Phosphate (Pi) is vital for plant growth, yield, and survival, but in most soils, it is poorly available to plants. To facilitate Pi acquisition, 80% of land plants associate with Glomeromycotina fungi in a 450-million-year-old arbuscular mycorrhiza (AM) symbiosis, in which the fungus provides mineral nutrients in exchange for carbon1. AM symbioses also improve plant stress resistance and soil stability, making AM a promising addition to sustainable agricultural practices2. Symbiotic plants acquire most of their phosphate through AM fungi (AMF)3. The fungi collect Pi via a subterranean hyphal network and release it inside the root cortex via tree-shaped arbuscules1. It has been observed for decades that AM symbiosis is suppressed when the plant Pi status is high, likely to conserve carbon4,5,6. However, the molecular mechanisms interconnecting plant Pi status with AM symbiosis development and function have largely remained elusive. Under Pi deficiency, plants activate a range of adaptive responses including transcriptomic, metabolic, and developmental changes7. A majority of these is controlled by PHOSPHATE STARVATION RESPONSE (PHR) proteins, first discovered in the AM-incompetent species Arabidopsis thaliana and the unicellular alga Chlamydomonas reinhardtii8. PHRs belong to the MYB transcription factor (TF) family and bind to PHR1 binding site (P1BS) motifs (GNATATNC) in the promoters of phosphate starvation-induced (PSI) genes8,9. Interestingly, in Lotus japonicus, P1BS motifs have also been found in the promoters of several genes induced during arbuscule development in root cortex cells10,11, often in combination with CTTC/MYCS motifs, which are bound by an AM-induced WRINKLED (WRI,) TF11,12. Therefore, we hypothesized that PHR may regulate Pi responsive AM development13. In contrast to Arabidopsis, L. japonicus and the important staple crop rice form AM symbioses14. The rice genome contains four genes encoding PHR proteins (PHR1-4), but based on promoter:GUS activity, PHR2 is most broadly expressed in roots and especially in tissues relevant for AM15,16. Thus, we focused on PHR2 in rice to investigate the role of this central phosphate starvation response regulator in AM.

We demonstrate that rice PHR2 is required for root colonization by AMF. Root colonization of phr2 mutants is drastically reduced at low Pi, while ectopic PHR2 expression partially rescues root colonization at high Pi. Even in non-colonized roots, the expression of almost 70% of genes that have been genetically shown to be relevant for AM development and function or that are induced during AM, is reduced in phr2 mutants compared to wild type. PHR2 targets essential genes for major and indispensable symbiotic processes, i.e. pre-contact signal exchange between the symbionts, accommodation of the fungus inside the root, and symbiotic nutrient exchange. In addition, PHR2 is required for root colonization, mycorrhizal phosphate uptake, and AM-mediated yield-promotion in field soil and is sufficient to promote root colonization at high Pi. Moreover, the role of PHRs in promoting AM is conserved in the legume L. japonicus. Thus, PHRs support AM development and function as part of the plant phosphate starvation response syndrome. At high phosphate AM cannot develop due to repression of PHR activity through so-called SPX proteins17,18. AM symbiosis is thus directly wired to the plant phosphate starvation response via the master regulator PHR.


PHR2 promotes root colonization by AMF

We examined root colonization by the model AMF Rhizophagus irregularis of wild type and phr2 mutants at low phosphate conditions (25 µM Pi; LP). Wild type roots were well colonized, but root colonization was severely impaired in a phr2 insertion mutant17 and an independent CRISPR-Cas9 generated phr2 mutant (‘phr2(C)19; Fig. 1A–D). We observed very few colonization attempts on mutant roots, mainly comprising hyphopodia or very few intraradical hyphae, resembling mutants in common symbiosis genes that encode proteins of a signaling cascade which is critically required for fungal root entry and AM development14. Only in very rare colonization units, arbuscules with wild-type-like morphology developed in the phr2 mutants (Fig. 1E–H and Supplementary Fig. 1).

Fig. 1: Effect of PHR2 mutation and overexpression on root colonization by AM fungi.
figure 1

Percent root length colonization (RLC) total (A), arbuscules (B), and vesicles (C) of the indicated genotypes inoculated with R. irregularis (AMF) for 7 weeks at low phosphate (25 µM Pi, LP) or high phosphate (500 µM Pi, HP). D Percent RLC of the indicated genotypes inoculated with AMF for 7 weeks at LP. Arb.: Arbuscules; Ves.: Vesicles. Confocal images of AMF in roots of wild type (E) and phr2 (F). Arbuscule phenotype in wild type (G) and phr2 (H) roots. E, extraradical hypha; H, hyphopodium; I, intraradical hypha; A, arbuscule. Scale-bars: E, F: 100 μm and G, H: 10 μm. Statistics: Individual data points and mean ± SE are shown. AC N = 5 independent plants; Brown-Forsythe and Welch’s One-Way ANOVA test with Games–Howell’s multiple comparisons test. Different letters indicate statistical differences. D N = 5 independent plants; Mann–Whitney test (two-tailed) between phr2(C) and wild type for Total (p = 0.0079), arbuscules (p = 0.0079) and vesicles (p = 0.0079). Asterisks indicate significance of difference: ** p ≤ 0.01. EH The phenotype was observed in 11 (6 + 5) independent plants in two independent experiments.

As PHR2 is critical for root colonization at LP, we examined whether ectopic expression of PHR2 driven by the 35S promoter (35S:PHR2)17 enables root colonization at higher Pi conditions. At LP, total colonization, arbuscules, and vesicles were slightly increased in the 35S:PHR2 line as compared to wild type. However, at medium (200 µM Pi, MP) and high Pi (500 µM Pi, HP) wild type and phr2 were hardly colonized, while 35S:PHR2 enabled 40 and 20% total root length colonization and 25 and 5% colonization with arbuscules, respectively (Fig. 1A–D and Supplementary Figs. 2 and 3). Together this indicates that PHR2 promotes AM development at Pi starvation and its inactivity may be responsible for the absence of AM at high phosphate, as described for other phosphate starvation responses17,20. The role of PHR2 in supporting arbuscule development is supported by the activity pattern of its promoter. Shi et al. showed that the PHR2 promoter is active across all tissue layers in non-colonized rice roots. In colonized roots, a stronger promoter activity was observed in arbuscule-containing cells with an overall increased GUS activity in large lateral roots18.

