Sugar-induced de novo cytokinin biosynthesis contributes to Arabidopsis growth under elevated CO2

Kiba, Takatoshi; Takebayashi, Yumiko; Kojima, Mikiko; Sakakibara, Hitoshi

doi:10.1038/s41598-019-44185-4

Download PDF

Article
Open access
Published: 23 May 2019

Sugar-induced de novo cytokinin biosynthesis contributes to Arabidopsis growth under elevated CO₂

Takatoshi Kiba ORCID: orcid.org/0000-0001-8651-0404^1,2,
Yumiko Takebayashi²,
Mikiko Kojima² &
…
Hitoshi Sakakibara^1,2

Scientific Reports volume 9, Article number: 7765 (2019) Cite this article

3774 Accesses
44 Citations
1 Altmetric
Metrics details

Subjects

Abstract

Carbon availability is a major regulatory factor in plant growth and development. Cytokinins, plant hormones that play important roles in various aspects of growth and development, have been implicated in the carbon-dependent regulation of plant growth; however, the details of their involvement remain to be elucidated. Here, we report that sugar-induced cytokinin biosynthesis plays a role in growth enhancement under elevated CO₂ in Arabidopsis thaliana. Growing Arabidopsis seedlings under elevated CO₂ resulted in an accumulation of cytokinin precursors that preceded growth enhancement. In roots, elevated CO₂ induced two genes involved in de novo cytokinin biosynthesis: an adenosine phosphate-isopentenyltransferase gene, AtIPT3, and a cytochrome P450 monooxygenase gene, CYP735A2. The expression of these genes was inhibited by a photosynthesis inhibitor, DCMU, under elevated CO₂, and was enhanced by sugar supplements, indicating that photosynthetically generated sugars are responsible for the induction. Consistently, cytokinin precursor accumulation was enhanced by sugar supplements. Cytokinin biosynthetic mutants were impaired in growth enhancement under elevated CO₂, demonstrating the involvement of de novo cytokinin biosynthesis for a robust growth response. We propose that plants employ a system to regulate growth in response to elevated CO₂ in which photosynthetically generated sugars induce de novo cytokinin biosynthesis for growth regulation.

Spatial co-transcriptomics reveals discrete stages of the arbuscular mycorrhizal symbiosis

Article Open access 08 April 2024

Legume rhizodeposition promotes nitrogen fixation by soil microbiota under crop diversification

Article Open access 04 April 2024

Plants with genetically encoded autoluminescence

Article 27 April 2020

Introduction

Being sessile, plants integrate environmental and internal cues and regulate physiological and morphological processes accordingly to optimize growth and development. Because multicellular higher plants consist of organs with different functions, for example photosynthesizing leaves and roots that absorb water and inorganic nutrients, the responses must be coordinated at the whole plant level. Local as well as long-distance signalling between cells and organs via signalling molecules such as sugars and plant hormones are vital for this coordination^1,2,3,4,5,6

Cytokinins (CKs) are a class of plant hormones that play a central role in the regulation of numerous aspects of plant growth and development acting as local and long-distance signals^7,8,9,10,11. Naturally occurring CKs are mostly N⁶-prenylated adenine derivatives; N⁶-(∆²-isopentenyl)adenine (iP), trans-zeatin (tZ) and their conjugates (iP-type and tZ-type CKs, respectively) are the major forms in Arabidopsis thaliana^10,11,12. CK activity is controlled at diverse levels, including CK quantity and modification. CK quantity is regulated mostly at the levels of de novo biosynthesis and degradation catalysed by adenosine phosphate-isopentenyltransferase (IPT) and CK oxidase/dehydrogenase (CKX), respectively^13,14,15,16. Side-chain modification to form tZ-type CKs by cytochrome P450 monooxygenase CYP735A specifies CK activity toward shoot growth^17,18. Recently, CK translocation via the vascular system was reported to also be important^19,20,21. Shoot-to-root translocation of CK via phloem is critical for root vascular patterning, whereas root-to-shoot translocation via xylem mediated by ABCG14 regulates shoot growth and development. Regulation of CK activity is relevant to various plant developmental processes and environmental responses such as shoot apical meristem activity, branching, stress and nutritional responses^{22,23,24,25,26,27,28}.

Because plants are autotrophs that rely on photosynthesis to gain most of their building materials and energy, carbon availability is a major factor defining plant growth and development^29,30,31,32. To maximize fitness, long-distance communication is required for plants to balance the growth of photosynthesizing leaves and that of carbon consuming roots in response to carbon availability^6,33. In various plant species, elevated CO₂ (i.e. high carbon availability) generally results in growth acceleration of both shoots and roots, although the root-to-shoot mass ratios are variable depending on species and environmental conditions^{25,26,29,34,35,36,37}. CKs have been implicated in growth acceleration because cell division and cell differentiation in the meristem are influenced by CKs and are often accompanied by CK accumulation^26,38. In addition, an increase in tZ-type CKs was detected in the xylem sap of cotton and tobacco plants grown under elevated CO₂, implying that tZ-type CKs have a role as root-to-shoot signals under elevated CO₂ conditions^25,39. However, how CKs accumulate and whether the accumulation and root-to-shoot translocation of CK is relevant to growth acceleration under elevated CO₂ (i.e. high carbon availability) remains to be determined.

In this study, we revealed that enhancement of de novo biosynthesis is responsible for CK accumulation under elevated CO₂ and that the enhancement is triggered by sugars derived from photosynthesis. Detailed growth analyses of mutants defective in cytokinin de novo biosynthesis (ipt3 ipt5 ipt7 and cyp735a1 cyp735a2) revealed that accumulation of tZ-type cytokinins through de novo biosynthesis plays a role in a robust growth response to elevated CO₂ by both shoots and roots. Altogether, these results suggest that the de novo tZ-type CK biosynthesis triggered by photosynthetically generated sugars contributes to growth enhancement under elevated CO₂ in Arabidopsis.

Results

Elevated CO₂ increases cytokinin precursor concentrations in shoots and roots

To examine the effects of elevated CO₂ on growth and CK levels, plants were grown under low [280 parts per million by volume (ppmv)] and high CO₂ (780 ppmv) on soil. Two hundred and eighty ppmv is the pre-industrial atmospheric concentration and 780 ppmv is a value close to the median of values predicted at the end of this century⁴⁰. When wild-type Arabidopsis Col-0 were germinated and grown under low or high CO₂ with a 12 h light/12 h dark photoperiod for four weeks, high CO₂-grown plants deposited more biomass and developed more leaf area and rosette leaves than low CO₂-grown plants did, as described previously (Supplementary Fig. S1^32,41,42). Using the same growth conditions, we analysed changes in the CK concentration following exposure to high CO₂. Sixteen-day-old Col-0 plants grown in low CO₂ were transferred to low or high CO₂, and CK concentrations in the whole shoot were followed for four days. Under these conditions, significant differences in shoot fresh weight between high and low CO₂-treated plants became evident from day 4 onward (Fig. 1a). The levels of iP-type CK precursors (iPR and iPRPs) and tZ-type CK precursors (tZR and tZRPs) in high CO₂-treated shoots increased after one day and stayed high until day 4 compared with those of low CO₂-treated plants (Fig. 1b,c). On the other hand, concentrations of other CK metabolites including inactivated iP-type CKs (iP7G and iP9G), and tZ-type CKs (tZ7G, tZ9G, tZOG, tZROG, and tZRPsOG) did not change consistently during the period of observation (Fig. 1b,c; Supplementary Table S1). Furthermore, the high CO₂-treatment did not significantly affect the levels of other plant hormones, including a gibberellin precursor (GA₂₄), IAA, and ABA (Fig. 1d,e; Supplementary Table S1). These results showed that iP-type and tZ-type CK precursors accumulate in the shoot prior to growth enhancement at high CO₂ under our experimental conditions.

