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Unique spatiotemporal requirements for intraflagellar transport genes during forebrain development

Primary cilia are organelles extended from virtually all cells and are required for the proper regulation of a number of canonical developmental pathways. The role in cortical development of proteins important for ciliary form and function is a relatively understudied area. Here we have taken a gene...

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Autores principales: Snedeker, John, Schock, Elizabeth N., Struve, Jamie N., Chang, Ching-Fang, Cionni, Megan, Tran, Pamela V., Brugmann, Samantha A., Stottmann, Rolf W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5349613/
https://www.ncbi.nlm.nih.gov/pubmed/28291836
http://dx.doi.org/10.1371/journal.pone.0173258
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author Snedeker, John
Schock, Elizabeth N.
Struve, Jamie N.
Chang, Ching-Fang
Cionni, Megan
Tran, Pamela V.
Brugmann, Samantha A.
Stottmann, Rolf W.
author_facet Snedeker, John
Schock, Elizabeth N.
Struve, Jamie N.
Chang, Ching-Fang
Cionni, Megan
Tran, Pamela V.
Brugmann, Samantha A.
Stottmann, Rolf W.
author_sort Snedeker, John
collection PubMed
description Primary cilia are organelles extended from virtually all cells and are required for the proper regulation of a number of canonical developmental pathways. The role in cortical development of proteins important for ciliary form and function is a relatively understudied area. Here we have taken a genetic approach to define the role in forebrain development of three intraflagellar transport proteins known to be important for primary cilia function. We have genetically ablated Kif3a, Ift88, and Ttc21b in a series of specific spatiotemporal domains. The resulting phenotypes allow us to draw several conclusions. First, we conclude that the Ttc21b cortical phenotype is not due to the activity of Ttc21b within the brain itself. Secondly, some of the most striking phenotypes are from ablations in the neural crest cells and the adjacent surface ectoderm indicating that cilia transduce critical tissue—tissue interactions in the developing embryonic head. Finally, we note striking differences in phenotypes from ablations only one embryonic day apart, indicating very discrete spatiotemporal requirements for these three genes in cortical development.
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spelling pubmed-53496132017-04-06 Unique spatiotemporal requirements for intraflagellar transport genes during forebrain development Snedeker, John Schock, Elizabeth N. Struve, Jamie N. Chang, Ching-Fang Cionni, Megan Tran, Pamela V. Brugmann, Samantha A. Stottmann, Rolf W. PLoS One Research Article Primary cilia are organelles extended from virtually all cells and are required for the proper regulation of a number of canonical developmental pathways. The role in cortical development of proteins important for ciliary form and function is a relatively understudied area. Here we have taken a genetic approach to define the role in forebrain development of three intraflagellar transport proteins known to be important for primary cilia function. We have genetically ablated Kif3a, Ift88, and Ttc21b in a series of specific spatiotemporal domains. The resulting phenotypes allow us to draw several conclusions. First, we conclude that the Ttc21b cortical phenotype is not due to the activity of Ttc21b within the brain itself. Secondly, some of the most striking phenotypes are from ablations in the neural crest cells and the adjacent surface ectoderm indicating that cilia transduce critical tissue—tissue interactions in the developing embryonic head. Finally, we note striking differences in phenotypes from ablations only one embryonic day apart, indicating very discrete spatiotemporal requirements for these three genes in cortical development. Public Library of Science 2017-03-14 /pmc/articles/PMC5349613/ /pubmed/28291836 http://dx.doi.org/10.1371/journal.pone.0173258 Text en © 2017 Snedeker et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Snedeker, John
Schock, Elizabeth N.
Struve, Jamie N.
Chang, Ching-Fang
Cionni, Megan
Tran, Pamela V.
Brugmann, Samantha A.
Stottmann, Rolf W.
Unique spatiotemporal requirements for intraflagellar transport genes during forebrain development
title Unique spatiotemporal requirements for intraflagellar transport genes during forebrain development
title_full Unique spatiotemporal requirements for intraflagellar transport genes during forebrain development
title_fullStr Unique spatiotemporal requirements for intraflagellar transport genes during forebrain development
title_full_unstemmed Unique spatiotemporal requirements for intraflagellar transport genes during forebrain development
title_short Unique spatiotemporal requirements for intraflagellar transport genes during forebrain development
title_sort unique spatiotemporal requirements for intraflagellar transport genes during forebrain development
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5349613/
https://www.ncbi.nlm.nih.gov/pubmed/28291836
http://dx.doi.org/10.1371/journal.pone.0173258
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