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Cell and molecular transitions during efficient dedifferentiation
Dedifferentiation is a critical response to tissue damage, yet is not well understood, even at a basic phenomenological level. Developing Dictyostelium cells undergo highly efficient dedifferentiation, completed by most cells within 24 hr. We use this rapid response to investigate the control featur...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7190356/ https://www.ncbi.nlm.nih.gov/pubmed/32255425 http://dx.doi.org/10.7554/eLife.55435 |
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author | Nichols, John ME Antolović, Vlatka Reich, Jacob D Brameyer, Sophie Paschke, Peggy Chubb, Jonathan R |
author_facet | Nichols, John ME Antolović, Vlatka Reich, Jacob D Brameyer, Sophie Paschke, Peggy Chubb, Jonathan R |
author_sort | Nichols, John ME |
collection | PubMed |
description | Dedifferentiation is a critical response to tissue damage, yet is not well understood, even at a basic phenomenological level. Developing Dictyostelium cells undergo highly efficient dedifferentiation, completed by most cells within 24 hr. We use this rapid response to investigate the control features of dedifferentiation, combining single cell imaging with high temporal resolution transcriptomics. Gene expression during dedifferentiation was predominantly a simple reversal of developmental changes, with expression changes not following this pattern primarily associated with ribosome biogenesis. Mutation of genes induced early in dedifferentiation did not strongly perturb the reversal of development. This apparent robustness may arise from adaptability of cells: the relative temporal ordering of cell and molecular events was not absolute, suggesting cell programmes reach the same end using different mechanisms. In addition, although cells start from different fates, they rapidly converged on a single expression trajectory. These regulatory features may contribute to dedifferentiation responses during regeneration. |
format | Online Article Text |
id | pubmed-7190356 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-71903562020-05-01 Cell and molecular transitions during efficient dedifferentiation Nichols, John ME Antolović, Vlatka Reich, Jacob D Brameyer, Sophie Paschke, Peggy Chubb, Jonathan R eLife Developmental Biology Dedifferentiation is a critical response to tissue damage, yet is not well understood, even at a basic phenomenological level. Developing Dictyostelium cells undergo highly efficient dedifferentiation, completed by most cells within 24 hr. We use this rapid response to investigate the control features of dedifferentiation, combining single cell imaging with high temporal resolution transcriptomics. Gene expression during dedifferentiation was predominantly a simple reversal of developmental changes, with expression changes not following this pattern primarily associated with ribosome biogenesis. Mutation of genes induced early in dedifferentiation did not strongly perturb the reversal of development. This apparent robustness may arise from adaptability of cells: the relative temporal ordering of cell and molecular events was not absolute, suggesting cell programmes reach the same end using different mechanisms. In addition, although cells start from different fates, they rapidly converged on a single expression trajectory. These regulatory features may contribute to dedifferentiation responses during regeneration. eLife Sciences Publications, Ltd 2020-04-07 /pmc/articles/PMC7190356/ /pubmed/32255425 http://dx.doi.org/10.7554/eLife.55435 Text en © 2020, Nichols et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Developmental Biology Nichols, John ME Antolović, Vlatka Reich, Jacob D Brameyer, Sophie Paschke, Peggy Chubb, Jonathan R Cell and molecular transitions during efficient dedifferentiation |
title | Cell and molecular transitions during efficient dedifferentiation |
title_full | Cell and molecular transitions during efficient dedifferentiation |
title_fullStr | Cell and molecular transitions during efficient dedifferentiation |
title_full_unstemmed | Cell and molecular transitions during efficient dedifferentiation |
title_short | Cell and molecular transitions during efficient dedifferentiation |
title_sort | cell and molecular transitions during efficient dedifferentiation |
topic | Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7190356/ https://www.ncbi.nlm.nih.gov/pubmed/32255425 http://dx.doi.org/10.7554/eLife.55435 |
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