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An integrated analysis of cell-type specific gene expression reveals genes regulated by REVOLUTA and KANADI1 in the Arabidopsis shoot apical meristem

In the Arabidopsis thaliana shoot apical meristem (SAM) the expression domains of Class III Homeodomain Leucine Zipper (HD-ZIPIII) and KANADI (KAN) genes are separated by a narrow boundary region from which new organs are initiated. Disruption of this boundary through either loss of function or ecto...

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Autores principales: Ram, Hasthi, Sahadevan, Sudeep, Gale, Nittaya, Caggiano, Monica Pia, Yu, Xiulian, Ohno, Carolyn, Heisler, Marcus G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7266345/
https://www.ncbi.nlm.nih.gov/pubmed/32294082
http://dx.doi.org/10.1371/journal.pgen.1008661
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author Ram, Hasthi
Sahadevan, Sudeep
Gale, Nittaya
Caggiano, Monica Pia
Yu, Xiulian
Ohno, Carolyn
Heisler, Marcus G.
author_facet Ram, Hasthi
Sahadevan, Sudeep
Gale, Nittaya
Caggiano, Monica Pia
Yu, Xiulian
Ohno, Carolyn
Heisler, Marcus G.
author_sort Ram, Hasthi
collection PubMed
description In the Arabidopsis thaliana shoot apical meristem (SAM) the expression domains of Class III Homeodomain Leucine Zipper (HD-ZIPIII) and KANADI (KAN) genes are separated by a narrow boundary region from which new organs are initiated. Disruption of this boundary through either loss of function or ectopic expression of HD-ZIPIII and KAN causes ectopic or suppression of organ formation respectively, raising the question of how these transcription factors regulate organogenesis at a molecular level. In this study we develop a multi-channel FACS/RNA-seq approach to characterize global patterns of gene expression across the HD-ZIPIII-KAN1 SAM boundary. We then combine FACS, RNA-seq and perturbations of HD-ZIPIII and KAN expression to identify genes that are both responsive to REV and KAN1 and normally expressed in patterns that correlate with REV and KAN1. Our data reveal that a significant number of genes responsive to REV are regulated in opposite ways depending on time after induction, with genes associated with auxin response and synthesis upregulated initially, but later repressed. We also characterize the cell type specific expression patterns of auxin responsive genes and identify a set of genes involved in organogenesis repressed by both REV and KAN1.
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spelling pubmed-72663452020-06-10 An integrated analysis of cell-type specific gene expression reveals genes regulated by REVOLUTA and KANADI1 in the Arabidopsis shoot apical meristem Ram, Hasthi Sahadevan, Sudeep Gale, Nittaya Caggiano, Monica Pia Yu, Xiulian Ohno, Carolyn Heisler, Marcus G. PLoS Genet Research Article In the Arabidopsis thaliana shoot apical meristem (SAM) the expression domains of Class III Homeodomain Leucine Zipper (HD-ZIPIII) and KANADI (KAN) genes are separated by a narrow boundary region from which new organs are initiated. Disruption of this boundary through either loss of function or ectopic expression of HD-ZIPIII and KAN causes ectopic or suppression of organ formation respectively, raising the question of how these transcription factors regulate organogenesis at a molecular level. In this study we develop a multi-channel FACS/RNA-seq approach to characterize global patterns of gene expression across the HD-ZIPIII-KAN1 SAM boundary. We then combine FACS, RNA-seq and perturbations of HD-ZIPIII and KAN expression to identify genes that are both responsive to REV and KAN1 and normally expressed in patterns that correlate with REV and KAN1. Our data reveal that a significant number of genes responsive to REV are regulated in opposite ways depending on time after induction, with genes associated with auxin response and synthesis upregulated initially, but later repressed. We also characterize the cell type specific expression patterns of auxin responsive genes and identify a set of genes involved in organogenesis repressed by both REV and KAN1. Public Library of Science 2020-04-15 /pmc/articles/PMC7266345/ /pubmed/32294082 http://dx.doi.org/10.1371/journal.pgen.1008661 Text en © 2020 Ram et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Ram, Hasthi
Sahadevan, Sudeep
Gale, Nittaya
Caggiano, Monica Pia
Yu, Xiulian
Ohno, Carolyn
Heisler, Marcus G.
An integrated analysis of cell-type specific gene expression reveals genes regulated by REVOLUTA and KANADI1 in the Arabidopsis shoot apical meristem
title An integrated analysis of cell-type specific gene expression reveals genes regulated by REVOLUTA and KANADI1 in the Arabidopsis shoot apical meristem
title_full An integrated analysis of cell-type specific gene expression reveals genes regulated by REVOLUTA and KANADI1 in the Arabidopsis shoot apical meristem
title_fullStr An integrated analysis of cell-type specific gene expression reveals genes regulated by REVOLUTA and KANADI1 in the Arabidopsis shoot apical meristem
title_full_unstemmed An integrated analysis of cell-type specific gene expression reveals genes regulated by REVOLUTA and KANADI1 in the Arabidopsis shoot apical meristem
title_short An integrated analysis of cell-type specific gene expression reveals genes regulated by REVOLUTA and KANADI1 in the Arabidopsis shoot apical meristem
title_sort integrated analysis of cell-type specific gene expression reveals genes regulated by revoluta and kanadi1 in the arabidopsis shoot apical meristem
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7266345/
https://www.ncbi.nlm.nih.gov/pubmed/32294082
http://dx.doi.org/10.1371/journal.pgen.1008661
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