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Daple coordinates organ-wide and cell-intrinsic polarity to pattern inner-ear hair bundles

The establishment of planar polarization by mammalian cells necessitates the integration of diverse signaling pathways. In the inner ear, at least two systems regulate the planar polarity of sensory hair bundles. The core planar cell polarity (PCP) proteins coordinate the orientations of hair cells...

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Detalles Bibliográficos
Autores principales: Siletti, Kimberly, Tarchini, Basile, Hudspeth, A. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5748220/
https://www.ncbi.nlm.nih.gov/pubmed/29229865
http://dx.doi.org/10.1073/pnas.1716522115
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author Siletti, Kimberly
Tarchini, Basile
Hudspeth, A. J.
author_facet Siletti, Kimberly
Tarchini, Basile
Hudspeth, A. J.
author_sort Siletti, Kimberly
collection PubMed
description The establishment of planar polarization by mammalian cells necessitates the integration of diverse signaling pathways. In the inner ear, at least two systems regulate the planar polarity of sensory hair bundles. The core planar cell polarity (PCP) proteins coordinate the orientations of hair cells across the epithelial plane. The cell-intrinsic patterning of hair bundles is implemented independently by the G protein complex classically known for orienting the mitotic spindle. Although the primary cilium also participates in each of these pathways, its role and the integration of the two systems are poorly understood. We show that Dishevelled-associating protein with a high frequency of leucine residues (Daple) interacts with PCP and cell-intrinsic signals. Regulated by the cell-intrinsic pathway, Daple is required to maintain the polarized distribution of the core PCP protein Dishevelled and to position the primary cilium at the abneural edge of the apical surface. Our results suggest that the primary cilium or an associated structure influences the domain of cell-intrinsic signals that shape the hair bundle. Daple is therefore essential to orient and pattern sensory hair bundles.
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spelling pubmed-57482202018-01-09 Daple coordinates organ-wide and cell-intrinsic polarity to pattern inner-ear hair bundles Siletti, Kimberly Tarchini, Basile Hudspeth, A. J. Proc Natl Acad Sci U S A PNAS Plus The establishment of planar polarization by mammalian cells necessitates the integration of diverse signaling pathways. In the inner ear, at least two systems regulate the planar polarity of sensory hair bundles. The core planar cell polarity (PCP) proteins coordinate the orientations of hair cells across the epithelial plane. The cell-intrinsic patterning of hair bundles is implemented independently by the G protein complex classically known for orienting the mitotic spindle. Although the primary cilium also participates in each of these pathways, its role and the integration of the two systems are poorly understood. We show that Dishevelled-associating protein with a high frequency of leucine residues (Daple) interacts with PCP and cell-intrinsic signals. Regulated by the cell-intrinsic pathway, Daple is required to maintain the polarized distribution of the core PCP protein Dishevelled and to position the primary cilium at the abneural edge of the apical surface. Our results suggest that the primary cilium or an associated structure influences the domain of cell-intrinsic signals that shape the hair bundle. Daple is therefore essential to orient and pattern sensory hair bundles. National Academy of Sciences 2017-12-26 2017-12-11 /pmc/articles/PMC5748220/ /pubmed/29229865 http://dx.doi.org/10.1073/pnas.1716522115 Text en Copyright © 2017 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle PNAS Plus
Siletti, Kimberly
Tarchini, Basile
Hudspeth, A. J.
Daple coordinates organ-wide and cell-intrinsic polarity to pattern inner-ear hair bundles
title Daple coordinates organ-wide and cell-intrinsic polarity to pattern inner-ear hair bundles
title_full Daple coordinates organ-wide and cell-intrinsic polarity to pattern inner-ear hair bundles
title_fullStr Daple coordinates organ-wide and cell-intrinsic polarity to pattern inner-ear hair bundles
title_full_unstemmed Daple coordinates organ-wide and cell-intrinsic polarity to pattern inner-ear hair bundles
title_short Daple coordinates organ-wide and cell-intrinsic polarity to pattern inner-ear hair bundles
title_sort daple coordinates organ-wide and cell-intrinsic polarity to pattern inner-ear hair bundles
topic PNAS Plus
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5748220/
https://www.ncbi.nlm.nih.gov/pubmed/29229865
http://dx.doi.org/10.1073/pnas.1716522115
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