PHR2 activates AM-relevant genes

To explain the role of PHR2 in AM, we performed RNA sequencing for non-inoculated (Mock) and R. irregularis-inoculated (AM) roots of phr2 at LP, 35S:PHR2 at HP, and wild type at both Pi conditions (Fig. 2 and Supplementary Fig. 4, and Supplementary Data 1). A larger number of genes differed in expression in phr2 or 35S:PHR2 vs. wild type in AM compared to Mock roots (Fig. 2A). The drastic transcriptome modulation upon AM indicated by principal component analysis in the wild type at LP was clearly reduced for phr2 (Fig. 2B). At HP, the transcriptomes of all 35S:PHR2 and wild-type samples clustered together, but they separated when analyzed separately from LP samples (Supplementary Fig. 5), suggesting a weaker but still remarkable effect of ectopic PHR2 expression on the AM root transcriptome at HP. Interestingly, the expression of AM-relevant genes is already compromised in phr2 Mock roots (without root colonization), similar to wild type at HP (Fig. 2C–F and Supplementary Data 2), including 16 genes with genetically determined and (for most of them) essential functions in AM (Fig. 2E). These include genes encoding receptors involved in the perception of fungal signals prior to root contact (CERK1, NFR5), common symbiosis genes involved in signal transduction and regulation of colonization (SYMRK, CCaMK, CYCLOPS, SLR1/DELLA, NSP1, NSP2, and VAPYRIN), genes involved in strigolactone biosynthesis for activation of the fungus in the rhizosphere prior to contact (CCD7, CCD8B), genes involved in the regulation of colonization (KIN2), genes responsive to karrikin signaling and involved in apocarotenoid biosynthesis (DLK2C, ZAS), and genes encoding periarbuscular membrane-localized ABCG and phosphate transporters for nutrient exchange (STR1, PT11, and PT13)21,22. In addition, the expression of one-fifth of AM-induced genes in wild type is reduced already in the absence of AMF in phr2 (Fig. 2F and Supplementary Data 3). Together, this suggests that PHR2 conditions the root for AM symbiosis at low phosphate and that the lower cumulative expression of AM-relevant genes impairs AM in phr2 mutants.

Fig. 2: The PHR2-dependent transcriptome of non-colonized roots contains genes required for AM development.
figure 2

A Number of up- and downregulated differentially expressed genes (DEGs) in phr2 vs WT (LP) and 35S:PHR2 vs WT (HP) for mock or R. irregularis-inoculated plants. B PCA plot for the transcriptome of indicated samples. C Hierarchical clustering of combined DEGs from mock-inoculated roots using normalized counts. Colored bars on the left of the heatmap depict individual clusters (based on the dendrogram). Z-scores represent scaled normalized counts. D Mean log2FC of phr2 vs WT (LP) and 35S:PHR2 vs WT (HP) for clusters obtained in (C). Dotted lines indicate mean log2FC values of −0.585 and 0.585 (used as a cut-off for selecting DEGs). Dashed boxes highlight the mean log2FC of clusters with overall reduced transcript accumulation in phr2 vs WT. E Z-scores for a subset of genes from (C) previously reported being functionally required in AM. Asterisks indicate that the gene is a DEG in the phr2 vs WT (LP) or 35S:PHR2 vs WT (HP) comparisons. F Venn diagram showing overlap of DEGs with increased transcript accumulation in wild type ‘AM vs Mock’ and DEGs with reduced transcript accumulation in ‘phr2 vs WT’ in Mock at LP. G Venn diagram showing the intersection of DEGs with reduced transcript accumulation in the ‘phr2 vs WT’ comparison for mock and AMF-inoculated samples with AM genelist (Supplementary Data 4) and DEGs upregulated in either smax1 (vs WT) or d3 smax1 (vs WT) Mock24. Statistics: Mean ± SE are shown in (D) where N = Number of genes in each cluster as obtained in (C). Error bars represent the SE of the mean.

We compiled a list of 205 genes, called ‘AM genelist’ (Supplementary Data 4), containing genes with a genetically determined or putative function in AM, based on phylogenomic and/or conserved expression patterns across AM-competent plant species23. Almost 70% of genes in the AM genelist were less expressed in phr2 vs. wild type, demonstrating that PHR2 is an important regulator of AM (Fig. 2G). Consistent with the low colonization of phr2 and the presence of PHR binding sites in the promoters of some of the orthologs in Lotus japonicus11, the activation of AM-induced genes was impaired, including a number of genes encoding (receptor) kinases, transcription factors, transporters, and enzymes with genetically determined function in AM (Supplementary Figs. 69 and Supplementary Data 57). Furthermore, many of these genes showed reduced expression in phr2 even in the absence of the fungus (Supplementary Fig. 7). qPCR recapitulated this expression pattern of a selected subset of important AM-relevant genes (Supplementary Fig. 9). Some of these were activated by 35S:PHR2 at HP and most of them at MP, consistent with the degrees of promotion of root colonization by 35S:PHR2 at these non-permissive conditions (Fig. 1A–D and Supplementary Figs. 2, 3, 9, 10). Furthermore, 213 DEGs that were less expressed in phr2 roots show increased expression in non-colonized smax1 or d3 smax1 roots, which display the opposite AM phenotype to phr2, i.e., they are colonized more extensively than wild type24, and 41 of these genes are additionally shared with the AM genelist (Fig. 2G and Supplementary Data 7). SMAX1 is a negative regulator of karrikin signaling and needs to be removed through proteasomal degradation after binding to a complex of the karrikin receptor KAI2 and the SCFMAX2- complex to enable AM in rice24,25. Thus, karrikin signaling and PHR2 seem to target partially overlapping genes for regulating AM.

PHR2 targets AM-relevant genes

To understand whether PHR2 directly targets chromatin regions containing AM-relevant genes, we performed chromatin immunoprecipitation followed by DNA sequencing (ChIP-Seq). Since we surprisingly found that PHR2 promotes the expression of AM-relevant genes already in the absence of AMF at LP, we chose to perform ChIP-Seq under this condition. For the two independent replicates, more than 60% of PHR2 binding sites were found upstream of ATG (Supplementary Fig. 11). Motif enrichment analysis of DNA sequences associated with PHR2 binding sites revealed the P1BS element (GNATATNC) among the top 2 enriched motifs in both ChIP replicates (Supplementary Data 8 and Supplementary Fig. 12). Peaks representing PHR2 binding sites were annotated to nearby genes and 435 genes were shared between the two replicates (referred to as “PHR2 targets”; Supplementary Fig. 13A and Supplementary Data 8). 77% of these PHR2 targets with reduced expression in phr2 contained P1BS/P1BS-like motifs in the sequence between the transcriptional start site (TSS) and 3000 bp upstream of the TSS (Supplementary Fig. 13B and Supplementary Data 9). ChIP-Seq quality was further validated by strong PHR2-binding peaks at P1BS elements in the promoter regions of the previously known PHR2-targets, GDPD2, IPS1, and SPX1/2/317,26,27 (Supplementary Fig. 14 and Supplementary Data 10). An overlap of PHR2 targets with DEGs reduced in phr2 vs wild type resulted in 162 overlapping genes, for which GO enrichment analysis revealed that most of these were involved in “Cellular response to phosphate starvation” and motif enrichment in the 3 kb region upstream of TSS revealed P1BS motif (GNATATNC) as the topmost hit (Fig. 3A, B and Supplementary Fig. 13C, D). 17 genes overlapped among the two ChIP replicates and the AM genelist, and these represent a significant enrichment of AM-relevant genes in high-confidence PHR2 targets, when compared to the whole rice genome (p-value of 6.4 × 10−11) (Supplementary Fig. 15). An overlap also showed 27 common genes (including genes from individual ChIP replicates), 15 of which were repressed in phr2 vs wild type and common to both ChIP replicates (Fig. 3A, C and Supplementary Data 10). These 15 genes contain 8 with established and crucial roles in AM. Except for PT11, which is required for mycorrhizal phosphate uptake and arbuscule maintenance, all these genes are indispensable for pre-contact signaling and necessary for or involved in important early events of fungal root entry (Fig. 3C), congruous with the phr2 AM phenotype. The remaining 12 genes that were hit in only one ChIP-Seq replicate included the genes CYCLOPS, SLR1/DELLA, required for root colonization and arbuscule formation22 (Fig. 3C) as well as GRAS16 and SMAX1, which are positive and negative regulators of AM respectively24,28.

