When performing real-time qPCR, one has to decide whether to use a one-step protocol that combines the RT reaction and PCR in one tube, or a two-step protocol where the RT reaction is performed separately from the PCR (Figure 1). Each method has its advantages and disadvantages that extend from the ease of logistics and cost of reaction to the resulting yield and sequence representation. One-step reactions are certainly easier to set up with less overall hands-on time, but don’t provide the flexibility and control possible with two-step reactions. One-step or two-step, which would you choose?
Figure 1. Comparison of workflows for one-step and two-step RT-qPCR Procedures. In the one-step protocol, in a single tube RNA is converted to cDNA and all of the cDNA is immediately used for qPCR quantification. No discrete cDNA product is generated. In a two-step protocol, cDNA is produced in the RT step, and a portion of that cDNA is used to set up a subsequent qPCR reaction.
One-step RT-qPCR: convenience with minimal handling
In one-step RT-qPCR, reverse transcription and PCR occur in the same tube. Gene-specific primers are used for generating the cDNA and for subsequent amplification. Major advantages of one-step reactions include limited sample handling and reduced bench time, which helps to decrease chances for pipetting errors and cross contamination. This method is quick to set up and makes processing multiple RNA samples easy when you are amplifying only a few genes of interest. It is also ideal for situations where the same genes must be amplified repetitively, such as in high-throughput detection of a specific target using well-established reaction conditions.
However, when using this protocol, you must take several concerns into account. For example, with one-step RT-qPCR, you are fully committed to the amount and quality of the RNA used in the reaction. With regards to RNA quality, it is important to remember that common contaminants such as fatty acids, buffer salts, phenol, or other components from sample isolation can compromise the efficiency of the RT reaction which is the most sensitive part of the procedure.
In addition, when using oligo(dT) or random hexamer primers with one-step RT-PCR, all of the RNA sample is converted to cDNA and all of the cDNA is used in the PCR. So if the copy number of your target sequence is high, signal may come up too early, or if there is not enough cDNA, you may not detect your target. If you want to adjust your template concentrations, or to amplify other genes at a later date using the one-step method, you must keep an aliquot of the original RNA sample and run the entire reaction again. Because of these factors, one-step reactions may require substantially more RNA in your initial samples if you are performing multiple amplifications. Variation between these different RT reactions can complicate assay interpretation significantly.
Furthermore, the combined RT and PCR reagents must allow these reactions to proceed together in one tube. This prevents use of the most optimal reagents and conditions for each individual reaction. So while all of the cDNA from the RT reaction is used in the PCR in a one-step RT-qPCR—theoretically providing very sensitive detection—the compromised reaction conditions affect efficiency and, thus, yield.
The specialized systems that allow both reactions to occur together are usually supplied through commercial kits, which can be expensive. However, one-step RT-qPCR reactions are smaller, using less reagent(s) compared to the two-step method.
Finally, one-step RT-qPCR requires careful evaluation to prevent primer dimer formation because the gene specific primers will be present not only during PCR cycling, but also during the lower temperature conditions of the RT reaction.
Two-step RT-qPCR: control and flexibility
In two-step RT-qPCR, reverse transcription and PCR are performed as two separate reactions, with RNA converted to cDNA first, using a choice of random hexamers, oligo dT primers, or even gene-specific primers. Use of random hexamers and/or oligo dT primers provides a cDNA archive of all RNA species in the sample. Either a portion of the RT reaction is diluted into the PCR, or the RT reaction can be extracted and precipitated, allowing control over the amount of cDNA input. This flexibility is an asset when working with genes of variable abundance. Any residual cDNA is available for future amplification reactions of other genes, or even for other applications. Use of the cDNA from the same RT reaction for multiple PCRs makes it easier to compare results across experiments because reaction variability and failure is limited to the PCR step, which simplifies any required troubleshooting.
