Ecdysteroid ligand–receptor selectivity – exploring trends to design orthogonal gene switches

書誌事項

公開日
2008-11-11
権利情報
  • http://onlinelibrary.wiley.com/termsAndConditions#vor
DOI
  • 10.1111/j.1742-4658.2008.06687.x
公開者
Wiley

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説明

<jats:p>A set of thirty‐two natural and ten semisynthetic ecdysteroids was assayed in murine 3T3 cells across ten different ecdysteroid receptor (EcR) ligand‐binding domains derived from nine arthropod species in an engineered gene switch format. Among the ecdysteroids tested, the most biologically widespread ecdysteroid, 20‐hydroxyecdysone (20E), was moderately and consistently potent across the tested EcRs. The most potent ligand–receptor combination (EC<jats:sub>50</jats:sub> = 0.3 n<jats:sc>m</jats:sc>) was ponasterone A (PoA) actuating the <jats:italic>Nephotettix cincticeps</jats:italic> EcR switch. The most robust ligand–receptor combination, as measured by potency and efficacy, was PoA actuating either the <jats:italic>Bombyx mori</jats:italic> EcR or a ‘VY’ (E274V/V390I/Y410E) mutant of <jats:italic>Choristoneura fumiferana</jats:italic> EcR. Parallel ecdysteroid structure–activity relationships were observed across species; addition of hydroxyl groups at positions 2, 3, 14, 20 and 22 incrementally enhanced potency, whereas hydroxylation at position 25 retarded potency. Nevertheless, several outlier ligand–EcR combinations, such as cyasterone actuating the VY <jats:italic>C. fumiferana</jats:italic> EcR mutant and canescensterone activating <jats:italic>Bemisia argentifolii</jats:italic> EcR, exhibited an inversion of relative potency, and therefore lend themselves to construction of orthogonal duplex gene switches. The potency inversion between these two ligand–receptor pairs can be accounted for by steroid–tail contact residues Tyr411 and Met502 in VY <jats:italic>C. fumiferana</jats:italic> EcR corresponding to two threonines in <jats:italic>B. argentifolii</jats:italic> EcR. Another potency inversion was also observed with cyasterone operating on the VY mutant of <jats:italic>C. fumiferana</jats:italic> EcR and polypodine B activating <jats:italic>Aedes aegypti</jats:italic> EcR. The ecdysteroid‐EcR dataset, generated in a non‐natural system, nevertheless invites conjecture regarding relative ecdysteroid potencies, plant species distribution of certain phytoecdysteroids, and the role of phytoecdysteroids as chemodefense against relevant insect herbivores.</jats:p>

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