Meis2 Is Required for Inner Ear Formation and Proper Morphogenesis of the Cochlea
Meis genes have been shown to control essential processes during development of the central and peripheral nervous system. Here we have explored the roles of the Meis2 gene during vertebrate inner ear induction and the formation of the cochlea. Meis2 is expressed in several tissues required for inne...
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Published in | Frontiers in cell and developmental biology Vol. 9; p. 679325 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Frontiers Media S.A
28.05.2021
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Subjects | |
Online Access | Get full text |
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Summary: | Meis
genes have been shown to control essential processes during development of the central and peripheral nervous system. Here we have explored the roles of the
Meis2
gene during vertebrate inner ear induction and the formation of the cochlea.
Meis2
is expressed in several tissues required for inner ear induction and in non-sensory tissue of the cochlear duct. Global inactivation of
Meis2
in the mouse leads to a severely reduced size of the otic vesicle. Tissue-specific knock outs of
Meis2
reveal that its expression in the hindbrain is essential for otic vesicle formation. Inactivation of
Meis2
in the inner ear itself leads to an aberrant coiling of the cochlear duct. By analyzing transcriptomes obtained from
Meis2
mutants and ChIPseq analysis of an otic cell line, we define candidate target genes for
Meis2
which may be directly or indirectly involved in cochlear morphogenesis. Taken together, these data show that
Meis2
is essential for inner ear formation and provide an entry point to unveil the network underlying proper coiling of the cochlear duct. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 This article was submitted to Morphogenesis and Patterning, a section of the journal Frontiers in Cell and Developmental Biology Edited by: Rosa Barrio, CIC bioGUNE, Spain Reviewed by: Andy Groves, Baylor College of Medicine, United States; Olivia Bermingham-McDonogh, University of Washington, United States |
ISSN: | 2296-634X 2296-634X |
DOI: | 10.3389/fcell.2021.679325 |