Unique and shared gene expression patterns in Atlantic salmon (Salmo salar) tooth development

• Published in: Development Genes and Evolution
• Main Authors: Huysseune, Ann, Takle, Harald, Soenens, Mieke, Taerwe, Karen, Witten, Paul Eckhard
• Format: Article in Journal/Newspaper
• Language: English
• Published: 2008
• Subjects: Atlantic salmon; Salmo salar
• Online Access: https://biblio.ugent.be/publication/684207; http://hdl.handle.net/1854/LU-684207; https://doi.org/10.1007/s00427-008-0237-9; https://biblio.ugent.be/publication/684207/file/684227

To validate the use of Atlantic salmon (Salmo salar L.) as a model species in research on the mechanism of continuous tooth replacement, we have started to collect data on the molecular control underlying tooth formation in this species. This study reports expression patterns in the lower jaw dentition of a number of key regulatory genes such as bmp2, bmp4, and sox9 and structural genes such as col1 alpha 1 and osteocalcin (= bgp, Bone Gla Protein) by means of in situ hybridization using salmon-specific, digoxygenin-labeled antisense riboprobes. We compare expression of these genes to that in other skeletogenic cells in the lower jaw (osteoblasts, chondroblasts, and chondrocytes). Our studies reveal both expression patterns that are in accordance to studies on mammalian tooth development and patterns that are specific to salmon, or teleosts. The epithelial expression of sox9 and a shift of the expression of bmp2 from epithelium to mesenchyme have also been observed during mammalian tooth development. Different from previous reports are the expressions of col1 alpha 1 and osteocalcin. In contrast to what has been reported for zebrafish, osteocalcin is not expressed in odontoblasts, nor in the osteoblasts involved in the attachment of the teeth. At the lower jaw, osteocalcin is expressed in mature and/or resting osteoblasts only. As expected, col1 alpha 1 is expressed in odontoblasts. Surprisingly, it is also strongly expressed in the inner dental epithelium, representing the first report of ameloblast involvement in collagen type I transcription. Whether the collagen is translated and secreted into the enameloid remains to be demonstrated.