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...
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Veröffentlicht in: | Scientific reports 2014-09, Vol.4 (1), p.6490, Article 6490 |
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Sprache: | eng |
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Zusammenfassung: | 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. |
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ISSN: | 2045-2322 2045-2322 |
DOI: | 10.1038/srep06490 |