- Research article
- Open Access
Functional analysis of COP1 and SPA orthologs from Physcomitrella and rice during photomorphogenesis of transgenic Arabidopsis reveals distinct evolutionary conservation
© Ranjan et al.; licensee BioMed Central Ltd. 2014
- Received: 24 April 2014
- Accepted: 24 June 2014
- Published: 1 July 2014
Plants have evolved light sensing mechanisms to optimally adapt their growth and development to the ambient light environment. The COP1/SPA complex is a key negative regulator of light signaling in the well-studied dicot Arabidopsis thaliana. COP1 and members of the four SPA proteins are part of an E3 ubiquitin ligase that acts in darkness to ubiquitinate several transcription factors involved in light responses, thereby targeting them for degradation by the proteasome. While COP1 is also found in humans, SPA proteins appear specific to plants. Here, we have functionally addressed evolutionary conservation of COP1 and SPA orthologs from the moss Physcomitrella, the monocot rice and the dicot Arabidopsis.
To this end, we analyzed the activities of COP1- and SPA-like proteins from Physcomitrella patens and rice when expressed in Arabidopsis. Expression of rice COP1 and Physcomitrella COP1 protein sequences predominantly complemented all phenotypic aspects of the viable, hypomorphic cop1-4 mutant and the null, seedling-lethal cop1-5 mutant of Arabidopsis: rice COP1 fully rescued the constitutive-photomorphogenesis phenotype in darkness and the leaf expansion defect of cop1 mutants, while it partially restored normal photoperiodic flowering in cop1. Physcomitrella COP1 partially restored normal seedling growth and flowering time, while it fully restored normal leaf expansion in the cop1 mutants. In contrast, expression of a SPA ortholog from Physcomitrella (PpSPAb) in Arabidopsis spa mutants did not rescue any facet of the spa mutant phenotype, suggesting that the PpSPAb protein is not functionally conserved or that the Arabidopsis function evolved after the split of mosses and seed plants. The SPA1 ortholog from rice (OsSPA1) rescued the spa mutant phenotype in dark-grown seedlings, but did not complement any spa mutant phenotype in light-grown seedlings or in adult plants.
Our results show that COP1 protein sequences from Physcomitrella, rice and Arabidopsis have been functionally conserved during evolution, while the SPA proteins showed considerable functional divergence. This may - at least in part - reflect the fact that COP1 is a single copy gene in seed plants, while SPA proteins are encoded by a small gene family of two to four members with possibly sub- or neofunctionalized tasks.
- Light signal transduction
- Flowering time
Since plants use sunlight as their primary source of energy they have evolved mechanisms of light sensing in order to optimally adjust their growth and development accordingly. Light-adapted responses are particularly obvious during seedling growth. Dark-grown seedlings usually exist under soil cover and therefore respond with etiolation, showing a long hypocotyl, small and closed cotyledons, an apical hook and a lack of chlorophyll synthesis. Light-grown seedlings, in contrast, are green and exhibit a short hypocotyl, open, expanded and green cotyledons and no apical hook. Other light-induced responses include phototropism, leaf expansion, the shade avoidance response and photoperiodic flowering [1, 2]. To sense the light, plants have several classes of photoreceptors: the red (R) and far-red (FR) sensing phytochromes, the blue (B)/UV-A responsive cryptochromes, phototropins and ZEITLUPE family members and the recently identified UV-B sensing UV-RESISTANCE LOCUS 8 (UVR8) protein [3–6].
