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Intrinsic Disorder in Plant Transcription Factor Systems: Functional Implications

Eukaryotic cells are complex biological systems that depend on highly connected molecular interaction networks with intrinsically disordered proteins as essential components. Through specific examples, we relate the conformational ensemble nature of intrinsic disorder (ID) in transcription factors t...

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Autores principales: Salladini, Edoardo, Jørgensen, Maria L. M., Theisen, Frederik F., Skriver, Karen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7767404/
https://www.ncbi.nlm.nih.gov/pubmed/33371315
http://dx.doi.org/10.3390/ijms21249755
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author Salladini, Edoardo
Jørgensen, Maria L. M.
Theisen, Frederik F.
Skriver, Karen
author_facet Salladini, Edoardo
Jørgensen, Maria L. M.
Theisen, Frederik F.
Skriver, Karen
author_sort Salladini, Edoardo
collection PubMed
description Eukaryotic cells are complex biological systems that depend on highly connected molecular interaction networks with intrinsically disordered proteins as essential components. Through specific examples, we relate the conformational ensemble nature of intrinsic disorder (ID) in transcription factors to functions in plants. Transcription factors contain large regulatory ID-regions with numerous orphan sequence motifs, representing potential important interaction sites. ID-regions may affect DNA-binding through electrostatic interactions or allosterically as for the bZIP transcription factors, in which the DNA-binding domains also populate ensembles of dynamic transient structures. The flexibility of ID is well-suited for interaction networks requiring efficient molecular adjustments. For example, Radical Induced Cell Death1 depends on ID in transcription factors for its numerous, structurally heterogeneous interactions, and the JAZ:MYC:MED15 regulatory unit depends on protein dynamics, including binding-associated unfolding, for regulation of jasmonate-signaling. Flexibility makes ID-regions excellent targets of posttranslational modifications. For example, the extent of phosphorylation of the NAC transcription factor SOG1 regulates target gene expression and the DNA-damage response, and phosphorylation of the AP2/ERF transcription factor DREB2A acts as a switch enabling heat-regulated degradation. ID-related phase separation is emerging as being important to transcriptional regulation with condensates functioning in storage and inactivation of transcription factors. The applicative potential of ID-regions is apparent, as removal of an ID-region of the AP2/ERF transcription factor WRI1 affects its stability and consequently oil biosynthesis. The highlighted examples show that ID plays essential functional roles in plant biology and has a promising potential in engineering.
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spelling pubmed-77674042020-12-28 Intrinsic Disorder in Plant Transcription Factor Systems: Functional Implications Salladini, Edoardo Jørgensen, Maria L. M. Theisen, Frederik F. Skriver, Karen Int J Mol Sci Review Eukaryotic cells are complex biological systems that depend on highly connected molecular interaction networks with intrinsically disordered proteins as essential components. Through specific examples, we relate the conformational ensemble nature of intrinsic disorder (ID) in transcription factors to functions in plants. Transcription factors contain large regulatory ID-regions with numerous orphan sequence motifs, representing potential important interaction sites. ID-regions may affect DNA-binding through electrostatic interactions or allosterically as for the bZIP transcription factors, in which the DNA-binding domains also populate ensembles of dynamic transient structures. The flexibility of ID is well-suited for interaction networks requiring efficient molecular adjustments. For example, Radical Induced Cell Death1 depends on ID in transcription factors for its numerous, structurally heterogeneous interactions, and the JAZ:MYC:MED15 regulatory unit depends on protein dynamics, including binding-associated unfolding, for regulation of jasmonate-signaling. Flexibility makes ID-regions excellent targets of posttranslational modifications. For example, the extent of phosphorylation of the NAC transcription factor SOG1 regulates target gene expression and the DNA-damage response, and phosphorylation of the AP2/ERF transcription factor DREB2A acts as a switch enabling heat-regulated degradation. ID-related phase separation is emerging as being important to transcriptional regulation with condensates functioning in storage and inactivation of transcription factors. The applicative potential of ID-regions is apparent, as removal of an ID-region of the AP2/ERF transcription factor WRI1 affects its stability and consequently oil biosynthesis. The highlighted examples show that ID plays essential functional roles in plant biology and has a promising potential in engineering. MDPI 2020-12-21 /pmc/articles/PMC7767404/ /pubmed/33371315 http://dx.doi.org/10.3390/ijms21249755 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Salladini, Edoardo
Jørgensen, Maria L. M.
Theisen, Frederik F.
Skriver, Karen
Intrinsic Disorder in Plant Transcription Factor Systems: Functional Implications
title Intrinsic Disorder in Plant Transcription Factor Systems: Functional Implications
title_full Intrinsic Disorder in Plant Transcription Factor Systems: Functional Implications
title_fullStr Intrinsic Disorder in Plant Transcription Factor Systems: Functional Implications
title_full_unstemmed Intrinsic Disorder in Plant Transcription Factor Systems: Functional Implications
title_short Intrinsic Disorder in Plant Transcription Factor Systems: Functional Implications
title_sort intrinsic disorder in plant transcription factor systems: functional implications
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7767404/
https://www.ncbi.nlm.nih.gov/pubmed/33371315
http://dx.doi.org/10.3390/ijms21249755
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