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Plant stem-cell organization and differentiation at single-cell resolution
Plants maintain populations of pluripotent stem cells in shoot apical meristems (SAMs), which continuously produce new aboveground organs. We used single-cell RNA sequencing (scRNA-seq) to achieve an unbiased characterization of the transcriptional landscape of the maize shoot stem-cell niche and it...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7776995/ https://www.ncbi.nlm.nih.gov/pubmed/33318187 http://dx.doi.org/10.1073/pnas.2018788117 |
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author | Satterlee, James W. Strable, Josh Scanlon, Michael J. |
author_facet | Satterlee, James W. Strable, Josh Scanlon, Michael J. |
author_sort | Satterlee, James W. |
collection | PubMed |
description | Plants maintain populations of pluripotent stem cells in shoot apical meristems (SAMs), which continuously produce new aboveground organs. We used single-cell RNA sequencing (scRNA-seq) to achieve an unbiased characterization of the transcriptional landscape of the maize shoot stem-cell niche and its differentiating cellular descendants. Stem cells housed in the SAM tip are engaged in genome integrity maintenance and exhibit a low rate of cell division, consistent with their contributions to germline and somatic cell fates. Surprisingly, we find no evidence for a canonical stem-cell organizing center subtending these cells. In addition, trajectory inference was used to trace the gene expression changes that accompany cell differentiation, revealing that ectopic expression of KNOTTED1 (KN1) accelerates cell differentiation and promotes development of the sheathing maize leaf base. These single-cell transcriptomic analyses of the shoot apex yield insight into the processes of stem-cell function and cell-fate acquisition in the maize seedling and provide a valuable scaffold on which to better dissect the genetic control of plant shoot morphogenesis at the cellular level. |
format | Online Article Text |
id | pubmed-7776995 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-77769952021-01-12 Plant stem-cell organization and differentiation at single-cell resolution Satterlee, James W. Strable, Josh Scanlon, Michael J. Proc Natl Acad Sci U S A Biological Sciences Plants maintain populations of pluripotent stem cells in shoot apical meristems (SAMs), which continuously produce new aboveground organs. We used single-cell RNA sequencing (scRNA-seq) to achieve an unbiased characterization of the transcriptional landscape of the maize shoot stem-cell niche and its differentiating cellular descendants. Stem cells housed in the SAM tip are engaged in genome integrity maintenance and exhibit a low rate of cell division, consistent with their contributions to germline and somatic cell fates. Surprisingly, we find no evidence for a canonical stem-cell organizing center subtending these cells. In addition, trajectory inference was used to trace the gene expression changes that accompany cell differentiation, revealing that ectopic expression of KNOTTED1 (KN1) accelerates cell differentiation and promotes development of the sheathing maize leaf base. These single-cell transcriptomic analyses of the shoot apex yield insight into the processes of stem-cell function and cell-fate acquisition in the maize seedling and provide a valuable scaffold on which to better dissect the genetic control of plant shoot morphogenesis at the cellular level. National Academy of Sciences 2020-12-29 2020-12-14 /pmc/articles/PMC7776995/ /pubmed/33318187 http://dx.doi.org/10.1073/pnas.2018788117 Text en Copyright © 2020 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Biological Sciences Satterlee, James W. Strable, Josh Scanlon, Michael J. Plant stem-cell organization and differentiation at single-cell resolution |
title | Plant stem-cell organization and differentiation at single-cell resolution |
title_full | Plant stem-cell organization and differentiation at single-cell resolution |
title_fullStr | Plant stem-cell organization and differentiation at single-cell resolution |
title_full_unstemmed | Plant stem-cell organization and differentiation at single-cell resolution |
title_short | Plant stem-cell organization and differentiation at single-cell resolution |
title_sort | plant stem-cell organization and differentiation at single-cell resolution |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7776995/ https://www.ncbi.nlm.nih.gov/pubmed/33318187 http://dx.doi.org/10.1073/pnas.2018788117 |
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