- Research article
- Open Access
Coordination of the maize transcriptome by a conserved circadian clock
BMC Plant Biology volume 10, Article number: 126 (2010)
The plant circadian clock orchestrates 24-hour rhythms in internal physiological processes to coordinate these activities with daily and seasonal changes in the environment. The circadian clock has a profound impact on many aspects of plant growth and development, including biomass accumulation and flowering time. Despite recent advances in understanding the circadian system of the model plant Arabidopsis thaliana, the contribution of the circadian oscillator to important agronomic traits in Zea mays and other cereals remains poorly defined. To address this deficit, this study investigated the transcriptional landscape of the maize circadian system.
Since transcriptional regulation is a fundamental aspect of circadian systems, genes exhibiting circadian expression were identified in the sequenced maize inbred B73. Of the over 13,000 transcripts examined, approximately 10 percent displayed circadian expression patterns. The majority of cycling genes had peak expression at subjective dawn and dusk, similar to other plant circadian systems. The maize circadian clock organized co-regulation of genes participating in fundamental physiological processes, including photosynthesis, carbohydrate metabolism, cell wall biogenesis, and phytohormone biosynthesis pathways.
Circadian regulation of the maize genome was widespread and key genes in several major metabolic pathways had circadian expression waveforms. The maize circadian clock coordinated transcription to be coincident with oncoming day or night, which was consistent with the circadian oscillator acting to prepare the plant for these major recurring environmental changes. These findings highlighted the multiple processes in maize plants under circadian regulation and, as a result, provided insight into the important contribution this regulatory system makes to agronomic traits in maize and potentially other C4 plant species.
Plants match their physiology to daily and seasonal environmental changes through the circadian clock, an internal timekeeping mechanism that regulates a wide range of plant behavior. Overt circadian rhythms in plants include rhythmic leaf movements, stomatal conductance, and growth . Rhythms are maintained with a period of approximately 24 hours in the absence of environmental cues and over the normal range of ambient temperatures. The circadian system enables plants to anticipate and synchronize their physiology to the recurring environmental changes brought on by day and night. The consequence of proper clock and environment synchronization is optimized fitness [2, 3]. Beyond the daily control of plant biology, circadian rhythms also allow plants to track seasonal change according to day length, or photoperiod [4, 5]. The interplay of the circadian clock and photoperiod allows photoperiod sensitive plants to initiate floral development in accordance with the season [6, 7]. Thus, the circadian clock is an endogenous timer that maintains normal plant biology on both daily and seasonal timescales.
The circadian clock is best described in the model plant Arabidopsis thaliana. Arabidopsis mutants with impaired clock function show reduced fitness arising from mismatch between internal rhythms and external environmental conditions [8, 9]. In addition, many circadian clock mutants exhibit alterations in flowering time associated with defects in day length perception . At the molecular level, Arabidopsis circadian physiology requires the products of so-called core clock genes, whose mutation widely disrupts circadian physiology . The core clock proteins regulate expression of one another in a network of feedback loops . The myb-like transcription factors CCA1 and LHY directly control TOC1, PRR7, and PRR9 expression [13, 14]. In turn, these pseudoresponse regulators define the expression patterns of CCA1 and LHY. In addition, the TCP transcription factor CHE serves as a transcriptional regulator of CCA1 . Additionally, the clock-specific photoreceptor and F-box protein ZTL controls TOC1 function through 26S proteasome-mediated protein degradation of TOC1 at night [16, 17]. The core circadian oscillator also requires the activity of ELF3 and LUX in the evening [18, 19]. This regulatory network generates phase-specific 24-hour oscillations in each core clock gene, with the state of the overall system reflecting time of day.
Orthologs of circadian clock components in plants outside of Arabidopsis have been best characterized in rice  and Lemna . The rice genome encodes single orthologs of CCA1 and GI, but two potential orthologs of ZTL. In addition, rice possesses five unique PRR orthologs, including a clear ortholog of TOC1 . Overexpression of these rice orthologs in Arabidopsis modifies circadian rhythms, which is consistent with the function of these proteins being conserved between rice and Arabidopsis . In addition, rice TOC1 and PRR7 partially complement the corresponding Arabidopsis toc1 and prr7 mutants . Circadian clock related genes have also been described in two species of the monocot Lemna, including LHY, GI, ELF3, TOC1, and the other PRRs . Knockdown and overexpression of LHY, ELF3, and GI in Lemna suggest the topology of the Lemna circadian system is conserved with Arabidopsis and rice .
Genome-wide expression assays have revealed details behind circadian clock regulation of overt plant physiology. In Arabidopsis, the core oscillator genes are only a fraction of the genes showing cyclic expression in constant conditions. Whole genome transcriptional profiling demonstrates that the steady state transcripts of ~30% of Arabidopsis genes cycle every 24 hours in constant conditions [25, 26]. Clock controlled phasing of these cyclic genes throughout a day activates or represses metabolic and signal transduction pathways, thereby yielding macroscopic circadian rhythms in plant physiology. Genes involved in related pathways share timing of peak expression; for example, genes encoding enzymes in secondary metabolite biosynthesis, nutrient assimilation, and hormone signaling are co-regulated by the circadian clock [27–29].
Approximately half of the world's grass species employ C4 photosynthesis, including the food crops maize, sugarcane, and sorghum, as well as the potential biofuel crops switchgrass and Miscanthus. C4 plants capture CO2 as the 4-carbon compound oxaloacetate in specialized mesophyll cells and the newly captured carbon is then transported into adjacent bundle sheath cells to enter the Calvin cycle through the action of Rubisco. Primary carbon fixation in C3 plants like Arabidopsis occurs in mesophyll cells through Rubisco-mediated incorporation of CO2 into the 3-carbon compound 3-phosphoglycerate. Direct CO2 capture by Rubisco reduces the photosynthetic efficiency of C3 plants because photosynthetic rate is limited both by CO2 diffusion from the atmosphere and by photorespiration that increases at low CO2 concentrations and high temperatures. The physical partitioning of CO2 capture and the Calvin cycle in C4 plants improves photosynthetic efficiency under low CO2 concentrations and reduces photorespiration by Rubisco at high temperatures and low CO2 concentrations. As a consequence, C4 crop plants assimilate biomass more efficiently than C3 plants at the high temperatures typical of agricultural settings .
Previous studies have shown the circadian clock serves to coordinate expression of genes encoding the photosynthesis apparatus in plants that carry out C3 photosynthesis . The circadian system of C4 plants remains uncharacterized. Therefore, examination of the maize circadian system is fundamental to understanding the impact of circadian regulation on C4 photosynthesis, as well as the many other areas of maize metabolism where circadian rhythms are important. In this study, transcriptional profiling revealed the maize circadian transcriptome and this provided an initial characterization of the aspects of maize physiology under circadian clock influence.