The molecular events during light signal transduction are best understood in the model species Arabidopsis. After activation by light, phytochrome and cryptochrome photoreceptors inhibit the activity of a key negative regulator of light signal transduction, the CULLIN4 (CUL4)-dependent E3 ubiquitin ligase complex CONSTITUTIVELY PHOTOMORPHOGENIC1/SUPPRESSOR OF PHYA-105 (COP1/SPA). In darkness, COP1/SPA acts to ubiquitinate activators of the light response, such as the transcription factors ELONGATED HYPOCOTYL5 (HY5), LONG HYPOCOTYL IN FR 1 (HFR1), B-BOX DOMAIN PROTEINS (BBX) proteins, PRODUCTION OF ANTHOCYANIN PIGMENT1 (PAP1) and PAP2 as well as several photoreceptors, thereby targeting them for degradation in the proteasome. In light-grown plants, in contrast, COP1/SPA activity is suppressed and the target proteins can accumulate and mediate light-regulated gene expression and photomorphogenesis [7–11]. Hence, mutants defective in COP1 or in all four members of the SPA gene family show constitutive photomorphogenesis, exhibiting features of light-grown seedlings in complete darkness [12, 13]. Besides controling seedling growth in response to light, the COP1/SPA complex is involved in multiple other light-induced responses, such as anthocyanin biosynthesis, leaf expansion, shade avoidance responses and photoperiodic flowering [7, 11, 14–19]. COP1/SPA also acts downstream of the UV-B receptor UVR8, but in contrast to R and B signaling - where COP1 acts as a repressor of light signaling - COP1/SPA functions as a positive regulator of the UV-B response .
The COP1/SPA complex likely forms a tetramer with two COP1 and two SPA proteins. COP1 and SPA proteins interact with each other via their respective coiled-coil domains [21–24]. COP1 and the four SPA proteins (SPA1-SPA4) share further structural similarity in that they contain related C-terminal WD-repeat domains which have dual roles in substrate recruitment and binding of DAMAGED DNA-BINDING PROTEIN1 (DDB1) of the CUL4 complex . In their N-termini, COP1 and SPA proteins have distinct sequences, with COP1 containing a RING finger domain and SPA proteins carrying a kinase-like domain [25, 26]. The mechanisms involved in light-mediated inhibition of COP1/SPA activity are not well understood but likely involve light-induced interaction of cryptochromes with SPA1, light-induced degradation of SPA1 and SPA2 as well as light-mediated nuclear exclusion of COP1 [27–33].
The four SPA proteins share highest sequence similarity to each other in their WD-repeat domain. Sequence conservation of the N-terminal domain is relatively low and mostly limited to the kinase-like domain. Based on sequence similarity, the four SPA proteins fall into two subgroups with SPA1 and SPA2 forming one subgroup and SPA3 and SPA4 forming the other subgroup . Genetic analysis of spa mutants indicated that the four SPA genes have partly redundant but also distinct functions in plant growth and development [13, 27, 34].
COP1 functions have also been described in other flowering plant species. In rice, the COP1 ortholog PETER PAN SYNDROME1 (PPS) shortens the juvenile phase, a phenotype not reported for Arabidopsis, and delays flowering in short and long day . The COP1 ortholog of pea, LIGHT-INDEPENDENT PHOTOMORHOGENESIS1 (LIP1), regulates seedling growth by affecting gibberellic acid levels [36, 37]. In apple, MdCOP1 affects anthocyanin levels in the fruit peel . COP1 also exists in non-plant lineages, e.g. humans, where hCOP1 acts as an E3 ubiquitin ligase to control the protein stability of a number of transcription factors, e.g. p53 or cJun . SPA genes, in contrast, appear to be specific to plants, which indicates that human COP1 functions without a need for SPA proteins. This suggests that SPA genes might have evolved to place COP1 activity under the control of light. Indeed, the N-terminus of SPA1 was shown to be involved in the blue-light dependent interaction of SPA1 with cryptochrome photoreceptors [31, 32].
Whole genome sequencing has shown that COP1 and SPA genes exist in early diverged land plants, such as in the moss Physcomitrella patens. There are a number of light responses known in Physcomitrella, such as chloroplast movement, phototropism, caulonema branching and gametophore growth  as well as UV-B responses akin to those in Arabidopsis . While COP1 is a single copy gene in rice and Arabidopsis , genome sequence information predicted a total of nine paralogs in P. patens[41, 42]. Both the rice and Physcomitrella genomes contain two SPA-related genes each [41–43]. Physcomitrella has functional phytochrome and cryptochrome photoreceptors [39, 44–47], allowing the possibility that PpCOP1 and PpSPA genes may also function in light signal transduction in Physcomitrella.
