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A global genetic interaction network by single-cell imaging and machine learning
Cellular and organismal phenotypes are controlled by complex gene regulatory networks. However, reference maps of gene function are still scarce across different organisms. Here, we generated synthetic genetic interaction and cell morphology profiles of more than 6,800 genes in cultured Drosophila c...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10206407/ https://www.ncbi.nlm.nih.gov/pubmed/37116498 http://dx.doi.org/10.1016/j.cels.2023.03.003 |
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author | Heigwer, Florian Scheeder, Christian Bageritz, Josephine Yousefian, Schayan Rauscher, Benedikt Laufer, Christina Beneyto-Calabuig, Sergi Funk, Maja Christina Peters, Vera Boulougouri, Maria Bilanovic, Jana Miersch, Thilo Schmitt, Barbara Blass, Claudia Port, Fillip Boutros, Michael |
author_facet | Heigwer, Florian Scheeder, Christian Bageritz, Josephine Yousefian, Schayan Rauscher, Benedikt Laufer, Christina Beneyto-Calabuig, Sergi Funk, Maja Christina Peters, Vera Boulougouri, Maria Bilanovic, Jana Miersch, Thilo Schmitt, Barbara Blass, Claudia Port, Fillip Boutros, Michael |
author_sort | Heigwer, Florian |
collection | PubMed |
description | Cellular and organismal phenotypes are controlled by complex gene regulatory networks. However, reference maps of gene function are still scarce across different organisms. Here, we generated synthetic genetic interaction and cell morphology profiles of more than 6,800 genes in cultured Drosophila cells. The resulting map of genetic interactions was used for machine learning-based gene function discovery, assigning functions to genes in 47 modules. Furthermore, we devised Cytoclass as a method to dissect genetic interactions for discrete cell states at the single-cell resolution. This approach identified an interaction of Cdk2 and the Cop9 signalosome complex, triggering senescence-associated secretory phenotypes and immunogenic conversion in hemocytic cells. Together, our data constitute a genome-scale resource of functional gene profiles to uncover the mechanisms underlying genetic interactions and their plasticity at the single-cell level. |
format | Online Article Text |
id | pubmed-10206407 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-102064072023-05-25 A global genetic interaction network by single-cell imaging and machine learning Heigwer, Florian Scheeder, Christian Bageritz, Josephine Yousefian, Schayan Rauscher, Benedikt Laufer, Christina Beneyto-Calabuig, Sergi Funk, Maja Christina Peters, Vera Boulougouri, Maria Bilanovic, Jana Miersch, Thilo Schmitt, Barbara Blass, Claudia Port, Fillip Boutros, Michael Cell Syst Article Cellular and organismal phenotypes are controlled by complex gene regulatory networks. However, reference maps of gene function are still scarce across different organisms. Here, we generated synthetic genetic interaction and cell morphology profiles of more than 6,800 genes in cultured Drosophila cells. The resulting map of genetic interactions was used for machine learning-based gene function discovery, assigning functions to genes in 47 modules. Furthermore, we devised Cytoclass as a method to dissect genetic interactions for discrete cell states at the single-cell resolution. This approach identified an interaction of Cdk2 and the Cop9 signalosome complex, triggering senescence-associated secretory phenotypes and immunogenic conversion in hemocytic cells. Together, our data constitute a genome-scale resource of functional gene profiles to uncover the mechanisms underlying genetic interactions and their plasticity at the single-cell level. Cell Press 2023-05-17 /pmc/articles/PMC10206407/ /pubmed/37116498 http://dx.doi.org/10.1016/j.cels.2023.03.003 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Heigwer, Florian Scheeder, Christian Bageritz, Josephine Yousefian, Schayan Rauscher, Benedikt Laufer, Christina Beneyto-Calabuig, Sergi Funk, Maja Christina Peters, Vera Boulougouri, Maria Bilanovic, Jana Miersch, Thilo Schmitt, Barbara Blass, Claudia Port, Fillip Boutros, Michael A global genetic interaction network by single-cell imaging and machine learning |
title | A global genetic interaction network by single-cell imaging and machine learning |
title_full | A global genetic interaction network by single-cell imaging and machine learning |
title_fullStr | A global genetic interaction network by single-cell imaging and machine learning |
title_full_unstemmed | A global genetic interaction network by single-cell imaging and machine learning |
title_short | A global genetic interaction network by single-cell imaging and machine learning |
title_sort | global genetic interaction network by single-cell imaging and machine learning |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10206407/ https://www.ncbi.nlm.nih.gov/pubmed/37116498 http://dx.doi.org/10.1016/j.cels.2023.03.003 |
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