Results and Discussion
Widespread circadian regulation of the maize transcriptome
To map the maize circadian transcriptome, mRNA levels in the aerial tissues of week-old maize B73 plants were determined by transcriptional profiling with the Affymetrix GeneChip® Maize Genome Array. The B73 inbred is widely used and is the source material for the complete maize genome sequence . Young plants were chosen as the experimental model because at this developmental stage all the tissues of the plant were easily sampled at once, unlike older maize plants that were too large to sample whole. Plants were exposed to 12 h light:12 h dark photocycles to set the circadian clock and then transferred to LL conditions for 48 additional hours. While in LL, aerial tissue was harvested every 4 hours and transcript levels in three pooled replicate samples were determined for the 13,339 maize genes represented on the microarray. The genes on this microarray account for approximately 41% of the entire maize genome, as the maize genome is predicted to have over 32,540 protein-encoding genes . Consequently, the genes with circadian expression identified here may represent nearly half of the number of predicted maize genes with rhythmic expression.
Following preprocessing and normalization of the raw hybridization values, genes on the array exhibiting circadian waveforms were identified by two well-established methods known as COSOPT and HAYSTACK [26, 32]. COSOPT is a method that fits gene expression profiles to a series of modified cosine models, with the agreement between the experimental data and the model reported by the MMC-β value . Lower values of MMC-β indicate a better fit to the cosine model. 952 genes were considered to exhibit a circadian waveform based on a MMC-β cutoff value of ≤ 0.05 (Figure 1A), which is a cutoff established by previously published reports for analogous circadian datasets in Arabidopsis and mouse [25, 26, 28, 33, 34]. The HAYSTACK tool identifies rhythmic waveforms by determining the agreement between expression profiles and a collection of models, which represent different types of potential circadian expression patterns . The degree of correlation between model and experimental waveforms is determined by Pearson's correlation coefficient, where an exact match corresponds to PCC = 1.0. Maize transcripts with expression patterns matching a model with a PCC value of 0.7 or greater were considered to have a circadian rhythm. Based on this criterion, HAYSTACK analysis called 702 transcripts as exhibiting a circadian rhythm (Figure 1A). PCC values of 0.7 or greater consistently selected good matches between models and experimental waveforms, but this cutoff is more relaxed than the 0.8 value applied previously for a large collection of Arabidopsis time courses .
Comparing the genes called rhythmic by COSOPT and HAYSTACK revealed that the two methods had 210 genes in common (Figure 1A), a proportion similar to that described for Arabidopsis circadian expression datasets . COSOPT identified almost twice as many unique rhythmic transcripts as found by HAYSTACK. This outcome was unexpected, since HAYSTACK has the potential to match a larger diversity of waveforms  and HAYSTACK has been shown to identify a larger proportion of rhythmically expressed transcripts in Arabidopsis datasets, most notably those with expression patterns in the spike class . Not surprisingly, HAYSTACK appeared to favor maize genes showing the spike and box waveforms over other waveform classes, like cosine that COSOPT was designed to find (Figure 1B). Thus, under these standard cutoffs COSOPT was more sensitive than HAYSTACK in finding transcripts that match a cosine waveform. Furthermore, the cosine waveform appeared to be the dominant pattern of expression in maize seedlings under LL conditions.
Collectively, COSOPT and HAYSTACK indicated 1,444 transcripts, or ~10% of the expressed genes on the microarray showed rhythmic expression (Additional file 1 Table S1); therefore, a substantial part of the maize transcriptome is subject to regulation by the circadian clock. Genes in this collection included known maize circadian clock-regulated transcripts such as putative maize flowering time genes gi1A and conz1 , the well-established circadian clock-regulated gene cat3 , and several lhcb genes  (Additional file 2 Figure S1). Assuming a maize genome of 32,540 genes , the full circadian transcriptome of maize potentially represents a minimum of 3,254 genes. This degree of clock regulation is comparable to that observed in Arabidopsis with a partial genome array  and in other model systems like Drosophila melanogaster, Neurospora crassa, and Mus musculus .
Preferential expression of maize circadian gene expression at dawn and dusk
A fundamental role of the clock is to anticipate day and night; as a result, the majority of circadian gene expression in Arabidopsis, rice, and poplar is timed, or phased, to precede or coincide with these recurring environmental shifts [26, 28]. To determine whether the maize circadian transcriptome was similarly organized, the cycling maize transcripts were sorted into six phase bins based on expression waveform. The six phase bins were distributed in 4-hour intervals throughout the 24-hour subjective day: dawn (ZT0 hours), midday (ZT4), late day (ZT8), dusk (ZT12), midnight (ZT16), and early morning (ZT20). K-means clustering successfully placed all transcripts into one of these six phase bins (Additional file 3 Figure S2), with the exception of four outliers. As expected, rhythmically expressed transcripts were preferentially phased to the transitions into or out of subjective day (Figure 1C). This distribution was significantly different from that expected by chance, as assessed by χ2 testing (χ2 = 109.83, P(χ2) = 4.45 × 10-22, df = 5, α = .05). The single largest phase bin was ZT12 with 335 of cycling genes, followed by ZT0 encompassing 314 transcripts (Figure 1C). The early morning phase bin was also predominant, containing 249 genes with peak expression at ZT20. The remaining transcripts were distributed almost equally over the remaining phase bins. This analysis indicated the maize circadian oscillator parses gene expression in accordance with predictable environmental changes associated with day and night.
Phase-specific distribution of key physiological processes
The genes on the array were annotated to identify the maize cellular processes under clock control. The annotation process involved matching the probe sets on the array to maize genes and then extracting the GO Slim classification for each transcript provided by the Maize Sequence Consortium (full method is described in "Methods" and outlined in Additional file 4 Figure S3). Of the cycling transcripts, 655 were assigned to GO Slim classifications for Cellular Component, Biological Process, and Molecular Function (Additional file 5 Table S2). The cycling dataset was evaluated for overrepresentation of GO Slim categories to determine whether the maize circadian clock preferentially regulated specific plant processes. Applying hypergeometric distribution analysis to the entire cycling dataset showed the Molecular Function GO Slim terms "catalytic activity" (GO: 0003824), "binding" (GO: 0005488), and "transporter activity" (GO: 0005215) were overrepresented in this group of transcripts (Table 1). Each of these GO Slim terms indicates transcripts encoding enzymes, receptors, and proteins involved in movement of macromolecules, small molecules, and ions are an important aspect of the maize circadian transcriptome. In the Biological Process classification, genes annotated with the GO Slim terms ""generation of precursor metabolites and energy" (GO: 0006091), "carbohydrate metabolic process" (GO: 0005975), and "photosynthesis" (GO: 0015979) were enriched in the circadian expressed gene set (Table 1). Together, these three GO Slim terms suggested the maize circadian clock makes an important contribution to fitness by regulating energy and carbohydrate metabolism. Similar GO Slim terms were also found to be overrepresented in the Arabidopsis circadian transcriptome , which demonstrates the involvement of the plant circadian clock in these processes is highly conserved.