To address the evolutionary conservation of COP1 and SPA protein sequences, we expressed COP1 and SPA coding sequences from rice and Physcomitrella in the respective cop1 and spa mutant backgrounds of Arabidopsis. Our results show that COP1 sequences are functionally much more conserved than SPA sequences, suggesting that gene duplication of SPA genes in the flowering plant lineage has contributed to divergence of SPA gene functions.
A comparison of Physcomitrella, rice and Arabidopsis COP1 and SPA protein sequences
While the COP1 gene family has expanded in Physcomitrella as compared to a single COP1 gene reported in flowering plant species, there are only two predicted SPA genes in Physcomitrella. These two PpSPA genes are very similar to each other (89% amino acid identity of the predicted proteins), suggesting that they represent recent duplication events based on an ortholog of AtSPA1/2 (Figure 1; Additional file 1: Figure S1A, B; Additional file 4: Figure S4). We named the two Physcomitrella SPA genes PpSPAa (Pp1s59_66V6.1) and PpSPAb (Pp1s30_295V6.1). There are two predicted rice SPA proteins of which each groups with one subclass from Arabidopsis (AtSPA1/2, AtSPA3/4) (Figure 1; Additional file 1: Figure S1A, B), evidencing that two paralogs were already present in the last common ancestor of monocots and dicots. The SPA1/SPA2-like rice SPA was more similar to Arabidopsis SPA1 than to Arabidopsis SPA2. We therefore refer to this rice SPA as rice SPA1-like or OsSPA1 (Os05g49590.1). The predicted SPA3/SPA4-like SPA from rice equally resembles Arabidopsis SPA3 and SPA4 protein sequences. We therefore refer to it as rice SPA3/4-like or OsSPA3/4 (Os01g52640.1). The predicted domain structures of Physcomitrella and rice SPA proteins are similar to those from Arabidopsis SPA proteins: they all contain an N-terminal kinase-like domain, a coiled-coil domain and seven WD40-repeats (Figure 1; Additional file 1: Figure S1C, Additional file 3: Figure S3, Additional file 4: Figure S4). Similar to Arabidopsis SPA proteins, the kinase-like domains from rice and Physcomitrella SPA proteins share only limited sequence conservation with bona fide Ser/Thr kinase consensus motifs because amino acid residues that are normally highly conserved in Ser/Thr kinases are not conserved in PpSPA and OsSPA proteins. Nevertheless, sequences in the kinase-like domain that are conserved among the four Arabidopsis SPA proteins are also highly conserved in OsSPA and PpSPA proteins (Additional file 4: Figure S4). All SPA sequences in Arabidopsis, rice and Physcomitrella contain a predicted coiled-coil domain (Additional file 3: Figure S3), though the sequence of the respective coiled-coil domain is not strongly conserved among Arabidopsis, rice or Physcomitrella SPA proteins. This suggests a structural rather than sequence-based conservation of this domain in the SPA proteins. The SPA protein sequences are most conserved within the WD40-repeat domain, with Physcomitrella SPAa and SPAb showing 65% amino acid identity with AtSPA1 - compared with 42% when aligning the complete protein sequences.
Rice and Physcomitrella also contain predicted orthologs of the Arabidopsis RUP genes. Arabidopsis RUP proteins consist of COP1/SPA-like WD40 repeats and function as negative regulators of UV-B signaling [49, 50]. The rice genome contains 1 ortholog of RUP, while Physcomitrella has two predicted RUPs (Figure 1; Additional file 1: Figure S1, Additional file 5: Figure S5).
