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Evolutionarily Ancient Association of the FoxJ1 Transcription Factor with the Motile Ciliogenic Program

It is generally believed that the last eukaryotic common ancestor (LECA) was a unicellular organism with motile cilia. In the vertebrates, the winged-helix transcription factor FoxJ1 functions as the master regulator of motile cilia biogenesis. Despite the antiquity of cilia, their highly conserved...

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Autores principales: Vij, Shubha, Rink, Jochen C., Ho, Hao Kee, Babu, Deepak, Eitel, Michael, Narasimhan, Vijayashankaranarayanan, Tiku, Varnesh, Westbrook, Jody, Schierwater, Bernd, Roy, Sudipto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3493443/
https://www.ncbi.nlm.nih.gov/pubmed/23144623
http://dx.doi.org/10.1371/journal.pgen.1003019
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author Vij, Shubha
Rink, Jochen C.
Ho, Hao Kee
Babu, Deepak
Eitel, Michael
Narasimhan, Vijayashankaranarayanan
Tiku, Varnesh
Westbrook, Jody
Schierwater, Bernd
Roy, Sudipto
author_facet Vij, Shubha
Rink, Jochen C.
Ho, Hao Kee
Babu, Deepak
Eitel, Michael
Narasimhan, Vijayashankaranarayanan
Tiku, Varnesh
Westbrook, Jody
Schierwater, Bernd
Roy, Sudipto
author_sort Vij, Shubha
collection PubMed
description It is generally believed that the last eukaryotic common ancestor (LECA) was a unicellular organism with motile cilia. In the vertebrates, the winged-helix transcription factor FoxJ1 functions as the master regulator of motile cilia biogenesis. Despite the antiquity of cilia, their highly conserved structure, and their mechanism of motility, the evolution of the transcriptional program controlling ciliogenesis has remained incompletely understood. In particular, it is presently not known how the generation of motile cilia is programmed outside of the vertebrates, and whether and to what extent the FoxJ1-dependent regulation is conserved. We have performed a survey of numerous eukaryotic genomes and discovered that genes homologous to foxJ1 are restricted only to organisms belonging to the unikont lineage. Using a mis-expression assay, we then obtained evidence of a conserved ability of FoxJ1 proteins from a number of diverse phyletic groups to activate the expression of a host of motile ciliary genes in zebrafish embryos. Conversely, we found that inactivation of a foxJ1 gene in Schmidtea mediterranea, a platyhelminth (flatworm) that utilizes motile cilia for locomotion, led to a profound disruption in the differentiation of motile cilia. Together, all of these findings provide the first evolutionary perspective into the transcriptional control of motile ciliogenesis and allow us to propose a conserved FoxJ1-regulated mechanism for motile cilia biogenesis back to the origin of the metazoans.
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spelling pubmed-34934432012-11-09 Evolutionarily Ancient Association of the FoxJ1 Transcription Factor with the Motile Ciliogenic Program Vij, Shubha Rink, Jochen C. Ho, Hao Kee Babu, Deepak Eitel, Michael Narasimhan, Vijayashankaranarayanan Tiku, Varnesh Westbrook, Jody Schierwater, Bernd Roy, Sudipto PLoS Genet Research Article It is generally believed that the last eukaryotic common ancestor (LECA) was a unicellular organism with motile cilia. In the vertebrates, the winged-helix transcription factor FoxJ1 functions as the master regulator of motile cilia biogenesis. Despite the antiquity of cilia, their highly conserved structure, and their mechanism of motility, the evolution of the transcriptional program controlling ciliogenesis has remained incompletely understood. In particular, it is presently not known how the generation of motile cilia is programmed outside of the vertebrates, and whether and to what extent the FoxJ1-dependent regulation is conserved. We have performed a survey of numerous eukaryotic genomes and discovered that genes homologous to foxJ1 are restricted only to organisms belonging to the unikont lineage. Using a mis-expression assay, we then obtained evidence of a conserved ability of FoxJ1 proteins from a number of diverse phyletic groups to activate the expression of a host of motile ciliary genes in zebrafish embryos. Conversely, we found that inactivation of a foxJ1 gene in Schmidtea mediterranea, a platyhelminth (flatworm) that utilizes motile cilia for locomotion, led to a profound disruption in the differentiation of motile cilia. Together, all of these findings provide the first evolutionary perspective into the transcriptional control of motile ciliogenesis and allow us to propose a conserved FoxJ1-regulated mechanism for motile cilia biogenesis back to the origin of the metazoans. Public Library of Science 2012-11-08 /pmc/articles/PMC3493443/ /pubmed/23144623 http://dx.doi.org/10.1371/journal.pgen.1003019 Text en © 2012 Vij 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Vij, Shubha
Rink, Jochen C.
Ho, Hao Kee
Babu, Deepak
Eitel, Michael
Narasimhan, Vijayashankaranarayanan
Tiku, Varnesh
Westbrook, Jody
Schierwater, Bernd
Roy, Sudipto
Evolutionarily Ancient Association of the FoxJ1 Transcription Factor with the Motile Ciliogenic Program
title Evolutionarily Ancient Association of the FoxJ1 Transcription Factor with the Motile Ciliogenic Program
title_full Evolutionarily Ancient Association of the FoxJ1 Transcription Factor with the Motile Ciliogenic Program
title_fullStr Evolutionarily Ancient Association of the FoxJ1 Transcription Factor with the Motile Ciliogenic Program
title_full_unstemmed Evolutionarily Ancient Association of the FoxJ1 Transcription Factor with the Motile Ciliogenic Program
title_short Evolutionarily Ancient Association of the FoxJ1 Transcription Factor with the Motile Ciliogenic Program
title_sort evolutionarily ancient association of the foxj1 transcription factor with the motile ciliogenic program
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3493443/
https://www.ncbi.nlm.nih.gov/pubmed/23144623
http://dx.doi.org/10.1371/journal.pgen.1003019
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