Hypergeometric distribution analysis further tested whether expression of genes in particular GO Slim terms showed a time-of-day specific enrichment. The photosynthesis GO Slim term was enriched in the genes phased to ZT4 (Table 1). The bias toward photosynthesis genes at ZT4 is clear when the abundance of these genes is plotted as a function of phase (Figure 2). The Arabidopsis circadian clock similarly organizes photosynthesis-associated genes to reach peak expression early in the day . Therefore, the circadian clock prepares maize plants for increasing illumination by up-regulating photosynthesis genes early in the light period. A phasing preference was also clear for the expression of genes associated with "cellular amino acid and derivative metabolic process" (GO: 0006519), which showed overrepresentation of genes with peak levels at ZT20 (Table 1, Figure 2). These results indicate maize protein synthesis may also have a pre-dawn phase. Interestingly, Arabidopsis genes associated with protein synthesis are preferentially expressed at around dawn when plants are exposed to thermocycles, but at midday in photocycles . Since the maize plants used here did not experience thermocycles, maize plants may organize proteins synthesis at a time of day distinct from Arabidopsis. These findings show the maize circadian clock coordinates the expression of major cellular processes to occur at defined times within a normal 24-hour day. The specific physiological processes where the circadian clock plays a large role in coordinating transcription are explored in more depth below.
Coordinated circadian expression of key C4 photosynthesis genes
The maize proteins encoded by the transcripts represented on the array were given a functional annotation by matching amino acid sequences to likely orthologs in rice and Arabidopsis (Additional file 6 Table S3). The functional annotation grouped genes into a high confidence set and a low confidence set based on the criteria described in "Methods" and outlined in Additional file 4 Figure S3. Importantly, the high confidence genes represent those genes where orthologs were identified in both Arabidopsis and rice. The genes in this high confidence set were used to explore the influence of the circadian clock on maize physiology, in particular maize metabolic and signaling pathways.
The contribution of the maize circadian clock to photosynthesis was of special interest for its potential to provide insight into circadian regulation of C4 photosynthesis. Many key enzymes involved in C4 photosynthesis were under circadian clock control and expression of these were generally phased around dawn (Table 2; Figure 3), similar to Arabidopsis C3 photosynthesis . A gene encoding PEPC, the C4 enzyme that initially captures carbon for photosynthesis  (Figure 3), showed early morning phasing (Table 2). This PEPC is a strong candidate for a genuine C4 enzyme, as its amino acid sequence is highly homologous to a PEPC from sorghum and the genome regions around the maize and sorghum genes are syntenic (data not shown). Circadian regulation of a maize pepc gene is a novel observation. However, the true impact of the circadian oscillator on PEPC protein abundance remains to be determined, as the rhythms in transcription may not be translated into changes in protein levels. Interestingly, the Arabidopsis transcript encoding a homologous PEPC has a nearly identical phase of expression as the maize pepc transcript (Table 2). A maize ppdk gene, which encodes the enzyme that furnishes PEPC substrates  (Figure 3), and a ca gene both reach peak expression at dawn (Table 2). Expression of an Arabidopsis homolog of PPDK also has a phase matching the maize ppdk gene. Therefore, the circadian regulatory networks in C4 and C3 plants similarly organize expression of photosynthesis components. Logically, the expression of pepc, ppdk, and ca immediately precedes stomatal opening and the onset of light that stimulates C4 metabolism . Other components of photosynthesis displayed similar anticipatory expression, including transcripts encoding RBCS3B, RCA, and several LHCB proteins, as well as GAPD and CS, which contribute to chlorophyll synthesis (Table 2). Similarly, a large proportion of the enzymes of the Calvin cycle on the array were circadian clock-regulated such that peak expression preceded or occurred at dawn (Figure 3, Table 2). Consistent with the apparently conserved nature of the circadian network structure, the phase of expression for this set of photosynthesis genes was essentially invariant between maize and Arabidopsis (Table 2). Thus, the maize system has incorporated the initial CO2 capture of C4 photosynthesis into the overall coordination of photosynthesis that is shared with C3 photosynthesis.
The state of the maize circadian system observed here is likely an incomplete representation of the network in field grown mature plants, since young maize seedlings are developing their C4 photosynthetic capacity. Burris and de Veau showed that while 9 day-old maize seedlings exhibited a 3 times higher rate of photorespiration than 3 month-old maize plants, consistent with limited C4 photosynthesis in seedlings compared to the mature plants, the rate of photorespiration in these maize seedlings was 5 to 7 times lower than mature wheat plants performing C3 photosynthesis . Their analysis demonstrates young maize seedlings have the capacity for C4 photosynthesis, albeit a modified version with a higher rate of photorespiration than mature plants. Therefore, 7 day-old maize seedlings represent a suitable model of C4 photosynthesis.
Circadian expression was evident for genes encoding enzymes involved in biosynthesis of carotenoids including PSY, BCH, and ZEO (also known as ABA DEFICIENT 1 in Arabidopsis) (Table 2, Figure 3). Carotenoids serve as photoprotective pigments and are also important structural components of light harvesting complexes. PSY catalyzes the first and rate-limiting step in the production of carotenoids and both BCH and ZEO lie downstream of PSY [44, 45]. Expression of these genes was phased to either early morning (ZT20) or midday (ZT4), clearly showing the maize circadian system orchestrates expression of upstream and downstream enzymes for carotenoid production to coincide with the time when these compounds are needed for photosynthesis and non-photochemical quenching. PSY is also circadian regulated in Arabidopsis , with a phase matching that found here for maize (Table 2), which again suggests strong conservation of the regulatory networks underlying the maize transcriptome. Protection from ROS produced by photosynthesis is provided by the action of catalase and superoxide dismutase enzymes. Genes encoding maize CAT3 and an ortholog of MSD1 exhibited circadian expression in maize seedlings (Table 2). Consistent with their role in scavenging ROS arising from photosynthesis, expression of the cat3 and msd1 genes reached peak levels during late day (ZT8) when ROS is more likely to accumulate (Figure 3). Overall, these findings show the circadian clock organizes maize C4 photosynthesis to ensure the plant makes maximal use of light energy available during the day.
