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Pitx1 determines the morphology of muscle, tendon, and bones of the hindlimb
The vertebrate forelimb and hindlimb are serially homologous structures; however, their distinctive morphologies suggest that different mechanisms are associated with each limb type to give rise to limb-type identity. Three genes have been implicated in this process; T-box transcription factors Tbx5...
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Published in: | Developmental biology 2006-11, Vol.299 (1), p.22-34 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The vertebrate forelimb and hindlimb are serially homologous structures; however, their distinctive morphologies suggest that different mechanisms are associated with each limb type to give rise to limb-type identity. Three genes have been implicated in this process; T-box transcription factors
Tbx5 and
Tbx4, which are expressed in the forelimb and hindlimb, respectively, and a paired-type homeodomain transcription factor
Pitx1, expressed in the hindlimb. To explore the roles of
Pitx1 and
Tbx4 in patterning the hindlimb, we have ectopically misexpressed these genes in the mouse forelimb using transgenic methods. We have developed a novel technique for visualising the structure and organisation of tissues in limbs in 3D using optical projection tomography (OPT). This approach provides unparalleled access to understanding the relationships between connective tissues during development of the limb. Misexpression of
Pitx1 in the forelimb results in the transformation and translocation of specific muscles, tendons, and bones of the forelimb so that they acquire a hindlimb-like morphology.
Pitx1 also upregulates hindlimb-specific factors in the forelimb, including
Hoxc10 and
Tbx4. In contrast, misexpression of
Tbx4 in the forelimb does not result in a transformation of limb-type morphology. These results demonstrate that
Pitx1, but not
Tbx4, determines the morphological identity of hindlimb tissues. |
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ISSN: | 0012-1606 1095-564X |
DOI: | 10.1016/j.ydbio.2006.06.055 |