- Open Access
Selection of reference genes for diurnal and developmental time-course real-time PCR expression analyses in lettuce
© Sgamma et al. 2016
Received: 7 December 2015
Accepted: 14 March 2016
Published: 22 March 2016
Real-time quantitative polymerase chain reaction (RT-qPCR) analysis is a low cost and sensitive technique that is widely used to measure levels of gene expression. Selecting and validating appropriate reference genes for normalising target gene expression should be the first step in any expression study to avoid inaccurate results.
In this study, ten candidate genes were tested for their suitability for use as reference genes in diurnal and developmental timecourse experiments in lettuce. The candidate reference genes were then used to normalise the expression pattern of the FLOWERING LOCUS T (FT) gene, one of key genes involved in the flowering time pathway whose expression is known to vary throughout the day and at different stages of development. Three reference genes, LsPP2A-1 (PROTEIN PHOSPHATASE 2A-1), LsPP2AA3 (PROTEIN PHOSPHATASE 2A REGULATORY SUBUNIT A3) and LsTIP41 (TAP42-INTERACTING PROTEIN OF 41 kDa), were the most stably expressed candidate reference genes throughout both the diurnal and developmental timecourse experiments. In the developmental experiment using just LsPP2A-1 and LsTIP41 as reference genes would be sufficient for accurate normalisation, whilst in the diurnal experiment all three reference genes, LsPP2A-1, LsPP2AA3 and LsTIP41, would be necessary. The FT expression pattern obtained demonstrates that the use of multiple and robust reference genes for RT-qPCR expression analyses results in a more accurate and reliable expression profile.
Reference genes suitable for use in diurnal and developmental timecourse experiments in lettuce were identified and used to produce a more accurate and reliable analysis of lsFT expression levels than previously obtained in such timecourse experiments.
One of the most common techniques for studying gene expression is real-time quantitative polymerase chain reaction (RT-qPCR) analysis because it is extremely sensitive, specific and cost-effective. However there are often methodological errors in RT-qPCR application and, as a consequence, in the interpretation of the results . One of the most common errors is the choice of inappropriate reference genes used to normalise the expression of target genes [1–3]. Ideally reference genes would be expressed at a constant level and would thus be representative of the cDNA concentration in each sample, but their expression is often affected by experimental treatments or can vary in different tissues, or over the time-course chosen for the experiment . In literature there are several genes that are commonly used as reference genes but results often show that each experimental design and each organism requires its own reference genes to be selected and used [2, 3, 5]. Several approaches can be used for a systematic validation of reference genes such as NormFinder, Best-keeper and geNorm [6–8]. These software-based approaches rank a plethora of candidate reference genes measuring their relative stability by comparing the expression of each gene in each sample in relation to the entire set of reference genes. The best approach is to follow the Minimum Information for Publication of Quantitative Real-Time PCR Experiments (MIQE) guidelines and to use multiple reference control genes, as the use of single reference gene is now considered inappropriate .
Recently, a study investigated 17 selected candidate genes and microRNAs (miRNAs) for their suitability to be used as reliable and stable reference genes in RTqPCR analysis of gene expression differences in abiotic stress experiments . Some of these were genes such as TAP42-INTERACTING PROTEIN OF 41 kDa (TIP41), ADENOSINE PHOSPHORIBOSYL TRANSFERASE 1 (APT1) and miRNA genes and were selected on the basis that they had been used as reference genes in previously published work [2, 11–13]. The results of the experiments using abiotic stresses such as drought, salinity, UV-C irradiation, heavy metal stress and abscisic acid treatments, showed differences in stability between the reference genes . Therefore in any RTqPCR experiment the identification of a good set of reference genes whose expression remains constant throughout the experimental conditions under study is extremely important in order to be able to obtain reliable results.
Lettuce (Lactuca sativa) is a leafy vegetable cultivated throughout the course of the year, it is harvested when plants reach maturity but before they bolt and flower . In order to avoid harvest loss and wastage it is therefore important to be able to predict and anticipate when the crop will start bolting. Understanding changes in gene expression profiles, in particular those of flowering time genes, throughout development will help to develop predictable cropping.
In this study we wanted to identify suitable reference genes that would have stable expression profiles over diurnal and developmental timecourse experiments in order to analyse the expression of flowering time genes over these timecourses. Ten reference genes were selected based on genes that had been identified in previous experiments in other species and the stability of their expression profiles over developmental and diurnal timecourses was tested. To demonstrate the reliability and suitability of the reference genes identified, the expression pattern of the FLOWERING LOCUS T (FT) gene, one of key genes involved in the flowering time pathway, was analysed in lettuce leaves sampled over the diurnal and developmental timecourse experiments using the selected reference genes for normalisation.
