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Dynamics of hunchback translation in real-time and at single-mRNA resolution in the Drosophila embryo
The Hunchback (Hb) transcription factor is crucial for anterior-posterior patterning of the Drosophila embryo. The maternal hb mRNA acts as a paradigm for translational regulation due to its repression in the posterior of the embryo. However, little is known about the translatability of zygotically...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8077512/ https://www.ncbi.nlm.nih.gov/pubmed/33722899 http://dx.doi.org/10.1242/dev.196121 |
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author | Vinter, Daisy J. Hoppe, Caroline Minchington, Thomas G. Sutcliffe, Catherine Ashe, Hilary L. |
author_facet | Vinter, Daisy J. Hoppe, Caroline Minchington, Thomas G. Sutcliffe, Catherine Ashe, Hilary L. |
author_sort | Vinter, Daisy J. |
collection | PubMed |
description | The Hunchback (Hb) transcription factor is crucial for anterior-posterior patterning of the Drosophila embryo. The maternal hb mRNA acts as a paradigm for translational regulation due to its repression in the posterior of the embryo. However, little is known about the translatability of zygotically transcribed hb mRNAs. Here, we adapt the SunTag system, developed for imaging translation at single-mRNA resolution in tissue culture cells, to the Drosophila embryo to study the translation dynamics of zygotic hb mRNAs. Using single-molecule imaging in fixed and live embryos, we provide evidence for translational repression of zygotic SunTag-hb mRNAs. Whereas the proportion of SunTag-hb mRNAs translated is initially uniform, translation declines from the anterior over time until it becomes restricted to a posterior band in the expression domain. We discuss how regulated hb mRNA translation may help establish the sharp Hb expression boundary, which is a model for precision and noise during developmental patterning. Overall, our data show how use of the SunTag method on fixed and live embryos is a powerful combination for elucidating spatiotemporal regulation of mRNA translation in Drosophila. |
format | Online Article Text |
id | pubmed-8077512 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-80775122021-05-06 Dynamics of hunchback translation in real-time and at single-mRNA resolution in the Drosophila embryo Vinter, Daisy J. Hoppe, Caroline Minchington, Thomas G. Sutcliffe, Catherine Ashe, Hilary L. Development Research Article The Hunchback (Hb) transcription factor is crucial for anterior-posterior patterning of the Drosophila embryo. The maternal hb mRNA acts as a paradigm for translational regulation due to its repression in the posterior of the embryo. However, little is known about the translatability of zygotically transcribed hb mRNAs. Here, we adapt the SunTag system, developed for imaging translation at single-mRNA resolution in tissue culture cells, to the Drosophila embryo to study the translation dynamics of zygotic hb mRNAs. Using single-molecule imaging in fixed and live embryos, we provide evidence for translational repression of zygotic SunTag-hb mRNAs. Whereas the proportion of SunTag-hb mRNAs translated is initially uniform, translation declines from the anterior over time until it becomes restricted to a posterior band in the expression domain. We discuss how regulated hb mRNA translation may help establish the sharp Hb expression boundary, which is a model for precision and noise during developmental patterning. Overall, our data show how use of the SunTag method on fixed and live embryos is a powerful combination for elucidating spatiotemporal regulation of mRNA translation in Drosophila. The Company of Biologists Ltd 2021-04-15 /pmc/articles/PMC8077512/ /pubmed/33722899 http://dx.doi.org/10.1242/dev.196121 Text en © 2021. Published by The Company of Biologists Ltd https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Research Article Vinter, Daisy J. Hoppe, Caroline Minchington, Thomas G. Sutcliffe, Catherine Ashe, Hilary L. Dynamics of hunchback translation in real-time and at single-mRNA resolution in the Drosophila embryo |
title | Dynamics of hunchback translation in real-time and at single-mRNA resolution in the Drosophila embryo |
title_full | Dynamics of hunchback translation in real-time and at single-mRNA resolution in the Drosophila embryo |
title_fullStr | Dynamics of hunchback translation in real-time and at single-mRNA resolution in the Drosophila embryo |
title_full_unstemmed | Dynamics of hunchback translation in real-time and at single-mRNA resolution in the Drosophila embryo |
title_short | Dynamics of hunchback translation in real-time and at single-mRNA resolution in the Drosophila embryo |
title_sort | dynamics of hunchback translation in real-time and at single-mrna resolution in the drosophila embryo |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8077512/ https://www.ncbi.nlm.nih.gov/pubmed/33722899 http://dx.doi.org/10.1242/dev.196121 |
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