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Chromatin accessibility dynamics and single cell RNA-Seq reveal new regulators of regeneration in neural progenitors
Vertebrate appendage regeneration requires precisely coordinated remodeling of the transcriptional landscape to enable the growth and differentiation of new tissue, a process executed over multiple days and across dozens of cell types. The heterogeneity of tissues and temporally-sensitive fate decis...
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/PMC7250574/ https://www.ncbi.nlm.nih.gov/pubmed/32338593 http://dx.doi.org/10.7554/eLife.52648 |
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author | Kakebeen, Anneke Dixie Chitsazan, Alexander Daniel Williams, Madison Corinne Saunders, Lauren M Wills, Andrea Elizabeth |
author_facet | Kakebeen, Anneke Dixie Chitsazan, Alexander Daniel Williams, Madison Corinne Saunders, Lauren M Wills, Andrea Elizabeth |
author_sort | Kakebeen, Anneke Dixie |
collection | PubMed |
description | Vertebrate appendage regeneration requires precisely coordinated remodeling of the transcriptional landscape to enable the growth and differentiation of new tissue, a process executed over multiple days and across dozens of cell types. The heterogeneity of tissues and temporally-sensitive fate decisions involved has made it difficult to articulate the gene regulatory programs enabling regeneration of individual cell types. To better understand how a regenerative program is fulfilled by neural progenitor cells (NPCs) of the spinal cord, we analyzed pax6-expressing NPCs isolated from regenerating Xenopus tropicalis tails. By intersecting chromatin accessibility data with single-cell transcriptomics, we find that NPCs place an early priority on neuronal differentiation. Late in regeneration, the priority returns to proliferation. Our analyses identify Pbx3 and Meis1 as critical regulators of tail regeneration and axon organization. Overall, we use transcriptional regulatory dynamics to present a new model for cell fate decisions and their regulators in NPCs during regeneration. |
format | Online Article Text |
id | pubmed-7250574 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-72505742020-05-28 Chromatin accessibility dynamics and single cell RNA-Seq reveal new regulators of regeneration in neural progenitors Kakebeen, Anneke Dixie Chitsazan, Alexander Daniel Williams, Madison Corinne Saunders, Lauren M Wills, Andrea Elizabeth eLife Developmental Biology Vertebrate appendage regeneration requires precisely coordinated remodeling of the transcriptional landscape to enable the growth and differentiation of new tissue, a process executed over multiple days and across dozens of cell types. The heterogeneity of tissues and temporally-sensitive fate decisions involved has made it difficult to articulate the gene regulatory programs enabling regeneration of individual cell types. To better understand how a regenerative program is fulfilled by neural progenitor cells (NPCs) of the spinal cord, we analyzed pax6-expressing NPCs isolated from regenerating Xenopus tropicalis tails. By intersecting chromatin accessibility data with single-cell transcriptomics, we find that NPCs place an early priority on neuronal differentiation. Late in regeneration, the priority returns to proliferation. Our analyses identify Pbx3 and Meis1 as critical regulators of tail regeneration and axon organization. Overall, we use transcriptional regulatory dynamics to present a new model for cell fate decisions and their regulators in NPCs during regeneration. eLife Sciences Publications, Ltd 2020-04-27 /pmc/articles/PMC7250574/ /pubmed/32338593 http://dx.doi.org/10.7554/eLife.52648 Text en © 2020, Kakebeen 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 Kakebeen, Anneke Dixie Chitsazan, Alexander Daniel Williams, Madison Corinne Saunders, Lauren M Wills, Andrea Elizabeth Chromatin accessibility dynamics and single cell RNA-Seq reveal new regulators of regeneration in neural progenitors |
title | Chromatin accessibility dynamics and single cell RNA-Seq reveal new regulators of regeneration in neural progenitors |
title_full | Chromatin accessibility dynamics and single cell RNA-Seq reveal new regulators of regeneration in neural progenitors |
title_fullStr | Chromatin accessibility dynamics and single cell RNA-Seq reveal new regulators of regeneration in neural progenitors |
title_full_unstemmed | Chromatin accessibility dynamics and single cell RNA-Seq reveal new regulators of regeneration in neural progenitors |
title_short | Chromatin accessibility dynamics and single cell RNA-Seq reveal new regulators of regeneration in neural progenitors |
title_sort | chromatin accessibility dynamics and single cell rna-seq reveal new regulators of regeneration in neural progenitors |
topic | Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7250574/ https://www.ncbi.nlm.nih.gov/pubmed/32338593 http://dx.doi.org/10.7554/eLife.52648 |
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