Name: Profiling of Pre-micro RNAs and microRNAs using Quantitative Real-time PCR (qPCR) Arrays (Video) | JoVE Journal
Uploaded: 2010-12-03T17:00:00.000+00:00
Duration: 10 min 58 s
Description: Learn automated QPCR array setup for profiling pre-microRNAs and microRNAs using robotic and manual methods. This protocol enables accurate expression analysis of large mRNA sets in molecular biology research.

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This work was supported by NIH grants DE018304, R01DE018281. K.T. is supported by T32 GM07092-34 and by a grant to the University of North Carolina at Chapel Hill from Howard Hughes Medical Institute (HHMI) through the Med into Grad Initiative. PC is supported by T32 CA009156.

The qPCR pre-miRNA profiling arrays can be set up as fully automated with a Tecan Freedom Evo robot (A) or by hand with the Matrix electronic multichannel pipette (B).
1)Prepare the master mix, primer plates and samples.
<ol>
	<li>Primer plates containing 186 primer pairs in 96-well format (total of 2 plates) at 0.5pM should be stored at -80°C. Thaw plates out at room temperature, vortex and centrifuge briefly before use.</li>
	<li>To prepare the master mix, thaw out SYBR Green 2x PCR Mix at room temperature. Each reaction uses 8ul master mix with 2ul primer. The composition of the master mix per reaction is 4ul SYBR mix, 3ul PCR grade water and 10-20 ng sample DNA or cDNA.</li>
	<li>For setup of each 96-well primer plate, four master mix tubes will be needed. Samples can be run 4 samples per plate (singlicate), 2 samples per plate (duplicate) or a single sample in quadruplicate.</li>
	<li>Prepare master mix by combining SYBR, water and sample in each of 4-2ml Eppendorf tubes. Each tube should contain enough master mix for approximately 100 reactions, allowing excess for pipetting waste. Vortex to mix.</li>
</ol>
A. Setup of pre-miRNA assay using the Freedom Tecan Evo robot.
<ol>
	<li>Following initialization of the robot and loading of the Evoware program, flush three times with 30mls each to clear system of air bubbles that will interfere with pipetting accuracy.</li>
	<li>Setup the robot platform to include the following:
	<ul>
		<li>Labeled 384-well plate</li>
		<li>96-well primer plate (1)</li>
		<li>Master mixes</li>
		<li>A trough containing 2% bleach</li>
		<li>A filled system fluid container</li>
		<li>Empty waste container</li>
	</ul>
	</li>
	<li>Begin automated robot run by selecting "Run" twice.</li>
	<li>At end of program, remove 384-well plate and seal with LightCycler 480 sealing foil and centrifuge briefly. Place sealed 384-well plate in position 1 of the hotel.</li>
	<li>Go to step 2.2 and repeat for primer plate 2 with new master mixes and a new 384-well plate. 
	<ol>
 	<li>Place sealed plate in position 2 of the hotel.</li>
 </ol>
 </li>
	<li>Open new Evoware program for Loading the Lightcycler from the hotel and select "Run" twice.
 <ol>
 	<li>Freedom Evo will automatically load each plate into the LightCycler and run the following SYBR-green I/HRM cycling program: 
		Pre (1 cycle): 
 50° for 5 minutes at ramp rate of 4.8°/sec
 95° for 5 minutes at ramp rate of 4.8°/sec
		 
