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First published online August 25, 2008
doi: 10.1242/10.1242/dev.019901


Development 135, 2995-2999 (2008)
Published by The Company of Biologists 2008


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On the trail of the `new head' in Les Treilles

Marianne Bronner-Fraser

Division of Biology 139-74, California Institute of Technology, Pasadena, CA 91125, USA.


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Fig. 1. Elements of cranial organization at the core of the `New Head Hypothesis'. The New Head Hypothesis (NHH) of Carl Gans and Glenn Nothcutt (Gans and Northcutt, 1983Go), as schematized in mouse (A-D) and human (E) embryos. (A-D) Schematics of embryonic day 9.5 (E9.5) mouse embryos, highlighting specific major tissue components of the NHH. The NHH posits that vertebrates exhibit unique characteristics, such as (A) an expanded alar plate of the forebrain; (B) formation of neurogenic sensory placodes from the surface cephalic ectoderm; (C) a migratory mesenchymal population of cranial neural crest cells that invade the branchial arches (BA) and surround the expanded forebrain and rostral primary sensory placodes; and (D) an expanded skeletal system to support the new rostrally expanded forebrain, rostral sensory capsules and BAs. (E) The hypothesized shift from a passive suction feeding protovertebrate to a predatory vertebrate with jaws made from modified BA elements necessitated a high degree of craniogenic developmental and functional integration. Abbreviations: BA, branchial arches; di, diencephalon; hb, hindbrain; mb, midbrain; olf, olfactory; op, optic; ot, otic; tel, telencephalon. (A-D) Modified, with permission, from Depew and Olsson (Depew and Olsson, 2008Go).

 

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© The Company of Biologists Ltd 2008