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Functional characterization of putative cilia genes by high-content analysis
Cilia are microtubule-based protrusions from the cell surface that are involved in a number of essential signaling pathways, yet little is known about many of the proteins that regulate their structure and function. A number of putative cilia genes have been identified by proteomics and comparative...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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The American Society for Cell Biology
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069013/ https://www.ncbi.nlm.nih.gov/pubmed/21289087 http://dx.doi.org/10.1091/mbc.E10-07-0596 |
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author | Lai, Cary K. Gupta, Nidhi Wen, Xiaohui Rangell, Linda Chih, Ben Peterson, Andrew S. Bazan, J. Fernando Li, Li Scales, Suzie J. |
author_facet | Lai, Cary K. Gupta, Nidhi Wen, Xiaohui Rangell, Linda Chih, Ben Peterson, Andrew S. Bazan, J. Fernando Li, Li Scales, Suzie J. |
author_sort | Lai, Cary K. |
collection | PubMed |
description | Cilia are microtubule-based protrusions from the cell surface that are involved in a number of essential signaling pathways, yet little is known about many of the proteins that regulate their structure and function. A number of putative cilia genes have been identified by proteomics and comparative sequence analyses, but functional data are lacking for the vast majority. We therefore monitored the effects in three cell lines of small interfering RNA (siRNA) knockdown of 40 of these genes by high-content analysis. We assayed cilia number, length, and transport of two different cargoes (membranous serotonin receptor 6-green fluorescent protein [HTR6-GFP] and the endogenous Hedgehog [Hh] pathway transcription factor Gli3) by immunofluorescence microscopy; and cilia function using a Gli-luciferase Hh signaling assay. Hh signaling was most sensitive to perturbations, with or without visible structural cilia defects. Validated hits include Ssa2 and mC21orf2 with ciliation defects; Ift46 with short cilia; Ptpdc1 and Iqub with elongated cilia; and Arl3, Nme7, and Ssna1 with distinct ciliary transport but not length defects. Our data confirm various ciliary roles for several ciliome proteins and show it is possible to uncouple ciliary cargo transport from cilia formation in vertebrates. |
format | Text |
id | pubmed-3069013 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-30690132011-06-16 Functional characterization of putative cilia genes by high-content analysis Lai, Cary K. Gupta, Nidhi Wen, Xiaohui Rangell, Linda Chih, Ben Peterson, Andrew S. Bazan, J. Fernando Li, Li Scales, Suzie J. Mol Biol Cell Articles Cilia are microtubule-based protrusions from the cell surface that are involved in a number of essential signaling pathways, yet little is known about many of the proteins that regulate their structure and function. A number of putative cilia genes have been identified by proteomics and comparative sequence analyses, but functional data are lacking for the vast majority. We therefore monitored the effects in three cell lines of small interfering RNA (siRNA) knockdown of 40 of these genes by high-content analysis. We assayed cilia number, length, and transport of two different cargoes (membranous serotonin receptor 6-green fluorescent protein [HTR6-GFP] and the endogenous Hedgehog [Hh] pathway transcription factor Gli3) by immunofluorescence microscopy; and cilia function using a Gli-luciferase Hh signaling assay. Hh signaling was most sensitive to perturbations, with or without visible structural cilia defects. Validated hits include Ssa2 and mC21orf2 with ciliation defects; Ift46 with short cilia; Ptpdc1 and Iqub with elongated cilia; and Arl3, Nme7, and Ssna1 with distinct ciliary transport but not length defects. Our data confirm various ciliary roles for several ciliome proteins and show it is possible to uncouple ciliary cargo transport from cilia formation in vertebrates. The American Society for Cell Biology 2011-04-01 /pmc/articles/PMC3069013/ /pubmed/21289087 http://dx.doi.org/10.1091/mbc.E10-07-0596 Text en © 2011 Lai et al. This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License (http://creativecommons.org/licenses/by-nc-sa/3.0). “ASCB®,“ “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society of Cell Biology. |
spellingShingle | Articles Lai, Cary K. Gupta, Nidhi Wen, Xiaohui Rangell, Linda Chih, Ben Peterson, Andrew S. Bazan, J. Fernando Li, Li Scales, Suzie J. Functional characterization of putative cilia genes by high-content analysis |
title | Functional characterization of putative cilia genes by high-content analysis |
title_full | Functional characterization of putative cilia genes by high-content analysis |
title_fullStr | Functional characterization of putative cilia genes by high-content analysis |
title_full_unstemmed | Functional characterization of putative cilia genes by high-content analysis |
title_short | Functional characterization of putative cilia genes by high-content analysis |
title_sort | functional characterization of putative cilia genes by high-content analysis |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069013/ https://www.ncbi.nlm.nih.gov/pubmed/21289087 http://dx.doi.org/10.1091/mbc.E10-07-0596 |
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