Brassinosteroid negatively regulates jasmonate inhibition of root growth in Arabidopsis

Abstract

Jasmonate (JA) inhibits root growth of Arabidopsis thaliana seedlings. The mutation in COI1 that plays a central role in JA signaling displays insensitivity to JA inhibition of root growth. To dissect JA signaling pathway, we recently isolated one mutant named psc1, which partially suppresses coi1 insensitivity to JA inhibition of root growth. As we identified the PSC1 gene as an allele of DWF4 that encodes a key enzyme in brassinosteroid (BR) biosynthesis, we hypothesized and demonstrated that BR is involved in JA signaling and negatively regulates JA inhibition of root growth. In our Plant Physiology paper, we analyzed effects of psc1 or exogenous BR on the inhibition of root growth by JA. Here we show that treatment with brassinazole (Brz), a BR biosynthesis inhibitor, increased JA sensitivity in both coi1-2 and wild type, which further confirms that BR negatively regulates JA inhibition of root growth. Since effects of psc1, Brz, and exogenous BR on JA inhibition of root growth were mild, we suggests that BR negatively finely regulates JA inhibition of root growth in Arabidopsis.

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Jasmonate (JA) regulates many plant developmental processes and stress responses.1,2 COI1 plays a central role in JA signaling and is required for all JA responses in Arabidopsis.3,4 coi1-1, a strong mutation in COI1, is male sterile and exhibits loss of all JA responses tested to date, such as JA inhibition of root growth, the expression of JA-induced genes, and susceptibility to insect attack and pathogen infection, and coi1-2, a weak mutant of COI1, shows similar JA responses to coi1-1 except for partially fertile that makes it able to produce a small quantity of seeds.5

To investigate COI1-mediated JA responses and dissect JA signaling pathway, we conducted genetic screens for suppressors of coi1-2. Previously, we identified cos1 that completely suppresses coil-2 insensitive to JA.6 Recently, we isolated the psc1 mutant that partially suppresses coi1-2 insensitivity to JA, and found that PSC1 is an allele of DWF4.7

Since the DWF4 gene encodes a key enzyme in brassinosteroid (BR) biosynthesis,8 we hypothesized that BR is involved in JA signaling. By physiological analysis, we showed that psc1 partially restored JA inhibition of root growth in coi1-2 background and displayed JA hypersensitivity in wild-type COI1 background, the effects of psc1 were eliminated by exogenous BR, and that exogenous BR could attenuated JA inhibition of root growth in wild type. These findings demonstrated that BR is involved in JA signaling and indicated that BR negatively regulates JA inhibition of root growth.

BR is a family of polyhydroxylated steroid hormones involved in many aspects of plant growth and development. The BR-deficient mutants exhibited severely retarded growth that was able to be rescued by exogenous BR.9 Brassinazole (Brz) is a BR biosynthesis inhibitor. The Arabidopsis seedlings treated with Brz displayed a BR deficient-mutant-like phenotype, which could be elimilated by exogenous BR.10

To determine wether treatment with Brz affects JA inhibition of root growth, the seedlings of wild type and coi1-2 were grown in MS medium supplemented with MeJA and/or Brz. As shown in Figure 1, the relative root length was obviously reduced in both coi1-2 and wild type when treated with Brz relative to without Brz, indicating that the repression of BR biosynthesis by Brz could increase JA sensitivity. These results further confirm BR negatively regulates JA inhibition of root growth.

It has been demonstrated that JA connects with other plant hormones including auxin, ethylene, abscisic acid, salicylic acid and gibberellin to form complex regulatory networks modulating plant developmental and stress responses.11–15 We found that BR negatively regulates JA inhibition of root growth, suggesting that a cross talk between JA and BR exists in planta, which extends our understandings on the JA signal transduction.

COI1 is a JA receptor16 and DWF4 catalyzes the rate-limiting step in BR-biosynthesis pathway.8 We found that JA inhibits DWF4 expression, this inhibition was dependent on COI1,7 indicating that DWF4 is downregulated by JA and is located downstream of COI1 in the JA signaling pathway.

Since the effects of psc1, Brz, and exogenous BR on JA inhibition of root growth were mild, and the DWF4 expression was partially repressed by JA (Ren et al. 2009, Fig. 1), we suggest that BR negatively finely regulates JA inhibition of root growth, and propose a model for these regulations. As shown in Figure 2A, JA signal passes COI1 repressing substrates, such as JAZs,17,18 i.e., JA activates degradation of substrates via SCF^COI1-26S proteasome,16–18 whereas substrates positively regulate root growth through other regulators. JA also partially inhibits DWF4 expression through COI1, reducing BR that is required for root growth.7,9 Mutation in COI1 interrupts JA signaling for failing in degradation of substrates and repression of DWF4 as well, resulting in JA-insensitivity (Fig. 2B). However, mutation in DWF4 or treatment with Brz causes a reduction in BR, which affects root growth, leading to JA-hypersensitivity in wild-type COI1 background (Fig. 2C and E) and partial restoration of JA sensitivity in coi1-2 background (Fig. 2D and F). Whereas, an application of exogenous BR could eliminate the effect of BR reduction resulted from repression of DWF4 by JA on root growth, attenuating JA sensitivity in wild type (Fig. 2G). Because the inhibition of DWF4 expression by JA is dependent on COI1, the coi1 mutant treated with exogenous BR do not show alteration in JA sensitivity (Fig. 2H).

Figures and Tables

Figure 1 Effect of Brz on JA inhibition of root growth. Brz increased JA inhibition of root growth in both coi1-2 and wild type (WT). Root length of 7-day-old seedlings grown in MS medium containing 0, 5 and 10 μM MeJA without (−) or with (+) 0.5 μM Brz was expressed as a percentage of root length in MS without (−) or with (+) 0.5 µM Brz. Error bars represent SE (n > 30).

Figure 2 A model for that BR negatively finely regulates JA inhibition of root growth in Arabidopsis. (A–D) Treatment with JA in wild type (A), coi1-2 (B), psc1 (C) and psc1coi1 (D). (E and F) Treatments with JA and Brz in wild type (E) and coi1-2 (F). (G and H) Treatments with JA and exogenous BR in wild type (G) and coi1-2 (H). Arrows indicate positive regulation or enhancement, whereas blunted lines indicate repression or negative regulation. Crosses indicate interruption or impairment. The letter “S” indicates substrates of SCF^COI1. Thicker arrows and blunted lines represent the central JA signaling pathway regulating JA inhibition of root growth. Broken arrows represent JA signaling pathway in which other regulators are involved. The intensity of gray boxes represents the degree of JA inhibition on root growth.

Acknowledgements

This research was funded by the National Science Foundation of China, the National Basic Research 973 Program of China and the Scientific Research Fund of Hunan Provincial Education Department.

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