Phytochromes sense red/far-red light and trigger a cascade of physiological responses in plant. Here, a phytochrome B homolog, GmPHYB1, was amplified from the soybean genome, and its expression profiles were obtained for various parts of the plant and at various developmental stages. The gene was ectopically expressed in Arabidopsis thaliana, driven by CaMV 35S promoter, to study the physiological functions of the gene product. The overexpressors of GmPHYB1 behaved similarly to those of AtPHYB, but with some subtle differences with respect to the acceleration of flowering under short day conditions and the growth of the hypocotyl under certain light fluence rate. The results suggested that this soybean PHYB homolog was well conserved both at the level of sequence and physiological function.
Citation: Wu F-Q, Zhang X-M, Li D-M, Fu Y-F (2011) Ectopic Expression Reveals a Conserved PHYB Homolog in Soybean. PLoS ONE 6(11): e27737. https://doi.org/10.1371/journal.pone.0027737
Editor: Pär K. Ingvarsson, University of Umeå, Sweden
Received: August 3, 2011; Accepted: October 24, 2011; Published: November 16, 2011
Copyright: © 2011 Wu et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This work was partly supported by Transgenic program (Nos 2009ZX08009-133B, 2011ZX08009-001 and 2011ZX08004-005) and the Chinese National Key Basic Research “973” Program (2010CB125906). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
For better growth and development, plants have evolved a series of photoreceptors to respond to light. One of the important kinds of photoreceptors is phytochromes (PHY), which are essential for red and far-red light sensing and involved in such responses as seed germination, photomorphogenesis, shade avoidance, flowering, and a number of other adaptive responses , , . PHY molecules are composed of a linear tetrapyrrole chromophore covalently linked to an apoprotein and function as dimers that undergo a reversible comformational change between the inactive (Pr) and the active (Pfr) form in response to red or far-red light, allowing the phytochrome to act as a switch that is turned on or turned off , , .
The PHY molecules are encoded by a small gene family, and have different members in different plants. The Arabidopsis thaliana genome includes five PHY genes (PHYA to PHYE), while the rice genome includes just three (PHYA to PHYC). Based on phylogenetic analysis, all phytochromes found in plants can be classified into two groups, the PHYA branch, including PHYA and PHYC, and the PHYB branch, including PHYB, PHYD and PHYE . The various phytochromes play overlapping, yet distinct roles. In A. thaliana, PHYB is the principal and primary mediator of red light responses and shade avoidance . It predominates in light-grown plants , promoting seed germination and de-etiolation in response to red light, inhibiting shade avoidance responses under a high ratio of red: far-red light (R:FR) . Such responses are important for the plants to survive in the ever-changing environmental conditions during its life cycle.
Some information is also available regarding the PHY of the rice  and tobacco . However, despite of some report of pea PHYA and PHYB  and soybean PHYA , , there has been limited molecular analysis of PHYB in legumes, especially in soybean (Glycine max (L.) Merr.), a paleopolyploid species with a complex genome .
Here we report the isolation of GmPHYB1, a soybean PHYB homolog, and the documentation of its expression profiles. The ectopic overexpression of GmPHYB1 in A. thaliana resulted in strong suppression of shade avoidance, early flowering under short days (SD), the shortening of the hypocotyls and the lengthening of the roots. We detail the impact on hypocotyl length of the expression of GmPHYB1 in A. thaliana plants grown under a variety of light fluence rate, and demonstrate that a number of genes related to flowering time and hypocotyl elongation show altered expression profiles. Our results suggested that both the sequence and function of GmPHYB1 are well conserved across evolutionarily diverse species.
The soybean genome includes a PHYB homolog
The EST sequence TC227575 represented in the DFCI Soybean Gene Index database (http://compbio.dfci.harvard.edu/tgi/cgi-bin/tgi/gimain.pl?gudb=soybean) was identified as a soybean PHYB homolog on the basis of its sequence similarity with A. thaliana PHYB (AtPHYB). Its sequence was used to design a pair of primers (Table S1) to amplify the soybean PHYB gene from a leaf mRNA template extracted from the soybean cultivar Kennong 18. The resulting sequence (hereafter GmPHYB1) encoded a predicted 1,137 residue protein which matched the translated Glyma09g03990 product (Phytozome; http://www.phytozome.net/soybean). GmPHYB1 shared a 76% level of peptide identity with AtPHYB, and included all the known functional domains of PHY (Figure S1). The GmPHYB1 sequence has been submitted to the GenBank/EMBL/DDBJ database (accession number EU428749).
A distance-based, neighbor-joining tree constructed by comparing the GmPHYB1 sequence with related peptide sequences (including GmPHYB2, the translated product of another soybean PHYB homolog, Glyma15g14980, found by screening the soybean genomic sequence database Phytozome) revealed its relationship with homologs from other plant species (Figure 1A). The tree showed two major clades, one corresponding to the monocotyledonous species, and the other to the dicotyledonous ones. The GmPHYB1 and GmPHYB2 sequences clustered with the latter, within the legume sub-clade alongside Lotus japonicus, Pisum sativum (alfalfa) and Pisum sativum (pea) PHYB homologs, which are particularly closely related to one another as all three are Galegoid legumes, while soybean is a Phaseoloid , . Thus interspecific divergence in the PHYB sequence appears to largely reflect phylogenetic relationships.