 Amp (45 cycles):
 95° for 15 sec at ramp rate of 4.8°/sec
		 62° for 30 sec at ramp rate of 2.5°/sec
		 (Single data acquisition during this step) 
		Melting curve:
 95° for 5 sec at ramp rate of 4.8°/sec
		 60° for 1 minute at ramp rate of 2.5°/sec
		 95° continuous at ramp rate of .11°/sec
		 with 5 acquisitions per °C 
		Cool :
 50° for 30 sec at ramp rate of 25°/sec
 </li>
 </ol>
</li>
</ol>
B.Setup of pre-miRNA assay using the Matrix electronic multichannel pipette:
<ol>
	<li>Place contents of master mix tube 1 into a reservoir.</li>
	<li>Set the electronic pipette to aspirate 16ul of master mix with 2-8ul dispense steps followed by a purge step.</li>
	<li>For master mix 1, dispense 8ul into every other well of the 384-well plate (set on 384-well tip spacing), beginning with well A1. (i.e. wells A1, C1, E1, etc.) For the second 8ul dispense, move to column 3 (i.e. wells A3, C3, E3, etc.) then purge over a waste container and dispose tips.</li>
	<li>Follow this pattern for the remaining 5 cycles until you reach well A23.</li>
	<li>Repeat for master mix 2, (beginning with well A2, C2, E2, etc.); master mix 3 (beginning at well B1, D1, F1, etc.); master mix 4 (beginning at B2, D2, F2, etc.).</li>
	<li>For aliquotting of primer plate, set electronic pipette to aspirate 2ul and dispense 2ul with a purge step following. Dispense 2ul of primers from column 1 of 96-well primer plate (A-H) into the 384-well plate, wells A1, C1, E1, etc. Purge over a waste container and dispose tips. Repeat for wells A2, C2, E2; B1, D1 ,F1; and B2, D2, F2, etc.</li>
	<li>Repeat for rows 2-12 of 96-well primers, moving over every 2 columns for each primer column, until full 384-well plate has been aliquotted.</li>
	<li>Seal plates with a LightCycler sealing foil and centrifuge briefly.</li>
	<li>Place plates into a LightCycler 480 and cycle the plates according to the following settings using the SYBR Green I/HRM detection format: 
	Pre (1 cycle):
 50° for 5 minutes at ramp rate of 4.8°/sec
	 95° for 5 minutes at ramp rate of 4.8°/sec
	 Amp (45 cycles):
 95° for 15 sec at ramp rate of 4.8°/sec
	 62° for 30 sec at ramp rate of 2.5°/sec
	 (Single data acquisition during this step)
	 Melting curve:
 95° for 5 sec at ramp rate of 4.8°/sec
	 60° for 1 minute at ramp rate of 2.5°/sec
	 95° continuous at ramp rate of .11°/sec
	 with 5 acquisitions per °C
	 Cool :
 50° for 30 sec at ramp rate of 25°/sec
 </li>
	<li>Repeat using primer plate 2, aliquotting into a fresh 384-well plate using freshly prepared master mixes.</li>
</ol>
Secrets to success:
An important characteristic when designing PCR arrays is that all 186 primer pairs have the same annealing temperature, so the plate can be run at the same optimal PCR run program settings.
Each new array should be checked using three controls prior to running samples. These controls are: 
1 run of all primers run with water or .1x TE to rule out primer contamination. 
1 run of alternating water/TE and positive control, to ensure no carryover. 
3 runs using the same positive control, to ensure reproducibility between runs. 
Master mixes should be freshly prepared, and plates should be run within 24 hrs for optimal results 
Primer plate foil should be removed slowly to reduce risk of contamination between wells. 
When using a robot with fixed tips, 2% bleach wash is necessary to wash the tips between each pipetting step, followed by a water flush. This prevents and eliminates carryover, which could otherwise contaminate data and lead to inconclusive results. 
After a plate is run through the Lightcycler, it should not be opened again in the PCR setup room. This helps prevent PCR contamination.
Representative Results:
qPCR results are typically represented by CT values as determined from the Lightcycler analysis software. A successful run usually consists of a range of CTs for samples, typically between 20-35 for samples that are positive. The water samples in a good run are always at a CT of &gt;40 and any samples or specific wells with a CT over 37 are considered negative or not detected. As a general rule, samples yielding a CT of &lt;10 are also unreliable and are excluded from further analysis. There are several ways to analyze qPCR data and the inclusion of internal controls in our assay helps control for variation of sample input. The pre-miR array includes a U6 control primer, which is often used as a reference gene to normalize CT values from different samples. This normalized value is referred to as the delta CT value (dCT). Results are often graphed as the raw CT, the dCT value or can be further analyzed to standardized values.
In Figure 1, analysis of the full pre-microRNA array of four different samples from a timecourse experiment is presented in heat map format. The relative expression of each pre-microRNA is shown and three major, distinct clusters emerged. The majority of pre-miRs analyzed underwent small, insignificant changes as expected (Figure 1A). However, a small portion of pre-microRNAs were significantly decreased (Figure 1B) or increased dramatically (Figure 1C) throughout the timecourse experiment. Levels of expression of each pre-microRNA were normalized to the 0h timepoint (sample 1) as a baseline level. In some instances, you may note that some of the clustered pre-microRNAs also cluster together in the heatmap analysis (ex: let-7a, Figure 1B). Depending on the experiment, clusters may emerge that are dependent on viral infection, cell type specific expression of pre-microRNAs or pre-miRs that are regulated by a common molecule or signaling pathway.
The pre-microRNA assay that we have developed also includes a number of known viral pre-microRNAs and genes encoded by Kaposi's Sarcoma Associated Herpesvirus (KSHV) and Epstein Barr Virus (EBV) in addition to the human pre-miRs. These can be used as positive or negative controls, depending on the cell line and viral status of the samples used. In Figure 2, the average CTs from a KSHV-negative sample run in quadruplicate are shown. Importantly, KSHV LANA was not detected in this sample by the highly sensitive qPCR array. However, U6--our internal control and let-7a--a highly expressed human pre-microRNA, were expressed at detectable levels. Finally, as expected, the negative control of PCR-grade water did not yield a qPCR product. 
Another indicator of a successful qPCR run is a good melting curve analysis, which can give insight into potential contamination in samples. To establish a melting temperature, the plate is heated slowly after the PCR is complete. As the DNA strands separate, SYBR green is released, and fluorescence signal decreases. The temperature at which this drop occurs is graphed, and is known as the melting temperature of the sample. Depending on the DNA sequence, samples melt at different temperatures from each other and from the water negative control, which should not have a melting temperature since no DNA is present. The PCR products from each primer pair should melt at similar temperatures. For example, Figure 3 shows a melting curve analysis for two different primers using the same sample in duplicate. It is clear that the melting temperature is different for the two primer pairs but the sample is melting at the exact same temperature for each replicate. Signs of a bad or potentially contaminated sample may include several melting peaks, suggesting the presence of two different sources of input.

