous for the FINmaj TMD mutation and the novel A-band titin missense mutation showed a phenotype completely different from previously described titinopathies. Our results further expand the complexity of muscular dystrophies caused by TTN mutations and suggest that the coexistence of second mutations may constitute a more common general mechanism explaining phenotype variability.

• Authors: Anni Evilä, Anna Vihola, Jaakko Sarparanta, Olayinka Raheem, Johanna Palmio, Satu Sandell, Bruno Eymard, Isabel Illa, Ricard Rojas-Garcia, Karolina Hankiewicz, Luis Negrão, Tuija Löppönen, Pekka Nokelainen, Mikko Kärppä, Sini Penttilä, Mark Screen, Tiina Suominen, Isabelle Richard, Peter Hackman, Bjarne Udd
• Journal: Annals of neurology (Ann Neurol) Vol. 75 Issue 2 Pg. 230-40 (Feb 2014) ISSN: 1531-8249 [Electronic] United States
• PMID: 24395473 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
• Copyright: © 2014 American Neurological Association.

Chemical References

• Connectin
• RNA, Messenger

Topics

• Adolescent
• Adult
• Aged
• Base Sequence
• Connectin (genetics)
• Distal Myopathies (genetics, pathology)
• Exons (genetics, immunology)
• Family Health
• Female
• Humans
• Magnetic Resonance Imaging
• Male
• Middle Aged
• Muscle, Skeletal (pathology)
• Mutation (genetics)
• Phenotype
• RNA, Messenger (genetics, metabolism)
• White People