Next, we employed a growth system in which Col-0 seedlings were germinated and grown on half-strength MS (1/2 MS) agar plates placed vertically to allow the analysis of both shoots and roots. Twelve-day-old wild-type seedlings grown under continuous light in low CO₂ were transferred to low or high CO₂, and the CK concentrations in shoots and roots were measured after 6 h and 24 h. The basal level of tZ, tZRPs and tZ-N-conjugates in this measurement (Supplementary Table S2) was very different from that in soil-grown plants (Supplementary Table S1). This is possibly due to differences in growth conditions and plant ages, as a similar trend has been observed previously¹⁷. Accumulation of tZ, and iP-type and tZ-type precursors became evident in shoots and roots as early as 6 h after commencing the high CO₂-treatment and continued until 24 h, whereas the levels of other CK metabolites did not consistently change (Fig. 2a,b; Supplementary Table S2).

It is known that the accumulation of CK precursors generally results in increased CK activity^7,43. To verify that CK signalling is activated in parallel with precursor accumulation, the expression of immediate-early CK responsive type-A ARR genes was analysed in whole seedlings treated as in Fig. 2a. As expected, ARR4, ARR6, and ARR15 were induced, with the timing of induction similar to that of CK precursor accumulation (Fig. 2c). Since recent studies on plant membrane binding and crystal structure analysis showed that precursors do not bind to Arabidopsis CK receptors^44,45, one would expect that active CKs (iP and tZ) are accumulated in response to an increase in CK precursor levels. However, active CKs were not always increased significantly in our experiments (for example, Supplementary Tables S1, S2). This lack of significant change in active CK levels has been reported previously^46,47 and we assume that it is because only a fraction of active CKs exists in a compartment where they can be perceived by CK receptors. Taken together, these results indicated that elevated CO₂ resulted in increased CK activity, which is triggered by CK precursor accumulation in shoots and roots.

Cytokinin biosynthetic genes, AtIPT3 and CYP735A2, are up-regulated in roots under elevated CO₂

Generally the accumulation of CK precursors reflects increased de novo biosynthesis^7,43. The initial step of de novo CK biosynthesis is catalysed by IPT^13,14, and the key step of tZ-type de novo CK biosynthesis requires CYP735A^17,18. We examined the expression levels of seven IPT (AtIPT1, AtIPT3, AtIPT4, AtIPT5, AtIPT6, AtIPT7, AtIPT8) and two CYP735A (CYP735A1 and CYP735A2) genes in Arabidopsis shoots and roots of Col-0 seedlings incubated at low or high CO₂ from 3 h, an earlier time point than when CK precursor accumulation was observed (up to 9 h). AtIPT4, AtIPT6, and AtIPT8 were not detected in shoots nor roots in our experimental conditions. In shoots, none of the genes examined were affected by high CO₂ except for AtIPT5 that was down-regulated at 9 h (Fig. 3a). In roots, the transcript level of CYP735A2 increased after 3 h and stayed high till 9 h and that of AtIPT3 steadily accumulated after the onset of high CO₂ treatment (Fig. 3b). On the other hand, the levels of the other transcripts remained unchanged or showed transient fluctuations (Fig. 3b). Down-regulation of AtIPT5 in both shoot and root might be caused by accumulated CK because AtIPT5 has been reported to be repressed by CK⁴⁸. Since CK levels are determined by the balance between de novo biosynthesis and degradation, we also analysed the expression of genes encoding CK-degrading enzymes, CKX. Among seven CKXs in Arabidopsis, the expression of six genes was detected but none of these genes were down-regulated in shoots and roots under high CO₂ treatment (Supplementary Fig. S2). Rather, the expression of CKX1, CKX4, CKX6, and CKX7 was transiently enhanced, possibly in response to CK accumulation (Supplementary Fig. S2). Similar CK precursor accumulation and induction of AtIPT3 and CYP735A2 were observed when seedlings were grown and treated under 12-h-light/12-h-dark cycles (Supplementary Fig. S3; Supplementary Table S3). These results suggested that the induction of AtIPT3 and CYP735A2 in roots plays a role in iP- and tZ-type CK precursor accumulation under elevated CO₂.

Photosynthetically generated sugars induce AtIPT3 and CYP735A2 in roots

Next, we tested the involvement of photosynthesis in the induction of AtIPT3 and CYP735A2 by incubating wild-type seedlings in the dark or by applying the photosynthesis inhibitor DCMU, which blocks electron flow from photosystem II. When seedlings were incubated in the dark or in the light with DCMU at 280 ppmv for 6 h, expression levels of AtIPT3 and CYP735A2 were reduced compared to the control (Fig. 4a,b). The induction of AtIPT3 and CYP735A2 in response to elevated CO₂ was completely abolished by these treatments (Fig. 4a,b), indicating that photosynthetic activity is required for the maintenance and induction of AtIPT3 and CYP735A2 expression.

Elevated CO₂-treatment reportedly increases endogenous sugar concentrations (e.g. fructose, glucose, and sucrose), whereas DCMU treatment reduces sugar levels^31,37,49. To examine whether the DCMU-triggered attenuation of AtIPT3 and CYP735A2 induction were caused by lowered levels of sugars, we supplemented DCMU-treated seedlings with sucrose. Sucrose reversed the effect of DCMU on AtIPT3 and CYP735A2 expression (Fig. 4c,d). We also tested the effects of other sugars on AtIPT3 and CYP735A expression. Seedlings were transferred to agar plates containing metabolizable sugars (sucrose and glucose) or non-metabolizable sugars (sorbitol and mannitol) and were incubated at 280 ppmv CO₂ in the dark. Metabolizable sugars were able to induce AtIPT3 and CYP735A expression (Fig. 4e,f). On the other hand, non-metabolizable sugars were ineffective in inducing AtIPT3 expression (Fig. 4e). CYP735A2 expression was induced by non-metabolizable sugars but to a much lower extent compared with metabolizable sugars (Fig. 4f). Since CYP735A2 seems to be moderately activated by osmotic stress⁵⁰, the induction by non-metabolizable sugars is probably due to osmotic effects.

CYP735A2 is known to be a CK-inducible gene^18,21. Thus we tested whether CYP735A2 induction by elevated CO₂ and sugars is the result of accumulated CKs by employing ipt3 ipt5 ipt7 (ipt357) and the cytokinin receptor mutants ahk2 ahk3 and ahk3 ahk4^51,52,53 that are defective in CK biosynthesis and signalling, respectively. Elevated CO₂ and sugars induced CYP735A2 expression in the mutants at a level comparable to Col-0 (Fig. 5a,b), indicating that sugars induce this gene independently of CK.

These results suggested that AtIPT3 and CYP735A2 are induced in roots under elevated CO₂ by sugars generated in shoots by photosynthesis. Consistent with this, sucrose treatment resulted in an accumulation of CK precursors in shoots and roots (Fig. 4g,h; Supplementary Table S4).