Functional analysis of COP1-like proteins from rice and Physcomitrella in the hypomorphic cop1-4mutant of Arabidopsis
In order to address the evolutionary conservation of COP1 and SPA function, we expressed the coding sequence of Physcomitrella, rice and - as a control - Arabidopsis COP1 and SPA genes in transgenic Arabidopsis cop1 and spa mutants, respectively, to subsequently evaluate whether the transgenes complement the respective mutant phenotypes. Though protein detection in the transgenic plants is desirable, we did not add an epitope tag to the coding sequence because a tag might negatively affect protein function. Among the nine PpCOP1 genes, we chose the one with the highest sequence similarity to AtCOP1, based on BLAST scores, for the complementation study (Pp1s135_17V6.1, PpCOP1a, Figure 1). The coding sequences of OsCOP1, PpCOP1a and AtCOP1 were placed under the control of the 35S constitutive promoter and introduced into the hypomorphic cop1-4 mutant and into the cop1-5 null mutant of Arabidopsis. While the cop1 null mutant is seedling lethal, the cop1-4 mutant is viable, producing a truncated COP1 protein lacking the C-terminal WD-repeat domain [12, 51].
Besides the constitutive photomorphogenesis in seedlings, cop1-4 mutants exhibit mutant phenotypes in the adult plant: cop1-4 mutant plants are small and dwarfed and they flower earlier than the wild type, particularly under short day conditions . Transgenic AtCOP1, OsCOP1 and PpCOP1a cop1-4 mutant lines were similar in size as the wild type and flowered at a similar time as the wild type (Figure 2C,D,E). For each of the three transgenes, about half of the transgenic T1 plants showed full rescue of the cop1-4 mutant adult phenotypes (Figure 2D,E). Hence, OsCOP1 and PpCOP1a, like AtCOP1, were able to fully complement the cop1-4 mutant phenotypes in adult plants.
Functional analysis of COP1–like proteins from rice and Physcomitrella in the cop1-5null mutant of Arabidopsis
Since all three transgenes rescued the seedling-lethal phenotype of cop1-5, we were able to analyze the activity of the transgene also in the adult stage. Transgenic OsCOP1 cop1-5, PpCOP1a cop1-5 and AtCOP1 cop1-5 plants were of similar size as the wild type (Figure 2C,D). With respect to flowering time, transgenic AtCOP1 cop1-5 lines flowered at a similar time as the Ws wild type while transgenic OsCOP1 cop1-5 and, in particular, PpCOP1a cop1-5 lines flowered earlier than the wild type and the AtCOP1 cop1-5 transgenic lines (Figure 2E). These results indicate that the COP1 sequences from rice and Physcomitrella only partially rescued this aspect of the cop1-5 mutant phenotype.
Rice and Physcomitrella SPA protein-coding sequences do not complement the light hypersensitivity-phenotype of the Arabidopsis spa1 spa3 spa4triple mutant
To analyze functional conservation of rice and Physcomitrella SPA1-related protein-coding sequences we expressed OsSPA1 and PpSPAb ORFs in an Arabidopsis spa mutant. The two Physcomitrella SPA proteins, SPAa and SPAb are highly similar to each other (89% amino acid sequence identity) and both share equal sequence similarity to the Arabidopsis SPA1. We therefore chose only one of these SPAs, SPAb, for our analyses. As controls, we included the Arabidopsis SPA1 and SPA4 ORFs because these two SPAs are representative for the partially distinct functions of the four SPA genes [13, 15, 34]. We transformed these constructs into the spa1 spa3 spa4 triple mutant because this mutant is a viable spa mutant showing defects in multiple phenotypes including seedling deetiolation, leaf expansion and flowering time control [13, 15]. Initially, we expressed the SPA coding sequences under the control of the 35S promoter. However, the Arabidopsis 35S::AtSPA1 and 35S::AtSPA4 constructs produced very low complementation rates (<10% of transgenic plants) in the spa triple mutant, an observation we had made before . We therefore proceeded to express the respective SPA coding sequences under the control of the endogenous Arabidopsis AtSPA1 and AtSPA4 5´ and 3´ regulatory sequences which previously produced very high complementation rates among transgenic spa mutant plants (>90%) [27, 52]. For linguistic simplicity, we will refer to these regulatory sequences as ´promoters´ from now on.
