News Release

Mammals’ noses come from reptiles’ jaws

Evolutionary development of facial bones studied in embryos and fossils

Peer-Reviewed Publication

University of Tokyo

Illustrations of facial development in mammals (right) and evolutionarily older species (non-mammalian tetrapods).

image: Experts at the University of Tokyo used cellular studies and reexaminations of fossilized skulls to develop a new, improved understanding of how mammals developed separate noses and upper jaws. This reorganization of the premaxilla and septomaxilla bones likely allowed mammals to form flexible noses that can “sniff.” view more 

Credit: Image by Hiroki Higashiyama, CC BY-SA 4.0

New examinations of skeletons and animal embryos have allowed researchers to discover how mammals developed protruding, flexible noses. This study contributes to uncovering the origin of mammals’ strong sense of smell and creates the potential for new animal models, like chickens or frogs, that are often used in lab experiments to investigate facial development disorders such as cleft palate.

 

The traditional scientific understanding of facial evolution is that both mammalian and reptilian jaws develop in almost the same way. Even though mammals have a unique nose, the evolution of this structure has remained unknown.

 

“Existing fossils of four-legged animals, both reptilian and mammalian ancestors, have the same number of upper jaw bones. It’s very easy to think that the bones are the same, but now we can study embryos and track cellular development to study these bones in much greater detail,” explained postdoctoral researcher Hiroki Higashiyama, who studies evolutionary development at the University of Tokyo Graduate School of Medicine. The research, recently published in Proceedings of the National Academy of Sciences, is the first to examine the evolution of facial structure using cellular studies comparing multiple embryos of multiple species.

 

Higashiyama and his colleagues in the laboratory of Professor Hiroki Kurihara designed experiments to track facial development in embryos of different species, including birds (chickens), reptiles (geckos) and mammals (mice). They focused on a group of cells known as the facial prominences in embryos that produce the physical structures of the face. Researchers stained the cells to track them as they moved and grew.  A group of cells called the frontonasal prominence forms the jaw tip in reptiles, but becomes the protruding nose in mammals. Mammals’ jaw tips form instead from a separate group of cells called the maxillary prominence. 

 

Using this new perspective from their cellular experiments, researchers then examined fossil specimens. 

 

As species’ ancestors accumulated more physical and genetic differences, the bone at the tip of reptiles’ upper jaw, the premaxilla, became smaller and migrated upwards and the bone that was behind it, the septomaxilla, became larger and moved forwards to become mammals’ jaw tip. Researchers say that the facial bones of egg-laying mammals, like the Australian platypus and echidna, provide additional living examples of transitional bone structures from the evolutionarily older reptile model to the more recently evolved mammalian structure. 

 

This separation of the nose and jaw gives mammals their unique ability to “sniff,” using muscles to flare the nostrils and deeply inhale odors from the environment.

 

“This finding is a key innovation in the evolution of our and other mammals’ motile nose, which contributes to mammals’ highly sensitive sense of smell,” said Higashiyama. 

 

Distinguishing and recognizing so many odors may have also helped mammals develop larger, more complex brains than earlier ancestor species.  

 

The recent research has provided physical evidence of the evolutionary shift in premaxilla and septomaxilla arrangement, but separate studies will be needed to identify the genetic causes. 

 

“Now we know the composition of facial prominences and embryonic development in multiple species, so we can compare facial development disorders in chickens or frogs to humans. We have mainly just improved textbook knowledge for now, but in the future, these animal models will be a practical application of our studies,” said Higashiyama. 

 

Mice are currently the only animal model to study cleft lip and palate. Mice are expensive to maintain and slower to develop, so additional animal models of facial development disorders could become a valuable research tool.

 

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Research Publication

Hiroki Higashiyama, Daisuke Koyabu, Tatsuya Hirasawa, Ingmar Werneburg, Shigeru Kuratani, Hiroki Kurihara. 2 November 2021. Mammalian face as an evolutionary novelty. PNAS 118 (44) e2111876118. DOI: 10.1073/pnas.2111876118

https://www.pnas.org/content/118/44/e2111876118

 

Related Links

Graduate School of Medicine: http://www.m.u-tokyo.ac.jp/english/

 

Research Contact

Hiroki Higashiyama, Ph.D. 

Department of Physiological Chemistry and Metabolism, Graduate School of Medicine, The University of Tokyo, 7-3-1, Hongo, Bunkyo-ku, Tokyo 113-0033, Japan.

Email: h-hiroki@m.u-tokyo.ac.jp

 

Press Officer Contact

Ms. Caitlin Devor

Division for Strategic Public Relations, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 133-8654, JAPAN

Tel: +81-080-9707-8178

Email: press-releases.adm@gs.mail.u-tokyo.ac.jp

 

About the University of Tokyo

The University of Tokyo is Japan’s leading university and one of the world’s top research universities. The vast research output of some 6,000 researchers is published in the world’s top journals across the arts and sciences. Our vibrant student body of around 15,000 undergraduate and 15,000 graduate students includes over 4,000 international students. Find out more at http://www.u-tokyo.ac.jp/en/ or follow us on Twitter at @UTokyo_News_en.

 

Funders

Japan Society for the Promotion of Science, JRPs-LEAD with German Research Foundation, City University of Hong Kong Start-up Grant, Core Research for Evolutional Science and Technology of the Japan Science and Technology Agency


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