(A) A neighbor-joining tree constructed with MEGA 4.0 software based on the full-length amino acid sequences. The bootstrap analysis (1000 replicates) was performed. Except for the arrows indicated, all bootstrap values = 100. Sequences examined are (accession number in parenthesis): Arabidopsis lyrata PHYB (AlB, Q5G889), Arabidopsis thaliana PHYB (AtB, P14713), Cardamine nipponica PHYB (CnB, C4TGD7), Cardamine resedifolia PHYB(CrB, C4TGE0), Glycine max PHYB1 (GmPHYB1, EU428749) and PHYB2 (GmPHYB2, Glyma15g14980), Lotus japonicus PHYB (LjB, A1IIA2), Medicago sativa PHYB (MsB, C7FHN7), Nicotiana plumbaginifolia PHYB (NpB, O24117), Nicotiana tabacum PHYB(NtB, P29130), Oryza sativa subsp. Japonica PHYB, (OsB, Q10MG9), Pisum sativum PHYB, (PsB, Q9SEW2), Populus trichocarpa PHYB1 (PtB1, Q9FPQ3) and PHYB2 (PtB2, Q9FPQ2), Solanum tuberosum PHYB, (StB, P34094), Sorghum bicolor PHYB(SbB, P93527), Stellaria longipes PHYB, (SlB, Q717V7), Triticum aestivum PHYB (TaB, A9JR06), Vitis riparia PHYB (VrB, B9U4G7) and Zea mays PHYB1 (ZmB1, Q6XFQ3) and PHYB2 (ZmB2, Q6XFQ2). (B) The gene structure of GmPHYB1, compared with that of AtPHYB (AT2G18790). Exons are represented by black boxes; introns by lines and UTRs by grey boxes.
To determine the structure of GmPHYB1, its cDNA sequence was aligned with its corresponding genomic DNA sequence, as retrieved from the Phytozome database. This revealed that the genomic sequence includes four exons (Figure 1B), as also is the case for the PHYB genes present in A. thaliana, potato , tomato, rice ,  and maize  PHYBs. Although the exon lengths in GmPHYB1 were comparable with those in AtPHYB, the soybean introns were considerably larger (Figure 1B).
The endogenous expression of GmPHYB1
The transcription of GmPHYB1 in various tissues/organs of soybean cv. Kennong 18 plants grown under SD conditions at 28°C for 12 days was assessed using quantitative real-time RT-PCR (qPCR) (Figure 2A). GmPHYB1 transcript was present in all of the sampled organs/tissues, consistent with the pattern of PHYB expression in A. thaliana and potato , , where the gene appears to be expressed in most parts of plants. GmPHYB1 was expressed at a relatively high level in the petiole, suggesting that it might have an important role in petiole elongation, as shown similarly for A. thaliana that phytochrome regulated petiole elongation of Arabidopsis . Transcript abundance increased gradually from day 7 to day 21 after flowering, the period during which the pod matured.
(A) Tissue/organ expression profiles. SL, seedling; SAM, shoot apex (including the apical meristem and immature leaves); EH, epicotyl; HH, hypocotyl; Pt, petiole; St, stem; F, flower buds; P1 to P3, pods (excluding seeds) at 7, 14, and 21 days after flowering. Stages defined as follows: unifoliolates, unifoliolates fully opened; flowering, onset of flowering; seed setting, initiation of seed growth. (B) Expression profiles in leaves and aerial parts of the plant at different developmental stages. U and T1–T4 indicated different leaves or aerial parts (Organs) when leaves opened fully (Stages). U, fully opened unifoliolates; T1, fully opened 1st trifoliolates; T2, fully opened 2nd trifoliolates; T3, fully opened 3rd trifoliolates; T4, fully opened 4th trifoliolates; F, flowering. Error bars denote the standard deviation.
The patterns of expression in the leaf and aerial parts of the plant at different developmental stages are shown in Figure 2B. The level of GmPHYB1 transcript was low in the unifoliolates and the 1st and 2nd trifoliolates, but increased gradually thereafter, reaching a peak of expression just prior to flowering. At the later developmental stages, the level was higher in the unifoliolates and the 1st and 2nd trifoliolates than in the 3rd and 4th trifoliolates. The level of expression in the aerial part of the plant was modest and rather constant until the full expansion of the 3rd trifoliolate.
The ectopic expression of GmPHYB1 in A. thaliana alters plant architecture
PHYB contributes most strongly to shade avoidance responses . The function of GmPHYB1 was explored by its overexpression driven by the CaMV 35S promoter in both wild type A. thaliana ecotype Col-0 and in the corresponding loss-of-function mutant phyB (phyB-9). The seedling stage of both transgenic lines developed a markedly shortened hypocotyl (Figure 3A). The ectopic expression of GmPHYB1 not only rescued the phenotype of the phyB mutant, but also strongly suppressed the plants' shade avoidance phenotype. On the whole, the transgenic plants, regardless of its background, showed a compact, semi-dwarf stature with the shortened petioles and floral stems (Figure 3B). In addition, overexpression led to prostrate rosette leaves, a deep green leaf color and larger leaf size (compared to the phyB mutant), and an increased branching angle between the main inflorescences and the petioles or the lateral branches (Figure 3C, D). A similar phenotype has been associated with PHYB overexpressors in A. thaliana , potato  and tobacco , consistent with a high degree of functional conservation among disparate PHYB homologs.
(A) Strong inhibition of hypocotyl length; (B) compact, semi-dwarf architecture with shortened petioles and floral stems; (C) increased angle between the main inflorescence and the lateral branch; (D) deep green leaf color, larger leaf size and shortened petioles.
