CRISPR/Cas9‐mediated knockout and overexpression studies reveal a role of maize phytochrome C in regulating flowering time and plant height

Summary

Maize is a major staple crop widely used for food, feedstocks and industrial products. Shade‐avoidance syndrome (SAS), which is triggered when plants sense competition of light from neighbouring vegetation, is detrimental for maize yield production under high‐density planting conditions. Previous studies have shown that the red and far‐red photoreceptor phytochromes are responsible for perceiving the shading signals and triggering SAS in Arabidopsis; however, their roles in maize are less clear. In this study, we examined the expression patterns of ZmPHYC1 and ZmPHYC2 and found that ZmPHYC1, but not ZmPHYC2, is highly expressed in leaves and is regulated by the circadian clock. Both ZmPHYC1 and ZmPHYC2 proteins are localized to both the nucleus and cytoplasm under light conditions and both of them can interact with themselves or with ZmPHYBs. Heterologous expression of ZmPHYCs can complement the Arabidopsis phyC‐2 mutant under constant red light conditions and confer an attenuated SAS in Arabidopsis in response to shading. Double knockout mutants of ZmPHYC1 and ZmPHYC2 created using the CRISPR/Cas9 technology display a moderate early‐flowering phenotype under long‐day conditions, whereas ZmPHYC2 overexpression plants exhibit a moderately reduced plant height and ear height. Together, these results provided new insight into the function of ZmPHYCs and guidance for breeding high‐density tolerant maize cultivars.

Introduction

Maize (Zea mays ssp. mays) is the world’s highest producing crop now and widely cultivated across all major continents, with an annual planting area of ~197 185 936 hectares (FAO statistics, http://www.fao.org/faostat/zh/#data/QC). Over the past few decades, increasing planting density has made an important contribution to the constant yield increases in the United States, China and other countries (Lee and Tollenaar, 2007; Mansfield and Mumm, 2014; Tollenaar and Lee, 2002). However, shade‐avoidance syndrome (SAS), which is triggered when plants sense a reduction of red‐to‐far‐red light ratios (R:FR < 1.0) in the dense canopy, is detrimental to maize yield production due to increased plant height (and ear height, and less lodging‐resistant), prolonged anthesis–silking interval (ASI), deteriorated tassel development and reduced carbohydrate transport to grains (Boccalandro et al., 2009; Dubois and Brutnell, 2011; Duvick, 2005a; Duvick, 2005b; Gonzalo et al., 2010; Ku et al., 2015). Therefore, dissecting the molecular mechanisms of SAS in maize could provide useful guidance for breeding of high‐density‐tolerant maize cultivars.

Previous studies in Arabidopsis and other plant species have shown that phytochromes (phys), the red/far‐red light photoreceptors, are responsible for perceiving the decline of red‐to‐far‐red light ratios (R:FR) under canopy shade conditions and subsequent triggering of SAS. Arabidopsis has five phy members, phyA‐phyE. Among them, phyA belongs to type I (light labile) phy, and phyB to phyE are type II (light stable) phys (Li et al., 2011). phyA is the primary photoreceptor for far‐red light and is responsible for mediating far‐red high‐irradiation response (FR‐HIR) and the very‐low‐fluence response (VLFR), and phyB‐phyE are the photoreceptors for red light‐mediated low‐fluence response (LFR), with phyB playing a major role (Franklin and Quail, 2010; Wang and Wang, 2015).

Phys exist in two forms: the red‐absorbing inactive Pr form and the far‐red‐absorbing biologically active Pfr form (Rockwell et al., 2006). The Pr and Pfr conformers can be converted to each other depends on the R:FR ratio. Under high R:FR, red light induces a Pr‐to‐Pfr conformational shift that promotes the translocation of Pfr‐phys into the nucleus to suppress SAS. Under low R:FR, FR converts the Pfr form of phys to the Pr form, and then SAS is induced. More recently, numerous studies showed that phys (mainly phyB) act to repress SAS through regulating the degradation or phosphorylation of phytochrome‐interacting factor (PIF) proteins and then downstream transcriptional regulatory networks (Leivar et al., 2012; Lorrain et al., 2008; Mansfield and Mumm, 2014; Mizuno et al., 2015; Xie et al., 2017).

Studies with loss‐of‐function phyC mutants in Arabidopsis have revealed that in addition to serving as a weak red light sensor in mediating seedling depolarization and cotyledon enlargement, phyC is also a flowering repressor under short‐day (SD) conditions (Franklin et al., 2003; Monte et al., 2003). In rice, phyC plays an important role in FR‐mediated inhibition of coleoptile elongation and the repression of flowering under long‐day (LD) conditions (Takano et al., 2005). A role for phyC in plant architecture development and flowering time has also been reported in other plants (Chen et al., 2014; Nishida et al., 2013; Saïdou et al., 2009; Takano et al., 2005).

The maize genome contains a pair of duplicated genes for PHYA, PHYB and PHYC, named PHYA1, PHYA2, PHYB1, PHYB2, PHYC1 and PHYC2 (Sheehan et al., 2004). Limited studies have shown that the maize elongated mesocotyl1 (elm1) mutant (which is defective in the ZmHY2 gene encoding phytochromobilin synthase) and the maize phyB1 phyB2 double mutant have elongated internodes and are prone to lodging (Kebrom et al., 2010; Kebrom et al., 2006; Sheehan et al., 2007), whereas overexpression of ZmPHYA1 causes increased plant and ear height in maize (Yu et al., 2018). In addition, phy‐mediated signalling has been shown to be involved in shade suppression of axillary bud outgrowth in maize (Kebrom et al., 2010; Kebrom et al., 2006; Whipple et al., 2011). However, the roles of ZmPHYC1 and ZmPHYC2 in regulating plant development, flowering time and SAS have not been reported yet.