PCR amplification efficiency and expression profiling of candidate reference genes
Candidate reference genes selected for testing
Arabidopsis thaliana homolog locus tag
Lettuce Genbank ID
Putative ubiquitin extension protein
Ubiquitin-like protein RUB2
Actin protein coding 12
Glyceraldehyde 3-phosphate dehydrogenase, cytosolic
Ubiquitin conjugating enzyme 9
Protein phosphatase 2A regulatory subunit A3
Protein phosphatase 2A-1
Candidate reference gene performance at optimum concentration
Stability of candidate reference genes
Validation of the reference genes
FT is one of the key genes involved in the flowering time pathway whose expression varies over a diurnal and developmental timecourse. We used the lettuce FT homologue (LsFT) to evaluate the reliability of the selected reference genes to normalise its expression in diurnal and developmental timecourse RT-qPCR analyses. LsPP2A-1, LsPP2AA3 and LsTIP41 were used as optimal reference genes in the diurnal time-course. LsPP2A-1 and LsTIP41 were used as optimal reference genes in the developmental time-course.
To illustrate the difference in the LsFT expression pattern that would be obtained if sub-optimal reference genes were used for normalisation, three commonly used (but the less stable) reference genes, LsUBQ1, LsUBQ7 and LsACT12 were used for a comparative analysis (Fig. 4c, d). In the diurnal time-course normalised LsFT expression exhibited a different pattern from Fig. 4a with only one peak, around ZT 12 (Fig. 4c). There was, however, little difference observed in the developmental timecourse experiment (Fig. 4b, d) which reflects the overall greater stability of all the candidate reference genes in this experiment compared to the diurnal experiment (Fig. 2a, b).
To validate the usefulness of LsPP2A-1, LsPP2AA3 and LsTIP41 as good reference genes for diurnal experiments, the expression level of another target gene, the lettuce FLAVIN-BINDING, KELCH REPEAT, F-BOX (FKF1) homologue (LsFKF1) , was studied in the diurnal time-course experiment. In the diurnal time-course normalised LsFKF1 expression increased from ZT 8 reaching a maximum level at ZT 12, after this point the expression decreased dramatically reaching very low level just before the dark period (Additional file 3: Figure S2).
Quantifying gene transcripts using RT-qPCR has become a very widespread technique and there is a great need for a reliable method to analyse and interpret the results . One of the main problems is selecting reliable reference genes to use for normalisation of the expression of the target gene [1–3].
Recently, the need to identify reliable reference genes was presented in a study by Borowski et al.  where 17 candidates were studied for their suitability as reference genes in abiotic stress experiments. Results showed that different abiotic treatments required different reference genes as the stability of the genes was different in different experimental situations. The identification of stable reference genes in different experimental contexts is therefore essential in order to obtain accurate and reliable gene expression data.
In the present study a geNorm approach was used to investigate 10 candidate genes for their potential to be used as reference genes in diurnal and developmental time-course expression experiments in lettuce. GeNorm M values showed that three reference genes, LsPP2A-1, LsPP2AA3 and LsTIP41, were more constantly expressed throughout both the diurnal and developmental timecourse experiments. These reference genes were stable and constantly expressed in all the samples showing that they are not influenced by developmental stage (even the onset of flowering) or diurnal cycles in lettuce. The geNorm V values suggested that in the developmental experiment using just two reference genes LsPP2A-1 and LsTIP41 would be sufficient for accurate normalisation, whilst in the diurnal experiment three reference genes (LsPP2A-1, LsPP2AA3 and LsTIP41) would be necessary.
Flowering is one of the major developmental changes that plants undergo during their development. It is tightly regulated and involves many changes in metabolic and developmental pathways [16–18]. Therefore finding reference genes that do not fluctuate during this process that can be used as reference genes to examine the expression of genes involved in the flowering pathway is very important. PP2AA3, is a catalytic subunit of serine/threonine protein phosphatase or PP2A-1, an enzyme that remove phosphatase groups from the given substrate [19, 20]. TIP-41 is a tonoplastic intrinsic protein, a type of membrane protein channel that allows the movement of water and amino acids from the tonoplastic interior to the cytoplasm . The constant expression of these genes throughout development and during the day is probably due to the essential role they play in cells at all developmental stages. We can speculate that these reference genes could be good candidate reference genes for similar time course studies in other species, for example it is interesting to note that these three reference genes (LsPP2A-1, LsPP2AA3 and LsTIP41) were also identified as three of the most stable genes in Affymetrix GeneChip developmental timecourse data , but the stability of these candidate reference genes would still need to be checked for particular species and the specific experimental conditions used.