Organization of carbohydrate metabolism gene expression by the maize circadian clock
The maize clock also regulates genes contributing to carbohydrate metabolism and carbon flux (Figure 3, Table 1). For example, the circadian clock controlled expression of two PFK encoding genes and peak expression for each occurred around dawn (Figure 3). Note that the annotation matched two different maize transcripts to the same Arabidopsis gene (PFK3), which explains the different phase values shown in Table 2. PFK enzymes mediate the central regulatory step of glycolysis. Two glycolysis enzymes of the FBAase class, which reversibly convert fructose bisphosphate to triose phosphate, were clock regulated such that one peaked in the morning (FBAase2) and another expressed in the evening (FBAase1). As in energy generation, the clock regulates genes involved in energy storage. AGPase is the major regulatory enzyme in starch biosynthesis, where it converts glucose 6-phosphate to ADP-glucose, the substrate for starch synthase . The transcript encoding AGPL, a subunit of AGPase, reached peak levels near dawn at ZT20 (Figure 3). Early morning accumulation of AGPase may be an anticipatory strategy to prepare the system for midday when photosynthate is in excess and starch biosynthesis commences. Similarly, two ss transcripts encoding starch synthases were maximally expressed early in the day (ZT0 and ZT4) like their Arabidopsis orthologs (Table 2). Thus, the maize circadian clock anticipated the need for carbon metabolism components and up-regulated expression of these genes so that enzymes would be present at the time when photosynthate would be available for energy production and storage. Together, the coordinated regulation of carbohydrate metabolism and C4 photosynthesis indicates that the circadian clock in maize organizes gene expression to ensure efficient and maximal energy production, use, and storage throughout the day.
Co-regulation of cell wall synthesis genes by the maize circadian clock
Cell walls are a major constituent of plant biomass, and their enlargement exhibits a biological rhythm [47, 48]. Consistent with rhythmic growth, the transcripts of several enzymes involved in cell wall biosynthesis were found to be circadian-regulated in maize (Table 2, Figure 3). CCR and CAD catalyze two of the final steps in the conversion of phenylpropanoid into monolignins to achieve wall hardening . Transcripts encoding both these enzymes were found to have cyclic expression peaking at dawn (Figure 3). The maize CAD is orthologous to Arabidopsis CAD4. Arabidopsis CAD4 is a class II CAD enzyme that acts on sinapaldehyde instead of coniferaldehyde ; therefore, the substrate for the maize CAD is likely to be sinapaldehyde (Figure 3). 4-CL acts early in phenylpropanoid synthesis and a maize gene encoding an ortholog of Arabidopsis 4-CL3 is rhythmically expressed with peak expression at ZT16, instead of ZT0 like the ccr and cad transcripts. Since the Arabidopsis 4-CL3 enzyme participates in flavonoid biosynthesis instead of contributing to lignin production , this maize 4-CL is likely not involved in lignin biosynthesis but flavonoid biosynthesis instead. The similar expression waveforms of ccr and cad in maize and Arabidopsis suggests the timing of this aspect of lignin biosynthesis is conserved (Table 2) . Several cellulose synthase genes shared nearly the same dawn phasing as the ccr and cad transcripts (Figure 3). Similarly, transcripts for two endoglucanases and a cellulase cycled at dawn in the maize dataset (Figure 3). Circadian dawn expression of cell wall-related enzymes correlates with the time of maximal plant growth rate reported for Arabidopsis [49, 51]; therefore, the maize circadian clock seems to regulate daily cell wall construction so that it coincides with growth trigged by phytohormone signaling.
Circadian clock regulation of maize GA, ethylene, and ABA biosynthesis genes
Several recent studies have shown a fundamental role of the Arabidopsis circadian clock is to indirectly control growth and development through transcriptional regulation of genes involved in phytohormone biosynthesis and response [25, 27, 29]. Placement of the maize cycling genes in the context of metabolic pathways revealed that the maize circadian clock also regulates genes involved in the synthesis of phytohormones fundamental to plant growth (Table 2).
GAs and ethylene are important positive regulators of plant cell growth. GAs promote longitudinal expansion of cells and ethylene promotes transverse cell expansion . Daily rhythmic growth exhibited by Arabidopsis is, in part, controlled through diurnal transcriptional control of genes encoding enzymes for synthesis of GAs and ethylene . For GAs, GA 12 biosynthesis is a prerequisite for the production of active GAs. In Arabidopsis, GA1, which encodes ENT-COPALYL DIPHOSPHATE SYNTHASE, and KAO2 act in the biosynthetic pathways that provide the GA 12 precursor of GA synthesis [53, 54]. Maize orthologs of GA1 and KAO2 were among the proteins encoded by circadian expressed transcripts (Table 2). Maize ga1 reached peak expression at subjective midday (Figure 4A), consistent with the phasing reported for GA synthesis genes in Arabidopsis seedlings under constant light conditions ; however, Arabidopsis GA1 does not exhibit circadian expression (Table 2). Maize kao2 showed peak circadian expression at ZT16, which was 12 hours later than maize ga1 and 8 hours later than its Arabidopsis counterpart (Figure 4A). Nevertheless, the robust circadian expression of ga1 and kao1 indicates the participation of the maize circadian clock in the coordination of maize growth through regulation of phytohormone biosynthesis. In support of this possibility, two putative ethylene biosynthesis genes also showed circadian expression: orthologs of Arabidopsis MTO3 and ACS6. MTO and ACS enzymes act sequentially to produce ACC, which is the precursor to ethylene . The dawn-phased expression of the maize acs6 and mto3 genes was in contrast to the non-circadian expression for their Arabidopsis orthologs (Table 2). The lack of correspondence in the phasing of GA and ethylene synthesis between maize and Arabidopsis may be a consequence of the constant light condition used here. Along with the circadian clock, diurnal light and dark cues serve an important role in determining the phase of phytohormone synthesis genes and ultimately the timing of cellular growth [26, 51]. Therefore, evaluation of maize expression in diurnal conditions will be important to fully comprehend the molecular basis for rhythmic growth in maize.
The plant stress hormone ABA antagonizes the growth promoting effects of GA and ethylene  and, like GAs and ethylene, ABA biosynthesis genes are part of a transcriptional regulatory network that exerts daily control over plant growth . The carotenoid biosynthesis pathway supplies precursors for the biosynthesis of ABA . As noted above, the transcript encoding PSY, the enzyme governing the first committed step in carotenoid synthesis, was under circadian control with peak expression in the early morning (Table 2, Figure 4A). Several genes downstream of PSY that are involved in ABA synthesis also showed dawn expression (Table 2, Figure 4A), which is consistent with ABA synthesis taking place in the early morning. Comparable circadian regulation of PSY and genes encoding downstream components of this pathway has been noted in Arabidopsis . The conserved circadian regulation of maize carotenoid biosynthesis genes observed here suggests that synthesis of ABA in maize leaves is under circadian control, which likely impacts the key role ABA plays in antagonizing cell growth and in stimulating stomatal closure . The latter role of ABA is associated higher-water use efficiencies in crop plants, since closure of stomata reduces water loss. Therefore, the maize circadian system is likely a critically important, but under appreciated, contributor to maize productivity in the field.
