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A systems-level approach reveals new gene regulatory modules in the developing ear
Author(s) -
Jingchen Chen,
Monica Tambalo,
Meyer Barembaum,
Ramya Ranganathan,
Marcos Simões-Costa,
Marianne BronnerFraser,
Andrea Streit
Publication year - 2017
Publication title -
development
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.15
H-Index - 36
eISSN - 1477-9129
pISSN - 0950-1991
DOI - 10.1242/dev.148494
Subject(s) - biology , reprogramming , inner ear , gene regulatory network , fate mapping , gene , genetics , cell fate determination , progenitor , embryonic stem cell , transcriptome , progenitor cell , otic vesicle , microbiology and biotechnology , transcription factor , lineage (genetic) , regulation of gene expression , gene expression , neuroscience , stem cell , in situ hybridization
The inner ear is a complex vertebrate sense organ, yet it arises from a simple epithelium, the otic placode. Specification towards otic fate requires diverse signals and transcriptional inputs that act sequentially and/or in parallel. Using the chick embryo, we uncover novel genes in the gene regulatory network underlying otic commitment and reveal dynamic changes in gene expression. Functional analysis of selected transcription factors reveals the genetic hierarchy underlying the transition from progenitor to committed precursor, integrating known and novel molecular players. Our results not only characterize the otic transcriptome in unprecedented detail, but also identify new gene interactions responsible for inner ear development and for the segregation of the otic lineage from epibranchial progenitors. By recapitulating the embryonic programme, the genes and genetic sub-circuits discovered here might be useful for reprogramming naïve cells towards otic identity to restore hearing loss.

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