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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...

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Autores principales: Riba, Andrea, Oravecz, Attila, Durik, Matej, Jiménez, Sara, Alunni, Violaine, Cerciat, Marie, Jung, Matthieu, Keime, Céline, Keyes, William M., Molina, Nacho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
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.
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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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