In this study, we investigated the expression patterns and molecular properties of ZmPHYC1 and ZmPHYC2. Heterologous expression in Arabidopsis revealed a conserved function of ZmPHYCs in regulating seedling photomorphogenesis, flowering time and SAS. Using CRISPR/Cas9 technology, we generated zmphyC1 zmphyC2 double knockout mutants and these mutants showed a moderate early‐flowering phenotype under LD conditions. Moreover, we found that overexpression of ZmPHYC2 caused a moderate reduction in plant height and ear height. Our results suggest that ZmPHYC1 and ZmPHYC2 can be used as potential targets for genetic engineering of maize to improve flowering time and plant architecture suitable for high‐density planting.

Results

ZmPHYC1 and ZmPHYC2 proteins have the conserved functional regions

The two homologs ZmPHYC genes [ZmPHYC1 (Zm00001d034038‐T002) and ZmPHYC2 (Zm00001d013262‐T004)] were isolated from maize B73 inbred line according to the corresponding annotated sequence. Multiple sequence alignment showed that ZmPHYC1 and ZmPHYC2 proteins have highly conserved domains including a PAS‐2 domain, a cGMP‐specific phosphodiesterases/adenyl cyclase/FhlA (GAF) domain, a phytochrome (PHY) domain, two PAS domains, a His Kinase A (HisKA) domain and a histidine kinase‐like ATPase (HATPase_c) domain (Figure S1). A phylogenetic tree with the sequences of PHYC proteins from Arabidopsis, rice and maize was constructed, and the results indicated that ZmPHYC1 and ZmPHYC2 belong to the type II phy proteins and they share the highest similarity with PHYC of rice (OsPHYC) (Figure 1a).

Figure 1.

Phylogenetic tree and ZmPHYC expression features. (a) Phylogenetic tree of maize phytochrome homologues. At, Os and Zm represent Arabidopsis thaliana, Oryza sativa, and Zea mays, respectively. Full‐length protein sequences of PHYC were obtained from the Gramene database (http://ensembl.gramene.org/genome_browser/index.html) and used to construct the phylogenetic tree with MEGA7 software using the neighbor‐joining method. ZmPHYC1 and ZmPHYC2 are marked with red rectangle. (b) RT‐qPCR analysis shows that ZmPHYC1 and ZmPHYC2 are expressed in multiple tissues. Six‐leaf stage seedling of the maize inbred line B73 were used to harvest different tissues for RNA extraction. (c and d) Diurnal expression patterns of ZmPHYC1 and ZmPHYC2 in maize inbred line ZC01 leaves under artificial LD (c) and SD (d) conditions. The gray shadows indicate the dark period. The leaves of three‐leaf stage ZC01 seedlings were harvested at different time points under LD or SD conditions. ZT, zeitgeber time. The data are relative to the control gene Tubulin 5 and represent means ± SD of three biological replicates. LD, long‐day; SD, short‐day.

Gene expression pattern and subcellular localizations of ZmPHYC1 and ZmPHYC2 proteins

To study the expression profiles of ZmPHYC genes in maize plants, tissues from different organs of B73 were collected from plants at the six‐leaf stage grown in a growth room. The results showed that both ZmPHYC genes were expressed in all organs examined and that ZmPHYC1 was expressed at higher levels than ZmPHYC2 in all organs (Figure 1b), which was in line with the transcriptomic data of maize B73 (Figure S2). The diurnal expression patterns of ZmPHYCs were also monitored under artificial LD and SD conditions (Figure 1c and d). Under both LD and SD conditions, the expression of ZmPHYC1, but not ZmPHYC2, showed an obvious diurnal oscillation pattern. Expression of ZmPHYC1 peaked at 4 h after dusk (20 h at zeitgeber time) under LD conditions or at the 4 h after dusk under SD conditions (Figure 1c). The distinct temporal expression patterns of the ZmPHYC1 and ZmPHYC2 suggest that subfunctionalization may have occurred between them.

To elucidate the localization pattern of ZmPHYCs in cells, we construct a ZmPHYCs‐GFP fusion protein constructs, which were then transiently expressed by infiltration in N. benthamiana leaves. As shown in Figure S3, the florescent signals of ZmPHYC1‐GFP and ZmPHYC2‐GFP fusion proteins were observed both in the nucleus and cytoplasm under light conditions.

ZmPHYC1 and ZmPHYC2 proteins can interact with themselves and ZmPHYBs

Previous studies have reported that phyC is predominantly exists as heterodimers or homodimer in plant cells for function (Chen et al., 2014; Monte et al., 2003; Takano et al., 2005). Thus, we examined the interactions of ZmPHYCs with themselves or with other phy proteins using LCI and BiFC assays in N. benthamiana leaf cells. As expected, LCI assays showed that ZmPHYCs could interact with other maize type II phy proteins, ZmPHYB1 and ZmPHYB2 (Figure S4a). Interestingly, ZmPHYC1 and ZmPHYC2 proteins could also interact with themselves and their homologues (Figure S4b). BiFC assays also verified that ZmPHYC proteins could interact with themselves and with ZmPHYB1 and ZmPHYB2 in the nucleus of N. benthamiana leaf epidermal cells (Figure S4c). No visible fluorescence signal was detected in the negative controls (Figure S4d). These observations suggest that the interaction with other phytochrome proteins may be required for ZmPHYCs to perform their functions.

