Publication: Role of skeletal muscle in ear development
Authors
Rot, Irena ; Baguma Nibasheka, Mark ; Costain, Willard J. ; Hong, Paul ; Tafra, Robert ; Mardesic Brakus, Snjezana ; Mrduljas Djujic, Natasa ; Saraga Babic, Mirna ; Kablar, Boris
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Publisher
Universidad de Murcia. Departamento de Biología Celular e Histología
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DOI
DOI: 10.14670/HH-11-886
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info:eu-repo/semantics/article
Description
Abstract
The current paper is a continuation of our
work described in Rot and Kablar, 2010. Here, we show
lists of 10 up- and 87 down-regulated genes obtained by
a cDNA microarray analysis that compared developing
Myf5-/-:Myod-/- (and Mrf4-/-) petrous part of the
temporal bone, containing middle and inner ear, to the
control, at embryonic day 18.5. Myf5-/-:Myod-/- fetuses
entirely lack skeletal myoblasts and muscles. They are
unable to move their head, which interferes with the
perception of angular acceleration. Previously, we
showed that the inner ear areas most affected in Myf5-/-
:Myod-/- fetuses were the vestibular cristae ampullaris,
sensitive to angular acceleration. Our finding that the
type I hair cells were absent in the mutants’ cristae was
further used here to identify a profile of genes specific to
the lacking cell type. Microarrays followed by a detailed
consultation of web-accessible mouse databases allowed
us to identify 6 candidate genes with a possible role in
the development of the inner ear sensory organs: Actc1,
Pgam2, Ldb3, Eno3, Hspb7 and Smpx. Additionally, we
searched for human homologues of the candidate genes
since a number of syndromes in humans have associated
inner ear abnormalities. Mutations in one of our
candidate genes, Smpx, have been reported as the cause
of X-linked deafness in humans. Our current study
suggests an epigenetic role that mechanical, and
potentially other, stimuli originating from muscle, play
in organogenesis, and offers an approach to finding
novel genes responsible for altered inner ear phenotypes.
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Citation
Histology and Histopathology, Vol.32, nº10, (2017)
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