The ectopic expression of GmPHYB1 accelerates flowering in A. thaliana under SD, but not under LD
Floral transition is regulated by environmental stimuli via signaling cascades . Phytochromes perceive the light signal and play an important role in photoperiodic flowering . The influence of GmPHYB1 on the regulation of flowering time was studied by measuring leaf number and flowering time in transgenic A. thaliana overexpressing GmPHYB1 grown under either long days (LD) or short days (SD).
A set of 18 independent Col-0 and 25 phyB transgenics was obtained. Within each of the two groups, all lines behaved consistently with respect to their flowering time (as well as for hypocotyl and root length, as discussed below), so a single line has been used from each group (referred to, respectively, as GmPHYB1 Col-0 and GmPHYB1 phyB) to present the data. Meanwhile, a matching pair of A. thaliana transgenic lines in which AtPHYB was expressed driven by the CaMV 35S promoter (referred to, respectively, as AtPHYB Col-0 and AtPHYB phyB) represented a control. The expression level of GmPHYB1 and AtPHYB gene in these plants was confirmed by qPCR (Figure S2).
Under LD conditions, there was little variation with respect to flowering time among the four transgenic lines and the two non-transgenics Col-0 and phyB (Figure 4A). The phyB mutant produced fewer rosette leaves and more cauline leaves than Col-0. The rosette leaf number formed by the AtPHYB overexpressor and the GmPHYB1 overexpressor was closer to that formed by Col-0 than by phyB (Figure 4B), suggesting that the expression of GmPHYB1 was able to rescue the mutant phenotype.
Leaf number (A, C) and number of days to flowering (B, D) under LD (A, B) and SD (C, D). Error bars denote the standard deviation; n = 20 plants. (E) Flowering phenotypes of the overexpressors of GmPHYB1 and AtPHYB under SD conditions.
Under SD conditions (Figure 4C), both the mutant and the transgenics flowered earlier than Col-0 (Figure 4E), but the flowering time of the transgenics was background-dependent. AtPHYB phyB plants flowered earlier than AtPHYB Col-0 ones, while the GmPHYB1 overexpressors in both backgrounds flowered earlier than either of the AtPHYB overexpressors. The leaf number under SD conditions (Figure 4D) was incompletely correlated with days to flowering (Figure 4C). For example, although AtPHYB Col-0 produced more rosette leaves than phyB, it nevertheless flowered earlier. It was noteworthy that the number of rosette leaves formed by AtPHYB Col-0 was almost double that formed by AtPHYB phyB, but there was little difference in rosette leaf number between GmPHYB1 Col-0 and GmPHYB1 phyB (Figure 4D).
GmPHYB1 mediates de-etiolation responses in A. thaliana under red light
In A. thaliana, PHY promotes de-etiolation in response to light, and hypocotyl elongation is considered the standard test of this light-responsiveness , . The effect of GmPHYB1 on this trait was tested by exposing seedlings of the set of four transgenic and two non-transgenic lines for five days to darkness, far-red, blue, red or white light.
Under the dark (DD) conditions, the six lines behaved indistinguishably, producing a so-called ‘skotomorphogenic’ phenotype  characterized by a long hypocotyl and closed, non-expanded yellow cotyledons (Figure 5A and Figure 5B).
(A) Five-day-old seedlings of Col-0, phyB, AtPHYB Col-0, AtPHYB phyB, GmPHYB1 Col-0 and GmPHYB1 phyB grown under DD, FR (23.5 µmol m−2 s−1), RL (1.3 µmol m−2 s−), BL (3.1 µmol m−2 s−1) or WL (80.8 µmol m−2 s−1) conditions. Asterisks indicated a 0.01 significant difference from its transgenic background (t-test). Error bars denote the standard deviation. n = 15. (B–F) Images of the corresponding seedlings (from left to right in each panel: Col-0, phyB, AtPHYB Col-0, AtPHYB phyB, GmPHYB1 Col-0, GmPHYB1 phyB). Bar = 0.5 cm.
Under far-red light (FR), the cotyledons of all the lines remained yellow, but hypocotyl length was clearly inhibited and the cotyledons were open and expanded (Figure 5A, 5C), consistent with the function of endogenous PHYA under far-red light. AtPHYB Col-0 seedlings produced a longer hypocotyl than any of the other lines (see later discussion below).
When exposed to blue light (BL), where cryptochromes would be expected to dominate the response, all six lines developed green, open cotyledons with a shortened hypocotyl. However, the reduction of hypocotyl length among these seedlings was slightly different and the GmPHYB1 overexpressors produced the shortest hypocotyl (Figure 5A, 5D).
Under red light (RL) (Figure 5A and Figure 5E), the phyB mutant developed a long hypocotyl along with green, but non-expanded cotyledons (Figure 5A, 5E). Col-0 seedlings produced a shorter hypocotyl than those of the phyB mutant. The overexpression of GmPHYB1 or AtPHYB greatly shortened hypocotyl length and expanded the size of the cotyledons (Figure 5A, 5E). The results proved that GmPHYB1, as AtPHYB, mediated de-etiolation responses under RL.
Under white light (WL), hypocotyl length was comparable with that produced under RL, implying that PHYB might play a major role in controlling hypocotyl length under WL. Furthermore, cotyledon size under WL was larger than when the seedlings were exposed to monochromatic light (FR, BL or RL), suggesting that PHYs and cryptochromes act additively in regulating cotyledon growth.
