Tropomodulin 1 directly controls thin filament length in both wild-type and tropomodulin 4-deficient skeletal muscle

David S. Gokhin*, Julien Ochala, Andrea A. Domenighetti, Velia M. Fowler

*Corresponding author for this work

Research output: Contribution to journalArticle

14 Scopus citations

Abstract

The sarcomeric tropomodulin (Tmod) isoforms Tmod1 and Tmod4 cap thin filament pointed ends and functionally interact with the leiomodin (Lmod) isoforms Lmod2 and Lmod3 to control myofibril organization, thin filament lengths, and actomyosin crossbridge formation in skeletal muscle fibers. Here, we show that Tmod4 is more abundant than Tmod1 at both the transcript and protein level in a variety of muscle types, but the relative abundances of sarcomeric Tmods are muscle specific.We then generate Tmod4−/− mice, which exhibit normal thin filament lengths, myofibril organization, and skeletal muscle contractile function owing to compensatory upregulation of Tmod1, together with an Lmod isoform switch wherein Lmod3 is downregulated and Lmod2 is upregulated. However, RNAi depletion of Tmod1 from either wild-type or Tmod4−/− muscle fibers leads to thin filament elongation by ∼15%. Thus, Tmod1 per se, rather than total sarcomeric Tmod levels, controls thin filament lengths in mouse skeletal muscle, whereas Tmod4 appears to be dispensable for thin filament length regulation. These findings identify Tmod1 as the key direct regulator of thin filament length in skeletal muscle, in both adult muscle homeostasis and in developmentally compensated contexts.

Original languageEnglish (US)
Pages (from-to)4351-4362
Number of pages12
JournalDevelopment (Cambridge)
Volume142
Issue number24
DOIs
StatePublished - Dec 15 2015

Keywords

  • Actin filament
  • Leiomodin
  • Myofibril
  • Pointed-end capping
  • Sarcomere

ASJC Scopus subject areas

  • Molecular Biology
  • Developmental Biology

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