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Plant lamin-like proteins mediate chromatin tethering at the nuclear periphery

BACKGROUND: The nuclear envelope not only serves as a physical barrier separating nuclear content from the cytoplasm but also plays critical roles in modulating the three-dimensional organization of genomic DNA. For both plants and animals, the nuclear periphery is a functional compartment enriched...

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Autores principales: Hu, Bo, Wang, Nan, Bi, Xiuli, Karaaslan, Ezgi Süheyla, Weber, Anna-Lena, Zhu, Wangsheng, Berendzen, Kenneth Wayne, Liu, Chang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6492433/
https://www.ncbi.nlm.nih.gov/pubmed/31039799
http://dx.doi.org/10.1186/s13059-019-1694-3
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author Hu, Bo
Wang, Nan
Bi, Xiuli
Karaaslan, Ezgi Süheyla
Weber, Anna-Lena
Zhu, Wangsheng
Berendzen, Kenneth Wayne
Liu, Chang
author_facet Hu, Bo
Wang, Nan
Bi, Xiuli
Karaaslan, Ezgi Süheyla
Weber, Anna-Lena
Zhu, Wangsheng
Berendzen, Kenneth Wayne
Liu, Chang
author_sort Hu, Bo
collection PubMed
description BACKGROUND: The nuclear envelope not only serves as a physical barrier separating nuclear content from the cytoplasm but also plays critical roles in modulating the three-dimensional organization of genomic DNA. For both plants and animals, the nuclear periphery is a functional compartment enriched with heterochromatin. To date, how plants manage to selectively tether chromatin at the nuclear periphery is unclear. RESULTS: By conducting dual-color fluorescence in situ hybridization experiments on 2C nuclei, we show that in Arabidopsis thaliana, specific chromatin positioning at the nuclear periphery requires plant lamin-like proteins CROWDED NUCLEI 1 (CRWN1), CRWN4, and DNA methylation in CHG and CHH contexts. With chromosome painting and Hi-C analyses, we show global attenuation of spatial chromatin compartmentalization and chromatin positioning patterns at the nuclear periphery in both the crwn1 and crwn4 mutants. Furthermore, ChIP-seq analysis indicates that CRWN1 directly interacts with chromatin domains localized at the nuclear periphery, which mainly contains non-accessible chromatin. CONCLUSIONS: In summary, we conclude that CRWN1 is a key component of the lamina-chromatin network in plants. It is functionally equivalent to animal lamins, playing critical roles in modulating patterns of chromatin positioning at the nuclear periphery. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13059-019-1694-3) contains supplementary material, which is available to authorized users.
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spelling pubmed-64924332019-05-08 Plant lamin-like proteins mediate chromatin tethering at the nuclear periphery Hu, Bo Wang, Nan Bi, Xiuli Karaaslan, Ezgi Süheyla Weber, Anna-Lena Zhu, Wangsheng Berendzen, Kenneth Wayne Liu, Chang Genome Biol Research BACKGROUND: The nuclear envelope not only serves as a physical barrier separating nuclear content from the cytoplasm but also plays critical roles in modulating the three-dimensional organization of genomic DNA. For both plants and animals, the nuclear periphery is a functional compartment enriched with heterochromatin. To date, how plants manage to selectively tether chromatin at the nuclear periphery is unclear. RESULTS: By conducting dual-color fluorescence in situ hybridization experiments on 2C nuclei, we show that in Arabidopsis thaliana, specific chromatin positioning at the nuclear periphery requires plant lamin-like proteins CROWDED NUCLEI 1 (CRWN1), CRWN4, and DNA methylation in CHG and CHH contexts. With chromosome painting and Hi-C analyses, we show global attenuation of spatial chromatin compartmentalization and chromatin positioning patterns at the nuclear periphery in both the crwn1 and crwn4 mutants. Furthermore, ChIP-seq analysis indicates that CRWN1 directly interacts with chromatin domains localized at the nuclear periphery, which mainly contains non-accessible chromatin. CONCLUSIONS: In summary, we conclude that CRWN1 is a key component of the lamina-chromatin network in plants. It is functionally equivalent to animal lamins, playing critical roles in modulating patterns of chromatin positioning at the nuclear periphery. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13059-019-1694-3) contains supplementary material, which is available to authorized users. BioMed Central 2019-04-30 /pmc/articles/PMC6492433/ /pubmed/31039799 http://dx.doi.org/10.1186/s13059-019-1694-3 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Hu, Bo
Wang, Nan
Bi, Xiuli
Karaaslan, Ezgi Süheyla
Weber, Anna-Lena
Zhu, Wangsheng
Berendzen, Kenneth Wayne
Liu, Chang
Plant lamin-like proteins mediate chromatin tethering at the nuclear periphery
title Plant lamin-like proteins mediate chromatin tethering at the nuclear periphery
title_full Plant lamin-like proteins mediate chromatin tethering at the nuclear periphery
title_fullStr Plant lamin-like proteins mediate chromatin tethering at the nuclear periphery
title_full_unstemmed Plant lamin-like proteins mediate chromatin tethering at the nuclear periphery
title_short Plant lamin-like proteins mediate chromatin tethering at the nuclear periphery
title_sort plant lamin-like proteins mediate chromatin tethering at the nuclear periphery
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6492433/
https://www.ncbi.nlm.nih.gov/pubmed/31039799
http://dx.doi.org/10.1186/s13059-019-1694-3
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