Rhythmic expression of putative maize flowering time, circadian clock, and phototropism genes
Several orthologs of Arabidopsis circadian clock and flowering time genes were present in the maize cycling gene set; however, the array had limited overall representation of genes in these categories. Included in the rhythmic collection was the gene encoding CONZ1, which the annotation matched to Arabidopsis COL1 (Table 2, Figure 4B). CONZ1 is a strong candidate for the functional ortholog of Arabidopsis CONSTANS and rice Heading date 1 . CONSTANS and Heading date 1 serve in control of flowering time to regulate the expression of the FT class of proteins. FT proteins act as florigen molecules that promote floral development at the shoot apical meristem . gi1A and gi1B are paralogous flowering time and circadian clock genes identified in the same study as conz1 . A probe set for gi1A was on the array and this transcript exhibited a waveform and phase similar to that of Arabidopsis GI expression (Figure 4B, Table 2) . Orthologs of Arabidopsis LDL1 and FCA were two other potential flowering time transcripts with rhythmic expression in the maize dataset (Figure 4B). LDL1 and FCA are known to act in the Arabidopsis autonomous flowering pathway . LDL1 is involved in modification of chromatin and, therefore, is not likely to be strictly involved in flowering time . Similarly, FCA plays a role in RNA-mediated silencing through DNA methylation . Circadian clock components present on the array included orthologs of Arabidopsis PRR7 and LUX (Table 2, Figure 4B). Expression of maize prr7 and lux exhibited the same phasing as their Arabidopsis orthologs (Table 2), indicating the conserved nature of the core maize circadian clock. Finally, the maize phot1 transcript, encoding a blue light photoreceptor of the phototropin family likely to be involved in phototropism, was robustly rhythmic with the identical phase as its Arabidopsis counterpart (Figure 4B). This restricted sampling of flowering time, circadian clock, and phototropism genes suggests that maize relies on conserved signaling networks for these key processes.
Identification of maize genes under circadian clock regulation and the predicted contribution of these genes to metabolism, growth, and development indicates the maize circadian clock plays an important role in coordinating the overall physiology of this C4 crop plant. In general, circadian regulation of the enzymes mediating C4 photosynthesis was predictable based on the Arabidopsis C3 model and without any apparent large-scale changes to accommodate the specialized C4 anatomy and enzymology. Recent investigation of the global effects of the circadian system on Arabidopsis physiology demonstrated that rhythms are critical to plant fitness and optimal growth . A more complete appreciation of the maize circadian clock will reveal where the circadian system impacts maize growth and development, as well as highlight novel approaches for optimization of crop production through targeted modification of the circadian system.
Plant materials and growth conditions
Seeds of inbred B73 were obtained from the Maize Genetics Cooperation Center. B73 is widely used and is the source material for the complete maize genome sequence . Seedlings were germinated and grown in 57 × 30 × 6 cm flats filled with Scotts Supersoil (scotts.com) inside a Conviron (conviron.com) growth chamber at constant 26°C and constant 70% humidity. High intensity cool white fluorescent bulbs provided illumination at a fluence rate of 200 μmoles m-2 s-1. Seedlings were grown for seven days under 12 hours of light followed by 12 hours of dark before being transferred to LL for two days at the same temperature and humidity.
RNA sample preparation and array hybridization
Tissue harvest began following transfer of seedlings to LL on the 8th day. The entire aerial portion (corresponding to all tissue above the prop roots) of five seedlings was harvested beginning at dawn and every 4 hours thereafter for the next 48 hours. Samples were immediately frozen in liquid nitrogen. Three separate experimental replicates were collected in this way. Tissue was ground to a fine powder under liquid nitrogen and total RNA isolated by Trizol extraction (Invitrogen; invitrogen.com) followed by Qiagen RNeasy columns and treatment with RNase-free DNase I (Qiagen; qiagen.com). cRNA was generated from total RNA of three pooled replicate samples with the GeneChip® One-Cycle Target Labeling kit according to the manufacturer's recommendations (Affymetrix, affymetrix.com). The University of California, Berkeley Functional Genomics Laboratory  hybridized samples to Affymetrix GeneChip® Maize Genome Arrays and scanned the washed arrays as suggested by manufacturer. Present, Marginal, and Absent calls for each probe set were determined with MAS5 analysis  and these are presented in Additional file 7 Table S4. Probe sets called "Absent" at more than nine time points were removed from the downstream analysis . Raw hybridization intensities were normalized across all twelve arrays using RMAExpress in Perfect Match mode [64, 65]. The raw microarray data is available online as experiment ZM28 at the Plant Expression Database .
Identification of maize transcripts with circadian expression waveforms
Rhythmic expression waveforms within the normalized dataset were identified by analysis with the COSOPT curve fitting algorithm and the pattern matching function HAYSTACK. The COSOPT algorithm is a cosine waveform fitting method that identifies transcripts with circadian expression by first performing an arithmetic linear-regression detrend of the normalized time series data for each transcript followed by testing detrended data for a fit to 101 cosine test models . An approximate goodness of fit value produced by COSOPT analysis is MMC-β, where lower values correspond to a better fit to an ideal cosine curve. Based on previous studies in Arabidopsis [25, 26, 28, 33] and our empirical tests, a MMC-β threshold of ≤ 0.05 was chosen to call a given probe set circadian. HAYSTACK is a model-based, pattern-matching tool that identifies rhythmic expression patterns by aligning time-series microarray data to a set of discrete diurnal and circadian models . HAYSTACK conducts a least square linear regression for each gene against all the models and calculates the best-fit model, phase-of-expression, and p-value for each gene. HAYSTACK was run on the normalized maize dataset with the following parameters: fold cutoff = 2, p-value cutoff = 0.05, background cutoff = 50, and PCC = 0.7 with the 552 model set described in Michael et al. 2008 . In general, goodness of fit between the model and experimental traces is revealed by the PCC value. We empirically determined that a PCC ≥ 0.7 produced good matches between model and experimental data. This cutoff was less stringent than that applied in previous studies investigating Arabidopsis circadian expression [26, 29].
Phase clustering of circadian waveforms
Probe sets with similar expression waveforms were grouped together by K-means clustering. The RMAExpress normalized values for probe sets with MMC-β ≤ 0.05 and those with PCC ≥ 0.7 were converted to normalized values with the following calculation: value = [(expression at single time point) - mean(all time points)]/[standard deviation(all time points)]. These values were used to fit the waveforms to six clusters representing each ZT phase with the K-means clustering algorithm built into the TIGR Multiexpression Viewer tool . Clustering ran for a total of 50 iterations and was considered complete when probe sets were no longer exchanged between clusters. In two independent trials, no greater than 7 iterations were required to build the clusters.
