CELF and PTB proteins modulate the inclusion of the β-tropomyosin exon 6B during myogenic differentiation

Alain Sureau1, Jérôme Saulière, Alain Expert-Bezançon

  • 1Centre de Génétique Moléculaire, FRE 3144, CNRS, Gif sur Yvette, France, Université Paris XI, Orsay, France.

Experimental Cell Research
|September 30, 2010
PubMed

Insights

CUG-BP and ETR-3-like factor (CELF) proteins promote exon 6B inclusion in beta-tropomyosin mRNA during muscle cell differentiation. Polypyrimidine tract binding protein (PTB) represses this splicing event, indicating an antagonistic regulatory mechanism.

Area of Science:

  • Molecular Biology
  • Cell Biology
  • RNA Splicing

Background:

  • Alternative splicing of beta-tropomyosin pre-mRNA is crucial for myogenic differentiation.
  • Exon 6B inclusion is observed in myotubes but excluded in myoblasts.

Purpose of the Study:

  • To investigate the regulatory mechanisms governing the alternative splicing of exon 6B in beta-tropomyosin.
  • To identify the roles of specific RNA-binding proteins in this process during myogenesis.

Main Methods:

  • Ex vivo studies using a quail myogenic cell line.
  • Overexpression of CUG-BP and ETR-3-like factor (CELF) proteins.
  • Utilizing a dominant-negative form of CELF4.
  • Investigating the role of polypyrimidine tract binding protein (PTB).

Main Results:

  • Beta-tropomyosin exon 6B is a novel target of CELF proteins.
  • CELF protein overexpression activates exon 6B splicing.
  • CELF proteins mediate the switch towards exon 6B inclusion during differentiation.
  • PTB is required for exon 6B splicing repression in myoblasts.
  • CELF and PTB proteins act antagonistically on exon 6B inclusion.

Conclusions:

  • Changes in CUGBP1 and PTB protein levels regulate exon 6B splicing during myogenesis.
  • Distinct PTB expression patterns contribute to the regulation of exon 6B splicing transition.

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