Overexpression of ZmPHYC1 and ZmPHYC2 rescues the phenotype of Arabidopsis phyC‐2 mutants

The Arabidopsis phyC‐2 mutant displays a long‐hypocotyl phenotype under continuous red light conditions (Franklin et al., 2003; Monte et al., 2003). To examine whether ZmPHYC1 and ZmPHYC2 could have PHYC functions, we tested whether they could complement the phyC‐2 phenotype by generating ZmPHYC1‐OE and ZmPHYC2‐OE plants in the Arabidopsis phyC‐2 mutant background (Figure S5a and b). In darkness, all of the ZmPHYCs‐OE lines had normal seedling development and exhibited similar hypocotyl lengths without significant differences (Figure 2a and b). When ZmPHYC1 and ZmPHYC2 were overexpressed in the phyC‐2 background, their hypocotyls were significantly reduced relative to phyC‐2 under continuous red light (Figure 2a and c). The result suggests that both ZmPHYC1 and ZmPHYC2 have conserved function as AtPHYC.

Figure 2.

Heterologous expression of ZmPHYC1 and ZmPHYC2 rescues the elongated hypocotyl phenotype of the Arabidopsis phyC‐2 mutant under constant red light (Rc) conditions. (a) Representative 4‐d‐old seedlings of ZmPHYC1‐OE and ZmPHYC2‐OE transgenic lines in the phyC‐2 mutant background either grown in the darkness (Dk) or under Rc (30 μmol photons m⁻² s⁻¹). Bars = 2 mm. (b and c) Quantification of hypocotyl lengths of the seedlings shown in (a). Data represent the mean and SD of at least 20 seedlings. Statistical significance analyses were performed between the transgenic plants and phyC‐2 mutant plants according to student’s t‐test. ∗ P < 0.01.

We also tested the effect of ZmPHYCs on flowering in the Arabidopsis phyC‐2 mutant background. Unexpectedly, the ZmPHYC1‐ and ZmPHYC2‐overexpression Arabidopsis plants flowered earlier than phyC‐2 in LD photoperiods (Figure S6), indicating a promoting role of ZmPHYC1 and ZmPHYC2 in the regulation of flowering time.

ZmPHYC1 and ZmPHYC2 are involved in the control of seedlings de‐etiolation under continuous red (Rc) and continuous blue (Bc) light conditions

To investigate the effect and the possible roles of ZmPHYCs in regulating seedling photomorphogenesis, we also overexpressed ZmPHYCs (ProUbi::ZmPHYCs‐GFP) in the Arabidopsis wild‐type Col‐0 background. Two independent overexpression lines for ZmPHYC1 (OE5 and OE8) and two independent overexpression lines ZmPHYC2 (OE4 and OE6) were selected and used to perform further analyses (Figure S5c and d). All the seedlings have no apparent differences in the dark (Figure 3a and b). However, the hypocotyls of all the transgenic lines were significantly shorter than those of Col‐0 in Rc and Bc conditions at the indicated light intensities, which indicates that both ZmPHYC1 and ZmPHYC2 can participate in inhibiting hypocotyl elongation growth in Arabidopsis under Rc and Bc (Figure 3a, c, e). Under FRc, ZmPHYCs‐OE seedlings failed to suppress the hypocotyl elongation (Figure 3d), indicating that ZmPHYCs do not play a major role in the control of hypocotyl elongation in FRc.

Figure 3.

Overexpression of ZmPHYC1 andZmPHYC2 confers a hypersensitive response to red and blue light, but not far‐red light. (a) Phenotype of Col‐0 (wild type), phyC‐2 mutant, ZmPHYC1‐OE and ZmPHYC2‐OE transgenic lines (in the wild‐type Col‐0 background) grown in continuous darkness (Dk), red (Rc, 30 μmol photons m⁻² s⁻¹), far‐red (FRc, 2.1 μmol photons m⁻² s⁻¹) or blue (Bc, 1.0 μmol photons m⁻² s⁻¹) light conditions for 4 days. Bars = 2 mm. (b‐e) Quantification of hypocotyl length of the seedling plants shown in (a). Data represent the mean and SD of at least 20 seedlings. Different letters indicate significant differences according to Bonferroni corrected (P < 0.05).

Further, we checked the fluence‐rate response of all the ZmPHYC1‐OE/Col and ZmPHYC2‐OE/Col transgenic lines under Rc, FRc and Bc conditions (Figure S7). Comparative fluence‐response curves for hypocotyl growth indicated that both ZmPHYC1‐OE and ZmPHYC2‐OE transgenic lines were hypersensitive to Rc from low‐fluence rates (1.6 μmol/m²/s) to high‐fluence rates (34 μmol/m²/s) tested (Figure S7, left panel). The growth suppression of hypocotyl length was only detected at low‐fluence rate (1.0 and 1.4 μmol/m²/s) of Bc (Figure S7, middle panel). However, there was no significant difference for the hypocotyl lengths in different genotype plants under different fluence rates of FRc (Figure S7, right panel). Taken together, these results demonstrate that ZmPHYCs are mainly involved in red and blue light‐mediated seedling photomorphogenesis.

Overexpression of ZmPHYC1 and ZmPHYC2 attenuates responses to EOD‐FR treatment in Arabidopsis

We next tested whether overexpression of ZmPHYCs could alleviate SAS in Arabidopsis. Seedlings of Col‐0, phyC‐2 and ZmPHYCs‐OE/Col‐0 plants were either grew under normal white light (WL) conditions or a simulated shade condition, in which the seedlings were given an end‐of‐day FR light treatment (EOD‐FR). When grown under normal WL conditions (high R:FR), the hypocotyl lengths had no significant difference between the transgenic lines and the wild‐type plants. While under EOD‐FR treatment, the ZmPHYC1 and ZmPHYC2 overexpression lines exhibited obviously shorter hypocotyls compared with the wild‐type plants (Figure 4a, b), indicating an attenuated shade‐avoidance response. RT‐qPCR analysis confirmed that the expression levels of four genes, LONG HYPOCOTYL IN FAR‐RED1 (HFR1), YUCCA2 (YUC2), ATHB‐2 (HB‐2) and PIF3‐LIKE1 (PIL1), known to be shade‐induced marker genes (Li et al., 2012; Zhang et al., 2013), were lower in the ZmPHYC1 or ZmPHYC2 overexpression lines than Col‐0 after EOD‐FR treatment (Figure 4c). Altogether, these results suggest that the ZmPHYCs act to repress SAS in Arabidopsis.