Photosynthetically generated sugars induce cytokinin precursor accumulation irrespective of the nitrate status

It is known that de novo CK biosynthesis is regulated by nitrate in Arabidopsis⁵⁴. Since carbon availability is reported to influence nitrate transporter gene expression and nitrate uptake^55,56, it is possible that carbon availability affects CK biosynthesis indirectly through nitrate-related pathways. To test this possibility, we measured CK levels in wild-type seedlings treated with high CO₂ or sucrose, and with and without nitrate. Twelve-day-old seedlings were treated with high CO₂ or sucrose on agar plates containing 10 mM KNO₃, 10 mM NH₄Cl, or no nitrogen source, and the CK concentrations in the whole seedling were measured after 24 h. The levels of CK precursors increased in all nitrogen conditions tested in response to high CO₂ or sucrose treatment (Fig. 6; Supplementary Tables S5 and S6), suggesting that sugars induce CK precursor accumulation independent of nitrate-related pathways.

The ipt3 cyp735a2 mutant still accumulates cytokinin precursors in response to elevated CO₂

Having shown the relevance of AtIPT3 and CYP735A2 in the elevated CO₂-enhanced de novo CK biosynthesis, we investigated whether these processes contribute to growth enhancement under elevated CO₂ by generating an ipt3 cyp735a2 double mutant. To this end, 12-day-old seedlings grown on agar plates were incubated at low or high CO₂ for seven days. Fresh weight (FW) was measured before and after the treatment, and relative growth rate (RGR) was calculated. Growth differences of Col-0 between low CO₂- and high CO₂-incubated seedlings were clearly observed; the FW and RGR of both the shoot and the root were significantly increased by the high CO₂ treatment (Supplementary Fig. S4a–c). However, no significant difference in the FW and RGR was observed between the double mutant and WT (Supplementary Fig. S4a–c). To understand this lack of growth phenotype, we analysed changes in iP- and tZ-type precursor CK levels in shoots and roots of the double mutant following exposure to high CO₂. Under low CO₂, the double mutant contained significantly reduced levels of iP-type CK precursors in shoots (Supplementary Fig. S4d; Supplementary Table S7). However, it accumulated both CK precursors in both organs in response to high CO₂-treatment, though the levels of accumulation were generally lower compared with WT (Supplementary Fig. S4d,e; Supplementary Table S7), indicating that AtIPT3 and CYP735A2 are not the only factors mediating the elevated CO₂-induced CK precursor accumulation. Together, these results suggest that the double mutant lacks a growth phenotype because it still is able to accumulate enough CKs for elevated CO₂-triggered growth enhancement.

The ipt3 ipt5 ipt7 and cyp735a1 cyp735a2 mutants are impaired in elevated CO₂-triggered growth enhancement

Since the ipt3 cyp735a2 double mutant still accumulated CKs in response to high CO₂ (Supplementary Fig. S4d,e), we employed higher order CK-biosynthetic mutants, ipt357 and cyp735a1 cyp735a2 (cypDM). The ipt357 mutant lacks three major IPT genes⁵⁷ and, thus, has a dramatically reduced ability to de novo synthesize both iP- and tZ-type CKs. The cypDM mutant lacks all CYP735A genes¹⁷ and, thus, is expected to accumulate iP-type CKs but not tZ-type CKs under elevated CO₂. To verify that elevated CO₂-induced de novo CK biosynthesis is attenuated in ipt357 and cypDM, the CK concentrations in shoots and roots were measured. Seedlings were grown and treated as in Fig. 2 (24 h high CO₂ treatment). In the ipt357 mutant, the accumulation level of all CKs was relatively low compared with the wild type. The iP-type CK precursor concentrations were unaffected in shoots and roots, but the levels of tZ-type precursor CKs increased slightly in shoots with a high CO₂ treatment (Fig. 7a,b; Supplementary Table S8). In the cypDM mutant, iP-type precursor CKs accumulated but tZ-type precursor CKs levels were consistently low in shoots and roots under elevated CO₂ (Fig. 7a,b; Supplementary Table S8). These observations confirmed the inability of the mutants to accumulate CKs of the expected types under elevated CO₂. These results showed that de novo CK biosynthesis, most likely mediated by IPT3, IPT5, IPT7, CYP735A1 and CYP735A2, plays an important role in CK accumulation in response to high CO₂.

We then investigated whether these mutants are impaired in growth enhancement under elevated CO₂. Seedlings were grown and treated on agar plates as in Supplementary Fig. S4, and the FW was measured before and after treatment, and the RGRs were calculated. In Col-0, the FW and RGR of both the shoot and the root were dramatically increased in response to high CO₂ (Fig. 7c,d; Supplementary Fig. S5). The ipt357 mutant also gained more FW both in shoots and roots in high CO₂ compared with the low CO₂ treatment, but the extent of the increase was smaller compared with that of Col-0 (Fig. 7c). RGR analysis revealed that shoots and roots of ipt357 grew faster in high CO₂ than in low CO₂ but at a lower rate compared with those of Col-0, whereas the RGR in low CO₂ was similar among all genotypes in this growth system (Fig. 7d). Interestingly, the cypDM mutant displayed essentially the same growth response defects to elevated CO₂ as the ipt357 mutant (Fig. 7c,d), showing that accumulation of tZ-type CKs is critical for the response.

We also analysed the growth response of soil-grown plants. The mutants were germinated and grown on soil together with Col-0 under low or high CO₂, and shoot growth was analysed at 17 and 31 days after germination (DAG) by measuring dry weight (DW). Note that it was not possible to evaluate root growth in this system. Although Col-0 plants grown in high CO₂ had significantly higher shoot biomass compared with those grown in low CO₂ at the beginning of analysis (17 DAG), they gained more biomass by further growth in high CO₂ (31 DAG, Supplementary Fig. S6). RGRs between 17 and 31 DAG were significantly higher in high CO₂-grown Col-0 plants than in the mutants (Fig. 7e). The number of rosette leaves counted on 31 DAG also significantly increased (Fig. 7f). Although the cypDM mutant gained more biomass under high CO₂ (Supplementary Fig. S6), no significant change in RGR in response to high CO₂ treatment was observed (Fig. 7e). The RGR of the ipt357 mutant was slightly enhanced by high CO₂ treatment (Fig. 7e). Rosette leaf numbers did not change in the cypDM mutant and were only marginally increased in the ipt357 mutant (5.4 more leaves in the wild type compared with 1.9 in ipt357) in response to high CO₂ (Fig. 7f). These results show that the ipt357 and cypDM mutants are impaired in the acceleration of shoot growth and development under elevated CO₂ during the growth period examined and that the cypDM mutant, which cannot accumulate tZ-type CKs, is severely compromised.

Together, these growth analyses suggest that CK accumulation, especially of the tZ-type, through de novo biosynthesis contributes to robust growth enhancement under elevated CO₂.

