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Notch/Her12 signalling modulates, motile/immotile cilia ratio downstream of Foxj1a in zebrafish left-right organizer
Foxj1a is necessary and sufficient to specify motile cilia. Using transcriptional studies and slow-scan two-photon live imaging capable of identifying the number of motile and immotile cilia, we now established that the final number of motile cilia depends on Notch signalling (NS). We found that des...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5608511/ https://www.ncbi.nlm.nih.gov/pubmed/28875937 http://dx.doi.org/10.7554/eLife.25165 |
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author | Tavares, Barbara Jacinto, Raquel Sampaio, Pedro Pestana, Sara Pinto, Andreia Vaz, Andreia Roxo-Rosa, Mónica Gardner, Rui Lopes, Telma Schilling, Britta Henry, Ian Saúde, Leonor Lopes, Susana Santos |
author_facet | Tavares, Barbara Jacinto, Raquel Sampaio, Pedro Pestana, Sara Pinto, Andreia Vaz, Andreia Roxo-Rosa, Mónica Gardner, Rui Lopes, Telma Schilling, Britta Henry, Ian Saúde, Leonor Lopes, Susana Santos |
author_sort | Tavares, Barbara |
collection | PubMed |
description | Foxj1a is necessary and sufficient to specify motile cilia. Using transcriptional studies and slow-scan two-photon live imaging capable of identifying the number of motile and immotile cilia, we now established that the final number of motile cilia depends on Notch signalling (NS). We found that despite all left-right organizer (LRO) cells express foxj1a and the ciliary axonemes of these cells have dynein arms, some cilia remain immotile. We identified that this decision is taken early in development in the Kupffer’s Vesicle (KV) precursors the readout being her12 transcription. We demonstrate that overexpression of either her12 or Notch intracellular domain (NICD) increases the number of immotile cilia at the expense of motile cilia, and leads to an accumulation of immotile cilia at the anterior half of the KV. This disrupts the normal fluid flow intensity and pattern, with consequent impact on dand5 expression pattern and left-right (L-R) axis establishment. |
format | Online Article Text |
id | pubmed-5608511 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-56085112017-09-25 Notch/Her12 signalling modulates, motile/immotile cilia ratio downstream of Foxj1a in zebrafish left-right organizer Tavares, Barbara Jacinto, Raquel Sampaio, Pedro Pestana, Sara Pinto, Andreia Vaz, Andreia Roxo-Rosa, Mónica Gardner, Rui Lopes, Telma Schilling, Britta Henry, Ian Saúde, Leonor Lopes, Susana Santos eLife Developmental Biology Foxj1a is necessary and sufficient to specify motile cilia. Using transcriptional studies and slow-scan two-photon live imaging capable of identifying the number of motile and immotile cilia, we now established that the final number of motile cilia depends on Notch signalling (NS). We found that despite all left-right organizer (LRO) cells express foxj1a and the ciliary axonemes of these cells have dynein arms, some cilia remain immotile. We identified that this decision is taken early in development in the Kupffer’s Vesicle (KV) precursors the readout being her12 transcription. We demonstrate that overexpression of either her12 or Notch intracellular domain (NICD) increases the number of immotile cilia at the expense of motile cilia, and leads to an accumulation of immotile cilia at the anterior half of the KV. This disrupts the normal fluid flow intensity and pattern, with consequent impact on dand5 expression pattern and left-right (L-R) axis establishment. eLife Sciences Publications, Ltd 2017-09-06 /pmc/articles/PMC5608511/ /pubmed/28875937 http://dx.doi.org/10.7554/eLife.25165 Text en © 2017, Tavares et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Developmental Biology Tavares, Barbara Jacinto, Raquel Sampaio, Pedro Pestana, Sara Pinto, Andreia Vaz, Andreia Roxo-Rosa, Mónica Gardner, Rui Lopes, Telma Schilling, Britta Henry, Ian Saúde, Leonor Lopes, Susana Santos Notch/Her12 signalling modulates, motile/immotile cilia ratio downstream of Foxj1a in zebrafish left-right organizer |
title | Notch/Her12 signalling modulates, motile/immotile cilia ratio downstream of Foxj1a in zebrafish left-right organizer |
title_full | Notch/Her12 signalling modulates, motile/immotile cilia ratio downstream of Foxj1a in zebrafish left-right organizer |
title_fullStr | Notch/Her12 signalling modulates, motile/immotile cilia ratio downstream of Foxj1a in zebrafish left-right organizer |
title_full_unstemmed | Notch/Her12 signalling modulates, motile/immotile cilia ratio downstream of Foxj1a in zebrafish left-right organizer |
title_short | Notch/Her12 signalling modulates, motile/immotile cilia ratio downstream of Foxj1a in zebrafish left-right organizer |
title_sort | notch/her12 signalling modulates, motile/immotile cilia ratio downstream of foxj1a in zebrafish left-right organizer |
topic | Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5608511/ https://www.ncbi.nlm.nih.gov/pubmed/28875937 http://dx.doi.org/10.7554/eLife.25165 |
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