Cited by 122Developmental Biology and Gene RegulationMorphological variations and asymmetryPaleontology and Evolutionary Biology

A molecular mechanism for the origin of a key evolutionary innovation, the bird beak and palate, revealed by an integrative approach to major transitions in vertebrate history: DEVELOPMENTAL MECHANISM FOR ORIGIN OF BIRD BEAK

Bhullar, Bhart-Anjan S., Morris, Zachary S., Sefton, Elizabeth M., Tok, Atalay, Tokita, Masayoshi, Namkoong, Bumjin, Camacho, Jasmin, Burnham, David A. +1 more·2015·Evolution

Abstract

The avian beak is a key evolutionary innovation whose flexibility has permitted birds to diversify into a range of disparate ecological niches. We approached the problem of the mechanism behind this innovation using an approach bridging paleontology, comparative anatomy, and experimental developmental biology. First, we used fossil and extant data to show the beak is distinctive in consisting of fused premaxillae that are geometrically distinct from those of ancestral archosaurs. To elucidate underlying developmental mechanisms, we examined candidate gene expression domains in the embryonic face: the earlier frontonasal ectodermal zone (FEZ) and the later midfacial WNT-responsive region, in birds and several reptiles. This permitted the identification of an autapomorphic median gene expression region in Aves. To test the mechanism, we used inhibitors of both pathways to replicate in chicken the ancestral amniote expression. Altering the FEZ altered later WNT responsiveness to the ancestral pattern. Skeletal phenotypes from both types of experiments had premaxillae that clustered geometrically with ancestral fossil forms instead of beaked birds. The palatal region was also altered to a more ancestral phenotype. This is consistent with the fossil record and with the tight functional association of avian premaxillae and palate in forming a kinetic beak.

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Crossref · 10.1111/evo.12684

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  • Taken together, the results support the fundamental prediction that macroevolutionary patterns are shaped by phenotypic modularity and integration, which are in turn determined by developmental processes.

    “Taken together, these results support the fundamental prediction that macroevolutionary patterns are shaped by phenotypic modularity and integration, which are in turn determined by developmental processes (7, 11, 13, 16, 23).”

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Authors
Bhullar, B.-A. S., Morris, Z. S., Sefton, E. M., Tok, A., Tokita, M., Namkoong, B., Camacho, J., Burnham, D. A., & Abzhanov, A.
Affiliations
  • Harvard University (US)
  • University of Kansas (US)
  • Natural History Museum (GB)
Venue
Evolution
Published
2015-06-30
Volume
69
Issue
7
Pages
1665-1677
ISSN
0014-3820 (ISSN-L)
OpenAlex
W1535284157
Cited by
122
References
6
Citations by year
2026: 6 · 2025: 6 · 2024: 7 · 2023: 6 · 2022: 8 · 2021: 8 · 2020: 25 · 2019: 12 · 2018: 12 · 2017: 13 · 2016: 10 · 2015: 9
FWCI
6.36
Type
journal article
Language
en
Open access
closed
Locations
  • Evolution (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • National Science Foundation (DEB 1110564, IOS 1257122)
  • American Museum of Natural History (Chapman Grant)
  • American Ornithologists' Union (Research Award)
  • Yale University (Research funds)
  • John Templeton Foundation (FQEB)
  • Harvard Museum of Comparative Zoology (Ernst Mayr Travel Grant)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
  • Physical Sciences › Mathematics › Geometry and Topology › Morphological variations and asymmetry
  • Physical Sciences › Earth and Planetary Sciences › Paleontology › Paleontology and Evolutionary Biology
Keywords
premaxilla, palate, major transitions, vertebrate evolution, Wnt signaling, gene expression domains, chickens, archosaurs, amniote evolution, skeletal phenotype
MeSH terms
Animals, Beak, Birds, Chick Embryo, Chickens, Biological Evolution, Fossils, Palate, Phenotype, Reptiles, Gene Expression Regulation, Developmental

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