GmPHYB1 regulates root elongation in A. thaliana under red light
PHY exerts a strong influence on primary root elongation in A. thaliana, as mutants lacking PHYB have reduced primary root elongation , , . Seedlings of the six lines exposed to either darkness (DD), far-red (FR) or blue light (BL) did not vary with respect to root length. However, exposure to either red (RL) or white light (WL) reduced root length in the phyB mutant, while the overexpression of GmPHYB1 as well as AtPHYB markedly increased root length (Figure 6). The observation supported the notion that GmPHYB1 was also involved in root elongation under RL.
Five-day-old seedlings of Col-0, phyB, AtPHYB Col-0, AtPHYB phyB, GmPHYB1 Col-0 and GmPHYB1 phyB grown under DD, FR (23.5 µmol m−2 s−1), RL (1.3 µmol m−2 s−1), BL (3.1 µmol m−2 s−1) or WL (80.8 µmol m−2 s−1) condition. Asterisks indicated a 0.01 significant difference from its transgenic background (t-test). Error bars denote the standard deviation. n = 15.
The effect of GmPHYB1 overexpression on the response to light fluence rate
Based on the radiation energy of light, phytochrome responses have been subdivided into different classes including low fluence response (LFR), very low fluence response (VLFR), high irradiance response to red light (HIR-R) and high irradiance response to far-red light (HIR-FR), and PHYB is mainly responsible for the LFR and HIR-R during photomorphogenesis , , , .
We first examined the PHYB HIR-R by measurement of hypocotyl length of 5-day-old seedlings grown under a range of continuous RL fluence rate (Figure 7A). Hypocotyl elongation in the GmPHYB1 overexpressors was strongly inhibited at a fluence rate of just 0.2 µmol m−2 s−1 (Figure S3A), while neither AtPHYB Col-0 nor AtPHYB phyB were inhibited until the fluence rate reached 0.6 and 2.9 µmol m−2 s−1, respectively. In contrast, hypocotyl elongation in phyB seedlings appeared to be independent of light fluence rate.
(A-C) Hypocotyl length of five-day-old seedlings of Col-0, phyB, AtPHYB Col-0, AtPHYB phyB, GmPHYB1 Col-0 and GmPHYB1 phyB grown under different fluence rate of RL (A), FR (B) or BL(C) conditions. (D) EOD-FR responses of Col-0, phyB, AtPHYB Col-0, AtPHYB phyB, GmPHYB1 Col-0 and GmPHYB1 phyB. Gray columns represented the hypocotyl length of 4-day-old seedlings grown under 8h-day/16h-night cycle; white columns represented hypocotyl length of four-day-old seedlings under the same short day conditions with an additional 15 min FR treatment at the end of the light (left axis). Red columns represented the percentage of increasement in the hypocotyl length of the treated seedlings compared with the untreated seedlings (right axis). Error bars denote the standard deviation. n = 15.
Exposure to either FR (Figure 7B) or BL (Figure 7C) inhibited hypocotyl elongation of the overexpressors of GmPHYB1 or AtPHYB as the light fluence rate was increased. At 20.3 µmol m−2 s−1 of FR, AtPHYB Col-0 seedlings developed a longer hypocotyl than those of the other five lines (Figure S3B), which had been observed in Figure 5A and Figure 5C. Additionally, hypocotyl elongation of the two GmPHYB1 overexpressors was clearly inhibited (2/3 length of Col-0 or phyB) when the fluence rate of BL reached 8.5 µmol m−2 s−1 (Figure S3C), though hypocotyl elongation of the AtPHYB overexpressors did not appear to be so strongly inhibited by BL.
PHYB-mediated LFR was assessed by measuring hypocotyl length following an end-of-day FR (EOD-FR) treatment . The hypocotyl of Col-0 seedlings showed a marked response to this treatment (Figure 7D), and the effect was even more pronounced in the GmPHYB1 and AtPHYB overexpressors, presumably due to the abundance of PHYB in these seedlings. In contrast, phyB mutant had no such response to the treatment.
The altered expression of genes related to flowering time & hypocotyle elongation in GmPHYB1 overexpressor
To study the mechanism of the overexpression of GmPHYB1 on early flowering under SD and the strong inhibition of hypocotyl elongation, the expression of a set of key flowering time genes and hypocotyl growth related genes was monitored by qPCR.
Under SD conditions, transcript abundance of FT (FLOWERING LOCUS T), SOC1 (SUPPRESSOR OF OVEREXPRESSION OF CONSTANS 1) and CO (CONSTANS)  in all of the transgenic lines was elevated, while FUL (FRUITFULL) and SEP3 (SEPALLATA3) ,  were also regulated in the overexpressors except in AtPHYB Col-0 (Figure 8). These results were basically in agreement with the phenotype observed above. The flowering time of Col-0 and phyB was delayed under SD, AtPHYB Col-0 had an intermediate flowering time, while the flowering of the other transgenics was accelerated.
The diurnal variation in transcript profiles of FT, SOC1, CO, FUL, SEP3, GA3OX1 and GA20OX1 in 10-day-old seedlings of Col-0, phyB, AtPHYB Col-0, AtPHYB phyB, GmPHYB1 Col-0 and GmPHYB1 phyB grown under SD conditions, as detected by qPCR. Error bars denote the standard deviation.