To demonstrate that these genes are good reference genes for RT-qPCR diurnal and developmental timecourse experiments in lettuce, the expression profile of LsFT was studied in these timecourse experiments. FT has been isolated and studied in several plants as well as in lettuce [22–27], and it has been shown to be repressed during the juvenile phase and promoted during the adult vegetative phase of development [28, 29]. In Arabidopsis, FT expression is promoted principally by CONSTANS at the end of a long day but other diurnal patterns have been observed in other plants [30–34]. In lettuce LsFT expression has been studied during development in sequentially growing leaves showing an increase in expression. FT diurnal expression was also studied and it showed a peak in expression at the beginning and at the end of the day with a trough in expression at ZT = 6 . These RTqPCR experiments however used only one reference gene, beta-tubulin (BTUB1), to normalise FT expression. Our results using the averaged value of three reference genes revealed a different FT diurnal expression pattern which peaks twice during the day at ZT 4–6 and at ZT 12–14 (Fig. 4a). This expression pattern differs to the diurnal pattern of LsFT previously observed by Fukuda et al.  and thus demonstrates the value of selecting multiple robust reference genes for RT-qPCR expression analyses.
To demonstrate that a poor selection of reference genes can affect the expression pattern obtained, three of the less stable reference genes from our analysis, LsUBQ1, LsUBQ7 and LsACT12 were used in a comparative analysis of the expression profile of LsFT in the same timecourse experiments (actin and ubiquitin being reference genes used most routinely in RT-qPCR studies ). This showed that using reference genes with low stability and high M values (such as LsUBQ1, LsUBQ7 and LsACT12 in the diurnal experiment) will give a very different outcome, however if they have low M values as in the developmental experiment where they were more stable then the result is not greatly affected.
Validation of LsPP2A-1, LsPP2AA3 and LsTIP41 as good reference genes for diurnal studies was confirmed using a second target gene, the clock-controlled FLAVIN-BINDING, KELCH REPEAT, F-BOX (FKF1) . Previous northern blotting analysis in Arabidopsis showed that FKF1 expression levels in LDs start to increase at ZT 7 and reach a peak around ZT 10, and then decrease before dark at ZT 16 . In our diurnal time-course the normalised expression of the lettuce homologue, LsFKF1, shows the same pattern verifying the suitability of the selected reference genes for such timecourse experiments.
In this study reference genes suitable for use in diurnal and developmental timecourse experiments in lettuce have been identified. The references genes selected have been used to generate a much more detailed and robust analysis of LsFT expression levels in both diurnal and developmental timecourse experiments than has been achieved to date.
Plant materials, experimental conditions and tissue collection
Lettuce (L. sativa) seeds were sown in Levington F2 compost and covered with vermiculite, before being stratified in the dark at 4 °C for 48 h to achieve uniform germination. After stratification, trays were moved into long day (LD) conditions in the glasshouse (8 h dark and 16 h light) with supplementary lighting provided by high pressure sodium lamps when natural light levels went below 300 W/m2. Constant day/night temperature of 18 °C/15 °C was maintained. Plants were re-potted into 12.7 cm pots when they reached the 3–4 leaf stage.
For the diurnal experiment 24 plants were moved one week after the plants had started bolting from the glasshouse into controlled environment cabinets set for 16 h LD (daily light integral = 7.5 mol m−2 d−1) and a constant temperature of 18 °C. The lighting in the cabinets was provided by 60 W fluorescent tubes. Every 2 h one leaf from four different plants was collected and then pool together for a total of 15 samples. Sampling was performed in duplicate.
For the developmental timecourse experiment, the youngest newly expanded leaf from 5 different plants was harvested. The first harvest was carried out when the plants were 31 days old followed by a harvest each week for 12 weeks, the samples were always collected at the same time of day which was 14 h after lights on. Plants bolted at a timepoint between samples 6 and 7. Sampling was performed in duplicate.
Total RNA isolation and cDNA synthesis
Total RNA was isolated from all samples collected using the Z6-extraction buffer method . RNA concentration and quality was evaluated by spectrometry using A260/A280 ratios, RNA integrity was also evaluated running 1–2 µg of total RNA on 2 % agarose gel. Samples were DNase treated using TURBO DNA-freeTM. PCR amplifications were performed to prove the absence of DNA contamination in the RNA samples using primers for L. sativa elongation factor alpha (LsELFα) [lettuce EST database—CGP2 project:CLS_S3_Contig4947] (Additional file 1: Table S1). PCR reactions used KOD Hot Start DNA Polymerase and consisted of an initial denaturation at 94 °C for 2 min, denaturation at 94 °C for 15 s, annealing for 30 s, and extension at 72 °C for 30 s for 30 cycles. First-strand cDNA was synthesised from 3 µg cleaned total RNA using iScript™ cDNA synthesis kit following the manufacturer’s guidelines and subsequently treated with RNase H.