Two-step RT-qPCR allows for individual optimization of the RT reaction and qPCR for efficiency and maximum sequence representation. These protocols typically produce higher yields of cDNA during the RT than one-step procedures. Because of the ability to optimize both reactions, and the higher cDNA yields, two-step reactions can be more sensitive than one-step reactions. The ability to separately optimize reactions is also beneficial when performing PCR on challenging sequences.
Beyond just having more control over the reactions and variability, the two-step method is particularly useful when the goal is to detect multiple messages from a single RNA sample or perform multiple PCR amplifications from a single cDNA sample.
So one-step or two?
The choice between one-step and two-step reactions comes down to the goal of your experiment. Use one-step RT-qPCR when you have a lot of sample, and/or a limited number of known targets that you may be repeatedly amplifying. It can be ideal for high-throughput detection applications that use an optimized reaction with well‑tested primers.
Use two-step RT-qPCR when your sample is precious and/or you need to examine multiple targets or targets that may not be well characterized and may require you to go back to test new targets. Two-step RT-qPCR will also give you the control to optimize in difficult PCR situations and when target abundance is variable.
Choosing between one-step and two-step RT-qPCR
|| Two-Step Protocol || One-Step Protocol |
Primers used in RT
- A mix of these
- Choice of primers
- Optimize reactions for maximum yield
- Modulate amount of RT that goes into PCR—controlling for target abundance
- Perform multiple PCR reactions on the same cDNA sample
Adjust for challenging PCR (e.g., GC-rich sequences)
- Experiment with different RT and Taq enzymes
- Quick setup and limited handling
- Easy processing of multiple samples for repetitive tests, or high-throughput screening
- Fewer pipetting steps, reducing potential errors
- Eliminates possibility of contamination between the RT and qPCR steps
- Requires more setup, hands-on, and machine time
- Additional pipetting increases the chances for experimental errors and contamination
- Uses more reagents
- Must “start over,” or save RNA aliquot and perform new RT to analyze new target or repeat amplifications
- Reaction conditions are not optimal—efficiency & thus quantification are affected
- Primer dimers a bigger potential problem
- amplifying multiple targets from a single RNA source
- when you plan to reuse cDNA for additional amplifications
- working with multiple RNA samples to amplify only a few targets
- assays performed repeatedly
Assays, probes, and controls for qPCR and PCR
PrimeTime® qPCR Assays
- 5′ nuclease, probe-based assays—the gold standard for quantitative gene expression studies
- Primer-based assays—designed for intercalating dye experiments
Create custom assays that are designed using our proprietary bioinformatics algorithms for any target and to your specific parameters. Alternatively, select one of our predesigned assays for human, mouse, and rat mRNA targets that are supported by our bioinformatics algorithms and up-to-date sequence/SNP information.
Learn more at www.idtdna.com/PrimeTime. For assistance with assay design, contact our scientific application specialists at firstname.lastname@example.org.
ZEN™ and TAO™ Double-Quenched Probes have a 5′ fluorophore, an internal quencher (ZEN or TAO quencher), and Iowa Black FQ as the 3′ quencher. These probes provide consistently earlier Cq values and improved precision, when compared to traditional, single-quenched qPCR probes.
Learn more at www.idtdna.com/qPCRprobes.
gBlocks® Gene Fragments
gBlocks Gene Fragments are double-stranded, 125–2000 bp DNA molecules. They are ideal for use as qPCR controls and standards, as well as for gene construction and editing applications. These affordable gene fragments are sequence-verified, ship in a few working days, and save laboratory time.
Learn more at www.idtdna.com/gBlocks.
Free tools for qPCR and PCR assay design
Explore IDT SciTools® Web Tools for free, online tools for qPCR probe design and analysis. The design engines for these tools use sophisticated formulas that, for example, take into account nearest neighbor analysis to calculate Tm, and provide the very best qPCR assay designs.
DECODED 4.2—Special qPCR Issue: Get this compendium of IDT DECODED newsletter articles with qPCR tips, troubleshooting advice, and researcher examples in one convenient volume.
PrimeTime® qPCR Application Guide: Download this useful resource that provides experimental overviews, protocols, data analysis, and troubleshooting chapters.
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