<img src="/files/ftp_upload/2210/2210fig1.jpg" alt="Heat map diagram showing gene expression analysis data, highlighting microRNA expression patterns." data-altupdatedat="1788235205000" data-alt="Figure 1"> Figure 1. Pre-microRNA signatures emerge through profiling using a novel qPCR-based array. The average deltaCTU6 was calculated and standardized values were loaded into ArrayMinerTM software, yielding 3 distinct clusters displayed as heatmaps. (A) Pre-microRNAs with small changes in expression are shown. Pre-microRNAs whose levels were significantly decreased (B) or increased (C) are also shown. Blue corresponds to lower levels of expression while red represents increased expression levels.
<img src="/files/ftp_upload/2210/2210fig2.jpg" alt="Real-time PCR result chart, CT values for U6, KSHV LANA, let-7a-1-1, and PCR H2O samples." data-altupdatedat="1788235205000" data-alt="Figure 2"> Figure 2. Inclusion of internal controls in the qPCR-based pre-microRNA array. The raw CT values for 3 different genes and a no template control are shown. U6 is used as an internal positive control while PCR H2O serves as our negative control. Let-7a-1-1 is a microRNA normally expressed in many different cell types while KSHV LANA can be used as either a positive or negative control, based on viral status of the cell line or tissue used.
<img src="/files/ftp_upload/2210/2210fig3.jpg" alt="Melting peaks graph; DNA primers analysis, fluorescence vs. temperature, PCR thermal analysis." data-altupdatedat="1788235205000" data-alt="Figure 3"> Figure 3. Melting peak analysis of pre-microRNA primers and lack of sample contamination. Melting curves were obtained using the Tm calling analysis in the LightCycler software. Two different primers (Primer A and B) for the same sample run in duplicate are shown. The melting temperature for each primer is distinct. However, the sample has only one peak, demonstrating the lack of sample contamination.

