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Tbx4 and tbx5 acting in connective tissue are required for limb muscle and tendon patterning.

Developmental cell | 2010

Proper functioning of the musculoskeletal system requires the precise integration of bones, muscles, and tendons. Complex morphogenetic events ensure that these elements are linked together in the appropriate three-dimensional configuration. It has been difficult, however, to tease apart the mechanisms that regulate tissue morphogenesis. We find that deletion of Tbx5 in forelimbs (or Tbx4 in hindlimbs) specifically affects muscle and tendon patterning without disrupting skeletal development, thus suggesting that distinct cues regulate these processes. We identify muscle connective tissue as the site of action of these transcription factors and show that N-Cadherin and beta-Catenin are key downstream effectors acting in muscle connective tissue and regulating soft-tissue morphogenesis. In humans, TBX5 mutations lead to Holt-Oram syndrome, which is characterized by forelimb musculoskeletal defects. Our results suggest that a focus on connective tissue is required to understand the etiology of diseases affecting soft tissue formation.

Pubmed ID: 20152185 RIS Download

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Associated grants

  • Agency: NICHD NIH HHS, United States
    Id: R37 HD033082
  • Agency: NICHD NIH HHS, United States
    Id: R01 HD033082-04
  • Agency: NICHD NIH HHS, United States
    Id: HD033082
  • Agency: Medical Research Council, United Kingdom
    Id: MC_U117562103
  • Agency: NICHD NIH HHS, United States
    Id: R01 HD033082
  • Agency: Medical Research Council, United Kingdom
    Id: MC_U117560477

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