GenomePlex^® Single Cell Whole Genome Amplification Kit (WGA4) - Protocol

Product Description
Reagents Provided
Storage/Stability
Procedure
Troubleshooting Guide
FAQs
Posters and Publications
Downstream applications
        Gel Electrophoresis & qPCR
        CGH Microarrays
        Short Tandem Repeats Analysis
        Single Nucleotide Ploymorphism (SNP)
       

Product Description

Whole genome amplification from a single cell is now possible with our optimized GenomePlex^® Single Cell Whole Genome Amplification Kit (WGA4). The single cell procedure differs very little from the previously described GenomePlex^® system, but for three procedural changes: (1) the kit includes a robust, optimized cell lysis protocol that is incorporated into the fragmentation steps; (2) the primers that have been optimized for increased sensitivity; and (3) the number of cycles have been increased to account for the minute amount of starting template. Single cells can be isolated by fluorescence-activated cell sorting (FACS), laser capture microdisection, dilution or any other applicable method. Single Cell WGA has been successfully applied to single cell Comparative Genome Hybridization, STR analysis of amniocentesis samples and genomic analysis of in vitro fertilized embryos, comparative genomic hybridization, etc.^1,2

Reagents Provided

Product Description	Catalog Number	10 Rxn	50 Rxn	500 Rxn
10x Single Cell Lysis & Fragmentation Buffer	L1043	350 µL	1.8 mL	18 mL
Proteinase K Solution	P4850	25 µL	110 µL	1 mL
1x Single Cell Library Preparation Buffer	L0918	25 µL	110 µL	1.1 mL
Library Stabilization Solution	L7292	12 µL	55 µL	550 µL
Library Preparation Enzyme	E0531	12 µL	55 µL	550 µL
10x Amplification Master Mix	A5604	85 µL	410 µL	5 x 820 µL
WGA DNA polymerase	W3891	55 µL	275 µL	2 x 1375 µL
Control DNA (5 ng/µL)	D7192	10 µL	10 µL	10 µL
Water, Molecular Biology Reagent	W4502	1.5 mL	2 x 1.5 mL	2 x 20 mL

Storage/Stability

All components should be stored at –20 °C. When thawed for use, components should be kept on ice. The stability of the Library Preparation Enzyme will be affected if stored warmer than –20 °C or allowed to remain for long periods at temperatures over 4 °C.

Procedure

The single cell WGA process is divided into lysis & fragmentation, OmniPlex library generation, and PCR amplification. These steps should be carried out sequentially without pause, as storage between steps may allow the ends of the library DNA to degrade. Such degradation will affect subsequent steps. The final WGA DNA should be stored at –20 °C and is as stable as any comparably stored genomic DNA sample.

We recommend that all experiments should be performed along with a positive control DNA sample, such as the Control Human Genomic DNA, Catalog Number D7192, included in this kit.

Single Cell Lysis and Fragmentation

1. Isolate a single cell into a PCR-ready vessel using laser capture micro-dissection, cell sorting, or other method. If sorted, the buffer should be of low ionic strength, such as Tris EDTA (TE) buffer, and in the minimal sort volume.
2. Add a sufficient volume of water to the single cell sample for a final volume of 9 µL.
3. Prepare a working Lysis and Fragmentation Buffer Solution by adding 2 µL of Proteinase K Solution (P4850) into 32 µL of the 10x Single Cell Lysis & Fragmentation Buffer. Vortex thoroughly.
4. Add 1 µL of the freshly prepared Proteinase K Solution-10x Single Cell Lysis & Fragmentation Buffer to the single cell sample. Mix thoroughly.
5. Incubate DNA mix at 50 °C for 1 hour, then heat to 99 °C for EXACTLY four minutes. Note that the incubation is very time sensitive. Any deviation may alter results. Cool on ice. Spin down sample prior to proceeding to Library Preparation.

Library Preparation

6. Add 2 µL of 1x Single Cell Library Preparation Buffer to each sample.
7. Add 1 µL of Library Stabilization Solution.
8. Mix thoroughly and place in thermal cycler at 95 °C for 2 minutes.
9. Cool the sample on ice, consolidate the sample by centrifugation, and replace on ice.
10. Add 1 µL of Library Preparation Enzyme, mix thoroughly, and centrifuge briefly.
11. Place sample in a thermal cycler and incubate as follows:
    16 °C for 20 minutes
    24 °C for 20 minutes
    37 °C for 20 minutes
    75 °C for 5 minutes
    4 °C hold

12. Remove samples from thermal cycler and centrifuge briefly. Samples may be amplified immediately or stored at –20 °C for three days.

