2014
DOI: 10.1073/pnas.1408960111
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Auxin transport sites are visualized in planta using fluorescent auxin analogs

Abstract: The plant hormone auxin is a key morphogenetic signal that controls many aspects of plant growth and development. Cellular auxin levels are coordinately regulated by multiple processes, including auxin biosynthesis and the polar transport and metabolic pathways. The auxin concentration gradient determines plant organ positioning and growth responses to environmental cues. Auxin transport systems play crucial roles in the spatiotemporal regulation of the auxin gradient. This auxin gradient has been analyzed usi… Show more

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Cited by 78 publications
(68 citation statements)
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References 43 publications
(59 reference statements)
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“…Dark-grown seedlings pretreated with or without RL were irradiated with a pulse of blue light (BL). After 2.5 h, the seedlings were incubated into growth medium containing a fluorescent auxin analog (NBD-NAA; Hayashi et al, 2014) at 5 mM for 15 min. The fluorescent signals derived from NBD-NAA were then quantified.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Dark-grown seedlings pretreated with or without RL were irradiated with a pulse of blue light (BL). After 2.5 h, the seedlings were incubated into growth medium containing a fluorescent auxin analog (NBD-NAA; Hayashi et al, 2014) at 5 mM for 15 min. The fluorescent signals derived from NBD-NAA were then quantified.…”
Section: Discussionmentioning
confidence: 99%
“…Recently, a fluorescent auxin analog (7-nitro-2,1,3-benzoxadiazole [NBD] -conjugated naphthalene-1-acetic acid [NAA]) has been developed to visualize auxin distribution (Hayashi et al, 2014). When dark-grown seedlings were treated with NBD-NAA, fluorescent signals were evenly distributed in the epidermis of hypocotyls of both the wild type and the pid quadruple mutant without phototropic stimulation (Fig.…”
Section: The Pid Family Is Necessary For the Promotion Of The Auxin Gmentioning
confidence: 99%
“…Both of these studies have strong evidence that sucrose is getting to the target tissues, but current methodologies make it difficult to get the needed temporal and spatial resolution to be sure that the sucrose effect is fully independent of auxin. New technologies like fluorescent-labeled auxin [18], sugar sensors [19,20] and methods to quantify auxin at the tissue-level [21] may resolve the extent to which these signals act in sequence, act independently or some synergistic combination of the two possibilities.…”
Section: Metabolic Interactions Long-range Signalling and Hormonesmentioning
confidence: 99%
“…To examine the subcellular localization of MA-5, fluorescence-labeled MA-5 (BODIPY-MA-5) was synthesized 11 and reacted with normal human fibroblasts ( Figure 2E, left panel). Fluorescence signals of BODIPY-MA-5 (green in Figure 2E, right panel) (10 nM) were clearly detected in the cytoplasm and colocalized (yellow in Figure 2E, right panel) with mitochondria labeled by Mitotracker (red in Figure 2E, right panel).…”
mentioning
confidence: 99%