Matching of probe sets to maize genes, assignment of GO Slim terms to genes, and functional annotation
Additional file 4 Figure S3 outlines the annotation scheme used to match probe sets to genes in the maize genome, identify GO Slim terms for maize genes, and functionally annotate maize genes. Transcripts represented on the Affymetrix GeneChip® Maize array were mapped to maize transcripts with a custom Perl script that used the DNA sequences provided by Affymetrix and BLASTn to query the ZmB73 4.53a filtered CDS sequences . After the maize gene ID was identified for each probe set, GO Slim terms and associated PlantCyc pathways  were extracted from the Maize Genome Consortium website . Maize gene IDs for each gene were used with a local implementation of BLASTp to identify likely rice orthologs in the Michigan State University Rice Pseudomolecule and Genome Annotation release 6.1 and likely Arabidopsis orthologs in TAIR9_pep_20090619 sequences. The output of these queries were separated into high and low confidence lists (Additional file 6 Table S3). Criteria for the high confidence list were amino acid identity of 40% or greater, Highest Scoring Segment Pair (HSP) of 50 amino acids or greater, and a match to putative orthologs in both Arabidopsis and rice. The low confidence list contains the remaining genes that encode proteins not meeting these three criteria. Putative functions of matched orthologs were derived from Kyoto Encyclopedia of Genes and Genomes . Phase of expression for Arabidopsis orthologs shown in Table 2 was determined with the DIURNAL tool from the "LL12" dataset and matches between model and data considered significant at PCC values ≥ 0.7 . Overrepresentation of GO Slim terms was calculated with hypergeometric distribution followed by a modified Bonfferoni correction for multiple testing as implemented in GeneMerge . GeneMerge produced an e-score comparable to a P-value that was used to determine significance of overrepresentation. GO Slim terms for the entire array were the population set and the indicated collection of cycling genes served as the study set. Overrepresented GO Slim terms were considered those with e-scores < 0.05.
ABSCISIC ACID 8-HYDROXYLASE
ADP-GLUCOSE PYROPHOSPHORYLASE LARGE SUBUNIT
CINNAMYL ALCOHOL DEHYDROGENASE
CIRCADIAN CLOCK ASSOCIATED 1
CCA1 HIKING EXPEDITION
CONSTANS OF ZEA MAYS1
EARLY FLOWERING 3
GA REQUIRING 1
ENT-KAURENOIC ACID HYDROXYLASE 2
KETOSE-BISPHOSPHATE ALDOLASE CLASS II
LYSINE-SPECIFIC DEMETHYLASE 1
LIGHT HARVESTING COMPLEX B
LATE ELONGATED HYPOCOTYL
- MALIC E:
Multiple Measures Corrected-β
MANGANESE SUPEROXIDE DISMUTASE1
METHIONINE OVER-ACCUMULATOR 3
Pearson Correlation Coefficient
phospho enol pyruvate
PHOSPHO ENOL PYRUVATE CARBOXYLASE
PYRUVATE; ORTHOPHOSPHATE DIKINASE
RUBISCO SMALL SUBUNIT
reactive oxygen species
RIBOSE PHOSPHATE ISOMERASE
RIBULOSE BISPHOSPHATE CARBOXYLASE OXYGENASE
TIMING OF CAB EXPRESSION 1
TRIOSE PHOSPHATE ISOMERASE
Uridine diphosphate glucose
McClung CR: Plant circadian rhythms. Plant Cell. 2006, 18: 792-803. 10.1105/tpc.106.040980.
Hotta CT, Gardner MJ, Hubbard KE, Baek SJ, Dalchau N, Suhita D, Dodd AN, Webb AA: Modulation of environmental responses of plants by circadian clocks. Plant Cell Environ. 2007, 30: 333-349. 10.1111/j.1365-3040.2006.01627.x.
Schultz TF, Kay SA: Circadian clocks in daily and seasonal control of development. Science. 2003, 301: 326-328. 10.1126/science.1085935.
Suarez-Lopez P, Wheatley K, Robson F, Onouchi H, Valverde F, Coupland G: CONSTANS mediates between the circadian clock and the control of flowering in Arabidopsis. Nature. 2001, 410: 1116-1120. 10.1038/35074138.
Yanovsky MJ, Kay SA: Molecular basis of seasonal time measurement in Arabidopsis. Nature. 2002, 419: 308-312. 10.1038/nature00996.
Imaizumi T, Kay SA: Photoperiodic control of flowering: not only by coincidence. Trends Plant Sci. 2006, 11: 550-558. 10.1016/j.tplants.2006.09.004.
Yanovsky MJ, Kay SA: Living by the calendar: how plants know when to flower. Nat Rev Mol Cell Biol. 2003, 4: 265-275. 10.1038/nrm1077.
Dodd AN, Salathia N, Hall A, Kevei E, Toth R, Nagy F, Hibberd JM, Millar AJ, Webb AA: Plant circadian clocks increase photosynthesis, growth, survival, and competitive advantage. Science. 2005, 309: 630-633. 10.1126/science.1115581.
Green RM, Tingay S, Wang ZY, Tobin EM: Circadian rhythms confer a higher level of fitness to Arabidopsis plants. Plant Physiol. 2002, 129: 576-584. 10.1104/pp.004374.
Harmon FG, Imaizumi T, Kay SA: The plant circadian clock: review of a clockwork Arabidopsis. Endogenous Plant Rhythms. Edited by: Hall AJW, McWatters HG. 2005, Oxford: Blackwell Publishing Ltd, 1-23.
McClung CR: Comes a time. Curr Opin Plant Biol. 2008, 11: 6-10.1016/j.pbi.2008.06.010.
Harmer SL: The circadian system in higher plants. Annu Rev Plant Biol. 2009, 60: 357-377. 10.1146/annurev.arplant.043008.092054.
Alabadi D, Oyama T, Yanovsky MJ, Harmon FG, Mas P, Kay SA: Reciprocal regulation between TOC1 and LHY/CCA1 within the Arabidopsis circadian clock. Science. 2001, 293: 880-883. 10.1126/science.1061320.
Farre EM, Harmer SL, Harmon FG, Yanovsky MJ, Kay SA: Overlapping and distinct roles of PRR7 and PRR9 in the Arabidopsis circadian clock. Curr Biol. 2005, 15: 47-54. 10.1016/j.cub.2004.12.067.
Pruneda-Paz JL, Breton G, Para A, Kay SA: A functional genomics approach reveals CHE as a component of the Arabidopsis circadian clock. Science. 2009, 323: 1481-1485. 10.1126/science.1167206.
Kim WY, Fujiwara S, Suh SS, Kim J, Kim Y, Han L, David K, Putterill J, Nam HG, Somers DE: ZEITLUPE is a circadian photoreceptor stabilized by GIGANTEA in blue light. Nature. 2007, 449: 356-360. 10.1038/nature06132.
Mas P, Kim WY, Somers DE, Kay SA: Targeted degradation of TOC1 by ZTL modulates circadian function in Arabidopsis thaliana. Nature. 2003, 426: 567-570. 10.1038/nature02163.
Thines B, Harmon FG: Ambient temperature response establishes ELF3 as a required component of the core Arabidopsis circadian clock. Proc Natl Acad Sci USA. 2010, 107: 3257-3262. 10.1073/pnas.0911006107.
