The Notch ligand Jagged1 is required for inner ear sensory development
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- 20 March 2001
- journal article
- Published by Proceedings of the National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 98 (7) , 3873-3878
- https://doi.org/10.1073/pnas.071496998
Abstract
Within the mammalian inner ear there are six separate sensory regions that subserve the functions of hearing and balance, although how these sensory regions become specified remains unknown. Each sensory region is populated by two cell types, the mechanosensory hair cell and the supporting cell, which are arranged in a mosaic in which each hair cell is surrounded by supporting cells. The proposed mechanism for creating the sensory mosaic is lateral inhibition mediated by the Notch signaling pathway. However, one of the Notch ligands, Jagged1 (Jag1), does not show an expression pattern wholly consistent with a role in lateral inhibition, as it marks the sensory patches from very early in their development--presumably long before cells make their final fate decisions. It has been proposed that Jag1 has a role in specifying sensory versus nonsensory epithelium within the ear [Adam, J., Myat, A., Roux, I. L., Eddison, M., Henrique, D., Ish-Horowicz, D. & Lewis, J. (1998) Development (Cambridge, U.K.) 125, 4645--4654]. Here we provide experimental evidence that Notch signaling may be involved in specifying sensory regions by showing that a dominant mouse mutant headturner (Htu) contains a missense mutation in the Jag1 gene and displays missing posterior and sometimes anterior ampullae, structures that house the sensory cristae. Htu/+ mutants also demonstrate a significant reduction in the numbers of outer hair cells in the organ of Corti. Because lateral inhibition mediated by Notch predicts that disruptions in this pathway would lead to an increase in hair cells, we believe these data indicate an earlier role for Notch within the inner ear.Keywords
This publication has 37 references indexed in Scilit:
- Expression of Math1 and HES5 in the Cochleae of Wildtype and Jag2 Mutant MiceJournal of the Association for Research in Otolaryngology, 2000
- Mouse Jagged1 Physically Interacts with Notch2 and Other Notch ReceptorsJournal of Biological Chemistry, 1999
- Fringe, Notch, and making developmental boundariesCurrent Opinion in Genetics & Development, 1999
- Notch Signaling: Cell Fate Control and Signal Integration in DevelopmentScience, 1999
- Mutations in the human Jagged1 gene are responsible for Alagille syndromeNature Genetics, 1997
- Cell fate specification in the inner earCurrent Opinion in Neurobiology, 1996
- Sequence of C. elegans lag-2 reveals a cell-signalling domain shared with Delta and Serrate of DrosophilaNature, 1994
- Single amino acid substitutions in EGF-like elements of notch and delta modify drosophila development and affect cell adhesion in vitroNeuron, 1992
- Temporal Bone Histopathologic Findings in Alagille's SyndromeJAMA Otolaryngology–Head & Neck Surgery, 1990
- Mutations altering the structure of epidermal growth factor-like coding sequences at the Drosophila Notch locusCell, 1987