<ol><li>Bustin, A. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((The+MIQE+Guidelines%3A+Minimum+Information+for+Publication+of+Quantitative+Real-Time+PCR+Experiments%5BTitle%5D)+AND+%22Clinical+Chem%22%5BJournal%5D)">The MIQE Guidelines: Minimum Information for Publication of Quantitative Real-Time PCR Experiments.</a> Clinical Chem. 55 (4), 611-622 (2009).</li>
<li>Frégeau, C. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Automated+Processing+of+Forensic+Casework+Samples+using+Robotic+Workstations+Equipped+with+Nondisposable+Tips+-+Contamination+Prevention%5BTitle%5D)+AND+%22J.+Forensic+Sci%22%5BJournal%5D)">Automated Processing of Forensic Casework Samples using Robotic Workstations Equipped with Nondisposable Tips - Contamination Prevention.</a> J. Forensic Sci. 53 (3), 53-533 (2008).</li>
<li>O'hara, A. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Pre-micro+RNA+Signatures+Delineate+Stages+of+Endothelial+Cell+Transformation+in+Kaposi+Sarcoma%5BTitle%5D)+AND+%22PLoS+Pathog%22%5BJournal%5D)">Pre-micro RNA Signatures Delineate Stages of Endothelial Cell Transformation in Kaposi Sarcoma.</a> PLoS Pathog. 5 (4), e1000389-e1000389 (2009).</li>
</ol>

No conflicts of interest declared.

QPCR is a highly sensitive assay that can be used to compare gene expression levels between samples in a study, as well as to determine positivity in the case of viruses. The benefit of using qPCR arrays is the ability to run many primers (in our case, 186 primer pairs) for each sample in a short period of time. Using a pipetting robot such as the Tecan Freedom Evo, the amount of time required to set an experiment up can be further reduced, and the accuracy and consistency of the robot can reduce and eliminate pipettin...

<table><tbody><tr><td>Freedom Evo 150</td><td>Tecan Group Ltd.</td><td>30017587</td><td></td></tr><tr><td>Matrix Electronic Multichannel Pipette</td><td>Thermo Fisher Scientific, Inc.</td><td>2001-MTX</td><td>(or any comparable Thermo Scientific multichannel that can pipette the volumes described above)</td></tr><tr><td>Matrix Integrity Filter Tips, Sterile</td><td>Thermo Fisher Scientific, Inc.</td><td>7435</td><td>(or comparable tip for multichannel used)</td></tr><tr><td>Lightcycler 480 SYBR Green 1 Master</td><td>Roche Group</td><td>04 707 516 001</td><td></td></tr><tr><td>Lightcycler 480 Instrument II</td><td>Roche Group</td><td>05015243001</td><td>384-well version</td></tr><tr><td>Lightcycler 480 Multiwell Plate 384, white</td><td>Roche Group</td><td>04729749001</td><td></td></tr><tr><td>LightCycler 480 Sealing Foil</td><td>Roche Group</td><td>04729757001</td><td></td></tr><tr><td>LightCycler 480 Multiple Plate Analysis Software</td><td>Roche Group</td><td>05075122001</td><td></td></tr><tr><td>Eliminase Decontaminant</td><td>Decon Laboratories</td><td>04-355-31</td><td></td></tr></tbody></table>

profiling of pre-micro rnas and micrornas using quantitative real-time pcr (qpcr) arrays

Profiling of Pre-micro RNAs and microRNAs using Quantitative Real-time PCR (qPCR) Arrays