Hazen SP, Schultz TF, Pruneda-Paz JL, Borevitz JO, Ecker JR, Kay SA: LUX ARRHYTHMO encodes a Myb domain protein essential for circadian rhythms. Proc Natl Acad Sci USA. 2005, 102: 10387-10392. 10.1073/pnas.0503029102.
Murakami M, Tago Y, Yamashino T, Mizuno T: Comparative overviews of clock-associated genes of Arabidopsis thaliana and Oryza sativa. Plant Cell Physiol. 2007, 48: 110-121. 10.1093/pcp/pcl043.
Miwa K, Serikawa M, Suzuki S, Kondo T, Oyama T: Conserved expression profiles of circadian clock-related genes in two Lemna species showing long-day and short-day photoperiodic flowering responses. Plant Cell Physiol. 2006, 47: 601-612. 10.1093/pcp/pcj027.
Murakami M, Ashikari M, Miura K, Yamashino T, Mizuno T: The evolutionarily conserved OsPRR quintet: rice pseudo-response regulators implicated in circadian rhythm. Plant Cell Physiol. 2003, 44: 1229-1236. 10.1093/pcp/pcg135.
Murakami M, Tago Y, Yamashino T, Mizuno T: Characterization of the rice circadian clock-associated pseudo-response regulators in Arabidopsis thaliana. Biosci Biotechnol Biochem. 2007, 71: 1107-1110. 10.1271/bbb.70048.
Serikawa M, Miwa K, Kondo T, Oyama T: Functional conservation of clock-related genes in flowering plants: overexpression and RNA interference analyses of the circadian rhythm in the monocotyledon Lemna gibba. Plant Physiol. 2008, 146: 1952-1963. 10.1104/pp.107.114611.
Covington MF, Maloof JN, Straume M, Kay SA, Harmer SL: Global transcriptome analysis reveals circadian regulation of key pathways in plant growth and development. Genome Biol. 2008, 9: R130-10.1186/gb-2008-9-8-r130.
Michael TP, Mockler TC, Breton G, McEntee C, Byer A, Trout JD, Hazen SP, Shen R, Priest HD, Sullivan CM, et al: Network discovery pipeline elucidates conserved time-of-day-specific cis-regulatory modules. PLoS Genet. 2008, 4: e14-10.1371/journal.pgen.0040014.
Covington MF, Harmer SL: The circadian clock regulates auxin signaling and responses in Arabidopsis. PLoS Biol. 2007, 5: e222-10.1371/journal.pbio.0050222.
Harmer SL, Hogenesch JB, Straume M, Chang HS, Han B, Zhu T, Wang X, Kreps JA, Kay SA: Orchestrated transcription of key pathways in Arabidopsis by the circadian clock. Science. 2000, 290: 2110-2113. 10.1126/science.290.5499.2110.
Michael TP, Breton G, Hazen SP, Priest H, Mockler TC, Kay SA, Chory J: A morning-specific phytohormone gene expression program underlying rhythmic plant growth. PLoS Biol. 2008, 6: e225-10.1371/journal.pbio.0060225.
Murchie EH, Pinto M, Horton P: Agriculture and the new challenges for photosynthesis research. New Phytol. 2009, 181: 532-552. 10.1111/j.1469-8137.2008.02705.x.
Schnable PS, Ware D, Fulton RS, Stein JC, Wei F, Pasternak S, Liang C, Zhang J, Fulton L, Graves TA, et al: The B73 maize genome: complexity, diversity, and dynamics. Science. 2009, 326: 1112-1115. 10.1126/science.1178534.
Straume M: DNA microarray time series analysis: automated statistical assessment of circadian rhythms in gene expression patterning. Methods Enzymol. 2004, 383: 149-166. full_text.
Edwards KD, Anderson PE, Hall A, Salathia NS, Locke JC, Lynn JR, Straume M, Smith JQ, Millar AJ: FLOWERING LOCUS C mediates natural variation in the high-temperature response of the Arabidopsis circadian clock. Plant Cell. 2006, 18: 639-650. 10.1105/tpc.105.038315.
Panda S, Antoch MP, Miller BH, Su AI, Schook AB, Straume M, Schultz PG, Kay SA, Takahashi JS, Hogenesch JB: Coordinated transcription of key pathways in the mouse by the circadian clock. Cell. 2002, 109: 307-320. 10.1016/S0092-8674(02)00722-5.
Mockler TC, Michael TP, Priest HD, Shen R, Sullivan CM, Givan SA, McEntee C, Kay SA, Chory J: The DIURNAL project: DIURNAL and circadian expression profiling, model-based pattern matching and promoter analysis. Cold Spring Harb Symp Quant Biol. 2007, 72: 353-363. 10.1101/sqb.2007.72.006.
Miller TA, Muslin EH, Dorweiler JE: A maize CONSTANS-like gene, conz1, exhibits distinct diurnal expression patterns in varied photoperiods. Planta. 2008, 227: 1377-1388. 10.1007/s00425-008-0709-1.
Redinbaugh MG, Wadsworth GJ, Scandalios JG: Characterization of catalase transcripts and their differential expression in maize. Biochim Biophys Acta. 1988, 951: 104-116.
Taylor WC: Transcriptional regulation by a circadian rhythm. Plant Cell. 1989, 1: 259-264. 10.1105/tpc.1.2.259.
Panda S, Hogenesch JB, Kay SA: Circadian rhythms from flies to human. Nature. 2002, 417: 329-335. 10.1038/417329a.
Hatch MD, Slack CR: The participation of phosphoenolpyruvate synthetase in photosynthetic CO 2 fixation of tropical grasses. Arch Biochem Biophys. 1967, 120: 224-225. 10.1016/0003-9861(67)90618-2.
Hatch MD, Slack CR: A new enzyme for the interconversion of pyruvate and phosphopyruvate and its role in the C4 dicarboxylic acid pathway of photosynthesis. Biochem J. 1968, 106: 141-146.
Slack CR: The photoactivation of a phosphopyruvate synthase in leaves of Amaranthus palmeri. Biochem Biophys Res Commun. 1968, 30: 483-488. 10.1016/0006-291X(68)90077-6.
de Veau EJ, Burris JE: Photorespiratory rates in wheat and maize as determined by O-labeling. Plant Physiol. 1989, 90: 500-511. 10.1104/pp.90.2.500.
Lindgren LO, Stalberg KG, Hoglund AS: Seed-specific overexpression of an endogenous Arabidopsis phytoene synthase gene results in delayed germination and increased levels of carotenoids chlorophyll, and abscisic acid. Plant Physiol. 2003, 132: 779-785. 10.1104/pp.102.017053.