Figure 4.

Overexpression of ZmPHYC1 and ZmPHYC2 confers an attenuated response to simulated shade treatment in Arabidopsis. (a) Phenotypes of Arabidopsis seedlings grew under normal white light (WL, 55.55 μmol photons m⁻² s⁻¹) or subjected to EOD‐FR treatment. Seedlings of Col‐0 wild type, phyC‐2, ZmPHYC1‐OE and ZmPHYC2‐OE (in the Col‐0 background) were grown under WL conditions for 2 d, and then were kept in WL or treated with FR light (30 μmol m⁻² s⁻¹) for 30 min at the end of the light period (EOD‐FR treatment) for 5 d before photographing. (b) Quantification of hypocotyl lengths for Col‐0, phyC‐2 mutant, and ZmPHYC1 or ZmPHYC2 transgenic lines grown as in (a). Data represent the mean and SD from at least 20 seedlings. Different letters indicate significant differences (P < 0.05) according to Bonferroni corrected. Bars = 2 mm. (c) Overexpression of ZmPHYC1 and ZmPHYC2 reduces the expression levels of shade response related genes in Arabidopsis. The expression of marker genes including HFR1, YUC2, HB2 and PIL1 was analyzed by RT‐qPCR in 4‐d‐old seedlings grown under WL or subjected to EOD‐FR treatment. ACT2 was used as the internal control. Data are means and SD of three independent biological replicates.

zmphyC1 zmphyC2 double knockout mutants display an early‐flowering phenotype under LD conditions

In order to further investigate the function of ZmPHYCs in maize growth and development, we generated zmphyC1 zmphyC2 double knockout mutants in the maize inbred line ZC01 background using the CRISPR/Cas9 technology (Figure 5a, b). Three homozygous lines, named KO#1, KO#3 and KO#7, were identified in the T₁ generation and selfed for two additional generations to produce T₃ seeds (Figure 5c). T₃ homozygous plants without CRISPR vector were planted in natural LD and SD conditions for phenotype observation and statistical analysis. Phenotypic investigation results showed that all the three zmphyC1 zmphyC2 double mutant lines flowered (anthesis) earlier than wild‐type and transformation control plants (CK, null segregates with wild‐type ZmPHYC1 and ZmPHYC2 genes) for 4 to 6 days under LD conditions (Figure 5d and e), without significant differences in the total leaf number between the mutant lines (except KO#3), CK (null segregate) and WT plants (Figure 5f). There were no obvious differences in plant height and ear height between the zmphyC1 zmphyC2 mutant lines compared with WT and CK plants, except for KO#3, which had a slight shorter plant height and ear height (Figure 5g and h). It was worth mentioning that the zmphyC1 zmphyC2 double mutants did not show an early‐flowering phenotype under SD conditions (Figure S8). These results suggest that ZmPHYCs mainly play a repressive role in flowering under LD conditions.

Figure 5.

The zmphyC1 zmphyC2 double knockout mutants display a modest early‐flowering phenotype under natural LD conditions. (a) Diagram showing the two target sites on the ZmPHYC1 and ZmPHYC2 genes, respectively. (b) Diagram illustrating the sgRNA expression cassettes targeting ZmPHYC1 and ZmPHYC2 genes via the dual‐sgRNAs CRISPR/Cas9 vector system. (c) Sequence analysis of the target sites in three homozygouszmphyC1 zmphyC2 double knockout lines. The wild type (WT) sequence is shown at the top. The target sites and protospacer‐adjacent motif (PAM) sequences are shown in the antisense strand and highlighted in red and boldface fonts, respectively. Red and black short dashed lines indicate deletions. Inversions and insertions are indicated by green and blue fonts, respectively. The sequence gap length is shown above or under the sequences. (d) Gross morphologies of WT, CK (null segregates with wild‐type ZmPHYC1 and ZmPHYC2 genes) and zmphyC1 zmphyC2 double knockout plants at flowering (anthesis) under natural LD conditions. Bars = 20 cm. (e‐h) Days to anthesis (e), leaf number (f), plant height (g), and ear height (h) in WT, CK and three knockout lines under natural LD conditions. Data represent the mean and SD from at least 10 maize plants. Different letters indicate significant differences (P < 0.05) according to Bonferroni corrected. (i and j) Transcript profiles of ZCN8 (i) and CONZ1 (j) in the WT (blue lines) and double zmphyC1 zmphyC2 mutant (red lines) plants. The data are relative to the control gene Tubulin 5 and represent means ± SD of three biological replicates. Plants were grown under artificial LD and SD conditions. The gray shadows indicate the dark period. ZT, zeitgeber time.

To understand how ZmPHYCs affect flowering at a molecular level, we examined the expression patterns of several known photoperiod and circadian clock genes, including ZCN8, CONZ1, ZmCCT9 and ZmCCA1 (Huang et al., 2018; Lazakis et al., 2011; Meng et al., 2011; Miller et al., 2008; Yang et al., 2013). Seven‐leaf stage of WT and zmphyC1 zmphyC2 mutants grew under artificial LD and SD conditions were used for RNA extraction and gene expression analysis. As shown in Figure 5i, ZCN8, which encodes the maize florigen and functions as a floral activator (Lazakis et al., 2011; Meng et al., 2011), exhibited increased expression in the zmphyC1 zmphyC2 mutants compared with WT plants for all the sampling points during LD conditions, which is in line with their phenotypes. Next, we examined the expression levels of CONZ1, a key factor of the photoperiod pathway in maize (Miller et al., 2008). The CONZ1 waveform in the zmphyC1 zmphyC2 mutant correlated well with that of ZCN8 under LD conditions, with peak expression at midnight (20 h) (Figure 5j). While under SD conditions, the expression of CONZ1 was nearly the same between the zmphyC1 zmphyC2 mutant and WT (Figure 5j). Interestingly, there was no significant difference in the expression of ZmCCT9 and ZmCCA1 between WT and the zmphyC1 zmphyC2 mutant plants (Figure S9), suggesting that the expression of ZmCCT9 and ZmCCA1 is not regulated by ZmPHYCs.