Photosynthetically generated sugars induce ABCG14 in roots

It has been reported that tZ-type CKs are translocated from root to shoot by the ABCG14 protein to act as shoot growth signals^17,20,21,58. To get insight into whether root-to-shoot translocation of CKs is relevant to the observed CK accumulation in shoots, ABCG14 expression in roots was investigated (Fig. 8). Interestingly, ABCG14 expression responded to high CO₂ and sugars in a similar manner to that of AtIPT3 and CYP735A2 (Fig. 8). Since ABCG14 has been reported to be CK-inducible²¹, we tested whether the CKs that accumulate in response to elevated CO₂ and sugars are relevant to ABCG14 induction. The ipt357 and the cytokinin receptor mutants ahk2 ahk3 and ahk3 ahk4^51,52,53 were analysed as in Fig. 5a,b. ABCG14 induction in response to elevated CO₂ and sugars was maintained in these mutants (Fig. 5c,d), indicating that sugars induce this gene independent of CK. Together, these results suggest that root-to-shoot translocation of CKs via ABCG14 might be involved in robust growth enhancement under elevated CO₂ by mediating tZ-type CK accumulation in the shoot.

Discussion

The availability of macronutrients such as nitrogen^{7,43,48,59,60}, phosphate^9,61,62,63 and sulphate^9,64 affects IPT expression as well as CK levels. Therefore, macronutrient availability has been proposed to regulate CK levels through de novo biosynthesis to control plant growth and development^9,27,65. Our investigation has revealed another pathway in which photosynthesis-derived sugars regulate de novo CK biosynthesis to control plant growth and development.

Our study suggests that de novo CK biosynthesis is triggered by photosynthetically generated sugars (Figs 1–6). There are several other reports indicating that sugars induce the expression of genes involved in the de novo synthesis of CKs. Transcriptome analyses show that glucose⁶⁶ and sucrose^67,68 treatments up-regulate AtIPT3 and CYP735A2. However, how sugars are perceived (as signalling molecules, energy sources or building blocks) to induce the expression of these genes is still not understood. Thus, it is possible that sugars act indirectly through the signalling pathways of macronutrients because the metabolism of carbon and macronutrients are tightly intertwined. Although our data suggests that sugars induce CK precursor accumulation independent of nitrate-related pathways (Fig. 6), Kamada-Nobusada et al.⁷ reported a pathway in which the internal nitrogen status regulates CK biosynthesis. Since the internal nitrogen status can also be modulated by carbon availability, we cannot rule out the possibility that sugars affect CK biosynthesis through this pathway. Further studies on sugar and internal nitrogen sensing and signalling mechanisms are required to resolve this problem. In any case, we propose that sugars generated by photosynthesis in shoots directly or indirectly promotes de novo CK biosynthesis.

Under our experimental conditions, AtIPT3 was the only gene of the AtIPT family induced by elevated CO₂ and sugars (Figs 3, 4). AtIPT3 expression is also regulated by various environmental signals to control CK levels; increases in nitrogen, phosphate, and sulphate availability induce AtIPT3 expression^9,43,48,63, whereas drought and salt stress repress AtIPT3 expression⁶⁹. Although it remains unclear – with the exception of nitrate – whether these signals regulate AtIPT3 expression directly^70,71, the available evidence suggests that AtIPT3 functions to integrate and translate various signals in the root into de novo CK biosynthetic activity. We also found that CYP735A2 and ABCG14 are high CO₂- and sugar-inducible (Figs 3, 4, 5, 8). Although CYP735A2 and ABCG14 are known to be CK-inducible genes^18,21, we showed that sugars induce these genes independent of CK (Fig. 5). These results indicate that CYP735A2 and ABCG14 are controlled by two independent signals: shoot-derived signals (sugars) and root internal cues (root-synthesized CKs) in the response to elevated CO₂. Thus, CYP735A2 and ABCG14 might act to integrate signals from shoots and roots and translate these signals into tZ-type CKs translocated from root to shoot. However, it remains to be determined whether ABCG14-mediated root-to-shoot translocation activity is regulated at the level of expression or by some other means.

In our expression analysis, AtIPT3 and CYP735A2 were the only genes induced under elevated CO₂ among the de novo CK biosynthetic genes (Fig. 3). However, the ipt3 cyp735a2 double mutant still accumulated CKs, although at a lower level than WT (Supplementary Fig. S4d,e). The ipt357 and cypDM mutants were unable to accumulate iP-type and tZ-type CKs, respectively, in response to high CO_2, suggesting that not only AtIPT3 and CYP735A2 but also AtIPT5, AtIPT7, and CYP735A1 are involved in the accumulation. Since these genes were not found to be regulated at the level of transcript accumulation, post-transcriptional regulation might be involved. Consistently, it has been reported that AtIPT3 farnesylation modulates this protein’s subcellular localization and enzymatic properties⁷². It should be noted that we cannot exclude that other genes involved in CK biosynthesis, modification, and/or degradation, and/or post-transcriptional regulation might be relevant to the accumulation of CKs.

In this study, the role of CKs in growth enhancement under elevated CO₂ was evaluated by analysing the growth of ipt357, a mutant deficient in iP- and tZ-type CKs, and cypDM, a mutant deficient in tZ-type CKs. Both mutants displayed similar growth response defects (Fig. 7), indicating that tZ-type CKs are required for robust growth enhancement of shoots and roots under elevated CO₂. A reduction in shoot growth acceleration in these mutants is consistent with previous reports that tZ-type CKs and their root-to-shoot translocation act to promote shoot growth^17,20,21. However, a reduction in root growth acceleration cannot be explained by CK action because CKs generally act to repress root growth^73,74. This result suggests that CK is not the major determinant of root growth rate. It is plausible that slowed root growth is a consequence of reduced photosynthesis (as sources of energy and building blocks) by smaller shoots, but it is also possible that complex crosstalk might exist between CK and sugars.

Here, we revealed that sugar-induced de novo biosynthesis of CKs plays a role in the robust growth enhancement under elevated CO₂. This finding provides some insight into the mechanisms that plants employ to optimise growth in a fluctuating environment. Taking into account that AtIPT3, CYP735A2, and ABCG14 are induced in the root by photosynthetically generated sugars (Figs 3, 4, 5, 8), it is tempting to speculate that there is a systemic growth regulatory mechanism in which photosynthetically generated sugars induce de novo tZ-type CK biosynthesis in the root and root-to-shoot translocation of the CK via ABCG14 for growth regulation of the shoot.

Materials and Methods

Plant material and growth conditions

Arabidopsis thaliana ecotype Columbia (Col-0) was used as the wild type. The cytokinin biosynthetic triple mutants ipt3 ipt5 ipt7⁵⁷, the cytokinin receptor double mutants ahk2 ahk3 and ahk3 ank4⁵³, and the cyp735a1-2 cyp735a2-2 double mutant¹⁷ were characterized previously. The ipt3 cyp735a2-1 and ipt3 cyp735a2-2 double mutants were generated by crosses between the ipt3 ipt5 ipt7 and the cyp735a1-2 cyp735a2-1 mutant, and cyp735a1-2 cyp735a2-2 mutants. For studies on soil-grown plants, stratified seeds were sown directly on nutrient-rich soil (Supermix A, Sakata, Japan), and grown in a CO₂-controlled growth chamber (LPH-0.5P-SH; Nippon Medical & Chemical Instrument) at 280 ppmv or 780 ppmv CO₂ under 150 µmol m⁻² s⁻¹ fluorescent light (12 h light/12 h dark) at 22 °C. For studies on seedlings, plants were grown on half-strength MS (1/2 MS) agar plates (pH 5.8; 1% agar) placed vertically at 22 °C in the CO₂-controlled growth chamber at 280 ppmv or 780 ppmv CO₂ under continuous light (120 µmol m⁻² s⁻¹) unless otherwise noted. To avoid any chamber effects, we used two growth chambers simultaneously with different CO₂ concentrations and repeated each experiment at least twice with different chamber and CO₂ concentration combinations. Although the data presented are from one representative experiment, similar results were obtained from different chamber and CO₂ concentration combinations.

