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A high-resolution gene expression atlas links dedicated meristem genes to key architectural traits
The shoot apical meristem (SAM) orchestrates the balance between stem cell proliferation and organ initiation essential for postembryonic shoot growth. Meristems show a striking diversity in shape and size. How this morphological diversity relates to variation in plant architecture and the molecular...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6886502/ https://www.ncbi.nlm.nih.gov/pubmed/31744902 http://dx.doi.org/10.1101/gr.250878.119 |
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author | Knauer, Steffen Javelle, Marie Li, Lin Li, Xianran Ma, Xiaoli Wimalanathan, Kokulapalan Kumari, Sunita Johnston, Robyn Leiboff, Samuel Meeley, Robert Schnable, Patrick S. Ware, Doreen Lawrence-Dill, Carolyn Yu, Jianming Muehlbauer, Gary J. Scanlon, Michael J. Timmermans, Marja C.P. |
author_facet | Knauer, Steffen Javelle, Marie Li, Lin Li, Xianran Ma, Xiaoli Wimalanathan, Kokulapalan Kumari, Sunita Johnston, Robyn Leiboff, Samuel Meeley, Robert Schnable, Patrick S. Ware, Doreen Lawrence-Dill, Carolyn Yu, Jianming Muehlbauer, Gary J. Scanlon, Michael J. Timmermans, Marja C.P. |
author_sort | Knauer, Steffen |
collection | PubMed |
description | The shoot apical meristem (SAM) orchestrates the balance between stem cell proliferation and organ initiation essential for postembryonic shoot growth. Meristems show a striking diversity in shape and size. How this morphological diversity relates to variation in plant architecture and the molecular circuitries driving it are unclear. By generating a high-resolution gene expression atlas of the vegetative maize shoot apex, we show here that distinct sets of genes govern the regulation and identity of stem cells in maize versus Arabidopsis. Cell identities in the maize SAM reflect the combinatorial activity of transcription factors (TFs) that drive the preferential, differential expression of individual members within gene families functioning in a plethora of cellular processes. Subfunctionalization thus emerges as a fundamental feature underlying cell identity. Moreover, we show that adult plant characters are, to a significant degree, regulated by gene circuitries acting in the SAM, with natural variation modulating agronomically important architectural traits enriched specifically near dynamically expressed SAM genes and the TFs that regulate them. Besides unique mechanisms of maize stem cell regulation, our atlas thus identifies key new targets for crop improvement. |
format | Online Article Text |
id | pubmed-6886502 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-68865022019-12-12 A high-resolution gene expression atlas links dedicated meristem genes to key architectural traits Knauer, Steffen Javelle, Marie Li, Lin Li, Xianran Ma, Xiaoli Wimalanathan, Kokulapalan Kumari, Sunita Johnston, Robyn Leiboff, Samuel Meeley, Robert Schnable, Patrick S. Ware, Doreen Lawrence-Dill, Carolyn Yu, Jianming Muehlbauer, Gary J. Scanlon, Michael J. Timmermans, Marja C.P. Genome Res Research The shoot apical meristem (SAM) orchestrates the balance between stem cell proliferation and organ initiation essential for postembryonic shoot growth. Meristems show a striking diversity in shape and size. How this morphological diversity relates to variation in plant architecture and the molecular circuitries driving it are unclear. By generating a high-resolution gene expression atlas of the vegetative maize shoot apex, we show here that distinct sets of genes govern the regulation and identity of stem cells in maize versus Arabidopsis. Cell identities in the maize SAM reflect the combinatorial activity of transcription factors (TFs) that drive the preferential, differential expression of individual members within gene families functioning in a plethora of cellular processes. Subfunctionalization thus emerges as a fundamental feature underlying cell identity. Moreover, we show that adult plant characters are, to a significant degree, regulated by gene circuitries acting in the SAM, with natural variation modulating agronomically important architectural traits enriched specifically near dynamically expressed SAM genes and the TFs that regulate them. Besides unique mechanisms of maize stem cell regulation, our atlas thus identifies key new targets for crop improvement. Cold Spring Harbor Laboratory Press 2019-12 /pmc/articles/PMC6886502/ /pubmed/31744902 http://dx.doi.org/10.1101/gr.250878.119 Text en © 2019 Knauer et al.; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by/4.0/ This article, published in Genome Research, is available under a Creative Commons License (Attribution 4.0 International), as described at http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Research Knauer, Steffen Javelle, Marie Li, Lin Li, Xianran Ma, Xiaoli Wimalanathan, Kokulapalan Kumari, Sunita Johnston, Robyn Leiboff, Samuel Meeley, Robert Schnable, Patrick S. Ware, Doreen Lawrence-Dill, Carolyn Yu, Jianming Muehlbauer, Gary J. Scanlon, Michael J. Timmermans, Marja C.P. A high-resolution gene expression atlas links dedicated meristem genes to key architectural traits |
title | A high-resolution gene expression atlas links dedicated meristem genes to key architectural traits |
title_full | A high-resolution gene expression atlas links dedicated meristem genes to key architectural traits |
title_fullStr | A high-resolution gene expression atlas links dedicated meristem genes to key architectural traits |
title_full_unstemmed | A high-resolution gene expression atlas links dedicated meristem genes to key architectural traits |
title_short | A high-resolution gene expression atlas links dedicated meristem genes to key architectural traits |
title_sort | high-resolution gene expression atlas links dedicated meristem genes to key architectural traits |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6886502/ https://www.ncbi.nlm.nih.gov/pubmed/31744902 http://dx.doi.org/10.1101/gr.250878.119 |
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