Removal of immunoglobulin-like domains from titin's spring segment alters titin splicing in mouse skeletal muscle and causes myopathy

Danielle Buck, John E. Smith, Charles S. Chung, Yasuko Ono, Hiroyuki Sorimachi, Siegfried Labeit, Hendrikus "Henk" Granzier

Research output: Contribution to journalArticle

18 Citations (Scopus)

Abstract

Titin is a molecular spring that determines the passive stiffness of muscle cells. Changes in titin's stiffness occur in various myopathies, but whether these are a cause or an effect of the disease is unknown. We studied a novel mouse model in which titin's stiffness was slightly increased by deleting nine immunoglobulin (Ig)-like domains from titin's constitutively expressed proximal tandem Ig segment (IG KO). KO mice displayed mild kyphosis, a phenotype commonly associated with skeletal muscle myopathy. Slow muscles were atrophic with alterations in myosin isoform expression; functional studies in soleus muscle revealed a reduced specific twitch force. Exon expression analysis showed that KO mice underwent additional changes in titin splicing to yield smaller than expected titin isoforms that were much stiffer than expected. Additionally, splicing occurred in the PEVK region of titin, a finding confirmed at the protein level. The titin-binding protein Ankrd1 was highly increased in the IG KO, but this did not play a role in generating small titin isoforms because titin expression was unaltered in IG KO mice crossed with Ankrd1-deficient mice. In contrast, the splicing factor RBM20 (RNA-binding motif 20) was also significantly increased in IG KO mice, and additional differential splicing was reversed in IG KO mice crossed with a mouse with reduced RBM20 activity. Thus, increasing titin's stiffness triggers pathological changes in skeletal muscle, with an important role played by RBM20.

Original languageEnglish (US)
Pages (from-to)215-230
Number of pages16
JournalJournal of General Physiology
Volume143
Issue number2
DOIs
StatePublished - Feb 2014

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Connectin
Muscular Diseases
Skeletal Muscle
Protein Isoforms
Immunoglobulin Domains
Kyphosis
Myosins
Muscle Cells
Immunoglobulins
Exons
Carrier Proteins

ASJC Scopus subject areas

  • Physiology

Cite this

Removal of immunoglobulin-like domains from titin's spring segment alters titin splicing in mouse skeletal muscle and causes myopathy. / Buck, Danielle; Smith, John E.; Chung, Charles S.; Ono, Yasuko; Sorimachi, Hiroyuki; Labeit, Siegfried; Granzier, Hendrikus "Henk".

In: Journal of General Physiology, Vol. 143, No. 2, 02.2014, p. 215-230.

Research output: Contribution to journalArticle

Buck, Danielle ; Smith, John E. ; Chung, Charles S. ; Ono, Yasuko ; Sorimachi, Hiroyuki ; Labeit, Siegfried ; Granzier, Hendrikus "Henk". / Removal of immunoglobulin-like domains from titin's spring segment alters titin splicing in mouse skeletal muscle and causes myopathy. In: Journal of General Physiology. 2014 ; Vol. 143, No. 2. pp. 215-230.
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