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NuA4 and H2A.Z control environmental responses and autotrophic growth in Arabidopsis

Nucleosomal acetyltransferase of H4 (NuA4) is an essential transcriptional coactivator in eukaryotes, but remains poorly characterized in plants. Here, we describe Arabidopsis homologs of the NuA4 scaffold proteins Enhancer of Polycomb-Like 1 (AtEPL1) and Esa1-Associated Factor 1 (AtEAF1). Loss of A...

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Autores principales: Bieluszewski, Tomasz, Sura, Weronika, Dziegielewski, Wojciech, Bieluszewska, Anna, Lachance, Catherine, Kabza, Michał, Szymanska-Lejman, Maja, Abram, Mateusz, Wlodzimierz, Piotr, De Winne, Nancy, De Jaeger, Geert, Sadowski, Jan, Côté, Jacques, Ziolkowski, Piotr A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8755797/
https://www.ncbi.nlm.nih.gov/pubmed/35022409
http://dx.doi.org/10.1038/s41467-021-27882-5
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author Bieluszewski, Tomasz
Sura, Weronika
Dziegielewski, Wojciech
Bieluszewska, Anna
Lachance, Catherine
Kabza, Michał
Szymanska-Lejman, Maja
Abram, Mateusz
Wlodzimierz, Piotr
De Winne, Nancy
De Jaeger, Geert
Sadowski, Jan
Côté, Jacques
Ziolkowski, Piotr A.
author_facet Bieluszewski, Tomasz
Sura, Weronika
Dziegielewski, Wojciech
Bieluszewska, Anna
Lachance, Catherine
Kabza, Michał
Szymanska-Lejman, Maja
Abram, Mateusz
Wlodzimierz, Piotr
De Winne, Nancy
De Jaeger, Geert
Sadowski, Jan
Côté, Jacques
Ziolkowski, Piotr A.
author_sort Bieluszewski, Tomasz
collection PubMed
description Nucleosomal acetyltransferase of H4 (NuA4) is an essential transcriptional coactivator in eukaryotes, but remains poorly characterized in plants. Here, we describe Arabidopsis homologs of the NuA4 scaffold proteins Enhancer of Polycomb-Like 1 (AtEPL1) and Esa1-Associated Factor 1 (AtEAF1). Loss of AtEAF1 results in inhibition of growth and chloroplast development. These effects are stronger in the Atepl1 mutant and are further enhanced by loss of Golden2-Like (GLK) transcription factors, suggesting that NuA4 activates nuclear plastid genes alongside GLK. We demonstrate that AtEPL1 is necessary for nucleosomal acetylation of histones H4 and H2A.Z by NuA4 in vitro. These chromatin marks are diminished genome-wide in Atepl1, while another active chromatin mark, H3K9 acetylation (H3K9ac), is locally enhanced. Expression of many chloroplast-related genes depends on NuA4, as they are downregulated with loss of H4ac and H2A.Zac. Finally, we demonstrate that NuA4 promotes H2A.Z deposition and by doing so prevents spurious activation of stress response genes.
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spelling pubmed-87557972022-01-20 NuA4 and H2A.Z control environmental responses and autotrophic growth in Arabidopsis Bieluszewski, Tomasz Sura, Weronika Dziegielewski, Wojciech Bieluszewska, Anna Lachance, Catherine Kabza, Michał Szymanska-Lejman, Maja Abram, Mateusz Wlodzimierz, Piotr De Winne, Nancy De Jaeger, Geert Sadowski, Jan Côté, Jacques Ziolkowski, Piotr A. Nat Commun Article Nucleosomal acetyltransferase of H4 (NuA4) is an essential transcriptional coactivator in eukaryotes, but remains poorly characterized in plants. Here, we describe Arabidopsis homologs of the NuA4 scaffold proteins Enhancer of Polycomb-Like 1 (AtEPL1) and Esa1-Associated Factor 1 (AtEAF1). Loss of AtEAF1 results in inhibition of growth and chloroplast development. These effects are stronger in the Atepl1 mutant and are further enhanced by loss of Golden2-Like (GLK) transcription factors, suggesting that NuA4 activates nuclear plastid genes alongside GLK. We demonstrate that AtEPL1 is necessary for nucleosomal acetylation of histones H4 and H2A.Z by NuA4 in vitro. These chromatin marks are diminished genome-wide in Atepl1, while another active chromatin mark, H3K9 acetylation (H3K9ac), is locally enhanced. Expression of many chloroplast-related genes depends on NuA4, as they are downregulated with loss of H4ac and H2A.Zac. Finally, we demonstrate that NuA4 promotes H2A.Z deposition and by doing so prevents spurious activation of stress response genes. Nature Publishing Group UK 2022-01-12 /pmc/articles/PMC8755797/ /pubmed/35022409 http://dx.doi.org/10.1038/s41467-021-27882-5 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Bieluszewski, Tomasz
Sura, Weronika
Dziegielewski, Wojciech
Bieluszewska, Anna
Lachance, Catherine
Kabza, Michał
Szymanska-Lejman, Maja
Abram, Mateusz
Wlodzimierz, Piotr
De Winne, Nancy
De Jaeger, Geert
Sadowski, Jan
Côté, Jacques
Ziolkowski, Piotr A.
NuA4 and H2A.Z control environmental responses and autotrophic growth in Arabidopsis
title NuA4 and H2A.Z control environmental responses and autotrophic growth in Arabidopsis
title_full NuA4 and H2A.Z control environmental responses and autotrophic growth in Arabidopsis
title_fullStr NuA4 and H2A.Z control environmental responses and autotrophic growth in Arabidopsis
title_full_unstemmed NuA4 and H2A.Z control environmental responses and autotrophic growth in Arabidopsis
title_short NuA4 and H2A.Z control environmental responses and autotrophic growth in Arabidopsis
title_sort nua4 and h2a.z control environmental responses and autotrophic growth in arabidopsis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8755797/
https://www.ncbi.nlm.nih.gov/pubmed/35022409
http://dx.doi.org/10.1038/s41467-021-27882-5
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