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The effect of auxin transport inhibition on Arabidopsis root development at low and high phosphate. Arabidopsis (Col-0) seedlings were grown for 16 d on nutrient medium containing low (1 M) and high (1 mM) phosphate content and varying concentrations of TIBA. Data are given for the length of the primary root (A), lateral root number (B), and lateral root density (C). Values shown represent the mean of 15 seedlings SE. Different letters are used to indicate means that differ significantly (P 0.05).

The effect of auxin transport inhibition on Arabidopsis root development at low and high phosphate. Arabidopsis (Col-0) seedlings were grown for 16 d on nutrient medium containing low (1 M) and high (1 mM) phosphate content and varying concentrations of TIBA. Data are given for the length of the primary root (A), lateral root number (B), and lateral root density (C). Values shown represent the mean of 15 seedlings SE. Different letters are used to indicate means that differ significantly (P 0.05).

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The postembryonic developmental program of the plant root system is plastic and allows changes in root architecture to adapt to environmental conditions such as water and nutrient availability. Among essential nutrients, phosphorus (P) often limits plant productivity because of its low mobility in soil. Therefore, the architecture of the root syste...

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... this effect appeared to be more dras- tic in low P conditions: Primary root elongation de- creased 2-fold in low P-treated seedlings grown in the presence of 10 7 m TIBA when compared with untreated controls, whereas a significant reduction of primary root elongation in seedlings grown at 1 mm P was only observed at concentrations of 10 5 m TIBA (Fig. 4A). Lateral root formation was similarly affected by treatments with 10 7 m TIBA at both high and low P concentrations, 41% and 50%, respectively (Fig. 4B). However, lateral root formation was completely abolished at 10 6 m TIBA in seedlings grown in 1 mm P, whereas at this concentration seedlings grown at low P still produce several ...
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... of 10 7 m TIBA when compared with untreated controls, whereas a significant reduction of primary root elongation in seedlings grown at 1 mm P was only observed at concentrations of 10 5 m TIBA (Fig. 4A). Lateral root formation was similarly affected by treatments with 10 7 m TIBA at both high and low P concentrations, 41% and 50%, respectively (Fig. 4B). However, lateral root formation was completely abolished at 10 6 m TIBA in seedlings grown in 1 mm P, whereas at this concentration seedlings grown at low P still produce several lateral roots (Fig. 4B). As a consequence of these changes, the negative effect of TIBA on lateral root density at 1 m P is significantly lower than at 1 mm ...
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... Lateral root formation was similarly affected by treatments with 10 7 m TIBA at both high and low P concentrations, 41% and 50%, respectively (Fig. 4B). However, lateral root formation was completely abolished at 10 6 m TIBA in seedlings grown in 1 mm P, whereas at this concentration seedlings grown at low P still produce several lateral roots (Fig. 4B). As a consequence of these changes, the negative effect of TIBA on lateral root density at 1 m P is significantly lower than at 1 mm P (Fig. ...
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... (Fig. 4B). However, lateral root formation was completely abolished at 10 6 m TIBA in seedlings grown in 1 mm P, whereas at this concentration seedlings grown at low P still produce several lateral roots (Fig. 4B). As a consequence of these changes, the negative effect of TIBA on lateral root density at 1 m P is significantly lower than at 1 mm P (Fig. ...
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... to be essential for lateral root development ( Reed et al., 1998;Casimiro et al., 2001). We used TIBA, an auxin transport inhibitor, to gain knowledge of the participation of auxin trans- port on lateral root development in response to P availability. Primary root elongation in low P seed- lings was more sensitive to TIBA than in high P seedlings (Fig. 4A); however, P-deprived plants showed lower sensitivity to the negative effect of TIBA on lateral root formation and lateral root den- sity when compared with high P-grown plants (Fig. 4, B and C). Because it is known that auxins inhibit primary root elongation and stimulate lateral root formation, these observations appear somewhat par- ...
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... port on lateral root development in response to P availability. Primary root elongation in low P seed- lings was more sensitive to TIBA than in high P seedlings (Fig. 4A); however, P-deprived plants showed lower sensitivity to the negative effect of TIBA on lateral root formation and lateral root den- sity when compared with high P-grown plants (Fig. 4, B and C). Because it is known that auxins inhibit primary root elongation and stimulate lateral root formation, these observations appear somewhat par- adoxical. However, it has recently been reported that treatment with auxin transport inhibitors results in suboptimal levels of auxins for lateral root initiation, but also in the ...

