Identification of dehydrocostus lactone and 4-hydroxy-β-thujone as auxin polar transport inhibitors

2013 ◽  
Vol 35 (7) ◽  
pp. 2251-2258 ◽  
Author(s):  
Junichi Ueda ◽  
Yuta Toda ◽  
Kiyotaka Kato ◽  
Yuichi Kuroda ◽  
Tsukasa Arai ◽  
...  
2013 ◽  
Vol 21 (2) ◽  
pp. 31-39
Author(s):  
Elżbieta Węgrzynowicz-Lesiak ◽  
Justyna Góraj ◽  
Kensuke Miyamoto ◽  
Junichi Ueda ◽  
Marian Saniewski

ABSTRACT Effects of auxin polar transport inhibitors: methyl 2-chloro-9-hydroxyfluorene-9-carboxylate (morphactin IT 3456), 2,3,5-triiodobenzoic acid (TIBA) and N-1-naphthylphthalamic acid (NPA) on elongation growth of the excised fourth internode of tulips (Tulipa gesneriana L.) cv. Apeldoorn were studied. After removal of flower bud, the continuing elongation of the excised fourth internode kept in water in normal or inverted position was observed, the elongation in inverted position being significantly higher than that in the normal position. On the other hand, the application of these inhibitors (0.2%, w/w in lanolin) in the place of removed flower bud substantially enhanced the elongation, the stimulation being much higher in the normal position than in the inverted one. When the inhibitors were applied in the middle or 1 cm from the base of the internode, the growth-promoting effect of these inhibitors was observed both in the upper and lower part of the internode, being greater in the upper part of the internode, regardless of the position of explants. Simultaneous application of indole-3-acetic acid (IAA) (0.1%, w/w in lanolin) at the place of the removed flower bud in the normal position with morphactin, TIBA and NPA applied in the middle or 1 cm from the base of the excised internode greatly stimulated the elongation, whereas almost no growthpromoting effect of these inhibitors was observed, in comparison to IAA. On the contrary, when IAA was applied on the base of the excised internode in the inverted position, the growth was inhibited, compared to that with lanolin only. The inhibitory effect of auxin was eliminated by the simultaneous application of morphactin, TIBA and NPA placed in the middle of the excised internode. These results suggest that auxin levels in the excised internode regulated by auxin polar transport play a crucial role in the regulation of its elongation growth.


2012 ◽  
Vol 20 (2) ◽  
pp. 161-171 ◽  
Author(s):  
Junichi Ueda ◽  
Justyna Góraj ◽  
Elżbieta Węgrzynowicz-Lesiak ◽  
Kensuke Miyamoto

Abstract Important role of auxin polar transport inhibitors such as TIBA (2,3,5- triiodobenzoic acid), NPA (N-(1-naphthyl)phthalamic acid) and morphactin (methyl 2-chloro-9-hydroxyfluorene-9-carboxylate) in stem growth of tulips was intensively studied. After the application of morphactin above the 3rd node of decapitated tulips, the stimulated growth of the 4th internode was clearly observed. On the other hand, NPA and TIBA were slightly effective in stimulating the 4th internode growth of tulips. Endogenous levels of IAA in the 4th internode after the treatment of auxin polar transport inhibitors were determined using gas-liquid chromatography-mass spectrometry (GC-MS) and gas-liquid chromatography-mass spectrometry selected ion monitoring system (GC-SIM) with deuterium labelled IAA (Indole-2,4,5,6,7-d5-3- acetic acid, d5-IAA) as an internal standard, resulted in significant accumulation of IAA in the 4th internode of tulips after the treatment of morphactin. In the treatment of NPA and TIBA, there was almost no such an accumulation of IAA. These results strongly suggest that stimulated growth of the 4th internode of tulips induced by the application of morphactin is the consequence of accumulated endogenous levels of IAA after the treatment. The possible mode of action of auxin polar transport inhibitors in tulip stem growth is also discussed.


2014 ◽  
Vol 67 (2) ◽  
pp. 85-92 ◽  
Author(s):  
Marian Saniewski ◽  
Justyna Góraj ◽  
Elżbieta Węgrzynowicz-Lesiak ◽  
Kensuke Miyamoto ◽  
Junichi Ueda

Effects of auxin polar transport inhibitors, 2,3,5-triio-dobenzoic acid (TIBA), 1-<em>N</em>-naphthylphthalamic acid (NPA) and methyl 2-chloro-9-hydroxyfluorene-9-carboxylate (morphactin IT 3456), as a lanolin paste, on root formation in cuttings of some species of Crassulaceae, such as <em>Bryophyllum daigremontianum, B. calycinum, Kalanchoe blossfeldiana </em>and <em>K. tubiflora</em>, were studied. Cuttings of these plants were easily rooted in water without any treatment. TIBA and morphactin IT 3456 completely inhibited root formation in the cuttings of these plants but NPA did not when these inhibitors were applied around the stem below the leaves. When TIBA and morphactin were applied around the stem near the top, but leaves were present below the treatment, the root formation was observed in <em>B. calycinum </em>and <em>K. blossfeldiana </em>but in a smaller degree than in control cuttings. These results strongly suggest that endogenous auxin is required for root formation in cuttings of Crassulaceae plants. The differential mode of action of NPA is discussed together with its effect on auxin polar transport.


1991 ◽  
Vol 3 (7) ◽  
pp. 677 ◽  
Author(s):  
Kiyotaka Okada ◽  
Junichi Ueda ◽  
Masako K. Komaki ◽  
Callum J. Bell ◽  
Yoshiro Shimura

2017 ◽  
Vol 114 (36) ◽  
pp. E7641-E7649 ◽  
Author(s):  
Riccardo Di Mambro ◽  
Micol De Ruvo ◽  
Elena Pacifici ◽  
Elena Salvi ◽  
Rosangela Sozzani ◽  
...  

In multicellular organisms, a stringent control of the transition between cell division and differentiation is crucial for correct tissue and organ development. In the Arabidopsis root, the boundary between dividing and differentiating cells is positioned by the antagonistic interaction of the hormones auxin and cytokinin. Cytokinin affects polar auxin transport, but how this impacts the positional information required to establish this tissue boundary, is still unknown. By combining computational modeling with molecular genetics, we show that boundary formation is dependent on cytokinin’s control on auxin polar transport and degradation. The regulation of both processes shapes the auxin profile in a well-defined auxin minimum. This auxin minimum positions the boundary between dividing and differentiating cells, acting as a trigger for this developmental transition, thus controlling meristem size.


2000 ◽  
Vol 14 (1) ◽  
pp. 9-13 ◽  
Author(s):  
Toru Shimazu ◽  
Kensuke Miyamoto ◽  
Takayuki Hoson ◽  
Seiichiro Kamisaka ◽  
Junichi Ueda

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