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New methods to image transcription in living fly embryos: the insights so far, and the prospects

The regulation of transcription is a fundamental process underlying the determination of cell identity and its maintenance during development. In the last decades, most of the transcription factors, which have to be expressed at the right place and at the right time for the proper development of the...

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Autores principales: Ferraro, Teresa, Lucas, Tanguy, Clémot, Marie, De Las Heras Chanes, Jose, Desponds, Jonathan, Coppey, Mathieu, Walczak, Aleksandra M., Dostatni, Nathalie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5021148/
https://www.ncbi.nlm.nih.gov/pubmed/26894441
http://dx.doi.org/10.1002/wdev.221
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author Ferraro, Teresa
Lucas, Tanguy
Clémot, Marie
De Las Heras Chanes, Jose
Desponds, Jonathan
Coppey, Mathieu
Walczak, Aleksandra M.
Dostatni, Nathalie
author_facet Ferraro, Teresa
Lucas, Tanguy
Clémot, Marie
De Las Heras Chanes, Jose
Desponds, Jonathan
Coppey, Mathieu
Walczak, Aleksandra M.
Dostatni, Nathalie
author_sort Ferraro, Teresa
collection PubMed
description The regulation of transcription is a fundamental process underlying the determination of cell identity and its maintenance during development. In the last decades, most of the transcription factors, which have to be expressed at the right place and at the right time for the proper development of the fly embryo, have been identified. However, mostly because of the lack of methods to visualize transcription as the embryo develops, their coordinated spatiotemporal dynamics remains largely unexplored. Efforts have been made to decipher the transcription process with single molecule resolution at the single cell level. Recently, the fluorescent labeling of nascent RNA in developing fly embryos allowed the direct visualization of ongoing transcription at single loci within each nucleus. Together with powerful imaging and quantitative data analysis, these new methods provide unprecedented insights into the temporal dynamics of the transcription process and its intrinsic noise. Focusing on the Drosophila embryo, we discuss how the detection of single RNA molecules enhanced our comprehension of the transcription process and we outline the potential next steps made possible by these new imaging tools. In combination with genetics and theoretical analysis, these new imaging methods will aid the search for the mechanisms responsible for the robustness of development. WIREs Dev Biol 2016, 5:296–310. doi: 10.1002/wdev.221 For further resources related to this article, please visit the WIREs website.
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spelling pubmed-50211482016-09-23 New methods to image transcription in living fly embryos: the insights so far, and the prospects Ferraro, Teresa Lucas, Tanguy Clémot, Marie De Las Heras Chanes, Jose Desponds, Jonathan Coppey, Mathieu Walczak, Aleksandra M. Dostatni, Nathalie Wiley Interdiscip Rev Dev Biol Advanced Reviews The regulation of transcription is a fundamental process underlying the determination of cell identity and its maintenance during development. In the last decades, most of the transcription factors, which have to be expressed at the right place and at the right time for the proper development of the fly embryo, have been identified. However, mostly because of the lack of methods to visualize transcription as the embryo develops, their coordinated spatiotemporal dynamics remains largely unexplored. Efforts have been made to decipher the transcription process with single molecule resolution at the single cell level. Recently, the fluorescent labeling of nascent RNA in developing fly embryos allowed the direct visualization of ongoing transcription at single loci within each nucleus. Together with powerful imaging and quantitative data analysis, these new methods provide unprecedented insights into the temporal dynamics of the transcription process and its intrinsic noise. Focusing on the Drosophila embryo, we discuss how the detection of single RNA molecules enhanced our comprehension of the transcription process and we outline the potential next steps made possible by these new imaging tools. In combination with genetics and theoretical analysis, these new imaging methods will aid the search for the mechanisms responsible for the robustness of development. WIREs Dev Biol 2016, 5:296–310. doi: 10.1002/wdev.221 For further resources related to this article, please visit the WIREs website. John Wiley & Sons, Inc. 2016-02-19 2016 /pmc/articles/PMC5021148/ /pubmed/26894441 http://dx.doi.org/10.1002/wdev.221 Text en © 2016 The Authors. WIREs Developmental Biology published by Wiley Periodicals, Inc. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Advanced Reviews
Ferraro, Teresa
Lucas, Tanguy
Clémot, Marie
De Las Heras Chanes, Jose
Desponds, Jonathan
Coppey, Mathieu
Walczak, Aleksandra M.
Dostatni, Nathalie
New methods to image transcription in living fly embryos: the insights so far, and the prospects
title New methods to image transcription in living fly embryos: the insights so far, and the prospects
title_full New methods to image transcription in living fly embryos: the insights so far, and the prospects
title_fullStr New methods to image transcription in living fly embryos: the insights so far, and the prospects
title_full_unstemmed New methods to image transcription in living fly embryos: the insights so far, and the prospects
title_short New methods to image transcription in living fly embryos: the insights so far, and the prospects
title_sort new methods to image transcription in living fly embryos: the insights so far, and the prospects
topic Advanced Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5021148/
https://www.ncbi.nlm.nih.gov/pubmed/26894441
http://dx.doi.org/10.1002/wdev.221
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