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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2017
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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. |
format | Online Article Text |
id | pubmed-5748220 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
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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