Overexpression of ZmPHYC2, but not ZmPHYC1, modestly reduces maize plant height

We also generated ZmPHYC1 and ZmPHYC2 overexpression lines in the maize inbred line ZC01. Two independent transgenic maize plants (OE3 and OE8 for ZmPHYC1, OE7 and OE12 for ZmPHYC2) with high expression levels of ZmPHYCs (Figure 6a, b) were selected and used for subsequent analyses. We observed that the plant height and ear height of the ZmPHYC2‐OE lines, but not that of the ZmPHYC1‐OE plants, were modestly reduced compared to WT plants, although they had similar total leaf numbers compared with WT (Figure 6c‐f). No significant differences in flowering time were observed in these overexpression lines under LD conditions, compared with the WT plants (Figure 6g).

Figure 6.

Overexpression of ZmPHYC2 reduces plant height and ear height in maize. (a and b) RT‐qPCR analysis show that ZmPHYC1 and ZmPHYC2 are highly expressed in the maize ZmPHYCs overexpression plants. Three‐leaf stage maize seedlings of wild type (WT), ZmPHYC1‐OE and ZmPHYC2‐OE transgenic plants were used to perform RT‐qPCR analysis. The mRNA level of Tublin5 was used as a reference. Data are means and SD of three independent biological replicates. (c) The plant height of WT and the transgenic plants overexpressing ZmPHYC2 in maize under natural long‐day (LD) conditions. Bar = 20 cm. (d‐g) Comparison of plant height (d), ear height (e), leaf number (f), and days to anthesis (g) between WT, ZmPHYC1‐OE and ZmPHYC2‐OE lines under natural LD conditions. Data represent the mean and SD from at least 10 maize plants. Different letters indicate significant differences (P < 0.05) according to Bonferroni corrected.

Discussion

ZmphyCs function as type II phytochromes in regulating seedling photomorphogenesis and SAS

In this study, we showed that heterologous expression of both ZmPHYC1 and ZmPHYC2 complemented the phenotype of Arabidopsis phyC‐2 mutant under constant red light conditions and that overexpression of ZmPHYC1 and ZmPHYC2 in Arabidopsis (wild‐type background) conferred a hypersensitive response (shorter hypocotyls) to red and blue light irradiation, but not to constant far‐red light (Figures 2 and 3), indicating that ZmphyC1 and ZmphyC2 indeed function as type II phytochromes, as the Arabidopsis and rice phyCs, which have been shown to play a minor role in early seedling development and shade‐avoidance responses in Arabidopsis and rice, respectively (Franklin et al., 2003; Takano et al., 2005). In addition, we showed that overexpression of ZmPHYCs in Arabidopsis significantly reduced the hypocotyl elongation under EOD‐FR treatment (Figure 4), indicating that ZmPHYCs also participate in SAS regulation in Arabidopsis. Together, these results suggest that both of ZmphyC1 and ZmphyC2 function as type II phytochormes and act similarly as AtphyC in mediating seedling photomorphogenesis and SAS. Consistent with this notion, we found that ZmPHYCs could form homodimers with themselves or with their homologs as well as form heterodimers with ZmPHYBs (Figure S4), similar to wheat PHYC (Chen et al., 2014). However, it was shown that Arabidopsis phyC could not bind to itself in vivo and it only forms heterodimers with phyB (Clack et al., 2009; Sharrock and Clack, 2004). Thus, whether homodimerization is a general feature for monocots and dicots PHYCs remains to be further investigated.

It is notable that we showed that although both ZmPHYC1 and ZmPHYC2 are actively expressed in all tissues examined, ZmPHYC1 has significantly higher expression levels than ZmPHYC2 (Figure 1b, S2). In addition, it appears that the expression of ZmPHYC1, but not ZmPHYC2, is subject to regulation by the circadian clock (Figure 1c and d). These results suggest that subfunctionalization may have occurred between them. Consistent with this, we found that overexpression of ZmPHYC2, but not ZmPHYC1, causes a modest reduction in the plant height and ear height in the transgenic maize plants (Figure 6). Future studies are required to elucidate the functional differentiation of ZmPHYC1 and ZmPHYC2 in regulating different developmental and physiological processes.

ZmPHYCs as potential targets for fine‐tuning plant height of maize cultivars for adapting to high‐density planting

Previous studies have shown that high‐density tolerant maize inbred and hybrids lines are characterized with several important morphological changes in plant architecture, including reduced ear height and increased culm strength for lodging resistance (Dubois and Brutnell, 2011; Gonzalo et al., 2010; Ku et al., 2015; Mansfield and Mumm, 2014). It is well known now that SAS causes exaggerated elongated growth, and the stalk lodging caused by high‐density planting is still a major challenge in maize production. The plant height and ear height of maize are controlled by many minor effective QTLs; thus, it is difficult and inefficient to reduce the plant height/ear height by pyramiding these QTLs through conventional maize breeding. In rice and wheat, the utilization of semi‐dwarf mutants sd1 and rht1 in the 1960s directly fostered the ‘First Green Revolution’ in crop breeding (Khush, 2001; Rutger and Mackill, 2001; Spielmeyer et al., 2002). However, in maize, some extreme dwarf mutants (such as d3, br2 etc.) could not be directly utilized in maize breeding due to strong negative effects (Multani et al., 2003; Winkler and Helentjaris, 1995). Therefore, elite semi‐dwarf maize breeding materials are still rare and highly desirable for breeding of high‐density tolerant maize cultivars that confer lodging resistant with minimal penalty on harvest index. In this study, we showed that overexpression of ZmPHYC2 conferred a modestly reduced plant height (and ear height), which may represent an ideal trait that can be introgressed into maize breeding lines to increase lodging resistance.