Fig. 3: PHR2 targets important AM symbiosis genes.
figure 3

A Overlap of PHR2 ChIP-Seq targets with RNASeq DEGs displaying reduced expression in Mock and AM roots of phr2 vs WT roots grown at LP and with AM genelist (Supplementary Data 4). B Consensus PHR2-binding motif for Set A + Set B genes based on ‘RSAT Plants’ oligo-analysis. C Fold change of RNAseq-based transcript accumulation in Mock and AM roots of phr2 vs WT grown at LP (left) and ChIP-Seq fold enrichment for PHR2 binding (right) for the 27 genes hit in at least one ChIP-Seq replicate and overlapping with phr2 vs WT down and AM genelist. Genes with assigned functional roles in AM, based on mutant phenotypes are displayed in red (bold for mutants, regular font for RNAi lines). D Illustration of promoters used in transactivation assays with positions of PHR1 binding site (P1BS) elements (black) and mutated P1BS elements (red). E PHR2 transactivates the promoters of GDPD2, CCD7, ZAS, and PT11 (553, 3540, 3377, and 1590 bp upstream of ATG, respectively) in a P1BS element-dependent manner in Nicotiana benthamiana leaves. promoter:GUS fusions were co-transformed with 35S:PHR2 or 35S:mCherry (negative control). ‘m’ indicates that all P1BS elements in the promoter were mutated. Individual dots show GUS activity in protein extracts from leaf disks from four independent plants. GUS: β-glucuronidase. F Quantity of 4-deoxyorobanchol and two isomers of methoxy-5-deoxystrigol in the root exudates of WT, phr2, and 35S:PHR2 grown at LP. G Percent root length colonization total (left), arbuscules (middle), and vesicles (right) of the indicated genotypes inoculated with R. irregularis for 6 weeks at low phosphate (25 µM Pi) and treated with 0.02% acetone solvent or the synthetic SL analog rac-GR24. Statistics: Individual data points and mean ± SE are shown. E N = 11–12 biological replicates representing independent Agrobacterium infiltrations, one per leaf into 3 leaves of 4 individual plants; Kruskal–Wallis test with Dunn’s posthoc comparison. F N = 6–7 independent plants; Brown–Forsythe and Welch’s One-Way ANOVA test with Games–Howell’s multiple comparisons test. G N = 5 independent plants; Brown–Forsythe and Welch’s One-Way ANOVA test with Games–Howell’s multiple comparisons test.

Specific binding of PHR2 to the P1BS/P1BS-like motif in the promoters of the 8 AM-relevant PHR2 targets detected in both ChIP-Seq replicates was confirmed by ChIP-qPCR except for CERK1 (Supplementary Figs. 16 and 17). Surprisingly, for the CERK1 promoter, we found moderate enrichment at a CTTC/MYCS motif nearby the P1BS motif. It is possible that a CTTC-binding protein (e. g. a WRI transcription factor12) forms a complex with PHR2 to regulate CERK1 transcription and that this CTTC/MYCS binding factor has a stronger affinity to the DNA than PHR2, leading to enrichment of this motif after PHR2 pulldown. Using transactivation assays in Nicotiana benthamiana leaves, we found that the promoter of the established PHR2 target GDPD2 and three previously uncharacterized AM-relevant PHR2 target promoters pCCD7, pZAS, and pPT11 are transactivated by PHR2 in a P1BS-dependent manner (Fig. 3D, E), confirming the ChIP-Seq results.

The binding of and transactivation of the promoter of the strigolactone (SL)-biosynthesis gene CCD7 by PHR2 (Fig. 3C–E) and the decreased expression of CCD7 and CCD8B in the phr2 mutant (Fig. 2E and Supplementary Figs. 9 and 10) are consistent with the observation that strigolactone biosynthesis is increased at Pi starvation29. Exuded SL in the rhizosphere activates AMF and is crucial for relevant levels of root colonization, while root colonization of ccd7 and ccd8 mutants with defects in SL biosynthesis is strongly reduced30,31,32,33. To understand the impact of mutating phr2 on SL exudation we quantified the canonical rice SL 4-deoxyorobanchol as well as 2 isomers of Methoxy-5-deoxystrigol in the root exudates of wild type, phr2, and 35S:PHR2 (Fig. 3F). The amount of all three compounds was reduced by at least half in phr2 root exudates as compared to the wild type, while the Methoxy-5-deoxystrigol isomers were slightly increased in the exudates of 35S:PHR2. This indicates that PHR2 indeed regulates SL biosynthesis and thereby the amount of SL in the root exudate. We examined whether exogenous supplementation of phr2 with SL can restore AM colonization. Treatment of roots with 100 nM of the synthetic SL analog, rac-GR24 led to a significant increase in total colonization and vesicles in phr2 roots but not in wild type roots, which probably exude saturating amounts of SL (Fig. 3G). Thus, part of the inability of phr2 to support AM is due to reduced SL exudation, while another part can be explained by reduced expression of other genes required for root colonization and AM functioning (Fig. 2E).

Transcript accumulation of gibberellin-related genes is altered in phr2

Gibberellin (GA) treatment inhibits AM development because AM formation requires DELLA, the proteolytic target of GA-signaling34,35. It was recently shown that GA is also involved in the suppression of AM in response to HP, as GA-deficient Nicotiana tabacum plants were less sensitive to AM inhibition by HP than wild type36. To understand whether GA signaling participates in the regulation of AM in response to phosphate downstream of PHR2, we mined the RNAseq and ChIP-Seq data for GA-biosynthesis and signaling genes. In addition to DELLA and the GIBBERELLIN INSENSITIVE DWARF 2 (GID2), encoding an F-box protein required for GA-perception being ChIP targets of PHR2 (Fig. 3C and Supplementary Fig. 18), we found that GA-related genes were enriched in genes deregulated in phr2 (Supplementary Fig. 18). GA biosynthesis genes have lower expression levels in Mock roots of phr2 mutants as compared to wild type, while the transcript levels of three genes encoding enzymes involved in de-activating GA (GA13ox2, GA2ox3, and GA2ox7) are increased in phr2 (Supplementary Fig. 18). Thus, the expression of several genes involved in GA metabolism is controlled by PHR2.

