Affiliation:
1. Center for Advanced Biotechnology and Medicine and Department of Pediatrics, Robert Wood Johnson Medical School, University of Medicine and Dentistry of New Jersey, Piscataway, New Jersey 08854
2. Department of Biomedical Sciences, Creighton University, Omaha, Nebraska 68178
Abstract
ABSTRACT
The development of the nervous system requires the concerted actions of multiple transcription factors, yet the molecular events leading to their expression remain poorly understood. Barhl1, a mammalian homeodomain transcription factor of the BarH class, is expressed by developing inner ear hair cells, cerebellar granule cells, precerebellar neurons, and collicular neurons. Targeted gene inactivation has demonstrated a crucial role for
Barhl1
in the survival and/or migration of these sensory cells and neurons. Here we report the regulatory sequences of
Barhl1
necessary for directing its proper spatiotemporal expression pattern in the inner ear and central nervous system (CNS). Using a transgenic approach, we have found that high-level and cell-specific expression of
Barhl1
within the inner ear and CNS depends on both its 5′ promoter and 3′ enhancer sequences. Further transcriptional, binding, and mutational analyses of the 5′ promoter have identified two homeoprotein binding motifs that can be occupied and activated by Barhl1. Moreover, proper
Barhl1
expression in inner ear hair cells and cerebellar and precerebellar neurons requires the presence of
Atoh1
. Together, these data delineate useful
Barhl1
regulatory sequences that direct strong and specific gene expression to inner ear hair cells and CNS sensory neurons, establish a role for autoregulation in the maintenance of
Barhl1
expression, and identify Atoh1 as a key upstream regulator.
Publisher
American Society for Microbiology
Subject
Cell Biology,Molecular Biology
Cited by
40 articles.
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