There were no regular changes in any of the hypocotyl growth related genes tested (PIFs and COPs, data not shown). However, a decline was noted in the rhythmic amplitude of the expression of GA3OX1 and GA20OX1 (both of which are involved in gibberellin synthesis) in the presence of overexpression of GmPHYB1 as well as AtPHYB (Figure 8). Some evidence has been presented to suggest that in light-grown plants, PHYs can inhibit the synthesis or action of gibberellin, which was known to stimulate hypocotyl elongation. Any interference in gibberellin synthesis which reduces the quantity of endogenous gibberellin may thus at least in part explain the observed inhibition of hypocotyl elongation in the transgenic plants.
AtPHYA is down-regulated in AtPHYB Col-0
AtPHYB Col-0 seedlings exhibited longer hypocotyls under far-red light (Figure 5A, 5C, 7B). To test whether this behavior reflected the altered expression of AtPHYA, its transcript abundance was monitored using qPCR. As Figure 9 showed, AtPHYA was up-regulated in the phyB mutant, and down-regulated in AtPHYB Col-0. This phenomenon of elongated hypocotyls under FR resulting from overexpression of PHYB had been previously demonstrated , , . However, the expression of AtPHYA was not affected by the overexpression of GmPHYB1, suggesting a functional difference between GmPHYB1 and AtPHYB.
Transcription of AtPHYA in 10-day-old seedlings of Col-0, phyB, AtPHYB Col-0, AtPHYB phyB, GmPHYB1 Col-0 and GmPHYB1 phyB grown under SD conditions, as detected by qPCR. Asterisk indicates a 0.01 significant difference from Col-0. Error bars denote the standard deviation.
In our study, a PHYB homolog, designated as GmPHYB1, was isolated in soybean, corresponding to the genomic locus Glyma09g03990. A second locus showing appreciable sequence similarity to PHYB was Glyma15g14980. This locus is quite likely a homolog of GmPHYB1, since soybean is a paleopolyploid , , in which a good many genes are represented by more than one copy . Supporting the hypothesis, the two soybean PHYB-like genes were located in two distinctive chromosomes (No. 9 & 15). So far, multiple copies of PHY homologs are known in the genome of maize, potato, tomato and poplar , , , . Four PHYA homologs were found in soybean genome . Two PHYA genes GmPHYA2  and GmPHYA3  have been functionally identified in the soybean genome, which correspond to two previously identified maturity loci, E4 and E3, respectively. GmPHYA1 gene was also isolated, while its function remained undetermined. However, both the protein sequences and the gene expression patterns suggested that GmPHYA1 might have a function similar to that of GmPHYA2 .
The GmPHYB1 sequence shows a high level of conservation with other plant PHYB sequences. Its exon/intron structure is identical to that of its A. thaliana and rice homologs , though the soybean introns were generally longer than those in A. thaliana (Figure 1B). The length of its gene product (1,137 residues) was consistent with the length of PHYB proteins characterized to date, and its level of peptide similarity with AtPHYB was over 70% (over 80% with PHYBs from other legume species). Finally, the GmPHYB1 protein included all the known conserved functional PHY domains, namely P1 (Gly/Ser-rich), P2/PAS, P3/GAF, P4/PHY, PAS1, PAS2, histidine kinase and a chromophore-binding site  (Figure S1).
In soybean, GmPHYB1 was expressed in the full range of tissues/organs sampled and at every developmental stage studied (Figure 2). Its overall level of expression in the aerial part of the plant increased as development proceeded (Figure 2B), but varied from organ to organ; in the unifoliolates, for example, expression peaked at the time of flowering, while in the trifoliolates, the peak occurred before flowering (Figure 2B). The implication is that GmPHYB1 is likely involved in a number of developmental processes, with each organ associated with a characteristic pattern of expression, reflecting the protein's specific function.
Photoreceptors are critical molecules that function at the interface between the organism and environmental cues, providing plants with signals for the control of germination, seedling development, shade avoidance, plant architecture, and photoperiodic flowering , , . The ectopic expression of GmPHYB1 in A. thaliana had a similar, but not fully identical effect on aspects of growth and development as produced by the overexpression of the native copy of PHYB. Thus, for example, the GmPHYB1 overexpressors displayed typical PHYB-related and red light specific phenotypes. The overexpression of GmPHYB1 (and the overexpression of AtPHYB) induced a similar expression pattern of genes related to flowering time and hypocotyl growth, suggesting that these two genes operate in a very similar manner to one another. Nevertheless, there were a number of subtle distinctions between the AtPHYB overexpressors and the GmPHYB1 overexpressors. Firstly, the latter induced a higher transcript abundance of the flowering time associated genes of CO, FT, SOC1, FUL and SEP3 (Figure 8), which might result in a more pronounced acceleration in flowering time under SD conditions (Figure 4). Secondly, a much lower fluence rate of red light was sufficient to induce hypocotyl shortening in the GmPHYB1 overexpressors (Figure 7A). Thirdly, the length of the hypocotyl formed by the GmPHYB1 overexpressors was much less than that formed by the AtPHYB overexpressors either when the fluence rate of blue light used was 8.5 µmol m−2 s−1 or 25.2 µmol m−2 s−1 (Figure 7C, S3C). The latter observation was suggestive of an interaction between PHY and the cryptochromes in the control of hypocotyl growth , , . It is well known that soybean is a heliophilous plant, while A. thaliana is a skiophilous one . Thus it is likely that the GmPHYB1 protein is more adapted to conditions of stronger incident radiation than AtPHYB; this might explain why the overexpression of GmPHYB1 in A. thaliana had a greater phenotypic effect than that of AtPHYB did. Finally, it is also possible that the interaction between PHYB and PHYA may differ qualitatively between soybean and A. thaliana, because the overexpression of AtPHYB down-regulated PHYA expression in Col-0, while the ectopic expression of GmPHYB1 did not (Figure 9).
