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WRINKLED1 Is Subject to Evolutionary Conserved Negative Autoregulation

High accumulation of storage compounds such as oil and starch are economically important traits of most agricultural crops. The genetic network determining storage compounds composition in crops has been the target of many biotechnological endeavors. Especially WRINKLED1 (WRI1), a well-known key tra...

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Autores principales: Snell, Per, Grimberg, Åsa, Carlsson, Anders S., Hofvander, Per
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6447653/
https://www.ncbi.nlm.nih.gov/pubmed/30984229
http://dx.doi.org/10.3389/fpls.2019.00387
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author Snell, Per
Grimberg, Åsa
Carlsson, Anders S.
Hofvander, Per
author_facet Snell, Per
Grimberg, Åsa
Carlsson, Anders S.
Hofvander, Per
author_sort Snell, Per
collection PubMed
description High accumulation of storage compounds such as oil and starch are economically important traits of most agricultural crops. The genetic network determining storage compounds composition in crops has been the target of many biotechnological endeavors. Especially WRINKLED1 (WRI1), a well-known key transcription factor involved in the allocation of carbon into oil, has attracted much interest. Here we investigate the presence of an autoregulatory system involving WRI1 through transient expression in Nicotiana benthamiana leaves. Different lengths of the Arabidopsis WRI1 promotor region were coupled to a GUS reporter gene and the activity was measured when combined with constitutive expression of different WRI1 homologs from Arabidopsis thaliana, oat (Avena sativa L.), yellow nutsedge (Cyperus esculentus L.), and potato (Solanum tuberosum L.). We could show that increasing levels of each WRI1 homolog reduced the transcriptional activity of the Arabidopsis WRI1 upstream region. Through structural analysis and domain swapping between oat and Arabidopsis WRI1, we were able to determine that the negative autoregulation was clearly dependent on the DNA-binding AP2-domains. A DNA/protein interaction assay showed that AtWRI1 is unable to bind to its corresponding upstream region indicating non-direct interaction in vivo. Taken together, our results demonstrate a negative feedback loop of WRI1 expression and that it is an indirect interaction most likely caused by downstream targets of WRI1. We also show that it is possible to release WRI1 expression from this autoregulation by creating semi-synthetic WRI1 homologs increasing the potential use of WRI1 in biotechnological applications.
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spelling pubmed-64476532019-04-12 WRINKLED1 Is Subject to Evolutionary Conserved Negative Autoregulation Snell, Per Grimberg, Åsa Carlsson, Anders S. Hofvander, Per Front Plant Sci Plant Science High accumulation of storage compounds such as oil and starch are economically important traits of most agricultural crops. The genetic network determining storage compounds composition in crops has been the target of many biotechnological endeavors. Especially WRINKLED1 (WRI1), a well-known key transcription factor involved in the allocation of carbon into oil, has attracted much interest. Here we investigate the presence of an autoregulatory system involving WRI1 through transient expression in Nicotiana benthamiana leaves. Different lengths of the Arabidopsis WRI1 promotor region were coupled to a GUS reporter gene and the activity was measured when combined with constitutive expression of different WRI1 homologs from Arabidopsis thaliana, oat (Avena sativa L.), yellow nutsedge (Cyperus esculentus L.), and potato (Solanum tuberosum L.). We could show that increasing levels of each WRI1 homolog reduced the transcriptional activity of the Arabidopsis WRI1 upstream region. Through structural analysis and domain swapping between oat and Arabidopsis WRI1, we were able to determine that the negative autoregulation was clearly dependent on the DNA-binding AP2-domains. A DNA/protein interaction assay showed that AtWRI1 is unable to bind to its corresponding upstream region indicating non-direct interaction in vivo. Taken together, our results demonstrate a negative feedback loop of WRI1 expression and that it is an indirect interaction most likely caused by downstream targets of WRI1. We also show that it is possible to release WRI1 expression from this autoregulation by creating semi-synthetic WRI1 homologs increasing the potential use of WRI1 in biotechnological applications. Frontiers Media S.A. 2019-03-28 /pmc/articles/PMC6447653/ /pubmed/30984229 http://dx.doi.org/10.3389/fpls.2019.00387 Text en Copyright © 2019 Snell, Grimberg, Carlsson and Hofvander. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Plant Science
Snell, Per
Grimberg, Åsa
Carlsson, Anders S.
Hofvander, Per
WRINKLED1 Is Subject to Evolutionary Conserved Negative Autoregulation
title WRINKLED1 Is Subject to Evolutionary Conserved Negative Autoregulation
title_full WRINKLED1 Is Subject to Evolutionary Conserved Negative Autoregulation
title_fullStr WRINKLED1 Is Subject to Evolutionary Conserved Negative Autoregulation
title_full_unstemmed WRINKLED1 Is Subject to Evolutionary Conserved Negative Autoregulation
title_short WRINKLED1 Is Subject to Evolutionary Conserved Negative Autoregulation
title_sort wrinkled1 is subject to evolutionary conserved negative autoregulation
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6447653/
https://www.ncbi.nlm.nih.gov/pubmed/30984229
http://dx.doi.org/10.3389/fpls.2019.00387
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