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Cell cycle gene regulation dynamics revealed by RNA velocity and deep-learning
Despite the fact that the cell cycle is a fundamental process of life, a detailed quantitative understanding of gene regulation dynamics throughout the cell cycle is far from complete. Single-cell RNA-sequencing (scRNA-seq) technology gives access to these dynamics without externally perturbing the...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9126911/ https://www.ncbi.nlm.nih.gov/pubmed/35606383 http://dx.doi.org/10.1038/s41467-022-30545-8 |
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author | Riba, Andrea Oravecz, Attila Durik, Matej Jiménez, Sara Alunni, Violaine Cerciat, Marie Jung, Matthieu Keime, Céline Keyes, William M. Molina, Nacho |
author_facet | Riba, Andrea Oravecz, Attila Durik, Matej Jiménez, Sara Alunni, Violaine Cerciat, Marie Jung, Matthieu Keime, Céline Keyes, William M. Molina, Nacho |
author_sort | Riba, Andrea |
collection | PubMed |
description | Despite the fact that the cell cycle is a fundamental process of life, a detailed quantitative understanding of gene regulation dynamics throughout the cell cycle is far from complete. Single-cell RNA-sequencing (scRNA-seq) technology gives access to these dynamics without externally perturbing the cell. Here, by generating scRNA-seq libraries in different cell systems, we observe cycling patterns in the unspliced-spliced RNA space of cell cycle-related genes. Since existing methods to analyze scRNA-seq are not efficient to measure cycling gene dynamics, we propose a deep learning approach (DeepCycle) to fit these patterns and build a high-resolution map of the entire cell cycle transcriptome. Characterizing the cell cycle in embryonic and somatic cells, we identify major waves of transcription during the G1 phase and systematically study the stages of the cell cycle. Our work will facilitate the study of the cell cycle in multiple cellular models and different biological contexts. |
format | Online Article Text |
id | pubmed-9126911 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-91269112022-05-25 Cell cycle gene regulation dynamics revealed by RNA velocity and deep-learning Riba, Andrea Oravecz, Attila Durik, Matej Jiménez, Sara Alunni, Violaine Cerciat, Marie Jung, Matthieu Keime, Céline Keyes, William M. Molina, Nacho Nat Commun Article Despite the fact that the cell cycle is a fundamental process of life, a detailed quantitative understanding of gene regulation dynamics throughout the cell cycle is far from complete. Single-cell RNA-sequencing (scRNA-seq) technology gives access to these dynamics without externally perturbing the cell. Here, by generating scRNA-seq libraries in different cell systems, we observe cycling patterns in the unspliced-spliced RNA space of cell cycle-related genes. Since existing methods to analyze scRNA-seq are not efficient to measure cycling gene dynamics, we propose a deep learning approach (DeepCycle) to fit these patterns and build a high-resolution map of the entire cell cycle transcriptome. Characterizing the cell cycle in embryonic and somatic cells, we identify major waves of transcription during the G1 phase and systematically study the stages of the cell cycle. Our work will facilitate the study of the cell cycle in multiple cellular models and different biological contexts. Nature Publishing Group UK 2022-05-23 /pmc/articles/PMC9126911/ /pubmed/35606383 http://dx.doi.org/10.1038/s41467-022-30545-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Riba, Andrea Oravecz, Attila Durik, Matej Jiménez, Sara Alunni, Violaine Cerciat, Marie Jung, Matthieu Keime, Céline Keyes, William M. Molina, Nacho Cell cycle gene regulation dynamics revealed by RNA velocity and deep-learning |
title | Cell cycle gene regulation dynamics revealed by RNA velocity and deep-learning |
title_full | Cell cycle gene regulation dynamics revealed by RNA velocity and deep-learning |
title_fullStr | Cell cycle gene regulation dynamics revealed by RNA velocity and deep-learning |
title_full_unstemmed | Cell cycle gene regulation dynamics revealed by RNA velocity and deep-learning |
title_short | Cell cycle gene regulation dynamics revealed by RNA velocity and deep-learning |
title_sort | cell cycle gene regulation dynamics revealed by rna velocity and deep-learning |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9126911/ https://www.ncbi.nlm.nih.gov/pubmed/35606383 http://dx.doi.org/10.1038/s41467-022-30545-8 |
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