Quantitative real-time PCR (QPCR) has emerged as an accurate and valuable tool in profiling gene expression levels.  One of its many advantages is a lower detection limit compared to other methods of gene expression profiling while using smaller amounts of input for each assay.  Automated qPCR setup has improved this field by allowing for greater reproducibility.  Its convenient and rapid setup allows for high-throughput experiments, enabling the profiling of many different genes simultaneously in each experiment.  This method along with internal plate controls also reduces experimental variables common to other techniques.  
We recently developed a qPCR assay for profiling of pre-microRNAs  (pre-miRNAs) using a set of 186 primer pairs.  MicroRNAs have emerged as a novel class of small, non-coding RNAs with the ability to regulate many mRNA targets at the post-transcriptional level.  These small RNAs are first transcribed by RNA polymerase II as a primary miRNA (pri-miRNA) transcript, which is then cleaved into the precursor miRNA (pre-miRNA).  Pre-miRNAs are exported to the cytoplasm where Dicer cleaves the hairpin loop to yield mature miRNAs.  Increases in miRNA levels can be observed at both the precursor and mature miRNA levels and profiling of both of these forms can be useful.  There are several commercially available assays for mature miRNAs; however, their high cost may deter researchers from this profiling technique.  Here, we discuss a cost-effective, reliable, SYBR-based qPCR method of profiling pre-miRNAs.  Changes in pre-miRNA levels often reflect mature miRNA changes and can be a useful indicator of mature miRNA expression.  However, simultaneous profiling of both pre-miRNAs and mature miRNAs may be optimal as they can contribute nonredundant information and provide insight into microRNA processing.  Furthermore, the technique described here can be expanded to encompass the profiling of other library sets for specific pathways or pathogens.

We will demonstrate the setup and analysis of pre-microRNA 96-well arrays for QPCR using a robot as well as by hand with a Thermo Scientific Matrix multichannel pipette.

Quantitative real-time PCR (QPCR) has emerged as an accurate and valuable tool in profiling gene expression levels.  One of its many advantages is a lower ...