The role of PHR in regulating AM is conserved in the dicotyledon Lotus japonicus

We used the model legume Lotus japonicus to understand whether the role of PHR in AM is conserved in dicotyledons. The L. japonicus genome contains three PHR genes, which we named PHR1A, PHR1B, and PHR1C (Supplementary Fig. 19). A LORE1 retrotransposon insertion line37 was obtained for PHR1A (Supplementary Fig. 19). Mutation of Ljphr1a was sufficient to cause a significant reduction in colonization by R. irregularis as compared to the wild type of hairy roots transformed with an empty vector and grown at LP. This indicates that the role of PHR in AM is conserved in L. japonicus. However, there may be redundancy among the three PHR proteins, and the AM phenotype may be stronger in double and triple phr mutants. Transgenic expression of PHR1A driven by a Ubiquitin promoter in phr1a hairy roots restored colonization to wild-type levels. Furthermore, Ubiquitin promoter-driven expression of PHR1A significantly increased root colonization at high phosphate as compared to the wild type (Fig. 4A). We examined, whether mutation of PHR1A leads to reduced expression of AM-relevant genes in L. japonicus, and monitored transcripts of selected candidate genes in Mock roots by RT-qPCR, namely the common symbiosis genes SYMRK, CCaMK, and CYCLOPS and the three SL biosynthesis genes D27, CCD7, and CCD8. Similar to rice phr2 mutants, the expression of SYMRK, CCaMK and CYCLOPS was reduced in roots of phr1a. However, no significant reduction in transcript accumulation of the SL biosynthesis genes was observed, even though one P1BS is located in the promoter of each of these genes (Supplementary Fig. 20). It is possible that one of the other PHRs regulates their expression. Alternatively, SL biosynthesis genes may not be regulated by PHRs in Lotus japonicus.

Fig. 4: PHR1A is required for full colonization of Lotus japonicus roots by R. irregularis.
figure 4

Percent intraradical hyphae (A), arbuscules (B), and vesicles (C) of hairy roots for indicated genotypes inoculated with R. irregularis (AMF) for 4 weeks at 250 µM Pi or 2500 µM Pi. EV, empty vector. D Relative transcript accumulation in mock-inoculated (Mock) hairy roots of the indicated genotypes in parallel with the experiment in Fig. 5A–C. Statistics: Individual data points and mean ± SE are shown. AC N = 5–13 independent plants; Brown–Forsythe and Welch’s One-Way ANOVA test with Games–Howell’s multiple comparisons test. Different letters indicate statistical differences between the samples. D N = 3 independent root systems; Mann–Whitney test (two-tailed). Different letters indicate statistical differences between statistical groups.

PHR2 promotes AM and yield in field soil

To assess the importance of rice PHR2 in supporting AM in field soil and in promoting plant performance via AM we conducted a greenhouse experiment with soil from a rice paddy field with (HP) or without (LP) Pi fertilization (Fig. 5 and Supplementary Figs. 2125). At LP, inoculation with R. irregularis caused a significant increase in several important agronomic parameters: total shoot phosphorus (P) and shoot P concentration, root fresh weight, and most importantly seed setting and 1000 grain weight in wild type and 35S:PHR2. However, these parameters remained unchanged or decreased in phr2 at LP (Fig. 5 and Supplementary Fig. 22), showing that phr2 is required for AM-mediated yield increase in field soil. At HP, total shoot phosphorus (P), root fresh weight, seed setting, and 1000 grain weight remained the same in wild type independent of AMF presence. However, in 35S:PHR2 these parameters increased in response to AM. Furthermore, 35S:PHR2 caused a significant response to AM for plant height, panicle length, and shoot dry weight at LP, HP, or both (Supplementary Fig. 22). Consistently, 35S:PHR2 enabled AM colonization in field soil even at HP, accompanied by increased expression of the AM marker genes AM1, AM3, AM14/ARK1, and PT1114 (Supplementary Figs. 2325).

Fig. 5: PHR2 affects AM-mediated phosphate uptake and yield in field soil.
figure 5

A Total shoot phosphorus (mg), B seed setting, and C 1000 grain weight of the indicated genotypes inoculated with R. irregularis (AM) or non-inoculated (Mock) and grown at LP (unfertilized) or HP (fertilized with superphosphate fertilizer, P2O5). Plants were grown in a greenhouse in soil from the Longhua field base in Shenzhen, China, and harvested at 110 days post transplanting (dpt) for trait quantification. Statistics: Individual data-points and mean ± SE are shown. N = 3–5 independent plants; Brown–forsythe and Welch’s One-Way ANOVA test with Games–Howell’s multiple comparison test was carried out. Different letters indicate statistical differences between genotypes and treatments.

Our data confirm previous observations that 35S:PHR2 reduces plant growth as compared to wild type (Fig. 5 and Supplementary Fig. 22). This may be due to Pi toxicity;15 changes in hormone biosynthesis and/or signaling or other pathways affecting development. Interestingly, AM mitigates this negative effect on rice performance, perhaps because it promotes the uptake of other nutrients, which consequently become less limiting and/or affects other pathways regulating plant growth.


Here we demonstrate that rice PHR2 is essential for the establishment of AM symbiosis under laboratory conditions, as well as for AM-mediated improvement of rice yield in LP paddy field soil.

PHR2 supports AM development at LP because it promotes the expression of a number of genes required for AM development and function already in the absence of AMF. This possibly occurs through the effect of PHR2 on chromatin accessibility, as recently shown in Arabidopsis38. We detected PHR2 targets using ChIP-Seq in the absence of AMF and these comprise strigolactone biosynthesis genes needed for strigolactone exudation to activate the fungus31,33, membrane receptors needed for perception of fungal signals39,40 and genes belonging to the common symbiosis signal transduction cascade, which is thought to relay the signals to the nucleus to activate gene expression, and which is required for fungal entry into the root14. Furthermore, PHR2 activates genes encoding transporters needed for nutrient exchange at the peri-arbuscular membrane, such as PT1141. Thus, PHR2 appears to be required for the activation of genes involved in several steps of arbuscular mycorrhiza development from initiation of root colonization to its functioning in nutrient exchange (Fig. 6).