ZmPHYCs are of value in fine‐tuning flowering time in breeding maize cultivars for adapting to local environments

Flowering time is another important agronomic trait, which determines the regional adaptation and yield of crop cultivars. Maize was domesticated in southwestern Mexico from its progenitor teosinte (Matsuoka et al., 2002), which has strong photoperiod sensitivity, requiring SD conditions to flower (Hung et al., 2012), whereas modern maize is often characterized as day‐neutral plant and cultivated all over the world within a broad range of latitudes. The widespread latitudinal expansion of modern maize benefits from the relaxation of photoperiod sensitivity for flowering for adapting to LD environments and different latitudes (Camus‐Kulandaivelu et al., 2006; Chardon et al., 2004). Phytochromes are known to play a major role in sensing the photoperiod and flowering time control in a wide range of plant species (Childs et al., 1995; Halliday et al., 1994; Hanumappa et al., 1999; Reed et al., 1993; Sawers et al., 2002; Sheehan et al., 2007). Recently, a role of PHYC in regulating flowering time has been well established in a number of plant species, including Arabidopsis, rice, wheat, barley, Brachypodium distachyon and pearl millet (Balasubramanian et al., 2006; Chen et al., 2014; Nishida et al., 2013; Saïdou et al., 2009; Takano et al., 2005; Woods et al., 2014). We showed in this study that the zmphyC1 zmphyC2 double knockout mutants exhibited a moderate early‐flowering phenotype under LD photoperiod (Figure 5), suggesting that ZmPHYCs function as a repressor in maize flowering under LD photoperiod. This result is consisting with the reported roles of PHYC in Arabidopsis and rice under noninductive photoperiod conditions [i.e. short days for Arabidopsis and long days for rice] (Monte et al., 2003; Takano et al., 2005). Surprisingly, we observed that overexpression of ZmPHYCs promoted flowering in the Arabidopsis phyC‐2 mutant background in LD conditions (Figure S6). We speculated that the differential roles of ZmPHYCs in regulating flowering time in maize and Arabidopsis are somewhat related to maize as an original SD plant, while Arabidopsis is classified as a typical LD plant. Consistent with this notion, loss‐of‐function mutations for PHYC in wheat have strong delayed flowering under LD photoperiod, indicating that PHYC functions as a flowering accelerator under the inductive photoperiod (Chen et al., 2014).

Despite being an important agronomic trait, the genetic control of flowering in maize is still not well studied. Although a large number of quantitative trait locus (QTLs) for flowering time have been mapped in maize, only Vegetative to generative transition 1 (Vgt1) and ZmCCTs have been well characterized and found to contribute to flowering‐time adaptation (Huang et al., 2018; Hung et al., 2012; Salvi et al., 2007; Yang et al., 2013). The best known gene ZmCCT10, encoding a CCT domain‐containing protein, is a homologue of the rice photoperiod response regulator Ghd7 (Hung et al., 2012). The insertion of a Harbinger‐like transposable element (TE) in the promoter of ZmCCT9 and a CACTA‐like TE in the promoter of ZmCCT10 dramatically reduced flowering time under LD environment, and these insertions are thought to be selected during spread of maize from its tropical origin to higher latitudes (Huang et al., 2018; Yang et al., 2013). Natural variations of PHYCs have been shown to be correlated with flowering time in Arabidopsis, wheat and pearl millet (Balasubramanian et al., 2006; Chen et al., 2014; Saïdou et al., 2009); thus, it will be interesting to examine whether ZmPHYCs are targets of domestication and genetic improvement for adapting to different local environments in the future. In this study, we showed that the zmphyc1 zmphyC2 double mutants display a modest early‐flowering phenotype (4–6 days), which represents a desirable feature that can be utilized in maize breeding to expand the geographical zone of maize cultivars with minimal impact on the biomass and harvest index. Thus, ZmPHYC1 and ZmPHYC2 could serve as valuable targets of molecular breeding of maize cultivars for adapting to different local environments.

Materials and methods

Plant materials and growth conditions

The Arabidopsis thaliana phyC‐2 mutant used in this study was described by Monte et al. (2003), and the wide‐type control plants were ecotype Columbia‐0 (Col‐0). Arabidopsis seeds were sown on one‐half‐strength Murashige and Skoog (MS) solid medium containing 1% sucrose and 0.8% agar after surface sterilization and stratified at 4 °C in the darkness for 3 day. Seeds were then exposed to white light for 6 h to induce germination before further treatments.

Nicotiana benthamiana seeds were directly sown into the soil and grew in the growth house under a 16‐h light/8‐h dark cycle at 25 °C for one month before being used for the bimolecular fluorescence complementation (BiFC) and luciferase complementation imaging (LCI) assays.

The wild‐type maize inbred line used in this study was ZC01, a private receptor inbred line conducted by the China National Seed Group Co., LTD (Wuhan, China). All the mutant and transgenic lines of maize were in the ZC01 background. For field experiments, ZC01 and zmphyC knockout mutants as well as ZmPHYCs‐OE transgenic lines were planted in Langfang (39°N, 116°E), Hebei Province, China, during the summer of 2019 and in Ledong (18°N, 116°E), Hainan Province, China, during the winter of 2018. The spacing between rows and plants was set to 30 cm and 15 cm, respectively. Ten plants were selected randomly for scoring of flowering time (days to anthesis, DTA) and several other important agronomic traits including total leaf number, plant height and ear height.