Selection of candidate reference genes and primer design
A total of 10 candidate reference genes were chosen based on previously published papers using reference genes for developmental and diurnal time-course expression studies in other species (Table 1). The reference genes selected were; PUTATIVE UBIQUITIN EXTENSION PROTEIN (UBQ1), UBIQUITIN-LIKE PROTEIN RUB2 (UBQ7), ACTIN 2 (ACT2), ACTIN PROTEIN CODING 12 (ACT12), TUBULIN ALPHA-3 (TUA-3), GLYCERALDEHYDE 3-PHOSPHATE DEHYDROGENASE, CYTOSOLIC (GAPDH), UBIQUITIN CONJUGATING ENZYME 9 (UBC9), TIP41-LIKE PROTEIN (TIP-41), PROTEIN PHOSPHATASE 2A REGULATORY SUBUNIT A3 (PP2AA3) and PROTEIN PHOSPHATASE 2A-1 (PP2-A1) [11, 36–42].
For each candidate reference gene, a blast search was carried out in the expressed sequence tag (EST) Compositae Genome Project Database (CGPDB 2013; http://cgpdb.ucdavis.edu/) against L. sativa coding DNA sequences using the Arabidopsis homolog as a query. The coding sequences of the matching contings were then retrieved and used to design primers using Primer3Plus (http://primer3plus.com/cgi-bin/dev/primer3plus.cgi) according to the following parameters: annealing temperature (Ta) of 60–67 °C with an ideal Ta of 65 °C, GC content of 45–55 %, an optimum primer length of 20–26 bp and a maximum product size of 200 bp. The secondary structure of the amplicons was examined using Mfold (http://mfold.rna.albany.edu/?q=mfold) so that amplicon sequences could be selected that didn’t have any secondary structure at the primer binding sites. Primer sequences and relevant information are shown in Additional file 1: Table S1.
The presence of any primer dimers and non-specific amplification was identified post-PCR through analysis of melting curve data and by sequencing the amplified products to confirm their identity.
Real-time quantitative PCR
RT-qPCR analysis was conducted using the Bio-Rad CFX384 TouchTM Real-time PCR machine (Bio-Rad). Each reaction contained 5 μl Sso Advanced™ SYBRH Green Supermix, 0.5 μl cDNA, and forward and reverse primers in the appropriate concentration (Additional file 1: Table S1), in a total volume of 10 µl made up with sterile distilled water. Amplification conditions were as follows: 95 °C for 3 min followed by 40 cycles of 10 s at 95 °C and 30 s at the primer specific Ta (Additional file 1: Table S1). The melting curve was obtained by melting the amplified template from 65 to 95 °C increasing the temperature by 0.5 °C per cycle. No-template controls were included. Three technical replicates were used for each sample. Amplification efficiencies for all primer pairs were evaluated using serial tenfold dilutions of pooled cDNA. MiQE guidelines were followed for analysis .
Reference gene stability
Each primer pair was screened for the best concentration to use in the PCR reaction. The geNorm algorithm  present in qBase Plus software version 2.5 (http://www.biogazelle.com/qbaseplus) was used to rank expression stability of the candidate reference genes across diurnal and developmental time-course samples. Using target- and run-specific amplification, geNorm generated an internal control gene stability measure (M) which represents the average pair-wise variation of each reference gene with all the other reference genes . The M value for a good reference gene is arbitrarily set as below 1.5 . The geNorm analysis, for the diurnal experiments, was initiated on 15 samples and 10 reference targets. The geNorm analysis, for the developmental experiments, was initiated on 12 samples and 10 reference targets. All samples were measured in the same run for a given reference target. MiQE guidelines were followed for analysis .
Validation of reference gene stability
To test and validate the stability of the selected reference genes the expression profile of L. sativa FT (LsFT) [DNA Data Bank of Japan: AB602322] and L. sativa FKF1 (LsFKF1)  were investigated in diurnal and developmental time-course experimental leaf tissue samples (Additional file 1: Table S1). RT-qPCR was performed as previously described with the appropriate primer concentration and annealing temperature (Additional file 1: Table S1). Normalised gene expression was determined using data from the three biological replicates by the geometric mean of the relative quantities for all and for the most stable reference genes according to geNorm results, and using target- and run-specific amplification with qBase Plus software version 2.5 (http://www.biogazelle.com/qbaseplus). MiQE guidelines were followed for analysis .
Availability of data and materials
The datasets supporting the conclusions of this article are included within the article and its additional file.
TS, AM, and SJ designed the experiments. TS performed the experiments. JP designed the primers used for the real time. TS, AM and SJ wrote the manuscript. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
We acknowledge funding for this work from the Biotechnology and Biological Sciences Research Council (BBSRC Grant No. BB/G007330/1).
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
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