In the adult stage, none of the constructs containing the OsSPA1 or PpSPAb coding sequences complemented the dwarfism or the early flowering time of the spa1 spa3 spa4 mutant (Figure 4B,C,D). Expression of the control constructs AtSPA1::AtSPA1 or AtSPA4::AtSPA4, in contrast, rescued these facets of the spa1 spa3 spa4 mutant phenotype to the expected degree [13, 15].
Functional analysis of SPA orthologs from rice and Physcomitrella in the constitutively photomorphogenic spa1 spa2 spa3mutant of Arabidopsis
The COP1/SPA complex of Arabidopsis is a well-characterized key negative regulator that actively suppresses the light signaling cascade in dark-grown plants by ubiquitinating transcription factors which mediate the various light responses. The E3 ubiquitin ligase activity is conserved in the mammalian ortholog of COP1 which, however, appears to function without a need for SPA proteins since SPA genes appear to be specific to plants. SPA protein sequences are distinct from COP1 in that they carry a kinase-like domain in the N-terminus [13, 26]. This kinase-like domain is conserved in Physcomitrella, rice and Arabidopsis SPA proteins and shows a similar divergence in sequence from bona fide Ser/Thr kinase motifs in all three species. This finding suggests on one hand that this kinase-like domain is of functional importance - though its exact role has so far remained elusive [31, 32, 34, 53] - and on the other hand that early in land plant evolution this domain was already divergent in sequence from normal protein kinases.
Our functional analysis clearly shows that PpCOP1a from Physcomitrella is able to mostly replace the functions of COP1 in Arabidopsis. Similarly, rice OsCOP1 was able to mostly complement all aspects of the Arabidopsis cop1 mutant phenotype. These findings suggest that COP1 is under strong negative selection in seed plants. Physcomitrella PpSPAb, in contrast, was incapable of complementing any of the spa mutant phenotypes in transgenic Arabidopsis, strongly suggesting that the PpSPAb protein is non-functional in Arabidopsis. Similarly, expression of the rice OsSPA1 protein in Arabidopsis spa mutants failed to complement any phenotypes of light-grown spa mutant plants and complemented the phenotype of dark-grown seedlings at a much reduced efficiency. These results suggest that SPA-like sequences underwent considerable functional divergence during evolution. However, since we cannot determine the PpSPAb and OsSPA1 protein levels in the transgenic Arabidopsis plants we cannot exclude the possibility that the apparent inactivity of PpSPAb and OsSPA1 in Arabidopsis are due to inefficient translation of the respective mRNAs or due to instability of the respective proteins in Arabidopsis when compared to the native Arabidopsis SPA1 protein. To fully understand the functional conservation between SPA1 from moss, rice and Arabidopsis, it will also be necessary to genetically identify OsSPA1 and PpSPA1 function in rice and Physcomitrella, respectively. Moreover, a protein-protein interaction analysis among the respective COP1 and SPA orthologs will be helpful in analyzing OsSPA1 and PpSPAb activity in Arabidopsis.
We can only speculate why the COP1 gene appears to be subject to much less functional divergence than SPA1. One likely reason is the fact that COP1 is a single-copy gene in flowering plants while SPA proteins are encoded by a small gene family comprising two to four members. Gene duplication is a powerful driving force of neo- and subfunctionalization during plant evolution . The four SPA genes of Arabidopsis are indeed not fully redundant but have partially distinct functions during Arabidopsis development [13, 15]. At least some of the functional divergence, the one between Arabidopsis SPA1 and SPA2, has been mapped to the respective SPA protein sequence rather than the promoter sequences . Hence, evidence strongly suggests that the four Arabidopsis SPA proteins are not identical in function but provide some degree of specificity to the COP1/SPA E3 ligase activity. The failure of PpSPAb and OsSPA1 to fully replace AtSPA1 in Arabidopsis supports that such functional divergence has occurred in the course of land plant evolution. While this is very reasonable, it is nevertheless significant that COP1 coding sequences did not functionally co-diverge with SPA sequences, especially considering that both proteins carry very similar WD40-repeat domains in their C-termini which both are able to bind and thereby recognize the same substrate proteins . Hence, COP1 must provide a core function to the COP1/SPA complex that hinders evolutionary divergence, and this core function is likely modified by divergent SPA proteins.
