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Common and unique cis-acting elements mediate xanthotoxin and flavone induction of the generalist P450 CYP321A1
How polyphagous herbivores up-regulate their counterdefense genes in response to a broad range of structurally different allelochemicals remains largely unknown. To test whether this is accomplished by having more allelochemical-response elements or the similar number of functionally more diverse el...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4178294/ https://www.ncbi.nlm.nih.gov/pubmed/25262756 http://dx.doi.org/10.1038/srep06490 |
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author | Zhang, Chunni Wong, Andrew Zhang, Yalin Ni, Xinzhi Li, Xianchun |
author_facet | Zhang, Chunni Wong, Andrew Zhang, Yalin Ni, Xinzhi Li, Xianchun |
author_sort | Zhang, Chunni |
collection | PubMed |
description | How polyphagous herbivores up-regulate their counterdefense genes in response to a broad range of structurally different allelochemicals remains largely unknown. To test whether this is accomplished by having more allelochemical-response elements or the similar number of functionally more diverse elements, we mapped out the cis-acting elements mediating the induction of the allelochemical-metabolizing CYP321A1 from the generalist Helicoverpa zea by xanthotoxin and flavone, two structurally distinct allelochemicals with very different encounter rate by this species. Seven xanthotoxin-responsive elements were localized by analyzing promoter activities of varying length of CYP321A1 promoter in H. zea fatbody cells. Compared with the 5 flavone-responsive elements mapped out previously, there are four common elements (1 essential element, 2 enhancers, and 1 negative element) mediating induction of CYP321A1 by both of the two allelochemicals. The remaining four elements (3 enhancers and 1 negative element), however, only regulate induction of CYP321A1 by either of the two allelochemicals. Co-administration of the two allelochemicals resulted in an induction fold that is significantly lower than the expected additive value of the two allelochemicals. These results indicate that xanthotoxin- and flavone-induced expressions of CYP321A1 are mediated mainly by the functionally more diverse common elements although the allelochemical-unique elements also play a role. |
format | Online Article Text |
id | pubmed-4178294 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-41782942014-09-30 Common and unique cis-acting elements mediate xanthotoxin and flavone induction of the generalist P450 CYP321A1 Zhang, Chunni Wong, Andrew Zhang, Yalin Ni, Xinzhi Li, Xianchun Sci Rep Article How polyphagous herbivores up-regulate their counterdefense genes in response to a broad range of structurally different allelochemicals remains largely unknown. To test whether this is accomplished by having more allelochemical-response elements or the similar number of functionally more diverse elements, we mapped out the cis-acting elements mediating the induction of the allelochemical-metabolizing CYP321A1 from the generalist Helicoverpa zea by xanthotoxin and flavone, two structurally distinct allelochemicals with very different encounter rate by this species. Seven xanthotoxin-responsive elements were localized by analyzing promoter activities of varying length of CYP321A1 promoter in H. zea fatbody cells. Compared with the 5 flavone-responsive elements mapped out previously, there are four common elements (1 essential element, 2 enhancers, and 1 negative element) mediating induction of CYP321A1 by both of the two allelochemicals. The remaining four elements (3 enhancers and 1 negative element), however, only regulate induction of CYP321A1 by either of the two allelochemicals. Co-administration of the two allelochemicals resulted in an induction fold that is significantly lower than the expected additive value of the two allelochemicals. These results indicate that xanthotoxin- and flavone-induced expressions of CYP321A1 are mediated mainly by the functionally more diverse common elements although the allelochemical-unique elements also play a role. Nature Publishing Group 2014-09-29 /pmc/articles/PMC4178294/ /pubmed/25262756 http://dx.doi.org/10.1038/srep06490 Text en Copyright © 2014, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-sa/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/ |
spellingShingle | Article Zhang, Chunni Wong, Andrew Zhang, Yalin Ni, Xinzhi Li, Xianchun Common and unique cis-acting elements mediate xanthotoxin and flavone induction of the generalist P450 CYP321A1 |
title | Common and unique cis-acting elements mediate xanthotoxin and flavone induction of the generalist P450 CYP321A1 |
title_full | Common and unique cis-acting elements mediate xanthotoxin and flavone induction of the generalist P450 CYP321A1 |
title_fullStr | Common and unique cis-acting elements mediate xanthotoxin and flavone induction of the generalist P450 CYP321A1 |
title_full_unstemmed | Common and unique cis-acting elements mediate xanthotoxin and flavone induction of the generalist P450 CYP321A1 |
title_short | Common and unique cis-acting elements mediate xanthotoxin and flavone induction of the generalist P450 CYP321A1 |
title_sort | common and unique cis-acting elements mediate xanthotoxin and flavone induction of the generalist p450 cyp321a1 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4178294/ https://www.ncbi.nlm.nih.gov/pubmed/25262756 http://dx.doi.org/10.1038/srep06490 |
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