The overall goal of this procedure is to allow for rapid and reliable automated setup of QPCR based arrays. This is accomplished by first preparing the primer sets for the array and setting up the sample master mixes to be screened. Next either an automated robotic PCR setup or a matrix electronic pipette system is used to accurately Eloqua sample master mix and primer sets into each well of a 384 well plate.Once prepared, the 384 well PCR reactions are run with the light cycler four 80 cyber based PCR program. The final step of the procedure is to analyze the QPCR data and determine relative expression levels for each primer pair tested, each of which targets a specific mRNA. Ultimately, results can be obtained that show changes in the expression of large sets of mRNAs.Specifically developed arrays can therefore target whole pre micro RNA profiles, specific pathways or molecules key to viral infection through QPCR based profiling. Hello, I'm Dirk DMA from the Department of Microbiology and Immunology at the University of North Carolina at Chapel Hill. Today we will show you how to set up real-time QQPC rra and we will show you two methods.One, using irregular pipette and one using a robot. We use this technology to measure pre microRNAs and mature microRNAs in human tumors. The demonstration today will be done by Pauline Chu and Kristen bu.So let's get started. To begin this procedure, retrieve primer plates containing 186 primer pairs in a 96. Well format at 0.5 picaMoles stored at minus 20 degrees Celsius.After thawing the plates out at room temperature, vortex and centrifuge them briefly. Also thaw cyber green two times PCR mix at room temperature for setup of each 96 well primer plates four master mix tubes will be needed. Prepare the master mix by combining four microliters of cyber green mix three microliters of PCR grade water and 10 to 20 nanograms of sample DNA or CDNA per reaction in each of four two milliliter einor tubes.Each tube should contain enough master mix for approximately 100 reactions, allowing excess for pipetting waste. Vortex the einor tubes to mix. Begin setup of the precursor micro RNA assay using the freedom Tecan EVO robot with initialization of the robot and loading of the EVO wear program.Then flush the robot three times with 30 milliliters of system liquid to clear the system of air bubbles that will interfere with pipetting accuracy. Next, set up the robot platform to include a 384 well plate and 96 well primer plate. The master mixes a trough containing 2%bleach, a filled system, fluid container, and an empty waste container.Begin the automated robot run by selecting run twice at the end of the program. Remove the 384 well plate and seal with light cycler four 80 ceiling foil. Then centrifuge the plate.Briefly place the sealed 384 well plate in position one of the hotel. Then repeat this process for primer plate two with new master mixes and a new 384 well plate. Place the resulting sealed 384 world plate in position two of the hotel.Open a new EVO wear program for loading the light cycler from the hotel and set the cycling parameters. Then select run twice. Freedom Evo will automatically load each plate into the light cycler and run the cyber green one HRM cycling program.Once complete. Review and analyze the results as described in the written protocol as an alternative to using the robot. A matrix electronic multichannel pipette can be used to begin place the contents of the master mix tube one into a reservoir.Set the electronic pipette to aspirate 16 microliters of master mix with two eight microliter dispense steps followed by a purge step. After setting the pipette aspirate 16 microliters of master mix and begin to dispense into a 384 wheel plate. Dispense the first eight microliters into every other row in column one using rows A to O, leaving the next column empty.Dispense the second eight microliters into the same rows of column three. Then purge over a waste container and dispose tips following this pattern of leaving alternate rows and alternate columns. Dispense across the plate for five more cycles to pipette master mix two.Utilize the same rows as master mix one, but begin with column two. Repeat this procedure for master mixes three and four, beginning with columns one and two respectively, but this time using rose B to P.Her quoting of the primer plate. Set an electronic pipette to aspirate two microliters and dispense two microliters with a purge step to follow.Transfer two microliters of primers from column one row A to H of a 96 well primer plate to every other rowing column one of the 384 well plate purge over a waste container and dispose tips. Repeat this pattern for quatt primer for the three remaining master mixes of columns one and two. Then continue this process for columns two to 12 of the 96 well primer plate moving over every two columns in the 384 well plate for each primer column.Next, seal the plates with a light cycler ceiling, foil and centrifuge. Briefly following centrifugation. Place the plates into a light cycler four 80 and cycle the plates using the cyber green one HRM detection format.Using the same cycling conditions as before, repeat this procedure using primer plate two Eloqua into a fresh 384 well plate using freshly prepared master mixes. Precursor micro RNA signatures emerge through profiling using a novel QPCR based array. The average delta CT as normalized to U six was calculated and standardized values were loaded into array.Minor software yielding three distinct clusters displayed as heat maps. The relative expression of each precursor micro RNA is shown red and blue represent an increase and decrease in relative expression respectively. The color intensity indicates the degree of expression change.The majority of precursor microRNAs underwent small insignificant changes as expected. However, a small portion of precursor microRNAs significantly increased throughout the time course experiment. Additionally, the relative level of some precursor microRNAs decreased dramatically.In some instances. They also cluster together in the heat map analysis. Depending on the experiment clusters may emerge that are dependent on viral infection, cell type specific expression of precursor microRNAs or precursor microRNAs that are regulated by a common molecule or signaling pathway.The average cycle thresholds or cts from a Posey sarcoma associated herpes virus negative sample running quad duplicate are shown. Importantly, Kaposi's sarcoma associated herpes virus latency associated nuclear antigen or KSHV Lana was not detected in this sample by the highly sensitive QPCR array. However, both the internal control U six and let seven a a highly expressed human precursor micro RNA, were expressed at detectable levels.Finally, as expected, the negative control of PCR grade water did not yield A-Q-P-C-R product. A melting curve analysis for two different primers. Using the same sampling duplicate is shown.It is clear that the melting temperature is different for the two primer pairs, but the sample is melting at the exact same temperature for each replicate. Signs of a bad or potentially contaminated sample may include several melting peaks suggesting the presence of two different sources of input. We have just shown you how to set up a real-time QPCR experiments using a robot.It's important that you include all the controls and as many housekeeping genes as possible. So thank you for watching and good luck with your experiments.

profiling-pre-micro-rnas-micrornas-using-quantitative-real-time-pcr

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Learn automated QPCR array setup for profiling pre-microRNAs and microRNAs using robotic and manual methods. This protocol enables accurate expression analysis of large mRNA sets in molecular biology research.

Profiling of Pre-micro RNAs and microRNAs using Quantitative Real-time PCR (qPCR) Arrays

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