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Optogenetic inhibition of Delta reveals digital Notch signalling output during tissue differentiation

Spatio‐temporal regulation of signalling pathways plays a key role in generating diverse responses during the development of multicellular organisms. The role of signal dynamics in transferring signalling information in vivo is incompletely understood. Here, we employ genome engineering in Drosophil...

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Autores principales: Viswanathan, Ranjith, Necakov, Aleksandar, Trylinski, Mateusz, Harish, Rohit Krishnan, Krueger, Daniel, Esposito, Emilia, Schweisguth, Francois, Neveu, Pierre, De Renzis, Stefano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6893285/
https://www.ncbi.nlm.nih.gov/pubmed/31668010
http://dx.doi.org/10.15252/embr.201947999
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author Viswanathan, Ranjith
Necakov, Aleksandar
Trylinski, Mateusz
Harish, Rohit Krishnan
Krueger, Daniel
Esposito, Emilia
Schweisguth, Francois
Neveu, Pierre
De Renzis, Stefano
author_facet Viswanathan, Ranjith
Necakov, Aleksandar
Trylinski, Mateusz
Harish, Rohit Krishnan
Krueger, Daniel
Esposito, Emilia
Schweisguth, Francois
Neveu, Pierre
De Renzis, Stefano
author_sort Viswanathan, Ranjith
collection PubMed
description Spatio‐temporal regulation of signalling pathways plays a key role in generating diverse responses during the development of multicellular organisms. The role of signal dynamics in transferring signalling information in vivo is incompletely understood. Here, we employ genome engineering in Drosophila melanogaster to generate a functional optogenetic allele of the Notch ligand Delta (opto‐Delta), which replaces both copies of the endogenous wild‐type locus. Using clonal analysis, we show that optogenetic activation blocks Notch activation through cis‐inhibition in signal‐receiving cells. Signal perturbation in combination with quantitative analysis of a live transcriptional reporter of Notch pathway activity reveals differential tissue‐ and cell‐scale regulatory modes. While at the tissue‐level the duration of Notch signalling determines the probability with which a cellular response will occur, in individual cells Notch activation acts through a switch‐like mechanism. Thus, time confers regulatory properties to Notch signalling that exhibit integrative digital behaviours during tissue differentiation.
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spelling pubmed-68932852019-12-16 Optogenetic inhibition of Delta reveals digital Notch signalling output during tissue differentiation Viswanathan, Ranjith Necakov, Aleksandar Trylinski, Mateusz Harish, Rohit Krishnan Krueger, Daniel Esposito, Emilia Schweisguth, Francois Neveu, Pierre De Renzis, Stefano EMBO Rep Reports Spatio‐temporal regulation of signalling pathways plays a key role in generating diverse responses during the development of multicellular organisms. The role of signal dynamics in transferring signalling information in vivo is incompletely understood. Here, we employ genome engineering in Drosophila melanogaster to generate a functional optogenetic allele of the Notch ligand Delta (opto‐Delta), which replaces both copies of the endogenous wild‐type locus. Using clonal analysis, we show that optogenetic activation blocks Notch activation through cis‐inhibition in signal‐receiving cells. Signal perturbation in combination with quantitative analysis of a live transcriptional reporter of Notch pathway activity reveals differential tissue‐ and cell‐scale regulatory modes. While at the tissue‐level the duration of Notch signalling determines the probability with which a cellular response will occur, in individual cells Notch activation acts through a switch‐like mechanism. Thus, time confers regulatory properties to Notch signalling that exhibit integrative digital behaviours during tissue differentiation. John Wiley and Sons Inc. 2019-10-31 2019-12-05 /pmc/articles/PMC6893285/ /pubmed/31668010 http://dx.doi.org/10.15252/embr.201947999 Text en © 2019 European Molecular Biology Laboratory Published under the terms of the CC BY 4.0 license This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Reports
Viswanathan, Ranjith
Necakov, Aleksandar
Trylinski, Mateusz
Harish, Rohit Krishnan
Krueger, Daniel
Esposito, Emilia
Schweisguth, Francois
Neveu, Pierre
De Renzis, Stefano
Optogenetic inhibition of Delta reveals digital Notch signalling output during tissue differentiation
title Optogenetic inhibition of Delta reveals digital Notch signalling output during tissue differentiation
title_full Optogenetic inhibition of Delta reveals digital Notch signalling output during tissue differentiation
title_fullStr Optogenetic inhibition of Delta reveals digital Notch signalling output during tissue differentiation
title_full_unstemmed Optogenetic inhibition of Delta reveals digital Notch signalling output during tissue differentiation
title_short Optogenetic inhibition of Delta reveals digital Notch signalling output during tissue differentiation
title_sort optogenetic inhibition of delta reveals digital notch signalling output during tissue differentiation
topic Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6893285/
https://www.ncbi.nlm.nih.gov/pubmed/31668010
http://dx.doi.org/10.15252/embr.201947999
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