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Direct ETTIN-auxin interaction controls chromatin states in gynoecium development
Hormonal signalling in animals often involves direct transcription factor-hormone interactions that modulate gene expression. In contrast, plant hormone signalling is most commonly based on de-repression via the degradation of transcriptional repressors. Recently, we uncovered a non-canonical signal...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7164952/ https://www.ncbi.nlm.nih.gov/pubmed/32267233 http://dx.doi.org/10.7554/eLife.51787 |
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author | Kuhn, André Ramans Harborough, Sigurd McLaughlin, Heather M Natarajan, Bhavani Verstraeten, Inge Friml, Jiří Kepinski, Stefan Østergaard, Lars |
author_facet | Kuhn, André Ramans Harborough, Sigurd McLaughlin, Heather M Natarajan, Bhavani Verstraeten, Inge Friml, Jiří Kepinski, Stefan Østergaard, Lars |
author_sort | Kuhn, André |
collection | PubMed |
description | Hormonal signalling in animals often involves direct transcription factor-hormone interactions that modulate gene expression. In contrast, plant hormone signalling is most commonly based on de-repression via the degradation of transcriptional repressors. Recently, we uncovered a non-canonical signalling mechanism for the plant hormone auxin whereby auxin directly affects the activity of the atypical auxin response factor (ARF), ETTIN towards target genes without the requirement for protein degradation. Here we show that ETTIN directly binds auxin, leading to dissociation from co-repressor proteins of the TOPLESS/TOPLESS-RELATED family followed by histone acetylation and induction of gene expression. This mechanism is reminiscent of animal hormone signalling as it affects the activity towards regulation of target genes and provides the first example of a DNA-bound hormone receptor in plants. Whilst auxin affects canonical ARFs indirectly by facilitating degradation of Aux/IAA repressors, direct ETTIN-auxin interactions allow switching between repressive and de-repressive chromatin states in an instantly-reversible manner. |
format | Online Article Text |
id | pubmed-7164952 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-71649522020-04-20 Direct ETTIN-auxin interaction controls chromatin states in gynoecium development Kuhn, André Ramans Harborough, Sigurd McLaughlin, Heather M Natarajan, Bhavani Verstraeten, Inge Friml, Jiří Kepinski, Stefan Østergaard, Lars eLife Developmental Biology Hormonal signalling in animals often involves direct transcription factor-hormone interactions that modulate gene expression. In contrast, plant hormone signalling is most commonly based on de-repression via the degradation of transcriptional repressors. Recently, we uncovered a non-canonical signalling mechanism for the plant hormone auxin whereby auxin directly affects the activity of the atypical auxin response factor (ARF), ETTIN towards target genes without the requirement for protein degradation. Here we show that ETTIN directly binds auxin, leading to dissociation from co-repressor proteins of the TOPLESS/TOPLESS-RELATED family followed by histone acetylation and induction of gene expression. This mechanism is reminiscent of animal hormone signalling as it affects the activity towards regulation of target genes and provides the first example of a DNA-bound hormone receptor in plants. Whilst auxin affects canonical ARFs indirectly by facilitating degradation of Aux/IAA repressors, direct ETTIN-auxin interactions allow switching between repressive and de-repressive chromatin states in an instantly-reversible manner. eLife Sciences Publications, Ltd 2020-04-08 /pmc/articles/PMC7164952/ /pubmed/32267233 http://dx.doi.org/10.7554/eLife.51787 Text en © 2020, Kuhn et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Developmental Biology Kuhn, André Ramans Harborough, Sigurd McLaughlin, Heather M Natarajan, Bhavani Verstraeten, Inge Friml, Jiří Kepinski, Stefan Østergaard, Lars Direct ETTIN-auxin interaction controls chromatin states in gynoecium development |
title | Direct ETTIN-auxin interaction controls chromatin states in gynoecium development |
title_full | Direct ETTIN-auxin interaction controls chromatin states in gynoecium development |
title_fullStr | Direct ETTIN-auxin interaction controls chromatin states in gynoecium development |
title_full_unstemmed | Direct ETTIN-auxin interaction controls chromatin states in gynoecium development |
title_short | Direct ETTIN-auxin interaction controls chromatin states in gynoecium development |
title_sort | direct ettin-auxin interaction controls chromatin states in gynoecium development |
topic | Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7164952/ https://www.ncbi.nlm.nih.gov/pubmed/32267233 http://dx.doi.org/10.7554/eLife.51787 |
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