It has been proposed that the function of PHYB is universal among flowering plants . The present data show that GmPHYB1 has much in common with AtPHYB, though there are subtle differences between them related to phenotypic intensity (e.g., earlier flowering under SD conditions and shorter hypocotyl length under certain light fluence rate) when the two genes were expressed in A. thaliana. A more precise determination of the function of GmPHYB1 will require experiments based on a transgene where the gene is driven by its native promoter in soybean. It would be of interest to determine the function of the second soybean PHYB gene, and possible interaction between the two.
Materials and Methods
Plant materials and growing conditions
The endogenous expression profiles of GmPHYB1 within various tissues/organs and at various developmental stages of the soybean cultivar Kennong18 were obtained from RNA harvested from plants raised at 28°C, with an 8h-light/16h-dark photoperiod, where the light fluence rate was 100–150 µmol m−2 s−1. Seedlings were harvested before the expansion of the unifoliolates leaves. Various tissues/organs including unifoliolates, trifoliolates, hypocotyls, epicotyls, cotyledons, petioles, shoot apex (including the apical meristem and immature leaves), stems, flowering buds, and the whole aerial organs of plants were individually sampled when the unifoliolates, the 1st, 2nd, 3rd or 4th trifoliolates had fully expanded or when plants reached flowering. Pods without seeds were sampled at 7, 14, and 21 days after flowering and at maturity.
Gene isolation, plasmid construction and production of transgenic A. thaliana plants
The fragment containing the coding sequence of GmPHYB1 was amplified with a pair of gene-specific primers (Table S1), and was then introduced into the pEASY-T1 vector (TransGen Biotech, CHN). Several independent clones were sequenced for bona fide sequence. The coding sequence of GmPHYB1 was subsequently cloned into entry vector pDONR207 (Invitrogen) and finally transferred to the expression vector pLeela via the LR Gateway recombination reaction (Invitrogen). A. thaliana plants were agroinfected with Agrobacterium tumefaciens strain pGV3101 MP90RK, using the floral dipping method . Basta-resistant T1 plants were self-pollinated through four generations to obtain the homozygous T4 transgenic lines for analysis.
Measurement of flowering time, hypocotyl and root length and EOD-FR experiment
At least three independent lines per transgene/background combination were assayed (although the data for just one has been presented here for clarity). Measurement of flowering time and hypocotyl and root length of A. thaliana was performed as describe by Xiao et al. . EOD-FR experiment followed the procedure elaborated by Robson et al. .
Quantitative real-time RT-PCR
Quantitative real-time RT-PCR (qPCR) with gene-specific primers (Table S1) was implemented using an ABI StepOne Real-Time PCR system (Applied Biosystems, USA), based on SYBR Premix ExTaq polymerase (TaKaRa, Japan). Expression data were analyzed using StepOne software (ABI, Applied Biosystems, USA) and transcript levels were calculated relative to the corresponding reference gene (Table S1). For the tissues/organs and developmental samples of soybean, the reference gene was GmUKN1  and for the gene expression in transgenic A. thaliana, it was At4g34270 . Two lines per each background in which GmPHYB1 was overexpressed were monitored (although for clarity only one line per background is presented here).
Multiple alignment of the complete sequences of AtPHYB (P14713) and GmPHYB1 (EU428749). The colored underlines indicate the functional domains of PHY. The asterisk indicated the chromophore-binding site. Shaded residues indicate amino acids matching the consensus.
Expression levels of GmPHYB1 and AtPHYB in the plants studied. 10-day-old seedlings of Col-0, phyB, AtPHYB Col-0, AtPHYB phyB, GmPHYB1 Col-0 and GmPHYB1 phyB grown under SD conditions, as detected by qPCR. Error bars denote the standard deviation.
The phenotype of seedlings grown under different light fluence rate. Five-day-old seedlings (from left to right: Col-0, phyB, AtPHYB Col-0, AtPHYB phyB, GmPHYB1 Col-0, GmPHYB1 phyB) grown under 0.2 µmol m−2 s−1 RL (A), in 20.3 µmol m−2 s−1 FR (B), or in 8.5 µmol m−2 s−1 BL (C). Bar = 0.5 cm.
We thank Dr Jianping Yang for his kind provision of the A. thaliana phyB-9 line engineered to overexpress AtPHYB.
Conceived and designed the experiments: YF-F. Performed the experiments: F-QW X-MZ D-ML. Analyzed the data: F-QW. Contributed reagents/materials/analysis tools: F-QW D-ML X-MZ. Wrote the paper: F-QW.
- 1. Bae G, Choi G (2008) Decoding of light signals by plant phytochromes and their interacting proteins. Annu Rev Plant Biol 59: 281–311.
- 2. Neff MM, Fankhauser C, Chory J (2000) Light: an indicator of time and place. Genes Dev 14: 257–271.
- 3. Smith H (2000) Phytochromes and light signal perception by plants--an emerging synthesis. Nature 407: 585–591.
- 4. Rockwell NC, Su YS, Lagarias JC (2006) Phytochrome structure and signaling mechanisms. Annu Rev Plant Biol 57: 837–858.
- 5. Quail PH (1991) Phytochrome: a light-activated molecular switch that regulates plant gene expression. Annu Rev Genet 25: 389–409.
- 6. Lagarias JC, Mercurio FM (1985) Structure function studies on phytochrome. Identification of light-induced conformational changes in 124-kDa Avena phytochrome in vitro. J Biol Chem 260: 2415–2423.