Rodriguez-Villalon A, Gas E, Rodriguez-Concepcion M: Phytoene synthase activity controls the biosynthesis of carotenoids and the supply of their metabolic precursors in dark-grown Arabidopsis seedlings. Plant J. 2009
Jin X, Ballicora MA, Preiss J, Geiger JH: Crystal structure of potato tuber ADP-glucose pyrophosphorylase. Embo J. 2005, 24: 694-704. 10.1038/sj.emboj.7600551.
Dowson-Day MJ, Millar AJ: Circadian dysfunction causes aberrant hypocotyl elongation patterns in Arabidopsis. Plant J. 1999, 17: 63-71. 10.1046/j.1365-313X.1999.00353.x.
Nozue K, Maloof JN: Diurnal regulation of plant growth. Plant Cell Environ. 2006, 29: 396-408. 10.1111/j.1365-3040.2005.01489.x.
Cosgrove DJ: Growth of the plant cell wall. Nat Rev Mol Cell Biol. 2005, 6: 850-861. 10.1038/nrm1746.
Raes J, Rohde A, Christensen JH, Van de Peer Y, Boerjan W: Genome-wide characterization of the lignification toolbox in Arabidopsis. Plant Physiol. 2003, 133: 1051-1071. 10.1104/pp.103.026484.
Nozue K, Covington MF, Duek PD, Lorrain S, Fankhauser C, Harmer SL, Maloof JN: Rhythmic growth explained by coincidence between internal and external cues. Nature. 2007, 448: 358-361. 10.1038/nature05946.
Nemhauser JL, Hong F, Chory J: Different plant hormones regulate similar processes through largely nonoverlapping transcriptional responses. Cell. 2006, 126: 467-475. 10.1016/j.cell.2006.05.050.
Tudzynski B: Biosynthesis of gibberellins in Gibberella fujikuroi: biomolecular aspects. Appl Microbiol Biotechnol. 1999, 52: 298-310. 10.1007/s002530051524.
Hedden P, Phillips AL: Gibberellin metabolism: new insights revealed by the genes. Trends Plant Sci. 2000, 5: 523-530. 10.1016/S1360-1385(00)01790-8.
Chae HS, Kieber JJ: Eto Brute? Role of ACS turnover in regulating ethylene biosynthesis. Trends Plant Sci. 2005, 10: 291-296. 10.1016/j.tplants.2005.04.006.
Nambara E, Marion-Poll A: Abscisic acid biosynthesis and catabolism. Annual Review of Plant Biology. 2005, 56: 165-185. 10.1146/annurev.arplant.56.032604.144046.
Schroeder JI, Allen GJ, Hugouvieux V, Kwak JM, Waner D: Guard cell signal transduction. Annu Rev Plant Physiol Plant Mol Biol. 2001, 52: 627-658. 10.1146/annurev.arplant.52.1.627.
Park DH, Somers DE, Kim YS, Choy YH, Lim HK, Soh MS, Kim HJ, Kay SA, Nam HG: Control of circadian rhythms and photoperiodic flowering by the Arabidopsis GIGANTEA gene. Science. 1999, 285: 1579-1582. 10.1126/science.285.5433.1579.
Colasanti J, Coneva V: Mechanisms of floral induction in grasses: something borrowed, something new. Plant Physiol. 2009, 149: 56-62. 10.1104/pp.108.130500.
Jiang D, Yang W, He Y, Amasino RM: Arabidopsis relatives of the human lysine-specific Demethylase1 repress the expression of FWA and FLOWERING LOCUS C and thus promote the floral transition. Plant Cell. 2007, 19: 2975-2987. 10.1105/tpc.107.052373.
Baurle I, Smith L, Baulcombe DC, Dean C: Widespread role for the flowering-time regulators FCA and FPA in RNA-mediated chromatin silencing. Science. 2007, 318: 109-112. 10.1126/science.1146565.
UC Berkeley Functional Genomics Laboratory. [http://microarrays.berkeley.edu]
Hubbell E, Liu WM, Mei R: Robust estimators for expression analysis. Bioinformatics. 2002, 18: 1585-1592. 10.1093/bioinformatics/18.12.1585.
Bolstad BM, Irizarry RA, Astrand M, Speed TP: A comparison of normalization methods for high density oligonucleotide array data based on variance and bias. Bioinformatics. 2003, 19: 185-193. 10.1093/bioinformatics/19.2.185.
Plant Expression Database. [http://www.plexdb.org/index.php]
MultiExperiment Viewer. [http://www.tm4.org/mev.html]
Plant Metabolic Network and PlantCyc. [http://www.plantcyc.org/]
MaizeSequence.org FTP Site. [http://ftp.maizesequence.org/current/]
Kyoto Encyclopedia of Genes and Genomes. [http://www.genome.jp/kegg/kegg2.html]
The DIURNAL project. [http://diurnal.cgrb.oregonstate.edu/]
Castillo-Davis CI, Hartl DL: GeneMerge--post-genomic analysis, data mining, and hypothesis testing. Bioinformatics. 2003, 19: 891-892. 10.1093/bioinformatics/btg114.
We thank Dr. Hector Candela-Anton, James Schnable, and Imran N. Amirani for writing perl scripts, as well as Dr. Robin Buell for help and advice on annotation with rice sequences. We also thank Bryan Thines for critical reading of the manuscript. This work is supported by United States Department of Agriculture grant CRIS 5335-21000-026-00D to FGH.
SK carried out the microarray analysis, annotation, comparative analysis, and drafted the manuscript. SCR helped draft the manuscript and created figures. FGH conceived the study, participated in its design and coordination, created figures, and drafted the manuscript. All authors read and approved the final manuscript.
Electronic supplementary material
Additional file 2: . COSOPT and HAYSTACK captured bona-fide rhythmically expressed transcripts including likely maize flowering time genes conz1 (purple circles) and gi1a (green squares), as well as established circadian clock-regulated genes cat3 (blue open triangles) and three lhcb transcripts (red closed symbols). Shaded squares represent subjective night. For each gene, the normalized expression values = [(expression at single time point) - mean(all time points)]/[standard deviation(all time points)]. (PDF 349 KB)
Additional file 3: Phase clusters of genes with similar circadian expression waveforms. Transcript expression profiles were placed into one of six phase bins by K-means clustering (see "Methods"). The number of transcripts in each phase cluster is indicated next to the time of peak expression in ZT for that group. Gray regions represent subjective night. (PDF 411 KB)
Additional file 6: Functional annotation of maize transcripts represented on the microarray by identification of orthologous proteins from Oryza sativaand Arabidopsis thaliana. High and low confidence genes were determined as described in "Methods". The high and low confidence gene sets are segregated into separate worksheets. (XLS 4 MB)
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Khan, S., Rowe, S.C. & Harmon, F.G. Coordination of the maize transcriptome by a conserved circadian clock. BMC Plant Biol 10, 126 (2010). https://0-doi-org.brum.beds.ac.uk/10.1186/1471-2229-10-126
- Circadian Clock
- Maize Genome
- Circadian System
- Circadian Regulation
- Rhythmic Expression