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Reciprocal Negative Regulation Between Lmx1a and Lmo4 Is Required for Inner Ear Formation

LIM-domain containing transcription factors (LIM-TFs) are conserved factors important for embryogenesis. The specificity of these factors in transcriptional regulation is conferred by the complexes that they form with other proteins such as LIM-domain-binding (Ldb) proteins and LIM-domain only (LMO)...

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Autores principales: Huang, Yanhan, Hill, Jennifer, Yatteau, Andrew, Wong, Loksum, Jiang, Tao, Petrovic, Jelena, Gan, Lin, Dong, Lijin, Wu, Doris K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for Neuroscience 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5990987/
https://www.ncbi.nlm.nih.gov/pubmed/29769265
http://dx.doi.org/10.1523/JNEUROSCI.2484-17.2018
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author Huang, Yanhan
Hill, Jennifer
Yatteau, Andrew
Wong, Loksum
Jiang, Tao
Petrovic, Jelena
Gan, Lin
Dong, Lijin
Wu, Doris K.
author_facet Huang, Yanhan
Hill, Jennifer
Yatteau, Andrew
Wong, Loksum
Jiang, Tao
Petrovic, Jelena
Gan, Lin
Dong, Lijin
Wu, Doris K.
author_sort Huang, Yanhan
collection PubMed
description LIM-domain containing transcription factors (LIM-TFs) are conserved factors important for embryogenesis. The specificity of these factors in transcriptional regulation is conferred by the complexes that they form with other proteins such as LIM-domain-binding (Ldb) proteins and LIM-domain only (LMO) proteins. Unlike LIM-TFs, these proteins do not bind DNA directly. LMO proteins are negative regulators of LIM-TFs and function by competing with LIM-TFs for binding to Ldb's. Although the LIM-TF Lmx1a is expressed in the developing mouse hindbrain, which provides many of the extrinsic signals for inner ear formation, conditional knock-out embryos of both sexes show that the inner ear source of Lmx1a is the major contributor of ear patterning. In addition, we have found that the reciprocal interaction between Lmx1a and Lmo4 (a LMO protein within the inner ear) mediates the formation of both vestibular and auditory structures. Lmo4 negatively regulates Lmx1a to form the three sensory cristae, the anterior semicircular canal, and the shape of the utricle in the vestibule. Furthermore, this negative regulation blocks ectopic sensory formation in the cochlea. In contrast, Lmx1a negatively regulates Lmo4 in mediating epithelial resorption of the canal pouch, which gives rise to the anterior and posterior semicircular canals. We also found that Lmx1a is independently required for the formation of the endolymphatic duct and hair cells in the basal cochlear region. SIGNIFICANCE STATEMENT The mammalian inner ear is a structurally complex organ responsible for detecting sound and maintaining balance. Failure to form the intricate 3D structure of this organ properly during development most likely will result in sensory deficits on some level. Here, we provide genetic evidence that a transcription factor, Lmx1a, interacts with its negative regulator, Lmo4, to pattern various vestibular and auditory components of the mammalian inner ear. Identifying these key molecules that mediate formation of this important sensory organ will be helpful for designing strategies and therapeutics to alleviate hearing loss and balance disorders.
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spelling pubmed-59909872018-06-22 Reciprocal Negative Regulation Between Lmx1a and Lmo4 Is Required for Inner Ear Formation Huang, Yanhan Hill, Jennifer Yatteau, Andrew Wong, Loksum Jiang, Tao Petrovic, Jelena Gan, Lin Dong, Lijin Wu, Doris K. J Neurosci Research Articles LIM-domain containing transcription factors (LIM-TFs) are conserved factors important for embryogenesis. The specificity of these factors in transcriptional regulation is conferred by the complexes that they form with other proteins such as LIM-domain-binding (Ldb) proteins and LIM-domain only (LMO) proteins. Unlike LIM-TFs, these proteins do not bind DNA directly. LMO proteins are negative regulators of LIM-TFs and function by competing with LIM-TFs for binding to Ldb's. Although the LIM-TF Lmx1a is expressed in the developing mouse hindbrain, which provides many of the extrinsic signals for inner ear formation, conditional knock-out embryos of both sexes show that the inner ear source of Lmx1a is the major contributor of ear patterning. In addition, we have found that the reciprocal interaction between Lmx1a and Lmo4 (a LMO protein within the inner ear) mediates the formation of both vestibular and auditory structures. Lmo4 negatively regulates Lmx1a to form the three sensory cristae, the anterior semicircular canal, and the shape of the utricle in the vestibule. Furthermore, this negative regulation blocks ectopic sensory formation in the cochlea. In contrast, Lmx1a negatively regulates Lmo4 in mediating epithelial resorption of the canal pouch, which gives rise to the anterior and posterior semicircular canals. We also found that Lmx1a is independently required for the formation of the endolymphatic duct and hair cells in the basal cochlear region. SIGNIFICANCE STATEMENT The mammalian inner ear is a structurally complex organ responsible for detecting sound and maintaining balance. Failure to form the intricate 3D structure of this organ properly during development most likely will result in sensory deficits on some level. Here, we provide genetic evidence that a transcription factor, Lmx1a, interacts with its negative regulator, Lmo4, to pattern various vestibular and auditory components of the mammalian inner ear. Identifying these key molecules that mediate formation of this important sensory organ will be helpful for designing strategies and therapeutics to alleviate hearing loss and balance disorders. Society for Neuroscience 2018-06-06 /pmc/articles/PMC5990987/ /pubmed/29769265 http://dx.doi.org/10.1523/JNEUROSCI.2484-17.2018 Text en Copyright © 2018 Huang et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License Creative Commons Attribution 4.0 International (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Articles
Huang, Yanhan
Hill, Jennifer
Yatteau, Andrew
Wong, Loksum
Jiang, Tao
Petrovic, Jelena
Gan, Lin
Dong, Lijin
Wu, Doris K.
Reciprocal Negative Regulation Between Lmx1a and Lmo4 Is Required for Inner Ear Formation
title Reciprocal Negative Regulation Between Lmx1a and Lmo4 Is Required for Inner Ear Formation
title_full Reciprocal Negative Regulation Between Lmx1a and Lmo4 Is Required for Inner Ear Formation
title_fullStr Reciprocal Negative Regulation Between Lmx1a and Lmo4 Is Required for Inner Ear Formation
title_full_unstemmed Reciprocal Negative Regulation Between Lmx1a and Lmo4 Is Required for Inner Ear Formation
title_short Reciprocal Negative Regulation Between Lmx1a and Lmo4 Is Required for Inner Ear Formation
title_sort reciprocal negative regulation between lmx1a and lmo4 is required for inner ear formation
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5990987/
https://www.ncbi.nlm.nih.gov/pubmed/29769265
http://dx.doi.org/10.1523/JNEUROSCI.2484-17.2018
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