N6-(5-phenylpentan-1-yl)adenine – a new non-competitive receptor-specific anti-cytokinin

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Resumo

For the first time, N6-(5-phenylpentan-1-yl)adenine, a synthetic adenine derivative with a receptor-specific anticytokinin effect, was obtained. This compound exhibits a pronounced anticytokinin effect, reducing cytokinin-induced expression of the GUS reporter gene, when interacting with the cytokinin receptor CRE1/AHK4 of the model plant Arabidopsis thaliana. This effect manifests itself much weaker with the related AHK2 receptor and is not observed at all with the AHK3 receptor. We have shown that N6-(5-phenylpentan-1-yl)adenine does not bind to the ligand-binding sites of the Arabidopsis cytokinin receptors, which does not allow it to be classified as a true cytokinin antagonist. Despite the currently unknown mechanism of action, this compound may find its use as a component of plant growth regulators. Like true anticytokinins, it enhances root growth of Arabidopsis seedlings, apparently suppressing the action of endogenous cytokinins on the “root” receptor CRE1/AHK4.

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Sobre autores

A. Zenchenko

Engelhardt Institute of Molecular Biology, Russian Academy of Sciences

Autor responsável pela correspondência
Email: kolomatchenkoa@yandex.ru
Rússia, Moscow

E. Savelieva

Timiryazev Institute of Plant Physiology, Russian Academy of Sciences

Email: kolomatchenkoa@yandex.ru
Rússia, Moscow

M. Drenichev

Engelhardt Institute of Molecular Biology, Russian Academy of Sciences

Email: kolomatchenkoa@yandex.ru
Rússia, Moscow

G. Romanov

Timiryazev Institute of Plant Physiology, Russian Academy of Sciences

Email: kolomatchenkoa@yandex.ru
Rússia, Moscow

V. Oslovsky

Engelhardt Institute of Molecular Biology, Russian Academy of Sciences

Email: kolomatchenkoa@yandex.ru
Rússia, Moscow

Bibliografia

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2. Fig. 1. Synthesis of N6-(5-phenylpentane‑1-yl)adenine. Reagents and conditions: i. R-OH, Ph3P, DIAD, THF, 20 °C, 48 h; ii. 5M PrNH2/MeOH, 20 °C, 24 h; iii. HCl, 100 °C, 3 hours

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3. Fig. 2. The effect of different concentrations of compound 3 on the intensity of expression of the construct Parr5: GUS activated by BA (0.1 µM) when interacting with the CRE1/AHK4 receptor. The control is the effect of 0.1 µM BA on the same receptor.

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