Fig. 6: Model depicting regulation of AM symbiosis by PHR2.
figure 6

When plants obtain sufficient phosphate (left), SPX proteins prevent nuclear translocation of PHR242, as well as PHR2 binding to promoters of phosphate starvation -induced genes including AM relevant genes17,42. This causes low exudation of strigolactone and poor expression of genes required for perception of Myc-Factors and fungal entry, thereby preventing full symbiosis development. Upon phosphate starvation, SPX proteins, are degraded42. Consequently, PHR2 is active, can bind to P1BS elements in promoters, and transcriptionally activate genes important for AM, such as CCD7 involved in strigolactone biosynthesis for activation of the fungus in the rhizosphere prior to contact31,32,33, genes encoding receptors involved in the perception of fungal signals prior to root contact such as CERK1 and SYMRK39,40,65,66, the transcription factor NSP267, ZAS involved in apocarotenoid biosynthesis promoting root colonization68, and the AM-specific phosphate transporter gene PT1141 (localized to the peri-arbuscular membrane (PAM)) required for Pi uptake from the fungus. (For simplicity, we focus here on 6 genes with important and genetically determined roles in AM that have been recovered in both ChIP-Seq replicates Fig. 3C, and were confirmed by ChIP-qPCR, Supplementary Fig. 17). Consequently, at low phosphate, roots exude increased amounts of strigolactone and can perceive fungal signals (middle), the fungus is activated to colonize the roots and the symbiosis can function through nutrient transporters localizing to the peri-arbuscular membrane (right). Thus, symbiosis establishment appears to be enabled as a part of the PHR2-regulated phosphate starvation response.

Shi et al. (2021)18 performed a large yeast-1-hybrid screen using 47 promoters of genes activated by AM predominantly in arbuscule-containing cells. They found that a large proportion of them was bound by PHR2, consistent with the previous observation that a number of their orthologs in L. japonicus carry the P1BS element in their promoter11. Interestingly, although transcripts of these genes were reduced in phr2 mutants in our study, which can be a symptom of reduced root colonization, we did not capture most of these genes in our ChIP-Seq experiment except for the AM-specific transporter genes PT11 and AMT3.1. We conducted ChIP-Seq from non-colonized roots and it is possible that additional AM-induced transcription factors are necessary to stabilize PHR2-binding to the promoters of these AM-induced genes. However, our ChIP-Seq approach enabled us to identify unexpected PHR2 targets involved in pre-contact symbiotic signaling and early stages of symbiosis, which were not present in the pre-selected set of promoters analyzed by Y1H18.

At HP the movement of PHR2 to the nucleus and its binding to promoters is inhibited by SPX proteins, which act as phosphate sensors17,18,42,43. Consistently, it appears that AM development is attenuated at HP due to SPX-mediated inhibition of PHR2-mediated transcriptional activation of AM-relevant genes. This is consistent with the finding that ectopic expression of PHR2, driven by a strong constitutive promoter allows AM development at HP, likely because PHR2 outnumbers SPX proteins when it is overexpressed. Importantly, a recent study18 showed that quadruple mutants in rice SPX genes have significantly increased root colonization independently of the phosphate concentration in the fertilizer, while ectopic SPX expression leads to significantly reduced root colonization. In contrast, Medicago truncatula SPX1 and SPX3 were shown to positively affect root length colonization by promoting the expression of SL biosynthesis genes. However, they also seemed to promote arbuscule degeneration and turnover, indicating a dual role of these proteins in regulating AM in M. truncatula44. The contrasting findings in rice and M. truncatula raise the possibility that different SPX family members play divergent roles in AM or that they differently affect AM in grasses vs legumes.

We show that the role of PHRs in AM is conserved in the model legume L. japonicus. It is therefore likely, that AM symbiosis is a part of the PHR-mediated phosphate starvation response syndrome at least across the angiosperms. It will be interesting to learn whether this hypothesis can be confirmed in other clades of the vascular and early-diverging non-vascular plants. In summary, we provide important insights into the regulation of AM by the plant phosphate status, which has a broad significance in agriculture and terrestrial ecosystems.


Plant material, growth conditions, and plant co-cultivation with AM fungi

Oryza sativa L. ssp. japonica genotypes used in this work were wild type (cv. ZH11) and CRISPR-Cas9 generated phr2(C)19 and wild type (cv. Nipponbare), phr2, 35S:PHR2, and 35S:PHR2-FLAG17. Rice seeds were sterilized by incubating in absolute ethanol for 2 min, then in sterilization solution (10% Clorox + 0.1% SDS) for 30 min and subsequently in autoclaved distilled water for 1 h. Seeds were germinated on agar plates and kept in the dark for 3 days at 27 °C and 60% air humidity in a controlled plant growth chamber. Subsequently, germinated seedlings were exposed to light and grown for 2 weeks in a long-day photoperiod (16 h light/8 h dark) in the same temperature and humidity conditions. 2-week-old seedlings were then transplanted to pots filled with quartz-sand and inoculated with 500 spores of Rhizophagus irregularis DAOM 197198 (Agronutrition, Toulouse, France) per plant and grown at the same conditions. Plants were fertilized with 50 ml sterilized half-Hoagland media at 25 µM Pi (low phosphate, LP), 200 µM Pi (medium phosphate, MP), and 500 µM Pi (high phosphate, HP) concentrations once a week and watered a second time per week with autoclaved distilled water.

For L. japonicus, ecotype Gifu wild type and phr1a mutants were used. The phr1a mutant corresponds to the LORE1 insertion line 3006305445. Seeds were scarified with sandpaper and surface sterilized with 0.1% SDS in 2% NaClO, washed 6 times with sterile water, and left to swell in sterile water with permanent inversion for 2 h. The seeds were germinated on 0.8% B5-Agar at 22 °C in darkness for 4 days and then in light for 3 days. Plates were then transferred to closed, sterilized cultivation pots (Duchefa, Os 140 Box, Green Filter), containing 450 g of sand and watered with modified B&D medium, containing 250 µM Pi (low phosphate) or 2.5 mM Pi (high phosphate)46. For arbuscular mycorrhiza colonization assays, plant roots were inoculated with 500 spores per plant of R. irregularis DAOM197198 (Agronutrition, Toulouse, France). The plants were grown for 4 weeks in a chamber set at 22 °C in a long-day photoperiod (16 h light/8 h dark) with 60% relative humidity.