Quantification of plant hormones

Cytokinin level was determined using an ultra-performance liquid chromatograph coupled with a tandem quadrupole mass spectrometer equipped with an electrospray interface as described previously⁷⁵. IAA and ABA levels were determined using an ultra-high-performance liquid chromatography (UHPLC)-electrospray interface (ESI) and a quadrupole-orbitrap mass spectrometer (UHPLC/Q-Exactive; Thermo Scientific) as described previously⁷⁶. In the results reported, the category iP-type CK precursors comprise iPR and iPRPs; inactivated iP-type CK comprise iP7G and iP9G; tZ-type CK precursors comprise tZR and tZRPs; and inactivated tZ-type CK comprise tZ7G, tZ9G, tZOG, tZROG, and tZRPsOG.

Gene expression analysis

Total RNA was extracted from root and shoot samples using the RNeasy Plant Mini kit (QIAGEN) in combination with the RNase-Free DNase set (QIAGEN). Total RNA was used for first strand cDNA synthesis by the SuperScript III First-Strand Synthesis System (Life Technologies) with oligo(dT)₂₀ primers. Quantitative reverse transcription-PCR (RT-PCR) was performed on a StepOnePlus Real-Time PCR system (Applied Biosystems) with the KAPA SYBR Fast qPCR kit (KAPA Biosystems). At4g34270 was used as an internal control because this gene has been shown to be one of the most stably expressed genes in Arabidopsis^77,78. Similar results were obtained using other internal control genes (At1g13320 and At2g28390) as described by Czechowski et al.⁷⁸. Primer sets are listed in Supplementary Table S9.

DCMU and sugar treatment

For 3-(3,4-dichlorophenyl)-1,1-dimethylurea (DCMU) treatment, 8-day-old Col-0 seedlings grown on 1/2 MS agar plates (1% agar) placed vertically under continuous fluorescent light (120 µmol m⁻² s⁻¹) at 22 °C in a CO₂-controlled growth chamber at 280 ppmv CO₂ were sprayed with 40 µM DCMU or mock solution (0.05% ethanol) and exposed to 280 ppmv or 780 ppmv CO₂ under 120 µmol m⁻² s⁻¹ light or in the dark. The DCMU stock solution was 40 mM in 50% ethanol. For DCMU and sucrose co-treatment, seedlings were treated with 40 µM DCMU or mock solution (0.05% ethanol) and then transferred to 1/2 MS agar plates (1% agar) containing 90 mM sucrose. For sugar treatment, seedlings were transferred to 1/2 MS agar plates (1% agar) containing 90 mM of sorbitol, mannitol, sucrose, glucose, or 45 mM sucrose.

High CO₂ and sugar treatment under different nitrogen conditions

Wild-type seedlings were pre-grown for 11 days on modified 1/2 MS agar plates (1% agar) containing 10 mM KNO₃, 10 mM NH₄Cl or 5 mM NH₄NO₃ as the sole nitrogen source in the CO₂-controlled growth chamber at 280 ppmv. Seedlings grown with 10 mM KNO₃, 10 mM NH₄Cl or 5 mM NH₄NO₃ were then transferred to new 1/2 MS agar plates (1% agar) containing 10 mM KNO₃, 10 mM NH₄Cl or no nitrogen source, respectively. After 24 h incubation at 280 ppmv, seedlings were subjected to high CO₂ and sugar treatments under the same nitrogen conditions.

Growth analysis under low or high CO₂

For growth analysis of soil-grown plants, stratified seeds were sown directly on nutrient-rich soil (Supermix A, Sakata, Japan), and grown in a CO₂-controlled growth chamber at 280 ppmv or 780 ppmv CO₂ under 150 µmol m⁻² s⁻¹ fluorescent light (12 h light/12 h dark) at 22 °C and 60% relative humidity. Shoots were harvested at 17 and 31 days after germination (DAG) and their dry weights were determined after drying them in an oven set at 80 °C for three days. Rosette leaf number was counted on 31 DAG.

For seedling growth analysis, surface sterilized seeds were sown on 1/2 MS agar plates (1% agar) containing 1% sucrose. After stratification, plates were placed vertically in a CO₂-controlled growth chamber (120 µmol m⁻² s⁻¹ continuous fluorescent light, 22 °C) at 280 ppmv. Five-day-old seedlings were transferred to 1/2 MS agar plates (1% agar without sucrose) and grown vertically for another 7 days at 280 ppmv. Then, the 12-day-old seedlings were exposed to 280 ppmv or 780 ppmv CO₂ for seven days. The shoots and roots were separated and their fresh weights were measured before (Supplementary Figs S4a; S5) and after exposure (Fig. 7c). Relative growth rate (RGR) was calculated from the dry and fresh weights as described elsewhere⁷⁹.

To avoid any chamber effects, we used two growth chambers simultaneously with different CO₂ concentrations and repeated each experiment at least twice with different chamber and CO₂ concentration combinations. Although the data presented are from one representative experiment, similar results were obtained from different chamber and CO₂ concentration combinations.

Statistical analysis

Data are given as means ± standard error (SE) or means ± standard deviation (SD) of one representative experiment. In order to examine whether hormone concentration, gene expression, or shoot growth were significantly different between treatments, Student’s t-test, two-way ANOVA, and Tukey’s honest significant difference (HSD) test were performed using KaleidaGraph ver. 4.1 software (Synergy Software).

Accession numbers

Sequence data for the genes described in this article can be found in The Arabidopsis Information Resource database (see http://www.arabidopsis.org) under the following accession numbers: CYP735A1 (At5g38450), CYP735A2 (At1g67110), AtIPT1 (At1g68460), AtIPT3 (At3g63110), AtIPT4 (At4g24650) AtIPT5 (At5g19040), AtIPT6 (Ay1g25410), AtIPT7 (At3g23630), AtIPT8 (At3g19160), CKX1 (At2g41510), AtCKX2 (At2g19500), CKX3 (At5g56970), CKX4 (At4g29740), CKX5 (At1g75450), CKX6 (At3g63440), CKX7 (At5g21482), ARR4 (At1g10470), ARR6 (At5g62920), ARR15 (At1g74890), ABCG14 (At1g31770).

Data Availability

The datasets generated during and/or analysed during the current study are available from the corresponding author on reasonable request.