Total RNA extraction and RT‐qPCR assay

Total RNA was isolated using TRIzol reagent (Invitrogen, USA), and reverse transcription reactions were performed following the manufacturer’s instructions of the FastQuant RT Kit (with gDNase) (Tiangen Biotech, China). Quantitative Real‐time PCR (RT‐qPCR) was performed using the SuperReal PreMix Plus Kit (SYBR Green) (Tiangen Biotech, China) on an Applied Biosystems Q3 real‐time PCR detection system according to the manufacturer’s manual. The transcript levels of Tubulin 5 (GRMZM2G099167) and ACT2 (AT3G18780) were used as internal controls for RT‐qPCR in maize and Arabidopsis, respectively. All the primer sequences used for RT‐qPCR above are shown in Table S1.

Expression profiling of ZmPHYCs

For maize tissue expression analysis, B73 seedlings were grown in the growth chamber under long‐day conditions (LD, 16‐h light/8‐h dark) at 28°C. Three weeks after planting, B73 seedlings were harvested and separated into roots, mesocotyls, coleoptiles and leaves for detection of the tissue expression patterns of ZmPHYCs. For circadian clock analysis, the leaves of ZC01 seedlings were harvested at different Zeitgeber times at the three‐leaf stage to measure the diurnal expression patterns of ZmPHYCs.

Plasmid construction

To generate constructs for the subcellular localization assay, the coding sequences of ZmPHYC1 and ZmPHYC2 without the terminators were amplified from cDNA of the maize inbred line B73 and cloned into the pCambia1305::GFP vector digested with XbaI. For transformation of Arabidopsis and maize, we cloned the coding regions of ZmPHYC1 and ZmPHYC2 into the CPB‐ProUbi::GFP vector (Zhao et al., 2016) through the PstI and BamHI sites to generate ProUbi::ZmPHYC1‐GFP and ProUbi::ZmPHYC2‐GFP constructs.

To generate constructs for the LCI assay, the full‐length coding regions of ZmPHYB1, ZmPHYB2, ZmPHYC1 and ZmPHYC2 were cloned into the pCAMBIA1300‐nLuc vector digested by the SalI/KpnI sites to generate ZmPHYB1‐nLuc, ZmPHYB2‐nLuc, ZmPHYC1‐nLuc and ZmPHYC2‐nLuc, respectively. The full‐length coding regions of ZmPHYC1 and ZmPHYC2 were cloned into the pCAMBIA1300‐cLuc vector digested by the SalI/KpnI sites to produce the corresponding construct ZmPHYC1‐cLuc and ZmPHYC2‐cLuc, respectively. The vectors for the LCI assay (pCAMBIA1300‐nLuc and pCAMBIA1300‐cLuc) were described previously in Chen et al. (2008).

To prepare constructs for the BiFC assay, the full‐length coding sequences of ZmPHYC1 and ZmPHYC2 were recombined into the p2YN vector at the PacI/SpeI sites to generate ZmPHYC1‐p2YN and ZmPHYC2‐p2YN, respectively. The full‐length coding sequences of ZmPHYB1, ZmPHYB2, ZmPHYC1 and ZmPHYC2 were recombined into the p2YC vector at the PacI/SpeI sites to generate ZmPHYB1‐p2YC, ZmPHYB2‐p2YC, ZmPHYC1‐p2YC and ZmPHYC2‐p2YC, respectively. The p2YN and p2YC vectors were described previously (Sun et al., 2017; Zheng et al., 2019).

All the plasmids above were constructed using an In‐Fusion HD Cloning Kit (Clontech) following the manufacturer’s protocol, and all the primers used for the constructs are shown in Table S1.

Subcellular localization analysis

The pCambia1305‐35S::ZmPHYC1‐GFP and pCambia1305‐35S::ZmPHYC2‐GFP constructs were introduced into Agrobacterium tumefaciens strain EHA105, respectively. N. benthamiana leaves were co‐injected with pCambia1305‐35S::ZmPHYC1‐GFP or pCambia1305‐35S::ZmPHYC2‐GFP together with a nuclear protein marker construct (Pro‐35S::mRFP‐AHL22) (Xiao et al., 2009). After injection, the N. benthamiana plants were incubated in darkness for 12 h and then transferred to greenhouse (16 h light/8 h dark) for 24 to 36 h. GFP and RFP signals were observed using a confocal microscopy (Zeiss LSM710).

Arabidopsis transformation and phenotypic analysis

The ProUbi::ZmPHYC1‐GFP and ProUbi::ZmPHYC2‐GFP constructs were transformed into Agrobacterium tumefaciens strain GV3101 and further transformed into Arabidopsis wild‐type (Col‐0) and phyC‐2 mutant using the floral dip method (Clough and Bent, 1998). At least 10 independent lines of each transformation were selected with 0.005% (volume ratio) Basta solution (Coolaber, China) and verified by RT‐qPCR analysis. Two independent transgenic lines of each transgene were selected for further studies.

For phenotypic analysis, Arabidopsis seedlings were moved to constant red light (Rc), or far‐red light (FRc), or blue light (Bc) conditions for 4 day at 22 °C before hypocotyl length measurement. Hypocotyl lengths were measured from the digital photographs using the ImageJ software (version 1.38). The different light intensities were designed as previously described (Franklin et al., 2003; Monte et al., 2003). For EOD‐FR treatment, 2‐day‐old seedlings were treated with FR light (30 μmol photons/m²/s) for 30 min at the end of the light period for 4 day before measurements were taken.