Quantification of root colonization and AM imaging

Rice roots were harvested at 7 weeks post-inoculation (wpi) into 10% KOH and boiled for 15 min followed by incubation in 10% acetic acid, ink staining, and 5% acetic acid de-staining as described46. Root pieces of 1 cm each were then mounted on a slide for observation under an inverted light microscope to quantify total AM colonization and % of AM structures using the gridline intersect method47. Furthermore, images of these stained roots were visualized using an OPTO EDU Binocular Compound Microscope (Opto-Edu, Beijing, China) fitted with 5MP USB 2.0 Color CMOS Digital Eyepiece Microscope Camera (AmScope, USA) and exported with Swift Easy View software (Motic, China). For visualization of AM structures inside root cells, roots were stained with Wheat Germ Agglutinin, Alexa Fluor™ 488 Conjugate46. Roots were then visualized with a Zeiss LSM 710 Confocal Microscope (Zeiss, Germany) at 20X for a root overview or at 100X (oil) for details of arbuscules and images extracted using the ZEN 2020 v3.3 software (Zeiss, Germany).

L. japonicus roots were stained with acid ink47. Root length colonization was quantified using a modified gridline intersect method48 at 10× magnification under a light microscope Leica, type 020-518500 DM/LS (Leica, Germany).

RNA extraction and RT-qPCR

Plant roots were harvested, frozen in liquid nitrogen, and stored at −80 °C. Frozen roots were ground into powder using mortar and pestle and the powder was immediately transferred to lysis extraction buffer and processed for RNA isolation using FastPure Plant Total RNA Isolation Kit (Polysaccharides & Polyphenolics–rich) (Vazyme, China). Isolated RNA was checked for the absence of genomic DNA contamination by PCR. RNA was quantified with a Nanodrop (Thermo Scientific, USA). First-strand cDNA synthesis was carried out with HiScript® III RT SuperMix for qPCR (+gDNA wiper) (Vazyme, China). qPCR was conducted with primers indicated in Supplementary Table 1 and ChamQ Universal SYBR® qPCR Master Mix (Vazyme, China) on a Bio-Rad CFX384 qPCR cycler (Bio-Rad Laboratories, Shanghai, China). Threshold cycle values were extracted using the CFX Maestro Software 2.0 (BioRad, USA).

RNA from Lotus japonicus roots was extracted using the Spectrum Plant Total RNA Kit (Sigma, USA). DNA contamination was removed by Invitrogen DNAse I amp. grade ( and RNA was tested for genomic DNA contamination by PCR. cDNA synthesis was performed with 600 ng RNA using the iScript cDNA synthesis kit (Bio-Rad, Germany). Real-time RT-PCR was performed with the qPCR GreenMaster high ROX mix (Jena Bioscience, Germany) and primers shown in Supplementary Table 1. The qPCR reaction was run on an iCycler (Bio-Rad, Germany) according to the manufacturer’s instructions. Thermal cycler conditions were: 95 °C 2 min, 45 cycles of 95 °C 30 s, 60 °C 30 s and 72 °C 20 s followed by dissociation curve analysis. Expression levels were calculated according to the ΔΔCt method49. For each genotype and treatment, three biological replicates were monitored and each sample was represented by two to three technical replicates.

RNASeq and data analysis

RNA was extracted as described above, checked for quality using an Agilent Bioanalyzer (Agilent, USA), and quantified in a Qubit 3.0 fluorometer (Invitrogen, USA). Samples with a RIN value of > 7 were used for library preparation (Illumina TruSeq Stranded Total RNA kit, Illumina, USA) and sequenced on an Illumina HiSeq 4000 to obtain 150 bp paired-end reads. Raw fastq files were processed through adaptor-trimming. Clean reads were tested with FastQC ( for base quality. Data were processed with a quasi-transcript mapping approach in SALMON50. SALMON 0.7.0 was operated in the Conda environment inside Linux ( Reads were mapped onto the Oryza sativa reference transcriptome downloaded from Phytozome v12 ( Read counts were obtained for rice transcripts at the gene level. Read counts were further processed through tximport in R/Bioconductor 3.13 (; R Core Team, 2013) for input into EdgeR for Data exploratory and differential expression analysis. Differentially expressed genes (DEGs) were obtained with the cut-off: absolute(log2Fold-Change) ≥ 0.5845 and FDR ≤ 0.05. Heatmaps were prepared using the heatmap.2 package in R/Bioconductor. AgriGO was utilized to find enriched GO terms for DEGs51. A list of genes implicated in AM was compiled based on previous studies in rice and other AM host plants and is referred to as “AM genelist” (Supplementary Data 4). For genes identified to have a role in AM development of symbiosis in other AM host plants, reciprocal blast was used to identify the best match in rice.

Chromatin immunoprecipitation (ChIP) and sequencing

Chromatin immunoprecipitation was performed as described52 with few modifications as follows: 3–4-week-old 35S-PHR2-FLAG transgenic rice roots were ground to a fine powder in liquid nitrogen and stored at −80 °C until further use. Subsequently, 3 g of tissue powder were resuspended in cold extraction buffer with 1.5% formaldehyde and incubated at room temperature for 10 min with shaking, followed by quenching for 5 min with 125 mM glycine and 750 mM Tris’s buffer. After Miracloth filtration and subsequent nuclei enrichment and lysis steps, the resulting chromatin was sheared in Bioruptor® Pico sonication device (Diagenode, USA) with settings of 30 s ON/30 s OFF for 40 cycles. Agarose gel check on sonicated chromatin (reverse cross-linked and DNA purified) suggested that most fragments ranged from 150 to 500 bp. Sonicated chromatin was concentrated using Microcon® Centrifugal Filters (Merck Millipore, USA). After centrifugation, sonicated chromatin supernatant was selected for immunoprecipitation. 20 µl chromatin was saved at –20 °C for input DNA, and 100 µl chromatin was used for immunoprecipitation by anti-Flag antibodies (F1804, Sigma) and IgG antibodies (ab171870, Abcam) respectively. The amount of each antibody used in each sample was 10 µg and antibody dilution was 1: 100. Antibody was used in the immunoprecipitation reactions at 4 °C overnight. The next day, 30 μL of protein beads were added and the samples were further incubated for 3 h. Next, the beads were washed once with 20 mM Tris/HCL (pH 8.1), 50 mM NaCl, 2 mM EDTA, 1% Triton X-100, 0.1% SDS; twice with 10 mM Tris/HCL (pH 8.1), 250 mM LiCl, 1 mM EDTA, 1% NP-40, 1% deoxycholic acid; and twice with TE buffer 1× (10 mM Tris-Cl at pH 7.5 + 1 mM EDTA). Bound material was then eluted from the beads in 300 μL of elution buffer (100 mM NaHCO3, 1% SDS), treated first with RNase A (final concentration 8 μg/mL) during 6 h at 65 °C and then with proteinase K (final concentration 345 μg/mL) overnight at 45 °C. To examine the quality of ChIP DNA to assess enrichment for PHR2 binding motif P1BS, a ChIP-qPCR was conducted, using immunoprecipitated (anti-Flag and IgG) DNA and input DNA and specific primers for sequence flanking the P1BS motif in the IPS1 promoter. qPCR reactions were run using the ChamQ SYBR Color qPCR Master Mix (Vazyme Biotech, China) on Bio-RAD CFX384 real-time system (BioRad, USA). The enrichment values were normalized to the input sample. After normalizing with input, fold enrichment was calculated using the “ΔΔCt” method by comparing with IgG negative control immunoprecipitated sample. Only samples showing more than five-fold enrichment compared to IgG for the IPS1 promoter17 negative control were used for sequencing. For ChIP-Seq, immunoprecipitated and input DNA were used to construct sequencing libraries following the protocol provided by the NEXTflex® ChIP-Seq Library Prep Kit for Illumina® Sequencing (NOVA-5143, Bioo Scientific) and sequenced on HiSeq X Ten (Illumina, USA) with PE 150 method.