- 7. Mathews S (2006) Phytochrome-mediated development in land plants: red light sensing evolves to meet the challenges of changing light environments. Mol Ecol 15: 3483–3503.
- 8. Franklin KA, Praekelt U, Stoddart WM, Billingham OE, Halliday KJ, et al. (2003) Phytochromes B, D, and E act redundantly to control multiple physiological responses in Arabidopsis. Plant Physiol 131: 1340–1346.
- 9. Furuya M (1989) Molecular properties and biogenesis of phytochrome I and II. Adv Biophys 25: 133–167.
- 10. Reed JW, Nagatani A, Elich TD, Fagan M, Chory J (1994) Phytochrome A and Phytochrome B Have Overlapping but Distinct Functions in Arabidopsis Development. Plant Physiol 104: 1139–1149.
- 11. Takano M, Inagaki N, Xie X, Yuzurihara N, Hihara F, et al. (2005) Distinct and cooperative functions of phytochromes A, B, and C in the control of deetiolation and flowering in rice. Plant Cell 17: 3311–3325.
- 12. Kern R, Gasch A, Deak M, Kay SA, Chua NH (1993) phyB of tobacco, a new member of the phytochrome family. Plant Physiol 102: 1363–1364.
- 13. Weller JL, Beauchamp N, Kerckhoffs LH, Platten JD, Reid JB (2001) Interaction of phytochromes A and B in the control of de-etiolation and flowering in pea. Plant J 26: 283–294.
- 14. Liu B, Kanazawa A, Matsumura H, Takahashi R, Harada K, et al. (2008) Genetic redundancy in soybean photoresponses associated with duplication of the phytochrome A gene. Genetics 180: 995–1007.
- 15. Watanabe S, Hideshima R, Xia Z, Tsubokura Y, Sato S, et al. (2009) Map-based cloning of the gene associated with the soybean maturity locus E3. Genetics 182: 1251–1262.
- 16. Schmutz J, Cannon SB, Schlueter J, Ma J, Mitros T, et al. (2010) Genome sequence of the palaeopolyploid soybean. Nature 463: 178–183.
- 17. Zhu H, Choi HK, Cook DR, Shoemaker RC (2005) Bridging model and crop legumes through comparative genomics. Plant Physiol 137: 1189–1196.
- 18. Goldblatt P (1981) Cytology and the phylogeny of Leguminosae;. In: Raven RMPaPH, editor. Kew, United Kingdom: Royal Botanic Gardens.
- 19. Heyer A, Gatz C (1992) Isolation and characterization of a cDNA-clone coding for potato type B phytochrome. Plant Mol Biol 20: 589–600.
- 20. Lazarova GI, Kubota T, Frances S, Peters JL, Hughes MJ, et al. (1998) Characterization of tomato PHYB1 and identification of molecular defects in four mutant alleles. Plant Mol Biol 38: 1137–1146.
- 21. Kay SA, Keith B, Shinozaki K, Chye ML, Chua NH (1989) The rice phytochrome gene: structure, autoregulated expression, and binding of GT-1 to a conserved site in the 5′ upstream region. Plant Cell 1: 351–360.
- 22. Sheehan MJ, Farmer PR, Brutnell TP (2004) Structure and expression of maize phytochrome family homeologs. Genetics 167: 1395–1405.
- 23. Goosey L, Palecanda L, Sharrock RA (1997) Differential patterns of expression of the Arabidopsis PHYB, PHYD, and PHYE phytochrome genes. Plant Physiol 115: 959–969.
- 24. Hisamatsu T, King RW, Helliwell CA, Koshioka M (2005) The involvement of gibberellin 20-oxidase genes in phytochrome-regulated petiole elongation of Arabidopsis. Plant Physiol 138: 1106–1116.
- 25. Wagner D, Tepperman JM, Quail PH (1991) Overexpression of Phytochrome B Induces a Short Hypocotyl Phenotype in Transgenic Arabidopsis. Plant Cell 3: 1275–1288.
- 26. Thiele A, Herold M, Lenk I, Quail PH, Gatz C (1999) Heterologous expression of Arabidopsis phytochrome B in transgenic potato influences photosynthetic performance and tuber development. Plant Physiol 120: 73–82.
- 27. Halliday KJ, Thomas B, Whitelam GC (1997) Expression of heterologous phytochromes A, B or C in transgenic tobacco plants alters vegetative development and flowering time. Plant J 12: 1079–1090.
- 28. Franklin KA, Quail PH (2010) Phytochrome functions in Arabidopsis development. J Exp Bot 61: 11–24.
- 29. Putterill J, Laurie R, Macknight R (2004) It's time to flower: the genetic control of flowering time. Bioessays 26: 363–373.
- 30. Kneissl J, Shinomura T, Furuya M, Bolle C (2008) A rice phytochrome A in Arabidopsis: The Role of the N-terminus under red and far-red light. Mol Plant 1: 84–102.
- 31. Correll MJ, Kiss JZ (2005) The roles of phytochromes in elongation and gravitropism of roots. Plant Cell Physiol 46: 317–323.
- 32. Salisbury FJ, Hall A, Grierson CS, Halliday KJ (2007) Phytochrome coordinates Arabidopsis shoot and root development. Plant J 50: 429–438.
- 33. Josse EM, Foreman J, Halliday KJ (2008) Paths through the phytochrome network. Plant Cell Environ 31: 667–678.
