Patterning by heritage in mouse molar row development
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
20709958
PubMed Central
PMC2932592
DOI
10.1073/pnas.1002784107
PII: 1002784107
Knihovny.cz E-zdroje
- MeSH
- biologické modely MeSH
- časové faktory MeSH
- fluorescenční mikroskopie metody MeSH
- hybridizace in situ MeSH
- mandibula embryologie růst a vývoj metabolismus MeSH
- moláry embryologie růst a vývoj MeSH
- myši inbrední C57BL MeSH
- myši transgenní MeSH
- myši MeSH
- odontogeneze * MeSH
- proteiny hedgehog genetika metabolismus MeSH
- techniky tkáňových kultur MeSH
- zelené fluorescenční proteiny genetika metabolismus MeSH
- zobrazování trojrozměrné metody MeSH
- zvířata MeSH
- Check Tag
- mužské pohlaví MeSH
- myši MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- proteiny hedgehog MeSH
- Shh protein, mouse MeSH Prohlížeč
- zelené fluorescenční proteiny MeSH
It is known from paleontology studies that two premolars have been lost during mouse evolution. During mouse mandible development, two bud-like structures transiently form that may represent rudimentary precursors of the lost premolars. However, the interpretation of these structures and their significance for mouse molar development are highly controversial because of a lack of molecular data. Here, we searched for typical tooth signaling centers in these two bud-like structures, and followed their fate using molecular markers, 3D reconstructions, and lineage tracing in vitro. Transient signaling centers were indeed found to be located at the tips of both the anterior and posterior rudimentary buds. These centers expressed a similar set of molecular markers as the "primary enamel knot" (pEK), the signaling center of the first molar (M1). These two transient signaling centers were sequentially patterned before and anterior to the M1 pEK. We also determined the dynamics of the M1 pEK, which, slightly later during development, spread up to the field formerly occupied by the posterior transient signaling center. It can be concluded that two rudimentary tooth buds initiate the sequential development of the mouse molars and these have previously been mistaken for early stages of M1 development. Although neither rudiment progresses to form an adult tooth, the posterior one merges with the adjacent M1, which may explain the anterior enlargement of the M1 during mouse family evolution. This study highlights how rudiments of lost structures can stay integrated and participate in morphogenesis of functional organs and help in understanding their evolution, as Darwin suspected long ago.
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Role of Cell Death in Cellular Processes During Odontogenesis
Developmental variability channels mouse molar evolution
Modeling Edar expression reveals the hidden dynamics of tooth signaling center patterning
The Impact of the Eda Pathway on Tooth Root Development
Transcriptomic signatures shaped by cell proportions shed light on comparative developmental biology
Migration of Founder Epithelial Cells Drives Proper Molar Tooth Positioning and Morphogenesis
Sprouty gene dosage influences temporal-spatial dynamics of primary enamel knot formation
Three-dimensional analysis of the early development of the dentition
Apoptotic signaling in mouse odontogenesis