ChIP-Seq data analysis

Sequencing yielded approximately 20 million paired-end reads of 150 bp per sample. Quality control of raw reads was performed in FASTQC. Adaptor trimming was carried out with TRIM-Galore 0.6.4 ( followed by mapping to reference genome in BWA-MEM253. MACS2 was used to identify narrow or broad peaks representing PHR2 binding sites (showing enrichment of FLAG-immunoprecipitated sequencing reads over input sequencing reads) from non-duplicated uniquely mapped reads54. Peaks were extracted with a threshold of 1.5-fold enrichment over INPUT and significance p-value ≤ 0.05. Fasta sequence for PHR2 binding sites and peak annotation to nearby genes were performed in samtools-1.14 and bedtools 2.29.2 respectively55,56. Read counts were normalized to CPM (Counts per Million mapped reads) and coverage was generated in deepTools 2 and visualized with IGV 2.8.957,58. Motif enrichment analysis for PHR2 binding sites was carried out in STREME ( Motif enrichment analysis for Set A + Set B genes in Fig. 3A was carried out in RSAT-oligo-analysis ( GO enrichment on Set A + Set B genes was performed in AgriGO. The search for P1BS or P1BS-like motifs in the sequences 3000 bp regions (upstream of TSS) for PHR2 target genes identified in the two ChIP-Seq replicates separately and for genes with repression in phr2, was performed with RSAT-dna-pattern (


ChIP was performed as mentioned above. Input DNA and FLAG- and IgG-immunoprecipitated DNA from three independent ChIP experiments were used for qPCR. qPCR was conducted with primers indicated in Supplementary Table 2 and TransScript® Green qRT-PCR SuperMix (TransGen Biotech, Beijing, China) on a Bio-Rad CFX384 qPCR cycler (Bio-Rad Laboratories, Shanghai, China).

rac-GR24 treatment

Plants inoculated with 500 spores of R. irregularis as described above were treated with a synthetic analog of strigolactone, rac-GR24 (Chiralix, CX23880). rac-GR24 was dissolved at 10 mM concentration in 100% acetone to make stocks and directly added to the Hoagland medium for use at 10 and 100 nM concentrations. The control solution was supplied with equal amounts of acetone. Plants were watered 2 times per week for 6 weeks. At 6 weeks, roots were harvested for acid-ink staining and quantification of colonization.

Plasmid construction

Genes and promoter regions were amplified with NEB Q5 polymerase from cDNA or genomic DNA of wild type (cv. Nipponbare), according to standard protocols and using primers indicated in Supplementary Table 3. Plasmids were constructed using Golden Gate cloning60 as indicated in Supplementary Table 4.

Transactivation assay

Transactivation assays in N. benthamiana leaves were performed as described in the following:61 Liquid cultures of A. tumefaciens Agl1, carrying the desired plasmids were set up (1 ml culture per ml used for infiltration of N. benthaminana leaves) and incubated at 28 °C with 180 rpm horizontal shaking. After 1.5 days the cultures were transferred to 15 ml or 50 ml Falcon tubes and spun down 30 min at 4500 rpm. The pellets were resuspended in 1 ml of Agrobacterium infiltration mix (AIM) (10 mM MES pH 5,6, 10 mM MgCl2, 150 µM acetosyringone). The OD600 value of 1:100 dilutions of the bacterial suspensions were measured and set to 1 by dilution with AIM. Then, 6 ml of a mixture were prepared by adding 1 ml of each culture carrying the desired plasmid for the respective mixture. Contained in the 6 ml per combination was also 1 ml of culture carrying the P19 plasmid, coding for a silencing suppressor. If less than five plasmids were included in one combination, a bacterial culture carrying the placeholder plasmid pMP200 was used, to ensure that the ratio among infiltrated cultures remained the same for all treatments.

The final mixtures were incubated for 1–2 h in the dark at room temperature. Each combination was then infiltrated in three leaves of respectively four N. benthamiana plants of the same age and size, by injecting the bacterial solution into the bottom side of the leaf with a syringe. The plants were watered up to twice a day if required and grown two days in a climate chamber with the following conditions: 24 °C, 60% humidity, 8 h dark, 16 h light. Then, three leaf disks of 1 cm diameter were collected from each transformed leaf and transferred to 2 ml Eppendorf tubes containing respectively one glass bead, frozen in liquid nitrogen and stored at −80 °C.

One set of the leaf disks frozen in liquid nitrogen was ground in a tissue lyser with racks precooled to −80 °C, 2×1 min at 30 Hz. Then, the tubes containing the powdered plant material were placed back into liquid nitrogen. Subsequently, 300 µl of extraction buffer were added to the tubes that were then thawn on ice until the powder had dissolved in the buffer. Then, the tubes were centrifuged at 4 °C for 15 min at 15000 rpm and 170 µl of the supernatant of each tube was transferred to one well of a non-skirted low profile 96-well plate, stored on ice. To a second 96-well plate 100 µl of assay buffer were added in each well corresponding to the wells on the first plate containing the leaf protein extract. The plate with the assay buffer was then sealed and put at 37 °C. In the meantime, five black 96-well plates, labeled corresponding to 5 timepoints (t0, t1 t2 t3 t4), were filled with 100 µl of 0.2 M Na2CO3. To start the assay 10 µl of the protein extract were transferred to the corresponding wells on the plate with the assay buffer and at five predefined time points (t0 = 0 min, t1 = 7 min, t2 = 14 min, t3 = 21 min, t4 = 28 min) 10 µl from the assay plate were transferred to the corresponding wells on the corresponding black plate. As a standard curve for the formed product 10 µl a dilution series of 4-MU (1, 0.5, 0.25, 0.125, 0.0625, 0.03125, 0.015625, and 0.0078125 µM) in extraction buffer were transferred to 100 µl of 0.2 M Na2CO3 in duplicate. To normalize the enzymatic activity to the amount of protein, a transparent 96-well plate was filled with 100 ml Bradford reagent per well and 1 µl from the respective wells containing the protein extract was added. To create a standard curve for the Bradford reaction, 2 µl of a dilution series of BSA in ddH2O (5, 2.5, 1.25, 0.625, 0.3125, 0.15625, 0.078125, and 0.0390625 mg/ml) were added to 100 µl of Bradford reagent in duplicate. The composition of buffers used for the transactivation assay is presented in Supplementary Table 5.