- 34. Chen M, Chory J, Fankhauser C (2004) Light signal transduction in higher plants. Annu Rev Genet 38: 87–117.
- 35. Franklin KA, Allen T, Whitelam GC (2007) Phytochrome A is an irradiance-dependent red light sensor. Plant J 50: 108–117.
- 36. Chen M, Galvao RM, Li M, Burger B, Bugea J, et al. (2010) Arabidopsis HEMERA/pTAC12 initiates photomorphogenesis by phytochromes. Cell 141: 1230–1240.
- 37. Sullivan JA, Deng XW (2003) From seed to seed: the role of photoreceptors in Arabidopsis development. Dev Biol 260: 289–297.
- 38. Elich TD, Chory J (1997) Biochemical characterization of Arabidopsis wild-type and mutant phytochrome B holoproteins. Plant Cell 9: 2271–2280.
- 39. Lee J, Lee I (2010) Regulation and function of SOC1, a flowering pathway integrator. J Exp Bot 61: 2247–2254.
- 40. de Folter S, Immink RG, Kieffer M, Parenicova L, Henz SR, et al. (2005) Comprehensive interaction map of the Arabidopsis MADS Box transcription factors. Plant Cell 17: 1424–1433.
- 41. Ferrandiz C, Gu Q, Martienssen R, Yanofsky MF (2000) Redundant regulation of meristem identity and plant architecture by FRUITFULL, APETALA1 and CAULIFLOWER. Development 127: 725–734.
- 42. Vandenbussche F, Verbelen JP, Van Der Straeten D (2005) Of light and length: regulation of hypocotyl growth in Arabidopsis. Bioessays 27: 275–284.
- 43. Herskowitz I (1987) Functional inactivation of genes by dominant negative mutations. Nature 329: 219–222.
- 44. Boylan M, Douglas N, Quail PH (1994) Dominant negative suppression of arabidopsis photoresponses by mutant phytochrome A sequences identifies spatially discrete regulatory domains in the photoreceptor. Plant Cell 6: 449–460.
- 45. Short TW (1999) Overexpression of Arabidopsis phytochrome B inhibits phytochrome A function in the presence of sucrose. Plant Physiol 119: 1497–1506.
- 46. Kim MY, Lee S, Van K, Kim TH, Jeong SC, et al. (2010) Whole-genome sequencing and intensive analysis of the undomesticated soybean (Glycine soja Sieb. and Zucc.) genome. Proc Natl Acad Sci U S A 107: 22032–22037.
- 47. Blanc G, Wolfe KH (2004) Widespread paleopolyploidy in model plant species inferred from age distributions of duplicate genes. Plant Cell 16: 1667–1678.
- 48. Hauser BA, Cordonnier-Pratt MM, Daniel-Vedele F, Pratt LH (1995) The phytochrome gene family in tomato includes a novel subfamily. Plant Mol Biol 29: 1143–1155.
- 49. Howe GT, Bucciaglia PA, Hackett WP, Furnier GR, Cordonnier-Pratt MM, et al. (1998) Evidence that the phytochrome gene family in black cottonwood has one PHYA locus and two PHYB loci but lacks members of the PHYC/F and PHYE subfamilies. Mol Biol Evol 15: 160–175.
- 50. Mathews S (2005) Phytochrome evolution in green and nongreen plants. J Hered 96: 197–204.
- 51. Abdurakhmonov IY, Buriev ZT, Logan-Young CJ, Abdukarimov A, Pepper AE (2010) Duplication, divergence and persistence in the Phytochrome photoreceptor gene family of cottons (Gossypium spp.). BMC Plant Biol 10: 119.
- 52. Casal JJ (2000) Phytochromes, cryptochromes, phototropin: photoreceptor interactions in plants. Photochem Photobiol 71: 1–11.
- 53. Ahmad M, Cashmore AR (1997) The blue-light receptor cryptochrome 1 shows functional dependence on phytochrome A or phytochrome B in Arabidopsis thaliana. Plant J 11: 421–427.
- 54. Sellaro R, Hoecker U, Yanovsky M, Chory J, Casal JJ (2009) Synergism of red and blue light in the control of Arabidopsis gene expression and development. Curr Biol 19: 1216–1220.
- 55. Foyer CH, Noctor G (1999) Leaves in the dark see the light. Science 284: 599–601.
- 56. Clough SJ, Bent AF (1998) Floral dip: a simplified method for Agrobacterium-mediated transformation of Arabidopsis thaliana. Plant J 16: 735–743.
- 57. Xiao C, Chen F, Yu X, Lin C, Fu YF (2009) Over-expression of an AT-hook gene, AHL22, delays flowering and inhibits the elongation of the hypocotyl in Arabidopsis thaliana. Plant Mol Biol 71: 39–50.
- 58. Robson P, Whitelam GC, Smith H (1993) Selected Components of the Shade-Avoidance Syndrome Are Displayed in a Normal Manner in Mutants of Arabidopsis thaliana and Brassica rapa Deficient in Phytochrome B. Plant Physiol 102: 1179–1184.
- 59. Hu R, Fan C, Li H, Zhang Q, Fu YF (2009) Evaluation of putative reference genes for gene expression normalization in soybean by quantitative real-time RT-PCR. BMC Mol Biol 10: 93.
- 60. Czechowski T, Stitt M, Altmann T, Udvardi MK, Scheible WR (2005) Genome-wide identification and testing of superior reference genes for transcript normalization in Arabidopsis. Plant Physiol 139: 5–17.