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Stenberg, O. E.

Publications and source records attributed to Stenberg, O. E..

2 recordsLinked to original sources

Rewinding the developmental tape shows how bears break a developmental rule

Mammals have evolved a broad variety of dental morphologies. Nevertheless, the development of the mammalian dentition is considered highly conserved. Molar size proportions exemplify this as a system where small changes in shared developmental mechanisms yield a defined range of morphological outcomes. The Inhibitory Cascade (IC) model states that as molars develop in a sequence, the first developing anterior molars inhibit the development of subsequent posterior ones. The IC model thus predicts a trend of linear tooth size change along the molar row, as has been observed in a wide range of mammalian taxa with otherwise differing dental morphology. Perhaps the starkest exceptions to the IC rule are bears, in which the second molar is the largest and the third molar is disproportionally small. Here we sought to illuminate when and how during development the bear dentition falls of the IC prediction. We examined molar proportions in seven bear species. The results indicate that development of bear molars deviates from IC expectation already during patterning. Yet, during the earlier cap stage, size proportions of bear molars still seem to adhere to the IC model predictions. Overall, these analyses are suggestive that irrespective of the final outcome, the process of initial splitting of the molar-forming region into individual teeth is conserved and follows the IC rule.

evolutionary biology↗

The developmental basis for scaling of mammalian tooth size

When evolution leads to differences in body size, organs generally scale along. A well-known example of the tight relationship between organ and body size is the scaling of mammalian molar teeth. To investigate how teeth scale during development and evolution, we compared molar development in mouse and rat from initiation through final size. Whereas the linear dimensions of the rat first lower molar are twice that of the mouse molar, their shapes are largely the same. We found that scaling of the molars starts early, and that the rat molar is patterned equally as fast but in a larger size than the mouse molar. Using transcriptomics, we discovered that a known regulator of body size, insulin-like growth factor 1 (Igf1), is more highly expressed in the rat molars compared to the mouse molars. Ex vivo and in vivo mouse models demonstrated that modulation of the IGF pathway reproduces several aspects of the observed scaling process. Furthermore, analysis of IGF1-treated mouse molars and computational modeling indicate that IGF signaling scales teeth by simultaneously enhancing growth and by inhibiting the cusp patterning program, thereby providing a relatively simple mechanism for scaling teeth during development and evolution. Finally, comparative data from shrews to elephants suggest that this scaling mechanism regulates the minimum tooth size possible, as well as the patterning potential of large teeth.

developmental biology↗