References

Mason, M. G., Ross, J. J., Babst, B. A., Wienclaw, B. N. & Beveridge, C. A. Sugar demand, not auxin, is the initial regulator of apical dominance. Proc. Natl. Acad. Sci. USA 111, 6092–6097 (2014).
Article CAS ADS Google Scholar
Kiba, T., Kudo, T., Kojima, M. & Sakakibara, H. Hormonal control of nitrogen acquisition: roles of auxin, abscisic acid, and cytokinin. J. Exp. Bot. 62, 1399–1409 (2011).
Article CAS Google Scholar
Oka-Kira, E. & Kawaguchi, M. Long-distance signaling to control root nodule number. Curr. Opin. Plant Biol. 9, 496–502 (2006).
Article CAS Google Scholar
Kircher, S. & Schopfer, P. Photosynthetic sucrose acts as cotyledon-derived long-distance signal to control root growth during early seedling development in Arabidopsis. Proc. Natl. Acad. Sci. USA 109, 11217–11221 (2012).
Article CAS ADS Google Scholar
Osugi, A. & Sakakibara, H. Q&A: How do plants respond to cytokinins and what is their importance? BMC Biol. 13, 102, https://doi.org/10.1186/s12915-015-0214-5 (2015).
Article CAS PubMed PubMed Central Google Scholar
Ljung, K., Nemhauser, J. L. & Perata, P. New mechanistic links between sugar and hormone signalling networks. Curr. Opin. Plant Biol. 25, 130–137 (2015).
Article CAS Google Scholar
Kamada-Nobusada, T., Makita, N., Kojima, M. & Sakakibara, H. Nitrogen-dependent regulation of de novo cytokinin biosynthesis in rice: The role of glutamine metabolism as an additional signal. Plant Cell Physiol. 54, 1881–1893 (2013).
Article CAS Google Scholar
Kudo, T., Kiba, T. & Sakakibara, H. Metabolism and long-distance translocation of cytokinins. J. Integr. Plant Biol. 52, 53–60 (2010).
Article CAS Google Scholar
Hirose, N. et al. Regulation of cytokinin biosynthesis, compartmentalization and translocation. J. Exp. Bot. 59, 75–83 (2008).
Article CAS Google Scholar
Sakakibara, H. Cytokinins: activity, biosynthesis, and translocation. Annu. Rev. Plant Biol. 57, 431–449 (2006).
Article CAS Google Scholar
Mok, D. W. & Mok, M. C. Cytokinin metabolism and action. Annu. Rev. Plant Physiol. Plant Mol. Biol. 52, 89–118 (2001).
Article CAS MathSciNet Google Scholar
Shaw, G. Chemistry of adenine cytokinins in Cytokinins : Chemistry, Activity, and Function (eds Mok, D. W. S. & Mok, M. C.) 15–34 (CRC Press, 1994).
Takei, K., Sakakibara, H. & Sugiyama, T. Identification of genes encoding adenylate isopentenyltransferase, a cytokinin biosynthesis enzyme, in Arabidopsis thaliana. J. Biol. Chem. 276, 26405–26410 (2001).
Article CAS Google Scholar
Kakimoto, T. Identification of plant cytokinin biosynthetic enzymes as dimethylallyl diphosphate: ATP/ADP isopentenyltransferases. Plant Cell Physiol. 42, 677–685 (2001).
Article CAS Google Scholar
Schmülling, T., Werner, T., Riefler, M., Krupková, E. & Manns, I. B. Y. Structure and function of cytokinin oxidase/dehydrogenase genes of maize, rice, Arabidopsis and other species. J. Plant Res. 116, 241–252 (2003).
Article Google Scholar
Nishiyama, R. et al. Analysis of cytokinin mutants and regulation of cytokinin metabolic genes reveals important regulatory roles of cytokinins in drought, salt and abscisic acid responses, and abscisic acid biosynthesis. Plant Cell 23, 2169–2183 (2011).
Article CAS Google Scholar
Kiba, T., Takei, K., Kojima, M. & Sakakibara, H. Side-Chain Modification of Cytokinins Controls Shoot Growth in Arabidopsis. Dev. Cell 27, 452–461 (2013).
Article CAS Google Scholar
Takei, K., Yamaya, T. & Sakakibara, H. Arabidopsis CYP735A1 and CYP735A2 encode cytokinin hydroxylases that catalyze the biosynthesis of trans-zeatin. J. Biol. Chem. 279, 41866–41872 (2004).
Article CAS Google Scholar
Bishopp, A. et al. Phloem-transported cytokinin regulates polar auxin transport and maintains vascular pattern in the root meristem. Curr. Biol. 21, 927–932 (2011).
Article CAS Google Scholar
Zhang, K. et al. Arabidopsis ABCG14 protein controls the acropetal translocation of root-synthesized cytokinins. Nat. Commun. 5, 3274, https://doi.org/10.1038/ncomms4274 (2014).
Article CAS PubMed Google Scholar
Ko, D. et al. Arabidopsis ABCG14 is essential for the root-to-shoot translocation of cytokinin. Proc. Nat. Acad. Sci. USA 111, 7150–7155 (2014).
Article CAS ADS Google Scholar
Tanaka, M., Takei, K., Kojima, M., Sakakibara, H. & Mori, H. Auxin controls local cytokinin biosynthesis in the nodal stem in apical dominance. Plant J. 45, 1028–1036 (2006).
Article CAS Google Scholar
Yanai, O. et al. Arabidopsis KNOXI proteins activate cytokinin biosynthesis. Curr. Biol. 15, 1566–1571 (2005).
Article CAS Google Scholar
Jasinski, S. et al. KNOX action in Arabidopsis is mediated by coordinate regulation of cytokinin and gibberellin activities. Curr. Biol. 15, 1560–1565 (2005).
Article CAS Google Scholar
Yong, J. W., Wong, S. C., Letham, D. S., Hocart, C. H. & Farquhar, G. D. Effects of elevated [CO₂] and nitrogen nutrition on cytokinins in the xylem sap and leaves of cotton. Plant Physiol. 124, 767–780 (2000).
Article CAS Google Scholar
Teng, N. et al. Elevated CO₂ induces physiological, biochemical and structural changes in leaves of Arabidopsis thaliana. New Phytol. 172, 92–103 (2006).
Article CAS Google Scholar
Sakakibara, H. Nitrate-specific and cytokinin-mediated nitrogen signaling pathways in plants. J. Plant Res. 116, 253–257 (2003).
Article CAS Google Scholar
Ha, S., Vankova, R., Yamaguchi-Shinozaki, K., Shinozaki, K. & Tran, L. S. Cytokinins: metabolism and function in plant adaptation to environmental stresses. Trends Plant Sci. 17, 172–179 (2012).
Article CAS Google Scholar
Tsutsumi, K., Konno, M., Miyazawa, S. I. & Miyao, M. Sites of Action of Elevated CO₂ on leaf development in rice: discrimination between the effects of elevated CO₂ and nitrogen deficiency. Plant Cell Physiol. 55, 258–268 (2014).
Article CAS Google Scholar
Terashima, I., Yanagisawa, S. & Sakakibara, H. Plant responses to CO₂: background and perspectives. Plant Cell Physiol. 55, 237–240 (2014).
Article CAS Google Scholar
Sato, S. & Yanagisawa, S. Characterization of metabolic states of Arabidopsis thaliana under diverse carbon and nitrogen nutrient conditions via targeted metabolomic analysis. Plant Cell Physiol. 55, 306–319 (2014).
Article CAS Google Scholar
Duan, Z. et al. Photoassimilation, assimilate translocation and plasmodesmal biogenesis in the source leaves of Arabidopsis thaliana grown under an increased atmospheric CO₂ concentration. Plant Cell Physiol. 55, 358–369 (2014).
Article CAS Google Scholar
Ruan, Y. L. Sucrose metabolism: gateway to Ddiverse carbon use and sugar signaling. Annu. Rev. Plant Biol. 65, 33–67 (2014).
Article CAS Google Scholar
Taylor, G. et al. Spatial and temporal effects of free-air CO₂ enrichment (POPFACE) on leaf growth, cell expansion, and cell production in a closed canopy of poplar. Plant Physiol. 131, 177–185 (2003).
Luomala, E. M., Laitinen, K., Sutinen, S., Kellomaki, S. & Vapaavuori, E. Stomatal density, anatomy and nutrient concentrations of Scots pine needles are affected by elevated CO₂ and temperature. Plant Cell Environ. 28, 733–749 (2005).
Article CAS Google Scholar
Takatani, N. et al. Effects of high CO₂ on growth and metabolism of Arabidopsis seedlings during growth with a constantly limited supply of nitrogen. Plant Cell Physiol. 55, 281–292 (2014).
Article CAS Google Scholar
Hachiya, T. et al. High CO₂ triggers preferential root growth of Arabidopsis thaliana via two distinct systems under low pH and low N stresses. Plant Cell Physiol. 55, 269–280 (2014).
Article CAS Google Scholar
Li, C. R., Gan, L. J., Xia, K., Zhou, X. & Hew, C. S. Responses of carboxylating enzymes, sucrose metabolizing enzymes and plant hormones in a tropical epiphytic CAM orchid to CO₂ enrichment. Plant Cell Environ. 25, 369–377 (2002).
Article CAS Google Scholar
Schaz, U., Dull, B., Reinbothe, C. & Beck, E. Influence of root-bed size on the response of tobacco to elevated CO₂ as mediated by cytokinins. Aob Plants 6, https://doi.org/10.1093/aobpla/plu010 (2014).
Article PubMed PubMed Central Google Scholar
IPCC, 2014. Climate change 2014: Synthesis report. Contribution of working groups I, II and III to the fifth assessment report of the intergovernmental panel on climate change [eds Core Writing Team, Pachauri, R. K. & Meyer, L. A.] (IPCC, 2014)