OsSPA1 was capable of restoring a wild-type phenotype in dark-grown spa triple mutant seedlings – though at low efficiency - but not in light-grown seedlings or adult plants. We consider two possible scenarios to explain this dark-specific complementation by OsSPA1: OsSPA1 activity may be reduced when compared to AtSPA1 and therefore be solely sufficient to restore SPA function in darkness but not in the light. This would be consistent with previous observations showing that mutations in a single SPA gene caused a mutant phenotype only in the light but not in darkness [24, 55]. Hence, full SPA activity is much more critical in light-grown seedlings than in dark-grown seedlings, probably because the light-induced inactivation of the COP1/SPA complex causes additional stress on the activity of the complex. Alternatively, OsSPA1 may be hyperinactivated by Arabidopsis photoreceptors and, therefore, lack any activity in the light. This behavior is found in the Arabidopsis SPA2 protein which also shows high activity primarily in dark-grown seedlings . Though the OsSPA1 sequence is more similar to Arabidopsis SPA1 than to SPA2, we do not exclude this possibility. Knocking out the OsSPA1 gene in rice would allow to distinguish between these two possibilities.
The degree of complementation by COP1 orthologs varied with respect to the different aspects of the cop1 mutant phenotype. Most evidently, expression of OsCOP1 or PpCOP1a in light-grown cop1-5 seedlings caused a reduced response to B and FR, a phenotype that is reminiscent of AtCOP1 overexpression rather than of reduced COP1 activity. This observation suggests that OsCOP1 and PpCOP1a maintain higher activity in the light than AtCOP1 and are therefore incompletely inactivated by Arabidopsis photoreceptors when compared to the native Arabidopsis COP1 protein. Hence, photoreceptor and COP1 sequences appear to have co-evolved to allow optimal adaptation of seedling growth to the ambient light environment. When analyzing adult growth and development, PpCOP1a and OsCOP1 fully complemented the cop1-5 leaf expansion phenotype while they only partially complemented the early-flowering phenotype of cop1-5. Since these phenotypes are mediated by distinct substrates, it is evident that the COP1-like proteins from rice and Physcomitrella do not polyubiquitinate all substrates of Arabidopsis COP1 equally well. Hence, functional conservation of COP1 may have varied with respect to the different substrates of COP1. Orthologs of known COP1/SPA substrates exist in P. patens, such as two PpHY5 and three PpCO-like (PpCOL) proteins [56–58]. A role of PpHY5 in moss light responses was described . Hence, if PpCOP1a acts as a light-regulated ubiquitin ligase in mosses as well, it may indeed mediate degradation of the PpHY5 protein. In the future, it will be interesting to elucidate whether there is a COP1/SPA E3 ligase in Physcomitrella and, if so, which substrates are recognized.
Our results show that COP1 protein sequences from Physcomitrella, rice and Arabidopsis are functionally conserved, while the sequences of the SPA proteins showed considerable functional divergence. This may - at least in part - reflect the fact that COP1 is a single copy gene in flowering plants, while SPA proteins are encoded by a small gene family of two to four members, thus possibly allowing sub- or neofunctionalization. Light responses are very distinct in mosses and angiosperms . Whether these differences reflect distinct signaling pathways including the recruitment of different transcription factors into the light signaling network needs to be resolved.
Sequences and ortholog prediction
Arabidopsis protein sequences correspond to the loci SPA1 (At2g46340.1), SPA2 (At4g11110.1), SPA3 (At3g15354.1), SPA4 (At1g53090.1) and COP1 (At2g32950.1) of the annotated Arabidopsis Col genome TAIR10 annotation . Rice proteins correspond to the loci OsCOP1 (Os02g53140.1), OsSPA1 (Os05g49590.1) and OsSPA3/4 (Os01g52640.3) of the Rice Genome Annotation Project Release 7 . However, based on an amino acid sequence alignment with all other SPAs from Arabidopsis, Physcomitrella and rice, the corresponding reference sequence of OsSPA3/4 (Os01g52640.3) lacks a part of the WD40 repeat domain. Here we used an alternatively spliced sequence, Os01g524630.1, from Genome Annotation Project Release 5 which contains additional WD40 repeats and in our opinion reflects the full-length OsSPA3/4 protein. Physcomitrella proteins correspond to the loci indicated in Figure 1. They are derived from the cosmoss.org Physcomitrella patens V1.6 genome annotation .
To conduct a phylogentic reconstruction of the COP1/SPA genes in Arabidopsis, rice and Physcomitrella, first an all-against-all blast search was performed. To find homologous sequences between these species, blastp + version 2.2.9  was used to build a blast database with protein sequences as indicated in Additional file 7: Table S1 and a blastp search was performed with an e-value cutoff of 10 by using the BLOSUM62 matrix. The resulting blastp results were then filtered by applying a changed version of formula (2) as indicated by . These filtered blastp results were then used with proteinortho version 4.26  to detect co-orthologs within and between these species by using the following options [-e = 0.01; -id = 11; -cov = 0.25; -conn = 0.1; -m = 0.75; -pairs; -selfblast; -blastdone]. The proteinortho results were filtered for COP1 (AT2G32950.1), SPA1 (AT2G46340.1), SPA2 (AT4G11110.1), SPA3 (AT3G15354.1), SPA4 (AT1G53090.1), RUP1 (AT5G52250.1), RUP2 (AT5G23730.1) and all resulting co-orthologs were used for further analysis and were screened for protein domains by InterProScan version 5 . The program ncoils (based on ) is used by InterProScan with default settings to predict coiled-coils domains. In addition to standard settings we used different sliding window parameters [14, 21, 28] for the coiled-coils domain predictions which are highlighted in Additional file 3: Figure S3. For the phylogenetic reconstruction RUP1 and RUP2 were chosen as an outgroup gene family since both also contain WD40 repeats like the COP1/SPA genes but lack functional domains further upstream. These genes could be used to root COP1/SPA phylogenetic trees.
A multiple sequence alignment (MSA) was calculated with MAFFT L-INS-i version 7.037b , ProbCons version 1.12 , Muscle version 3.8.31  and T-coffee version 8.99  with default settings and subsequently combined into an optimal alignment using the combiner function of T-coffee. The MSA was visualized and manually curated using Jalview version 2.8  (Additional file 2: Figure S2, Additional file 4: Figure S4, Additional file 5: Figure S5). The JTT + G + I + F model was selected as the best fitting amino acid substitution model according to the Bayesian Information Criterion in ProtTest version 3.3 . To reconstruct the phylogeny we used MrBayes 3.2.2  and RAxML version 8.0.2 .
For MrBayes we initiated two runs of four Markov-chain Monte Carlo (MCMC) chains of 2 × 107 generations each from a random starting tree, sampling every 1,000 generations [additional settings: rates = invgamma, ngammacat = 4, aamodelpr = JTT]. A 25% burn-in was chosen and convergence was assessed by standard deviation of split frequencies falling below 0.005.
RAxML conducted 1,000 non-parametric bootstrap inferences with the rapid hill-climbing mode using the PROTGAMMAIJTTF model [additional settings: -d -b -#1000]. The bootstrap replicates were used to build a consensus tree applying the majority rule option (-m PROTGAMMAIJTTF -J MR). Phylogenetic trees were rooted by the RUP outgroup gene family and visualized with Figtree version 1.4.0 (http://tree.bio.ed.ac.uk/software/figtree/).
Plant material, light sources and growth conditions
All mutant genotypes used were described previously: cop1-4 (Col-0), cop1-5 (Ws) , spa1-7 spa3-1 spa4-1 and spa1-7 spa2-1 spa3-1 (both Col) . Light sources, seedling growth conditions and determination of seedling and adult traits were described previously .
Plasmid constructions, plant transformations and selection of transgenic plants
All ORF clones were designed based on the sequence information provided in the databases described above. To generate COP1 expression clones, AtCOP1, OsCOP1 and PpCOP1a ORFs were amplified using gene-specific primers with attached attB sites and the amplified sequences were subsequently cloned into the pDONR221 entry vector by Gateway cloning according to the manufacturer´s instructions. AtCOP1 and PpCOP1a ORFs were amplified from cDNA derived from Arabidopsis seedlings or Physcomitrella gametophores, respectively. OsCOP1 was amplified from a full-length cDNA clone obtained from National Institute for Agrobiological Sciences (NIAS), Japan. The obtained Entry clones were recombined with the pGJ2169 GW binary destination vector (kindly provided by George Coupland) containing the 35S promoter before the Gateway cassette. The final destination vectors were transformed into homozygous cop1-4 and heterozygous cop1-5/+ mutants. Transgenic plants were selected on Basta herbicide. In the cop1-4 background, at least 25 independent transgenic lines per construct were analyzed in the T1 (flowering time, leaf size) and T2 (seedling deetiolation) generations. In the cop1-5 background, lines homozygous for cop1-5 and the respective transgene were generated by selecting for kanamycin resistance (cop1-5), the absence of the native COP1 transcript and the presence of the introduced transgene (Basta resistance).
SPA expression clones were constructed as follows: First, 2260 bp or 1309 bp of the Arabidopsis SPA1 or SPA4 5´ regulatory regions preceding the ATG start codon, respectively (pSPA1, pSPA4), were amplified from previously constructed plasmids using primers containing HindIII or SdaI restriction sites, respectively, and subsequently cloned into unique HindIII or SdaI restriction sites, respectively, of the pGWB1 destination vector . These modified pGWB1 destination vectors now have Gateway cassettes after the pSPA1 or pSPA4 promoters, respectively. Second, Entry clones carrying the ORFs of SPA sequences were generated after amplifying the ORF of AtSPA1 and AtSPA4 from Arabidopsis cDNA, the OsSPA1 ORF from a full-length cDNA clone obtained from NIAS, Japan, and the Physcomitrella SPAb ORF from cDNA synthesized from Physcomitrella gametophores (for all primer sequences, see Additional file 8: Table S2). Third, the modified pGWB1 destination vectors described above were recombined with the Entry clones containing the ORFs from AtSPA1, OsSPA1, PpSPAb and AtSPA4, respectively, using Gateway LR technology to generate pSPA1::AtSPA1/OsSPA1/PpSPAb vectors and pAtSPA4::AtSPA4/PpSPAb vectors. These binary vectors were transformed into Arabidopsis spa1 spa3 spa4 and spa1 spa2 spa3 mutants.
RNA isolation and transcript analysis
RNA was isolated and reverse-transcribed as described previously . SPA ORFs were amplified by semi-quantitative RT-PCR using gene-specific primers (Additional file 8: Table S2). PCR products were resolved by agarose electrophoresis and subsequent staining with ethidium bromide.
Availability of supporting data
The data sets supporting the results of this article are included within the article and its additional files.
We are grateful to the National Institute for Agrobiological Sciences (NIAS) in Japan for providing full-length OsCOP1 and OsSPA1 cDNA clones and to George Coupland for the gift of the pGJ2169 GW vector. We thank Sebastian Meller for excellent help in identifying transgenic cop1-5 mutant lines and Klaus Menrath and the greenhouse staff for expert care of our plants. This work was funded by the Deutsche Forschungsgemeinschaft (SFB635) to U.H. Aashish Ranjan was a recipient of a Ph.D. fellowship from the International Graduate School of Genetics and Functional Genomics from the state Northrhine-Westphalia, Germany. Stephen Dickopf was supported by a Ph.D. fellowship from the International Max-Planck Research School and the University of Cologne.
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