Vertebrates come in a dazzling array of shapes and sizes, from blue whales to pygmy bats, their overt morphology determined largely by the skeleton. The head skeleton in particular has undergone remarkable diversification, as is beautifully illustrated in Darwin’s examination of beak morphology in Galapagos finches. This week in PLoS Biology, Justin Crump, Mary Swartz, and Charles Kimmel explore the mechanism by which cell signals induce specific patterns of cartilage and bone that form the vertebrate head.
In zebrafish mutated for a gene called integrina5, the authors report, a specific region of the jaw support (hyosymplectic) cartilage fails to develop. Integrins are cell surface proteins that promote cell adhesion and signaling. Crump et al. show that Integrina5 promotes the development of an outpocketing known as the first endodermal pouch, which in turn acts as a template and helps to pattern a specific region of the hyosymplectic cartilage.
But the pouch may have more far-reaching effects. Since integrina5 mutants also have region-specific defects in cranial muscles and nerves, the first pouch may serve to organize an entire functional unit in a region of the head. As the hyosymplectic element has undergone considerable change during evolution--from a jaw-support element in fish to a tiny, sound-conducting bone called the stapes in mammals--Crump et al. speculate that such a local, interconnected strategy of development would facilitate evolution of the vertebrate head. Changes in signaling from the pouch would allow a particular skeletal element to vary in shape or size, in coordination with the muscles and nerves that move the skeletal element and independent of other regions of the head.
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