Song, X., Kristie, D. N. & Reekie, E. G. Why does elevated CO₂ affect time of flowering? An exploratory study using the photoperiodic flowering mutants of Arabidopsis thaliana. New Phytol. 181, 339–346 (2009).
Article CAS Google Scholar
Aoyama, S. et al. Ubiquitin ligase ATL31 functions in leaf senescence in response to the balance between atmospheric CO₂ and nitrogen availability in Arabidopsis. Plant Cell Physiol. 55, 293–305 (2014).
Article CAS Google Scholar
Takei, K. et al. AtIPT3 is a key determinant of nitrate-dependent cytokinin biosynthesis in Arabidopsis. Plant Cell Physiol. 45, 1053–1062 (2004).
Article CAS Google Scholar
Lomin, S. N. et al. Plant membrane assays with cytokinin receptors underpin the unique role of free cytokinin bases as biologically active ligands. J. Exp. Bot. 66, 1851–1863 (2015).
Article CAS Google Scholar
Hothorn, M., Dabi, T. & Chory, J. Structural basis for cytokinin recognition by Arabidopsis thaliana histidine kinase 4. Nat. Chem. Biol. 7, 766–768 (2011).
Article CAS Google Scholar
Tokunaga, H. et al. Arabidopsis lonely guy (LOG) multiple mutants reveal a central role of the LOG-dependent pathway in cytokinin activation. Plant J. 69, 355–365 (2012).
Article CAS Google Scholar
Ashikari, M. et al. Cytokinin oxidase regulates rice grain production. Science 309, 741–745 (2005).
Article CAS ADS Google Scholar
Miyawaki, K., Matsumoto-Kitano, M. & Kakimoto, T. Expression of cytokinin biosynthetic isopentenyltransferase genes in Arabidopsis: tissue specificity and regulation by auxin, cytokinin, and nitrate. Plant J. 37, 128–138 (2004).
Article CAS Google Scholar
Haydon, M. J., Mielczarek, O., Robertson, F. C., Hubbard, K. E. & Webb, A. A. Photosynthetic entrainment of the Arabidopsis thaliana circadian clock. Nature 502, 689–692 (2013).
Article CAS ADS Google Scholar
Kilian, J. et al. The AtGenExpress global stress expression data set: protocols, evaluation and model data analysis of UV-B light, drought and cold stress responses. Plant J. 50, 347–363 (2007).
Article CAS Google Scholar
Riefler, M., Novak, O., Strnad, M. & Schmülling, T. Arabidopsis cytokinin receptor mutants reveal functions in shoot growth, leaf senescence, seed size, germination, root development, and cytokinin metabolism. Plant Cell 18, 40–54 (2006).
Article CAS Google Scholar
Nishimura, C. et al. Histidine kinase homologs that act as cytokinin receptors possess overlapping functions in the regulation of shoot and root growth in Arabidopsis. Plant Cell 16, 1365–1377 (2004).
Article CAS Google Scholar
Higuchi, M. et al. In planta functions of the Arabidopsis cytokinin receptor family. Proc. Natl. Acad. Sci. USA 101, 8821–8826 (2004).
Article CAS ADS Google Scholar
Maeda, Y. et al. A NIGT1-centred transcriptional cascade regulates nitrate signalling and incorporates phosphorus starvation signals in Arabidopsis. Nat. Commun. 9, 1376, https://doi.org/10.1038/s41467-018-03832-6 (2018).
Article CAS ADS PubMed PubMed Central Google Scholar
Lejay, L. et al. Oxidative pentose phosphate pathway-dependent sugar sensing as a mechanism for regulation of root ion transporters by photosynthesis. Plant Physiol. 146, 2036–2053 (2008).
Article CAS Google Scholar
Lejay, L. et al. Regulation of root ion transporters by photosynthesis: Functional importance and relation with hexokinase. Plant Cell 15, 2218–2232 (2003).
Article CAS Google Scholar
Miyawaki, K. et al. Roles of Arabidopsis ATP/ADP isopentenyltransferases and tRNA isopentenyltransferases in cytokinin biosynthesis. Proc. Natl. Acad. Sci. USA 103, 16598–16603 (2006).
Article CAS ADS Google Scholar
Osugi, A. et al. Systemic transport of trans-zeatin and its precursor have differing roles in Arabidopsis shoots. Nat. Plants 3, 17112, https://doi.org/10.1038/nplants.2017.112 (2017).
Article CAS PubMed Google Scholar
Takei, K., Sakakibara, H., Taniguchi, M. & Sugiyama, T. Nitrogen-dependent accumulation of cytokinins in root and the translocation to leaf: Implication of cytokinin species that induces gene expression of maize response regulator. Plant Cell Physiol. 42, 85–93 (2001).
Article CAS Google Scholar
Walch-Liu, P., Neumann, G., Bangerth, F. & Engels, C. Rapid effects of nitrogen form on leaf morphogenesis in tobacco. J. Exp. Bot. 51, 227–237 (2000).
Article CAS Google Scholar
Horgan, J. M. & Wareing, P. F. Cytokinins and the growth responses of seedlings of Betula pendula Roth. and Acer pseudoplatanus L. to nitrogen and phosphorus deficiency. J. Exp. Bot. 31, 525–532 (1980).
Article CAS Google Scholar
Salama, A. M. S. E. A. & Wareing, P. F. Effects of mineral nutrition on dndogenous cytokinins in plants of sunflower (Helianthus annuus L.). J. Exp. Bot. 30, 971–981 (1979).
Article CAS Google Scholar
Woo, J. et al. The response and recovery of the Arabidopsis thaliana transcriptome to phosphate starvation. BMC Plant Biol. 12, 62, https://doi.org/10.1186/1471-2229-12-62 (2012).
Article CAS PubMed PubMed Central Google Scholar
Ohkama, N. et al. Regulation of sulfur-responsive gene expression by exogenously applied cytokinins in Arabidopsis thaliana. Plant Cell Physiol. 43, 1493–1501 (2002).
Article CAS Google Scholar
Lopez-Bucio, J., Cruz-Ramirez, A. & Herrera-Estrella, L. The role of nutrient availability in regulating root architecture. Curr. Opin. Plant Biol. 6, 280–287 (2003).
Article CAS Google Scholar
Kushwah, S. & Laxmi, A. The interaction between glucose and cytokinin signal transduction pathway in Arabidopsis thaliana. Plant Cell Environ. 37, 235–253 (2014).
Article CAS Google Scholar
Stokes, M. E., Chattopadhyay, A., Wilkins, O., Nambara, E. & Campbell, M. M. Interplay between sucrose and folate modulates auxin signaling in. Arabidopsis. Plant Physiol. 162, 1552–1565 (2013).
Article CAS Google Scholar
Gutierrez, R. A. et al. Qualitative network models and genome-wide expression data define carbon/nitrogen-responsive molecular machines in Arabidopsis. Genome Biol. 8, R7, https://doi.org/10.1186/gb-2007-8-1-r7 (2007).
Article CAS PubMed PubMed Central Google Scholar
Nishiyama, R. et al. Transcriptome analyses of a salt-tolerant cytokinin-deficient mutant reveal differential regulation of salt stress response by cytokinin deficiency. PLoS One 7, e32124, https://doi.org/10.1371/journal.pone.0032124 (2012).
Article CAS ADS PubMed PubMed Central Google Scholar
Wang, R., Xing, X., Wang, Y., Tran, A. & Crawford, N. M. A genetic screen for nitrate regulatory mutants captures the nitrate transporter gene NRT1.1. Plant Physiol. 151, 472–478 (2009).
Article CAS Google Scholar
Ho, C. H., Lin, S. H., Hu, H. C. & Tsay, Y. F. CHL1 functions as a nitrate sensor in plants. Cell 138, 1184–1194 (2009).
Article CAS Google Scholar
Galichet, A., Hoyerova, K., Kaminek, M. & Gruissem, W. Farnesylation directs AtIPT3 subcellular localization and modulates cytokinin biosynthesis in Arabidopsis. Plant Physiol 146, 1155–1164 (2008).
Article CAS Google Scholar
Kuderova, A. et al. Effects of conditional IPT-Dependent cytokinin overproduction on root architecture of Arabidopsis seedlings. Plant Cell Physiol. 49, 570–582 (2008).
Article CAS Google Scholar
Kiba, T. et al. The type-A response regulator, ARR15, acts as a negative regulator in the cytokinin-mediated signal transduction in Arabidopsis thaliana. Plant Cell Physiol. 44, 868–874 (2003).
Article CAS Google Scholar
Kojima, M. et al. Highly sensitive and high-throughput analysis of plant hormones using MS-probe modification and liquid chromatography tandem mass spectrometry: an application for Hhmone profiling in Oryza sativa. Plant Cell Physiol. 50, 1201–1214 (2009).
Article CAS Google Scholar
Shinozaki, Y. et al. Ethylene suppresses tomato (Solanum lycopersicum) fruit set through modification of gibberellin metabolism. Plant J. 83, 237–251 (2015).
Dekkers, B. J. et al. Identification of reference genes for RT-qPCR expression analysis in Arabidopsis and tomato seeds. Plant Cell Physiol. 53, 28–37 (2012).
Article CAS Google Scholar
Czechowski, T., Stitt, M., Altmann, T., Udvardi, M. K. & Scheible, W. R. Genome-wide identification and testing of superior reference genes for transcript normalization in Arabidopsis. Plant Physiol. 139, 5–17 (2005).
Article CAS Google Scholar
Hoffmann, W. A. & Poorter, H. Avoiding bias in calculations of relative growth rate. Ann. Bot. 90, 37–42 (2002).
Article Google Scholar

