PUBLICATION
Tfap2a Promotes Specification and Maturation of Neurons in the Inner Ear through Modulation of Bmp, Fgf and Notch Signaling
- Authors
- Kantarci, H., Edlund, R.K., Groves, A.K., Riley, B.B.
- ID
- ZDB-PUB-150318-1
- Date
- 2015
- Source
- PLoS Genetics 11: e1005037 (Journal)
- Registered Authors
- Riley, Bruce
- Keywords
- Embryos, Vesicles, Neurons, Neuronal differentiation, Neuroblasts, Notch signaling, Neurogenesis, Ears
- MeSH Terms
-
- Animals
- Bone Morphogenetic Protein 7/biosynthesis
- Bone Morphogenetic Protein 7/genetics*
- Cell Differentiation/genetics
- Chickens
- Ear, Inner/growth & development
- Ear, Inner/metabolism
- Fibroblast Growth Factors/genetics
- Fibroblast Growth Factors/metabolism
- Ganglion Cysts/embryology
- Ganglion Cysts/genetics*
- Gene Expression Regulation, Developmental
- Neurogenesis/genetics*
- Receptors, Notch/genetics
- Receptors, Notch/metabolism
- Signal Transduction/genetics
- Transcription Factor AP-2/biosynthesis*
- Transcription Factor AP-2/genetics
- Zebrafish/genetics
- Zebrafish/growth & development
- Zebrafish Proteins/biosynthesis*
- Zebrafish Proteins/genetics*
- PubMed
- 25781991 Full text @ PLoS Genet.
Citation
Kantarci, H., Edlund, R.K., Groves, A.K., Riley, B.B. (2015) Tfap2a Promotes Specification and Maturation of Neurons in the Inner Ear through Modulation of Bmp, Fgf and Notch Signaling. PLoS Genetics. 11:e1005037.
Abstract
Neurons of the statoacoustic ganglion (SAG) transmit auditory and vestibular information from the inner ear to the hindbrain. SAG neuroblasts originate in the floor of the otic vesicle. New neuroblasts soon delaminate and migrate towards the hindbrain while continuing to proliferate, a phase known as transit amplification. SAG cells eventually come to rest between the ear and hindbrain before terminally differentiating. Regulation of these events is only partially understood. Fgf initiates neuroblast specification within the ear. Subsequently, Fgf secreted by mature SAG neurons exceeds a maximum threshold, serving to terminate specification and delay maturation of transit-amplifying cells. Notch signaling also limits SAG development, but how it is coordinated with Fgf is unknown. Here we show that transcription factor Tfap2a coordinates multiple signaling pathways to promote neurogenesis in the zebrafish inner ear. In both zebrafish and chick, Tfap2a is expressed in a ventrolateral domain of the otic vesicle that includes neurogenic precursors. Functional studies were conducted in zebrafish. Loss of Tfap2a elevated Fgf and Notch signaling, thereby inhibiting SAG specification and slowing maturation of transit-amplifying cells. Conversely, overexpression of Tfap2a inhibited Fgf and Notch signaling, leading to excess and accelerated SAG production. However, most SAG neurons produced by Tfap2a overexpression died soon after maturation. Directly blocking either Fgf or Notch caused less dramatic acceleration of SAG development without neuronal death, whereas blocking both pathways mimicked all observed effects of Tfap2a overexpression, including apoptosis of mature neurons. Analysis of genetic mosaics showed that Tfap2a acts non-autonomously to inhibit Fgf. This led to the discovery that Tfap2a activates expression of Bmp7a, which in turn inhibits both Fgf and Notch signaling. Blocking Bmp signaling reversed the effects of overexpressing Tfap2a. Together, these data support a model in which Tfap2a, acting through Bmp7a, modulates Fgf and Notch signaling to control the duration, amount and speed of SAG neural development.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping