Bidirectional promoters in seed development and related hormone/stress responses
© Kourmpetli et al.; licensee BioMed Central Ltd. 2013
Received: 16 July 2013
Accepted: 15 November 2013
Published: 22 November 2013
Bidirectional promoters are common in genomes but under-studied experimentally, particularly in plants. We describe a targeted identification and selection of a subset of putative bidirectional promoters to identify genes involved in seed development and to investigate possible coordinated responses of gene pairs to conditions important in seed maturation such as desiccation and ABA-regulation.
We combined a search for 100–600 bp intergenic regions in the Arabidopsis genome with a cis-element based selection for those containing multiple copies of the G-box motif, CACGTG. One of the putative bidirectional promoters identified also contained a CE3 coupling element 5 bp downstream of one G-box and is identical to that characterized previously in the HVA1 promoter of barley. CE3 elements are significantly under-represented and under-studied in Arabidopsis. We further characterized the pair of genes associated with this promoter and uncovered roles for two small, previously uncharacterized, plant-specific proteins in Arabidopsis seed development and stress responses.
Using bioinformatics we identified putative bidirectional promoters involved in seed development and analysed expression patterns for a pair of plant-specific genes in various tissues and in response to hormones/stress. We also present preliminary functional analysis of these genes that is suggestive of roles in seed development.
Bidirectional promoters are common in genomes  and have more recently been identified and examined in silico in the completed genomes of plants, including Arabidopsis [2, 3]. The relevance and potential of these promoters in biotechnology has been documented [4–6], particularly for use in gene-stacking approaches where more than one gene is required to confer a particular trait trangenically or more than one trait is being conferred e.g. resistance to a suite of pests . While researchers can engineer polar promoters to be bidirectional [4, 6], if we can characterize naturally occurring bidirectional promoters in plants these could provide a valuable alternative or at least a source of information on their mode of action in planta.
As well as applied and biotechnological relevance, the existence of bidirectional promoters has been recognized as a fundamental and complex means of transcriptional control [8, 9]. Research in yeast revealed that the existence of bidirectional promoters was not only pervasive but the source of the majority of cryptic transcription in the organism and therefore the means of transcriptional regulation [10, 11].
Except for isolated examples of detailed experimental analyses of bidirectional promoters [12–15], virtually all the work published to date is bioinformatics-based and while this work has certainly highlighted the prevalence and potential importance of bidirectional promoters in areas from fundamental transcriptional control research to clinical relevance in cancer research [8, 9, 16], it still remains to explore the functional relevance of this gene organization experimentally by focusing on specific gene pairs of interest. The bioinformatics/computational-based criteria used to isolate a workable set of genes can vary depending on the desired outcome of the analyses and can involve coding and non-coding features – in this case we used both to identify putative bidirectional promoters regulating genes involved in seed development. Analysis of the divergently transcribed genes associated with a targeted set of bidirectional promoters is likely to lead to discovery of novel genes involved in development and/or previously undescribed relationships between genes of different functional categories in common or complementary processes/responses.
We used bioinformatics to search and identify a subset of putative bidirectional promoters that we predicted would regulate genes with roles in seed development. ABA is integral to plant seed development as a general process but mechanistically ABA mediates the conferral of desiccation tolerance and dormancy on seeds . As such therefore there is extensive crosstalk between the stress responses of drought and cold as well as antagonistic interactions with the germination process . The response to ABA is mediated by promoter motifs based on the ACGT core called ABREs (abscisic acid responsive elements) and including the G-box element (CACGTG). This element has been found in previously identified cases of bidirectional promoters which regulate genes involved in ABA response and seed development [19–21], as well as in promoters of genes regulated by light [22, 23]. The identity of the nucleotides flanking the ACGT has been found to be an important determinant of the element’s specificity [24, 25]. The use of cis-elements such as ABREs in identifying genes involved in ABA and stress response has been previously described . The G-box ABRE is often found in combination with other motifs, coupling elements (CE) that can be derived from or distinct from the ACGT core and are also involved in the seed/ABA regulation and responses to osmotic and cold-temperature stresses [18, 27]. In addition, specific motifs associated with regulation by cold and dehydration have been classified as DRE/CRTs (dehydration response element/c-repeat) derived from a CCGAC core sequence [28, 29].
Previous work characterized two genes highly expressed in maturing seeds [30, 31]. These genes are transcribed from an intergenic region (between start codons) of 411 bp which contains three copies of the G-box (CACGTG) motif involved in ABA-regulated seed development [20, 30, 31] (Additional file 1: Figure S1A). These genes, At4g16155 and At4g16160, encode a plastid outer envelope protein, OEP16-S, and a lipoamide dehydrogenase, ptLPD2, also localized to the plastid (in this case the stroma) . Recent functional analyses of these genes revealed roles in metabolic fluctuation and arsenate sensitivity, respectively [32, 33]. In addition, a divergent arrangement of a seed-expressed oleosin gene, OLE1, and a peptide methionine sulfoxide reductase, PMSR, At4g25130 and At4g25140 respectively, was reported initially in Brassica napus and then characterised in Arabidopsis[21, 34, 35]. This promoter of 499 bp (between start codons) contained two copies of the G-box motif (Additional file 1: Figure S1B). The PMSR protein is plastid-localised and involved in oxidative stress response while mutations in OLE1 conferred cold tolerance [36, 37].
We combined a search for a bidirectional gene arrangement with ABRE and associated cis-elements in the Arabidopsis genome and subsequently focused on a pair of plant-specific genes of unknown function that we characterised in detail. The identity and localisation of the genes identified in the bioinformatics search suggest that this gene arrangement might enable a means of concerted or complementary responses to stresses or environmental stimuli, such as drought or hormones, while the localization of the gene products to varied organelles could reflect a means of coordinating the complex intracellular interactions induced by stress conditions.
Arabidopsis thaliana genes were downloaded from ENSEMBL plants 17, with headers including gene ID, transcript ID, coding sequence, chromosome name, transcript start, transcript end and strand. Putative bidirectional promoters were identified using in-house Perl scripts that searched header information for transcripts on opposite strands of the same chromosome that had start sites within 100–600 bp of one another. (The start sites of transcripts on the reverse strand were taken as ENSEMBL’s ‘transcript end’ position). Putative bi-directional promoter sequences were retrieved from ENSMBL plant 17 chromosomes and searched for the presence of the CACGTG motif.
We used the AtGenExpress Visualisation Tool (AVT; http://jsp.weigelworld.org/expviz/expviz.jsp) to extract gene expression data where indicated using the datasets for development, abiotic stress, hormones and light [38–40].
Homologous sequences to genes At3g03150 and At3g03160 were identified using standard BLAST searching tools (http://0-www.ncbi.nlm.nih.gov.brum.beds.ac.uk/BLAST/). The Accession numbers of homologous sequences used for amino acid alignments are shown in Additional file 2: Table S1). Alignments were done using CLUSTALX and BioEdit [41, 42]. Localisation prediction programs used were PSORT  and TargetP . Searches for promoter motifs were done using PLACE  and transmembrane prediction was performed using the TMHMM Server v2.0 .
Plant material and growth conditions
Arabidopsis thaliana wild-type (Col-0) and T-DNA insertion plants were grown in a control environment with a 16 h photoperiod, 120–140 μmol/m2/sec light intensity, 40-50% relative humidity and a temperature of 21 ± 2°C. For crosses with dehiscent anthers, closed flower buds were emasculated 48–72 h before pollination.
For silique analysis, the five longest green siliques were collected from each plant (wild-type, T-DNA insertion line or cross between the two), opened under a dissecting microscope and the number of normal seeds, early and late aborted seeds as well as unfertilized ovules was determined.
Arabidopsis seedlings were grown vertically for three weeks at 22°C on a medium containing 0.5xMS salts, 0.5xMS vitamins, 0.5 gl-1 4-morpholineethanesulfonic acid (MES), 0.5% (w/v) sucrose and 0.7% agar, pH 5.7. For each treatment seedlings were transferred into a petri dish with a sterile filter paper that was soaked in either liquid MS medium, 10 μM ABA in 0.1% methanol or 0.1% methanol. Three seedlings from each treatment were collected for further analysis after 3 h and 24 h. For the dehydration stress, seedlings were left in an open petri dish at room temperature for 1.5 h. Primers for the KIN1 and RD29 genes were taken from Kim et al..
The full-length coding region of At3g03150 was amplified from the SALK ORF-trimmed pUNI clone (u23027) with Gateway compatible primers and cloned into a pDONR207 entry vector (Invitrogen). This was used to make a C-terminal GFP fusion in GFP-C-BIN and subsequent transient transformation of tobacco cells. Tobacco leaves (Nicotiana benthamiana) were infiltrated with a solution of saturated Agrobacterium resuspended in 10 mM MgCl2, 10 mM MES, 100 μM acetosyringone to OD600 0.4) and observed for GFP localisation 10 days after infiltration. Mitochondria tracker CMX Ros red (Molecular Bioprobe) was used at 400 nM in water for 45 min and washed 3 times for 5 min in water. Observation was carried out on an inverted SP2 confocal (Leica) using a 40x oil immersion lens. Sequential scans were taken with GFP excited at 488 nm with an Argon Ion laser and the Mito tracker at 543 nm from a green helium neon laser.
Transcript analysis by RT-PCR and qRT-PCR
Total RNA was extracted from the flower tissues of insertion lines and from flower, silique, root, rosette and cauline leaf and stem tissues of wild-type Arabidopsis and cDNA was made using the BioScript kit (Bioline) following the manufacturer’s instructions. Primers for amplification of At3g03150 from cDNA were 150 F and R; for At3g03160, 160 F and R; for At5g17165, 165 F and R and for At5g17190, 190 F and R. Actin was used as control using primers Actin2F and Actin2R.
Total RNA was extracted from ABA/stress treated seedlings of A. thaliana using TriSure™ (Bioline) and treated with DNase I (NEB), according to the manufacturer’s instructions. 700 ng of RNA from each sample were used in a 20 μl cDNA synthesis reaction with the Tetro cDNA Synthesis Kit (Bioline), following the manufacturer’s instructions. Quantification of At3g03150 and At3g03160 transcript levels by real-time PCR was performed using 1 ul of a 1:20 dilution of cDNA template in a 20 ul reaction containing SYBR Green JumpStart™ Taq ReadyMix™ (Sigma-Aldrich) and primers 150 qF and 150 qR, or 160 qF and 160 qR at a final concentration of 0.5 uM. Each reaction was performed in triplicate in a PTC-200 Peltier thermal cycler (MJ Research) using the following conditions: denaturation at 95°C for 3 min followed by 40 cycles of denaturation at 95°C for 30 sec, annealing at 55°C for 30 sec and extension at 72°C for 30 sec. 18S was used the reference gene with primers 18S F and 18S R All primers are listed in Additional file 3: Table S2.
The At3g03150-At3g03160 promoter sequence (between the two ATG start codons) was amplified from Col-0 genomic DNA using primers AtPromF and AtPromR (Additional file 3: Table S2) and a proofreading DNA polymerase (Velocity, Bioline). The amplified genomic fragment was then cloned into pJET1.2 vector using the CloneJET PCR Cloning Kit (Thermo Scientific) and confirmed by sequencing. The promoter fragment was amplified from pJET1.2 vector in both orientations using primers with suitable attB sites attached to them and cloned into Gateway® entry vector pDONR221 (Invitrogen). The primers used were 150promF and R for At3g03150 160promF and R for At3g03160. Each promoter entry clone was introduced into pKGWFS7 destination vector using single site recombination, in order to access the ability of the intergenic region to drive GUS expression in both orientations.
Arabidopsis Col-0 plants were transformed with Agrobacterium tumefaciens GV3101 strain harboring either one of the two promoter-pKGWFS7 plasmids using a standard floral dipping method . T1 seed collected from the transformed plants was plated on kanamycin selection plates. Surviving seedlings were transferred to soil and used for further analysis.
Siliques were harvested at stages just after fertilisation and up to endosperm cellularistion, fixed in 90% acetone at −20°C, infiltrated (under vacuum for 1 mintue) with GUS staining solution (50 mM Na2HPO4, 50 mM NaH2PO4, pH 7.0, 2 mM potassium ferricyanide, 2 mM potassium ferrocyanide, 2 mM EDTA, 1 mg/ml X-Gluc) and incubated at 37°C for overnight. The same staining solution was used to infiltrate fresh tissues of seedlings, leaves and inflorescences. After staining, tissue was cleared with 70% ethanol and stored at 4°C.
GUS-stained ovules and ovules for phenotypic analyses were mounted in chloral hydrate and analysed with DIC optics as described in Boisnard-Lorig et al., . Images were captured using a digital camera and assembled with Adobe Photoshop software (Adobe Systems, Mountain View, CA).
Insertion lines characterization
SALK T-DNA lines SALK_121507 and SALK_025090  were obtained through NASC (Nottingham Arabidopsis Stock Centre) and genotyped by PCR as recommended using the LBb1.3 primer and gene specific primers 507 F and R; 262 F and R (Additional file 3: Table S2).
Genetic transmission through male and female gametes
In order to determine the gametophytic transmission efficiency (TE) of the T-DNA, reciprocal crosses between wild-type Col-0 and SALK_121507 or SALK_025090 plants were performed. Seed was collected from individual siliques and the F1 generation was screened for the presence of the T-DNA insertion. The TE through each gamete (TEMALE and TEFEMALE) was calculated according to Howden et al..
Pollen of wild-type and T-DNA insertion lines was stained with DAPI (4′,6-diamidino-2-phenylindole; 1 mg/ml) and examined for any morphological differences. FDA (fluorescein diacetate) staining was used to access viability (10% solution in acetone/0.3 M mannitol). Pollen germination assays were performed according to Boavida and McCormick .
Identifying putative ABA-regulated/seed-expressed bidirectional promoters in Arabidopsis
Putative bidirectional gene pairs identified with 100–600 bp between transcription start sites (TSS) and containing at least two G-Box elements
maternal effect embryo arrest 4 (MEE4)
vicinal oxygen chelate (VOC) metalloenzyme
nuclear factor Y, subunit C10
Cystathionine beta-synthase (CBS)
Ribosomal protein L20
unknown protein 6 (UP6)
ER lumen protein retaining receptor family
LRR kinase (FEI1)
putrescine-binding transporter protein
unknown function (DUF639)
Ribosomal protein S7e family
RING/FYVE/PHD zinc finger
DWARF 5 (DWF5) -STEROL DELTA7 REDUCTASE
PHOTOSYSTEM I SUBUNIT H2
ChlADR aldehyde reductase
Glycoprotein membrane GPI-anchored
CCAAT motif binding complex
Ubiquitin c-terminal hydrolase
Ubiquitin c-terminal hydrolase
Auxin efflux carrier
RNA pol II transcription elongation factor
Tetratricopeptide repeat (TPR)-like
NOP10; EDA27 (RNA binding)
Ser/Thr kinases - Ataurora2 (AUR2)
acetyl-CoA carboxylase subunit
Cysteine proteinase superfamily
Amino acid dehydrogenase
galacturonosyltransferase 7 (GAUT7)
60S ribosomal protein L23aA
AtPOP4 (RNA processing)
Phosphoenolpyruvate carboxylase family
peroxin11 (PEX11) family
eukaryotic initiation factor 3 ⊠ subunit
lecithin:cholesterol acyltransferase 3
unknown function (DUF827)
rRNA small subunit methyltransferase B
Tetratricopeptide repeat (TPR)-like
plastid DNA-binding protein; MFP1
unknown function, DUF599
2OG and Fe(II)-dependent oxygenase
eukaryotic release factor 1-3
Kinase phosphorylation domain
Tetratricopeptide repeat (TPR)-like
HRF1 family protein
Plastid-lipid associated (PAP)
SD3 (Segregation Distortion 3); TIM21
raffinose synthase family pseudogene
S/R-Rich Protein Splicing Factors
nudix hydrolase homolog 14
Ribosomal protein L19 family
glycerol-3-phosphate permease gene family
RNA-binding (RRM/RBD/RNP motifs) family
starch synthase 4 (SS4)
DEG5 - photosystem II repair
Aldolase-type TIM barrel family
chromomethylase 2 (CMT2)
AMP-dependent synthetase and ligase family
PsbQ subunit photosystem II
kinesin-like motor protein
Leucine-rich repeat (LRR) family
Pectin lyase-like superfamily
chloroplast methionine sulfoxide reductase
cold acclimation protein (CAP160)
unknown function (DUF2296)
Tetratricopeptide repeat (TPR)-like
K + UPTAKE PERMEASE 5 (KUP5)
SYN1 (RAD21-like) gene
Peptide-N4-asparagine amidase A protein
prenylated RAB acceptor 1.A2
folylpolyglutamate synthetase isoform
Mito ATP-Mg/Pi transporter
Eukaryotic aspartyl protease
RNase L inhibitor protein-related
Protein phosphatase 2C family protein
TORMOZEMBRYO DEFECTIVE (TOZ)
ZPR1 zinc-finger domain protein
Ubiquitin c-terminal hydrolase
Ubiquitin c-terminal hydrolase
ACCUMULATION OF PHOTOSYSTEM ONE 3
isoform of alternative oxidase
GT43 glycosyltransferase family
FMN-linked oxidoreductase superfamily
The cellular localisation of each gene product was noted based on predictions using the TargetP tool and individual gene profiles available on TAIR. Proteins are predicted to lie in all main cell compartments and divergent gene pairs could be in the same or different locations. However, 25% were predicted to be localized to the plastid, 20% to the endomembrane/secretory system, 14% to the mitochondria and the remaining 40% to other components including cytoplasm and nucleus. At the functional or activity level, 33% encode enzymes. Previous studies have noted an enrichment for enzymes/metabolism and organellar localisation in the human genome [53, 54] and the seed development process is naturally accompanied by extensive metabolic fluctuation [33, 55, 56]. 24% of genes are potentially involved in direct gene expression regulation, DNA/RNA binding and processing. Some of the genes identified have already been shown to be involved in embryo/endosperm development (At1g04630 and At2g20490 were identified as MEE4 and EDA27, respectively, by Pagnussat et al. and other genes are more obviously associated with some form of light-regulation (At4g21280, PsbQ subunit) . Interestingly, MEE4 shares its bidirectional promoter with AtPOP5 which was shown to physically interact with AtPP30, involved in female gametophyte development, in an RNase P/MRP complex . The TORMOZ and AURORA genes (At5g16750 and At2g25880) are involved in embryo development [60, 61]; SYN1 (At5g05490) is essential for meiosis ; SD3 and DWF5 are membrane proteins involved in seedling development [63, 64]. Other genes have been shown experimentally to be responsive to drought or ABA such as LEA4-1 and OEP16-S (At1g32560 and At4g16160; [33, 65]; Additional file 1: Figure S2B and Additional file 1: Figure S1A). The gene pairs were also examined for the extent of co-expression using AtGenExpress Visualisation Tool [38–40] which showed that while in some cases the genes showed very similar patterns of expression, there were also cases where the expression patterns of both genes differed significantly in terms of both temporal and spatial patterns and also in terms of their response to various stresses (Additional file 1: Figure S2). Several parameters can be taken into account when assessing if a gene pairs’ products might be directly linked functionally such as the extent of co-expression and the subcellular co-localization of the gene pair products. Only three gene pairs have products that are predicted to be targeted to the same organelle (not counting cytosolic predictions). At1g52230 and At1g52220, encoding the PSI subunit H and an unknown protein respectively, have identical expression patterns according to AtGenExpress (Additional file 1: Figure S2A) and are localized in the thylakoid system of the plastid. Furthermore we found that a previous analyses of a chloroplast protein interaction network  had predicted an interaction between these proteins and that the localization of the unknown At1g52220 product to the thylakoid was confirmed as well as a physical interaction with the D subunit of PSI.
CE3 coupling elements are rare in the Arabidopsis genome [26, 67] and while CE3-like elements have been described [47, 68], this is the first report of a consensus CE3 element in Arabidopsis. Therefore we chose to focus on the only pair of genes containing both a DRE and a CE3 element (Highlighted in Table 1). In addition, this pair At3g03150-At3g03160 has SALK T-DNA insertion lines available within the coding regions to enable preliminary functional analyses of the genes.
At3g03150 and At3g03160 are transcribed from a putative bidirectional promoter and encode novel plant-specific proteins
The protein sequence of At3g03150 had no familiar domains or motifs that would indicate a function. Localization prediction using PSORT and TargetP programs indicated (with 75% and 91% probability, respectively) mitochondrial localization. The predicted cleavage site matches consensus sites and the targeting region is rich in serine. Overall the 120 amino acid protein is composed of almost 15% serine and threonine residues. Over 37% are PEST residues of which 16% are serine alone. A high PEST content is indicative of proteins with high turnover and indicates that the protein may be unstable. The gene’s structure is particularly striking showing the presence of one intron of over 1.2 kb and with the first exon discretely encoding the target sequence. To test the validity of the localization prediction of At3g03150, a translational protein fusion with GFP at the C-terminal of the protein was constructed to test for mitochondrial localization. Results in Additional file 1: Figure S3A confirm localization of the protein to the mitochondrion.
The divergent gene, At3g03160, is also of unknown function but contains three transmembrane domains (TMHMM Server v2.; ; Additional file 1: Figure S3B) and is homologous to a dehydration-induced transcript from the resurrection plant Xerophyta humilis (Figure 1C). The intergenic promoter contains a consensus DRE (Figure 1A). TargetP predicts a signal peptide and so it is likely the protein is part of the secretory pathway.
In addition, there are orthologues of At3g03150 in vascular plants only while At3g03160 has orthologues in Selaginella and Physcomitrella patens (Figure 1B,C). The strong preservation of certain blocks of sequence between At3g03150 and orthologues identified in Genbank, even before the emergence of the flowering plants (represented by the pine sequence), suggests that these putative active sites are well-conserved across a broad evolutionary time-frame (Figure 1B). The level of amino acid identity between At3g03160 orthologues across the embryophyta (land plants) is striking (Figure 1C).
Both genes have paralogues on chromosome 5 and appear to be the result of a genomic duplication previously identified [71, 72]. The corresponding region on chromosome 5 preserves the divergent arrangement of the genes but with two other genes, At5g17170 and At5g17180, intervening (Additional file 1: Figure S3C). These intervening genes are single-copy. At3g03160 is homologous to At5g17190. In the case of At5g17165, the modular nature of the gene structure with the first exon encoding the targeting peptide is maintained.
BLAST analysis against the rice and Brassica genomes revealed that the bidirectional arrangement of these two genes is only conserved in Brassica rapa. The duplication corresponding to At3g03160/At5g17190 and At3g03150/At5g17165 occurred before Brassica/Arabidopsis split and a further duplication in Brassica produced two At3g03150 and two At3g03160 paralogues (Figure 1B,C).
Both genes share a similar general expression pattern but are not identical
The expression patterns of the paralogues At5g17165 and At5g17190, respectively, were also checked by RT-PCR with gene-specific primers. At5g17165 produced a transcript spanning the two exons which was detectable at a level significantly less than that of At3g03150 except in flower tissues (Additional file 1: Figure S3D). At5g17190, like At3g03160 is also highly expressed in roots and developing seeds (Additional file 1: Figure S3D).
The genes respond differently to stresses
Data pertaining to stress and hormone treatments was also extracted from AtGenExpress (Figure 3C). This showed obvious ABA responsiveness in At3g03150 but also a weaker response of At3g03160 at 10 μM ABA. At3g03150 responded to drought treatments at 3 and 6 hours but no discernible response was seen for At3g03160 – however there is an obvious reduction in At3g03160 expression on seed imbibition suggesting that the gene may respond negatively to hydration in this context.
Both genes play a role in seed development
Seed counts from siliques of wild-type Col-0 and T-DNA insertion lines for At3g03150 and At3g03160
% Unfertilised ovules
% Early aborted seeds
% Late aborted seeds
% Normal dev. seeds
Selfing of the SALK_121507 heterozygotes produced a consistent ratio of wild-type to heterozygote of 1:0.7 in progeny populations suggesting that it was a gametophytic mutant. This was tested further by crossing the heterozygote to wild-type plants as both pollen donor and recipient. Screening of the F1 population of the reciprocal out-crosses to the wild-type for the presence of the T-DNA insertion revealed that there is a slight reduction in the transmission efficiency both through the male and the female (TEmale = 70.5%, TEfemale = 88%, Additional file 4: Table S3). The fact that, despite the significant transmission through both gametophytes, homozygous plants for the T-DNA insertion were never recovered after selfing indicates that this mutation causes zygotic lethality.
Though recognized as being a common phenomenon in animal and plant genomes based on bioinformatics analyses, there is currently no example in the literature that uses a targeted analysis of bidirectional promoters with associated functional characterization of the genes involved. Here we have conducted a targeted search for putative bidirectional promoters involved in seed development using limited examples from the literature and characterized one of the promoters and associated gene pairs in detail, including preliminary functional analyses. This approach could complement conventional screening approaches in the search for genes involved in seed-associated processes [57, 74–77] and/or for genes regulated by hormones and stresses  and our dataset contains some genes also identified in these screens [26, 57]. The bidirectional promoter structure suggests co-ordination of expression and indeed much of the bioinformatics analysis to date includes evidence of co-expression of diverging genes based on the large volume of transcriptomic data available. AtGenExpress analysis of the 70 bimotif flanking genes shows some that mirror each other and others that are very different (Additional file 1: Figure S1; Additional file 5: File S1). Bioinformatics analyses have tended to focus on the co-expression or even common GO categorization. With the large datasets this is understandable but if focusing on specific subsets it might be possible to tease apart other cases where protein function or expression pattern is not obviously similar. Co-expression does not necessarily mean spatial and temporal expression similarities but could also involve a coordinated response to stress that could be tissue-distinct, and indeed even organelle -distinct. These coordinated responses may be mediated through promoter cis-elements. It has been found that by integrating known cis-elements with co-expression increases the reliability of associated gene function prediction . Though 40% of the genes in Table 1 are predicted to be mitochondrial or plastid-localised, there are only three cases where both genes are predicted to be localized to the same organelle. In the case of the oleosin and PMSR genes, the AtGenExpress expression profiles diverge considerably with oleosin being seed-specific and PMSR expressed ubiquitously (Additional file 1: Figure S1B). In addition, oleosin is ABA-induced – often characteristic of a gene highly expressed in maturing seeds – while PMSR responds to oxidative stress, a natural consequence of seed maturation [36, 56]. While the At3g03150-At3g03160 intergenic region contains two ABRE palindromic CACGTG hexamers, the adjacent nucleotides vary in either orientation (which has shown to be an important determinant of binding specificity; [24, 25]) and the CE3 element is unidirectional. As might be expected therefore this variation is reflected in expression patterns and function, though both genes appear to affect aspects of seed development.
The bidirectional arrangement might be a particularly efficient way to mediate concerted or complementary response to stresses or environmental stimuli such as light or hormones. Bondino and Valle  pointed out that plants being sessile may need sophisticated means of coordinating gene expression responses to various stresses. In addition to the promoters coordinating responses to varied stresses and developmental signals, the localization of the gene products to varied organelles reflect a means of coordinating the intracellular interactions. Stresses such as drought, cold and salinity have shared and distinct signaling pathways, some of which are ABA-dependent . In the case of At3g03150-At3g03160, the former is strongly regulated by ABA and located in the mitochondrion while the latter has a weaker response to ABA and is membrane-bound (though may be regulated by drought based on the presence of a DRE element and homology to a X. humilis desiccation-induced transcript) . In the case of At1g07645 in Table 1 it is also homologous to a desiccation-induced X. humilis metalloenzyme but its expression was not affected in Arabidopsis seedlings under drought conditions . Zhang et al. searched for ABRE cis-elements in promoters to identify genes involved in associated stress responses but did not include any selection for potential bidirectionality in the promoters. Despite this, within the list of the top 40 predicted ABA/stress responsive genes in this study, 4 pairs of genes and another gene (23%) are also on our list in Table 1 and a further two pairs of divergent genes are also included (these were not on our list because the distance was slightly larger between genes and the ABRE search was not restricted to the CACGTC motif).
Co-regulation or co-ordination of the expression of multiple genes has been described in other arrangements and contexts. Operon structures, once thought exclusive to prokaryotes, have been found in biosynthetic pathways in plants (summarized by DellaPenna and O’ Conner ) coordinating the expression of genes with distinct functions but in a common biosynthetic pathway. Bidirectional promoters may constitute another means of coordinated expression in eukaryotes .
Analyses of the gene pairs spanning a putative bidirectional promoter may also help uncover functions for the vast array of unknown genes that remain to be characterised . An initially “unknown” gene identified with a TSS 200 bp upstream and divergent to the PARKIN gene (a ubiquitin E3 ligase determining aspects of parkinsonism), PACRG (PArkin Co-Regulated Gene; ), was shown to share a common molecular pathway . We were intrigued to find that in the case of the At1g52230 and At1g52220 gene pair, encoding the PSI subunit H and an unknown protein respectively, identified here (Table 1), a previous construction of a chloroplast protein interaction network had predicted an interaction between these proteins and a physical interaction of At1g52220 with a PSI subunit was confirmed .
There are still thousands of genes for which there is no definitive function assigned and this can only be done by careful experimental examination of individual genes in the laboratory at multiple levels – gene sequence, expression and function. In the Arabidopsis genome at least 40% of genes still have no determined function  and 20% of the mitochondrial proteome consisted of unknown proteins, many plant-specific . Analyses of previously uncharacterised and plant-specific genes such as mitochondrial At3g13150 and transmembrane At3g03160 help accelerate these potential discoveries. Though we do not know what the activities of the encoded proteins are, we have described preliminary evidence of a common involvement in aspects of seed development.
Bidirectional promoters are common in genome sequence but understudied experimentally, particularly in plants. Focusing on the G-box promoter motif, CACGTG, we performed a targeted identification of a subset of putative bidirectional promoters to identify genes involved in seed development and to investigate possible coordinated responses of gene pairs to conditions important in seed maturation such as desiccation and ABA-regulation. We further characterized a pair of genes sharing an intergenic region that also contained a CE3 element and describe preliminary functional data implicating two small, previously uncharacterized, plant-specific proteins in Arabidopsis seed development and stress responses.
The authors would like to thank other members of the B/BASH bioinformatics unit in University of Leicester, Richard Badge and Matthew Blades. Work in the SD group is supported by the University of Leicester, The Leverhulme Trust and BBSRC. TP was a University of Leicester MSc. Molecular Genetics project student. We also acknowledge the work of Annabel Sturgess funded by a summer internship from The Genetics Society.
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