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... Generally, highly weathered soils under humid tropical environments show low fertility, high acidity, and high iron (Fe) and aluminum (Al) oxide contents. In these soils, the movement of the H 2 PO 4 ion, the main form of phosphorus (P) taken up by plants, is very slow due to physical-chemical mechanisms binding it to the colloid surface, which is more evident in tropical soils (López-Bucio et al., 2002). When low-P soils are first fertilized, farmers must apply more P than what is taken up by crops, but continuous phosphate application gradually saturates the pathways through which phosphate is adsorbed and penetrates in soil colloids (Barrow & Debnath, 2014). ...
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... In particular, although BB consistently showed increased LR density with increasing P availability, the cultivar Okinawa showed increased LR density with decreasing P (Villordon et al. 2020). For Arabidopsis, it has been demonstrated that LR density can vary depending on available P in the growth medium (L opez-Bucio et al. 2002;Williamson et al. 2001). ...
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... Auxin is an important phytohormone that promotes plant LR growth and development, and Pi can regulate LR development by altering auxin biosynthesis, signal transduction, polar transport and sensitivity Nacry et al., 2005;Perez-Torres et al., 2008). Studies have shown that the concentration of auxin increases in both whole taproots and new LRs of Arabidopsis thaliana but decreases in old LRs under a low-Pi environment (Jiang et al., 2007;Lopez-Bucio et al., 2002;Nacry et al., 2005). In addition, auxin in maize (Zea mays) is redistributed under Hetero-NP or Hetero-LP conditions, thereby regulating root morphology (Wang et al., 2020). ...
... Phytohormones such as IAA, ABA and GA are known to play important roles in regulating RSA under low Pi stress (Jia et al., 2022;Kumar et al., 2021;Liu, 2021). Auxin is considered to be the main regulator of LR development, promotes the differentiation of LR primordial cells and regulates the morphogenesis of LRs (Jiang et al., 2007;Liu et al., 2013;Liu, 2021;Lopez-Bucio et al., 2002;Nacry et al., 2005;Wang et al., 2020). In the present study, the difference in auxin concentration between the Hetero-NP and Hetero-LP treatments may be because the supply of heterogeneous Pi promotes the redistribution of auxin, which participates in the regulation of the development of LRs. ...
... Under low P stress, the concentrations of phytohormones such as IAA, ABA, JA, SA and GA change, and the levels of genes involved in phytohormone synthesis, signal transduction, response and metabolism also increase . Several key elements of the auxin pathway play important roles in LR proliferation in response to low P stress in A. thaliana, such as PIN, ARF, AUX/IAA, LBD, GH3, small auxin-up RNAs (SAUR), and the auxin receptor TIR1 (Lopez-Bucio et al., 2002;Okushima et al., 2007;Perez-Torres et al., 2008;Scheible and Rojas-Triana, 2015). In this study, the transcription level of ILL6 (potri.002g082400), ...
... For the coordination of auxin and phosphate signalling, specifically the formation of lateral roots in response to low P i , genes encoding MYB-CC domains, including PHR1, were also found to be targets of ARF TFs [81]. The fact that PSR was suppressed in auxin repressor iaa28-1 mutant would also suggest that some ARFs act as suppressors of PHR1or related CC-MYC [137]. Huang et al. [81] found that the binding of ARF7 and ARF19 to auxin-response elements of the PHR1 promoter is essential for the induction of PSI genes under low P i availability, and phosphate uptake was reduced when ARF7 and ARF19 function was abolished. ...
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... One common strategy plants employ for increasing P-uptake is the production of longer and more branched roots, which can increase the surface area of the root system and improve the plant's ability to explore the soil for nutrients. For example, several studies have shown that plants grown under low P-conditions produce longer and more branched roots than those grown under high P-conditions [60,61]. ...
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... The vigor of the parent plant, combined with balanced nutrition, can positively induce the rhizogenesis of the cuttings, defining the concentration of carbohydrates, nitrogenous substances, amino acids, auxins, phenolic compounds, among other rooting promoting substances (López-Bucio et al., 2002;Cunha et al., 2009). Cunha et al. (2009) describe in Table 1 the macro and micronutrient demands in Eucalyptus globulus during root formation of woody species. ...
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