Download references

Acknowledgements

We are grateful to Prof. Tatsuo Kakimoto (Osaka Univ.) for providing the ipt3 ipt5 ipt7, ahk2 ahk3, and ahk3 ahk4 mutants. We thank Dr. Ko Noguchi (Tokyo Univ.) for advice concerning statistical analysis. Hormone analyses were supported by the Japan Advanced Plant Science Network. This work was, in part, supported by the Grant-in-Aid for Scientific Research on Innovative Areas (No. 21114005, JP16H01477, JP17H06473, JP18H04793) from the Ministry of Education, Culture, Sports, Science & Technology of Japan.

Author information

Authors and Affiliations

Department of Applied Biosciences, Graduate School of Bioagricultural Sciences, Nagoya University, Nagoya, 464-8601, Japan
Takatoshi Kiba & Hitoshi Sakakibara
RIKEN Center for Sustainable Resource Science, 1-7-22, Suehiro, Tsurumi, Yokohama, 230-0045, Japan
Takatoshi Kiba, Yumiko Takebayashi, Mikiko Kojima & Hitoshi Sakakibara

Authors

Takatoshi Kiba
View author publications
You can also search for this author in PubMed Google Scholar
Yumiko Takebayashi
View author publications
You can also search for this author in PubMed Google Scholar
Mikiko Kojima
View author publications
You can also search for this author in PubMed Google Scholar
Hitoshi Sakakibara
View author publications
You can also search for this author in PubMed Google Scholar

Contributions

T.K. and H.S. conceived the research. T.K., Y.T. and M.K. conducted the experiments. T.K., Y.T. and M.K. and H.S. analysed and discussed the data. T.K. and H.S. wrote the manuscript.

Corresponding authors

Correspondence to Takatoshi Kiba or Hitoshi Sakakibara.

Ethics declarations

Competing Interests

The authors declare no competing interests.

Additional information

Publisher’s note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary information

Supplementary Figures and Tables

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

Reprints and permissions

About this article

Cite this article

Kiba, T., Takebayashi, Y., Kojima, M. et al. Sugar-induced de novo cytokinin biosynthesis contributes to Arabidopsis growth under elevated CO₂. Sci Rep 9, 7765 (2019). https://doi.org/10.1038/s41598-019-44185-4

Download citation

Received: 19 October 2018
Accepted: 08 May 2019
Published: 23 May 2019
DOI: https://doi.org/10.1038/s41598-019-44185-4

This article is cited by

CEP peptide and cytokinin pathways converge on CEPD glutaredoxins to inhibit root growth
- Michael Taleski
- Kelly Chapman
- Michael A. Djordjevic
Nature Communications (2023)
Differential effects of root-level exposure to triazine xenobiotics on root development plasticity in Arabidopsis thaliana
- Diana Alberto
- Fanny Ramel
- Ivan Couée
Acta Physiologiae Plantarum (2022)
Sucrose interferes with endogenous cytokinin homeostasis and expression of organogenesis-related genes during de novo shoot organogenesis in kohlrabi
- Tatjana Ćosić
- Václav Motyka
- Slavica Ninković
Scientific Reports (2021)

Comments

By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.