LCI and BiFC assays

All constructs for LCI and BiFC assays were individually transformed into Agrobacterium tumefaciens strain EHA105 and then infiltrated into the leaves of N. benthamiana with different combinations as indicated in the figures. For BiFC assay, the N. benthamiana leaves were co‐infiltrated with a combination of Agrobacterium tumefaciens strain EHA105 carrying the indicated plasmid pairs and the 35S::mRFP‐AHL22 plasmid (Xiao et al., 2009). Samples were incubated in darkness for 24 h after the infiltration and then transferred to WL conditions (16‐h light/8‐h dark) for 24 to 36 h. For imaging the luciferase luminescence, the leaves were detached and photographed using the NightShade LB985 Plant Imaging System (Berthold Technologies) with a 60 s exposure time, 4 × 4 binning, slow readout and high gain after spraying with 20 mg/mL potassium luciferin (Gold Biotech, USA). For imaging the fluorescence of the reunion in BiFC, the N. benthamiana leaves were observed under confocal microscopy (Zeiss LSM710). All these experiments were independently repeated at least three times.

Generation and analysis of CRISPR/Cas9 knockout lines of zmphyC1 zmphyC2

The CRISPR/Cas9 knockout vector was constructed according to a previously described protocol (Wu et al., 2019). Briefly, two targets (target 1 and target 2) were designed in the first exons of ZmPHYC1 and ZmPHYC2 genes according to the reported criteria of 5′‐GG‐(N)18‐NGG‐3′ (Figure 5a). Given the ZmPHYC1 and ZmPHYC2 genes are highly homologous to each other, two identical target sequences in the exons of these two candidate genes were selected for Cas9 cleavage. The sequences for the guide RNAs, driven by the maize ubiquitin U6‐1 and U6‐2 promoters, respectively (Figure 5b), were inserted into the CPB vector (Zhao et al., 2016) using the HindⅢ restriction site and an In‐Fusion HD Cloning Kit (TaKaRa). The primer pair U6‐1‐1F and sgR‐R was used to assemble the first sgRNA expression cassette, and the primer pair U6‐2‐2F and sgR‐R was used to assemble the second sgRNA expression cassette. The primers are shown in Table S1. The resulting vector was confirmed by sequencing and introduced into the recipient line ZC01 via Agrobacterium tumefaciens‐mediated transformation. For genotyping, the target sequences of each ZmPHYC gene were amplified from ZC01 and the transgenic lines, and then PCR products were directly sequenced. The mutated sequences of each ZmPHYC gene in the transgenic lines were revealed by aligning the sequences between the transgenic lines and ZC01. Knockout lines with deletion or frameshift mutations were self‐pollinated to produce homozygous knockout mutants. The primers used above for construction and identifications are shown in Table S1.

Generation of ZmPHYC overexpression transgenic lines in maize

To get the ZmPHYC overexpression transgenic lines in maize, the Agrobacterium tumefaciens strain EHA105 carrying the ProUbi::ZmPHYCs‐GFP construct was used to transform the maize inbred line ZC01 as above described. The positive transgenic individuals of different lines were selected by spraying with the Basta solution (0.2 g/L). Two independent high expression transgenic lines for each ZmPHYC gene were verified by RT‐qPCR analysis and selected for further research. The primers used above for identifications are shown in Table S1.

Statistical analysis

All real‐time PCRs and other quantitative analysis were repeated at least three times. The significant differences of hypocotyl length and flowering time between the ZmPHYCs‐OE/phyC‐2 transgenic Arabidopsis plants and the phyC‐2 mutant plants were analysed by Student’s t‐test. To evaluate the significant differences of hypocotyl length among the various Arabidopsis genotypes treated or untreated with EOD‐FR and the differences of phenotypes among transgenic maize lines, the multiple comparisons were adopted by the LSD method with R package agricolae (R Core Team, 2018). The statistical significance of multiple comparisons was defined by using a Bonferroni‐corrected P‐value < 0.05.

Conflict of interest

The authors declare no conflict of interest.

Author contributions

H.W. designed the project. Q.L. and G.W. conducted the experiments. Y.Z., B.W. and B.Z. participated in some experiments. Q.L. and G.W. analysed the data and wrote the manuscript. H.W. and C.C. revised the manuscript. All the authors read and approved the manuscript.

Supporting information

Figure S1 Multiple sequence alignment of the protein sequences of ZmPHYC1, ZmPHYC2, OsPHYC and AtPHYC.

Figure S2 A heat map illustrating the expression levels of the ZmPHYC genes in different tissues from various developmental stages.

Figure S3 ZmPHYC1 and ZmPHYC2 proteins are localized in both the nucleus and cytoplasm in N. benthamiana epidermal cells under light conditions.

Figure S4 ZmPHYCs can interact with themselves and ZmPHYBs in plant cells.

Figure S5 Expression analysis of the ZmPHYC transgenes in the selected Arabidopsis transgenic lines.

Figure S6 ZmPHYC1‐ and ZmPHYC2‐overexpression plants in the phyC‐2 mutant background shows accelerated flowering compared with the phyC‐2 mutant.

Figure S7 Fluence‐rate response curves for hypocotyl length under Rc, Bc and FRc light conditions.

Figure S8 The zmphyC1 zmphyC2 double knockout mutants do not show an early‐flowering phenotype under natural SD conditions.

Figure S9 Transcript profiles of ZmCCT9 and ZmCCA1 genes in the wild type (blue lines) and zmphyC1 zmphyC2 double mutant (red lines).

Table S1 Primers used in this study.

Li, Q. , Wu, G. , Zhao, Y. , Wang, B. , Zhao, B. , Kong, D. , Wei, H. , Chen, C. and Wang, H. (2020) CRISPR/Cas9‐mediated knockout and overexpression studies reveal a role of maize phytochrome C in regulating flowering time and plant height. Plant Biotechnol. J., 10.1111/pbi.13429