Root exudate collection

Dehusked rice seeds were surface sterilized by incubating in absolute Ethanol for 2 min, then immersing twice in 3.5% Sodium hypochlorite solution for 15 min and rinsing three times with demineralized sterile water (15 min per rinse). Seeds were germinated on 1.5% 1/2 MS-agar at 22 °C in darkness for 1 week. Subsequently, germinated seedlings were exposed to light and grown for two weeks in a long-day photoperiod (16 h light/8 h dark) with 60% relative humidity in the same temperature conditions. Two seedlings were transferred to 7×7×8 cm pots filled with autoclaved sand (seven replicates of two seedlings per genotype). The plants were grown for 3 weeks in a chamber set at 22 °C in a long-day photoperiod (16 h light/8 h dark) with 60% relative humidity. Each pot was supplied with demineralized sterile water for two weeks and then with 1/2 Hoagland’s solution containing 25 µM phosphate for one week. Root exudates were collected by adding and draining 150 mL water (containing 5% ethanol) through each pot. The exudates were frozen using liquid nitrogen and stored at −80 °C until use.

Strigolactone quantification

Isolation of strigolactones from root exudates was carried out as reported previously24. The analyte 4-deoxyorobanchol and the internal standard rac-GR24 were obtained from Olchemim (Olomouc, Czech Republic). The extracts were analyzed on a QTrap 6500+ mass spectrometer (Sciex, Darmstadt, Germany) operating in the positive electrospray ionization (ESI+) mode. The following ESI source parameters were used: ion spray voltage (5500 V), source temperature (550 °C), turbo gas (55 psi), heater gas (65 psi). MS/MS analysis was performed in the multiple reaction monitoring (MRM) mode and individual MS parameters were optimized by collision-induced dissociation after individually infusing the pure references (rac-GR24, 4-deoxyorobanchol) or the exudate extract (putative methoxy-5-deoxy strigol isomers) via a syringe pump into the mass spectrometer. For compound quantification, the specific mass transition of 4-deoxyorobanchol (331.0 → 185.0), putative methoxy-5-deoxy strigol isomers (361.0 → 97.0), and internal standard rac-GR24 (299.0 → 96.9) were used. The exudate extracts were separated on an ExionLC UHPLC system (Shimadzu, Duisburg, Germany), equipped with two ExionLC AD pump systems, an ExionLC degasser, an ExionLC AD autosampler, an ExionLC AD column oven and an ExionLC controller. Chromatographic separation was performed at a flow rate of 0.45 mL/min on 100 × 2.1 mm, 100 Å, 1.7 μm Kinetex C18 column (Phenomenex, Aschaffenburg, Germany) at 45 °C. The solvents used for chromatography were aqueous formic acid (0.1%) as eluent A and acetonitrile (0.1% formic acid) as eluent B. The following gradient was used based on reports from the literature24 with slight modifications: 0.0–1.0 min (15% B), 1.0–5.0 min (40% B), 5.0–8.0 min (65% B), 8.0–9.0 min (65% B), 9.0–10.0 min (100% B), 10.0–11.0 min (100% B), 11.0–12.0 min (15% B), 12.0–13.0 min (15% B). The Analyst software (version 1.6.3) was used for data acquisition and processing.

Phylogenetic analysis of PHR proteins

Arabidopsis AtPHR1 was used to find close homologs in other plant species. Following this, Clustal Omega 1.2.4 ( was used for multiple sequence alignment (MSA) of amino acid sequences for PHR proteins and homologous MYB TFs from AM-incompetent species (Arabidopsis thaliana and Brassica rapa), monocotyledon AM-host species (Oryza sativa, Zea mays, and Sorghum bicolor) and dicotyledon AM-host species (Lotus japonicus, Medicago truncatula, and Solanum lycopersicum).

Based on the MSA, a tree was constructed using “Minimum evolution with 1000 bootstrap” in MEGA ( This tree was further modified in MEGA using “Maximum likelihood”.

Greenhouse experiment

The soil was collected from a rice field at Longhua base in Shenzhen, China, which was inundated for a long period and then land-prepared prior to rice seeding. A long-inundated and land-prepared field was chosen to ensure soil with very low amounts of infective AM fungal propagules41,62,63. The soil properties were as follows: pH 5.5, total nitrogen 1.73 g·kg−1, total phosphorus 0.72 g·kg−1, total potassium 29.3 g·kg−1, organic carbon 22.5 g·kg−1, alkali hydrolysable nitrogen 216 mg·kg−1, Olsen phosphorus 36.7 mg·kg−1, available potassium 115.0 mg·kg−1.The experiment was conducted in the greenhouse of Shenzhen Research Institute, Chinese University of Hong Kong, Shenzhen, Guangdong, China (22° 32 ′N, 113° 56 ′E). The temperature, sunlight, and humidity of the greenhouse used in the experiment are shown in Fig. Supplementary Fig. 16. Rice seeds were germinated and grown for 2 weeks on MS-agar. The seedlings were then transplanted to pots (each plant was put into a 4 cm × 4 cm area and 15 cm height pot) filled with collected field soil and were mock-inoculated or inoculated with R. irregularis (1500 spores; Agronutrition, Toulouse, France). Pure AMF spores (applied to a thin quartz sand layer) were placed at the depth of 2.5 cm from the soil surface in inoculated samples while for non-inoculated samples only a thin sand layer was included. Plants were grown in a greenhouse at around 22–32 °C (Supplementary Fig. 16) till 110 days post transplanting (dpt) and irrigated with tap water once surface soil dried so that the water layer of 2–3 cm got restored. All plants were fertilized once with urea (100 mg per pot) and potash (75 mg per pot) at 40 dpt before panicle initiation. HP samples were fertilized with superphosphate fertilizer, P2O5 at 75 mg/pot (every 20 days) while LP plants were not fertilized with superphosphate at all. Plants reached the panicle initiation stage at around 40–45 dpt and flowering started at around 75–80 dpt. At 110 days post transplanting, plant height and panicle length were determined and roots were harvested for quantification of root fresh weight, AM colonization, and gene expression analysis by RT-qPCR. Plants were air-dried for 1 week and quantified for shoot dry weight, seed setting (percentage of filled grains per total grains) and 1000 grain weight ([total grain weight per plant/total no. of grains per plant] * 1000). Further, shoots were oven-dried at 80 °C and ground to powder for shoot phosphorus determination according to the previous description64.

Statistics and graphics

Data were statistically analyzed and presented graphically using R statistical environment ( or Prism 8.0 (GraphPad, USA), respectively.

Reporting summary

Further information on research design is available in the Nature Research Reporting Summary linked to this article.