Abstract:Plants count on a wide variety of metabolic, physiological, and developmental responses to adapt their growth to variations in mineral nutrient availability. To react to such variations plants have evolved complex sensing and signaling mechanisms that allow them to monitor the external and internal concentration of each of these nutrients, both in absolute terms and also relatively to the status of other nutrients. Recent evidence has shown that hormones participate in the control of these regulatory networks.… Show more
“…65 Nitrate application was also shown to increase cytokinin biosynthesis and expression of its signaling components, leading to morphological effects on both roots and shoots (reviewed in ref. 24), whereas the reduction in shoot apical dominance in pea was suggested to be a result of reduced auxin transport out of the apex under conditions of B deficiency. 19 Notably, many of the phytohormones are coordinated with other phytohormones in their effects on plant development, and have multiple cross-talk junctions between them, forming a complex network of coordinated effects (reviewed in ref.…”
Section: Other Phytohormones and Plant Responses To Environmental Cuesmentioning
confidence: 99%
“…However, more research is needed to confer or rebut this hypothesis, since in many cases similar developmental responses may be triggered by different signaling mechanisms. 24 To conclude, further studies are clearly needed to determine the junction points of the co-regulation of SLs and light in lightregulated processes, in both shoots and roots. Moreover, the cross-talk between SLs and light-associated pathways might follow a feedback loop, because carotenoid biosynthesis has been shown to be light-dependent (reviewed in ref.…”
“…Key words: strigolactones, light, nutrient status, root, shoot, branching, lateral roots, root hairs development and architecture (reviewed in ref. [22][23][24] and to be mediators of the effects of environmental cues on plant development; one classic example is auxin's role in the plant's shadeavoidance response (reviewed in ref. 25).…”
“…65 Nitrate application was also shown to increase cytokinin biosynthesis and expression of its signaling components, leading to morphological effects on both roots and shoots (reviewed in ref. 24), whereas the reduction in shoot apical dominance in pea was suggested to be a result of reduced auxin transport out of the apex under conditions of B deficiency. 19 Notably, many of the phytohormones are coordinated with other phytohormones in their effects on plant development, and have multiple cross-talk junctions between them, forming a complex network of coordinated effects (reviewed in ref.…”
Section: Other Phytohormones and Plant Responses To Environmental Cuesmentioning
confidence: 99%
“…However, more research is needed to confer or rebut this hypothesis, since in many cases similar developmental responses may be triggered by different signaling mechanisms. 24 To conclude, further studies are clearly needed to determine the junction points of the co-regulation of SLs and light in lightregulated processes, in both shoots and roots. Moreover, the cross-talk between SLs and light-associated pathways might follow a feedback loop, because carotenoid biosynthesis has been shown to be light-dependent (reviewed in ref.…”
“…Key words: strigolactones, light, nutrient status, root, shoot, branching, lateral roots, root hairs development and architecture (reviewed in ref. [22][23][24] and to be mediators of the effects of environmental cues on plant development; one classic example is auxin's role in the plant's shadeavoidance response (reviewed in ref. 25).…”
“…In fact, nutrient supplies can strongly affect phytohormone gradients, as demonstrated by Fe triggering AUXIN INFLUX CARRIER1 (AUX1)-mediated auxin accumulation in LR tips and subsequent LR elongation (Giehl et al, 2012). Indeed, the deficiency of many nutrients has been reported to affect the levels of one or more hormones in plants (for review, see Rubio et al, 2009). However, for most nutrients, it is not yet known the extent to which and at which developmental steps these hormonal changes impact on RSA.…”
Section: The Effect Of Nutrient Availability On Lr Formationmentioning
“…Given that the amount of iP type CKs was higher in Cuscuta at stage 1 than that which the haustoria induced in vitro, the role of iP type CKs is not restricted to haustoria formation. In addition, iP type CKs may increase in nutrient-depleted plants, especially when nutrients are added (Takei et al 2004;Rubiom et al 2009). Cuscuta seedlings before parasitization clearly do not have an opportunity obtain any nutrients from the environment, and stage 1 is the first time to acquire nutrients after germination.…”
Section: Plant Hormonal Changes In Cuscutamentioning
The holostemparasitic plant Cuscuta parasitizes various plants and sucks nutrients from the host stem. We used Cuscuta japonica as the parasite and Momordica charantia as the host plant, and described their interaction. The parasitized Momordica stems started swelling as a hypertrophic response within 3 days after parasitization. Concurrently, the Cuscuta stem grew rapidly and developed bigger scale leaves than usual. Parasitized Momordica stems reduced photosynthetic activity. Histological observation revealed no programmed cell death but an increased number of vascular bundles in the Momordica stem, especially near the Cuscuta hyphae. The defensive response of Momordica mainly involved the SA pathway. Drastic increase of tZ-and DZ-type cytokinins in Momordica stems would play an important role for hypertrophy. Cuscuta had higher cZ endogenously and our results imply that each subtype of CK might play different roles during parasitization process. Comprehensive plant hormone analysis provides new insights into plant interaction studies.
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