Amplification

13. Add the following reagents to the entire 14 µL reaction:
    7.5 µL of 10x Amplification Master Mix
    48.5 µL of Water, Molecular Biology Reagent
    5.0 µL of WGA DNA Polymerase
14. Mix thoroughly, centrifuge briefly, and begin thermocycling. The following profile has been optimized for a PE 9700 or equivalent thermal cycler:
    Initial Denaturation     95 °C for 3 minutes

    Perform 25 cycles as follows:
    Denature                 94 °C for 30 seconds
    Anneal/Extend         65 °C for 5 minutes
    Hold                        4 °C

After cycling is complete, maintain the reactions at 4 °C or store at –20 °C until ready for analysis or purification. The stability of WGA DNA is equivalent to genomic DNA stored under the same conditions.

Purification of the final product is recommended before being used in subsequent applications. GenomePlex^® WGA amplified DNA may be purified with the GenElute™ PCR Cleanup Kit, Catalog Number NA1020, or standard purification methods that isolate single and double stranded DNAs. Once purified, the DNA can be quantified by measuring absorbance, assuming that 1 A₂₆₀ unit is equivalent to 50 ng/µL DNA. Measurement techniques such as PicoGreen^® dye will often underestimate the actual WGA DNA yield, since single stranded DNA might be generated during amplification.

Product Profile

All lots are functionally tested by the amplification of a 100 pg sample of standard human genomic DNA that must yield 4 µg of product. The quality and representation of amplification is determined by real-time PCR using primer sets for eight separate loci. Negative (no template) controls must yield no detectable product

References

1. Paz N, Zabala A, Royo F, García-Orad Á, Zugaza JL, Parada LA. Combined Fluorescent-Chromogenic In Situ Hybridization for Identification and Laser Microdissection of Interphase Chromosomes. PLoS ONE. 8(4):e60238. https://doi.org/10.1371/journal.pone.0060238

2. Seifertova E, Zimmerman LB, Gilchrist MJ, Macha J, Kubickova S, Cernohorska H, Zarsky V, Owens ND, Sesay AK, Tlapakova T, et al. 2013. Efficient high-throughput sequencing of a laser microdissected chromosome arm. BMC Genomics. 14(1):357. https://doi.org/10.1186/1471-2164-14-357

3. Yoshido A, ?íchová J, Kubí?ková S, Marec F, Sahara K. 2013. Rapid turnover of the W chromosome in geographical populations of wild silkmoths, Samia cynthia ssp.. Chromosome Res. 21(2):149-164. https://doi.org/10.1007/s10577-013-9344-1

4. Kitada K, Taima A, Ogasawara K, Metsugi S, Aikawa S. 2010. Chromosome-specific segmentation revealed by structural analysis of individually isolated chromosomes. Genes Chromosom. Cancer.n/a-n/a. https://doi.org/10.1002/gcc.20847

5. Navin N, Kendall J, Troge J, Andrews P, Rodgers L, McIndoo J, Cook K, Stepansky A, Levy D, Esposito D, et al. 2011. Tumour evolution inferred by single-cell sequencing. Nature. 472(7341):90-94. https://doi.org/10.1038/nature09807

6. Treff NR, Su J, Tao X, Levy B, Scott Jr. RT. 2010. Accurate single cell 24 chromosome aneuploidy screening using whole genome amplification and single nucleotide polymorphism microarrays. Fertility and Sterility. 94(6):2017-2021. https://doi.org/10.1016/j.fertnstert.2010.01.052

7. Hiura H, Sugawara A, Ogawa H, John RM, Miyauchi N, Miyanari Y, Horiike T, Li Y, Yaegashi N, Sasaki H, et al. 2010. A tripartite paternally methylated region within the Gpr1-Zdbf2 imprinted domain on mouse chromosome 1 identified by meDIP-on-chip. 38(15):4929-4945. https://doi.org/10.1093/nar/gkq200

8. Treff NR, Levy B, Su J, Northrop LE, Tao X, Scott RT. 2010. SNP microarray-based 24 chromosome aneuploidy screening is significantly more consistent than FISH. Molecular Human Reproduction. 16(8):583-589. https://doi.org/10.1093/molehr/gaq039

9. van Arensbergen J, Garcia-Hurtado J, Moran I, Maestro MA, Xu X, Van de Casteele M, Skoudy AL, Palassini M, Heimberg H, Ferrer J. 2010. Derepression of Polycomb targets during pancreatic organogenesis allows insulin-producing beta-cells to adopt a neural gene activity program. Genome Research. 20(6):722-732. https://doi.org/10.1101/gr.101709.109

10. Barker DL. 2004. Two Methods of Whole-Genome Amplification Enable Accurate Genotyping Across a 2320-SNP Linkage Panel. Genome Research. 14(5):901-907. https://doi.org/10.1101/gr.1949704

11. Gribble S, Ng BL, Prigmore E, Burford DC, Carter NP. 2004. Chromosome paints from single copies of chromosomes. Chromosome Res. 12(2):143-151. https://doi.org/10.1023/b:chro.0000013167.12527.f0

12. Thorstenson YR, Hunicke-Smith SP, Oefner PJ, Davis RW. 1998. An Automated Hydrodynamic Process for Controlled, Unbiased DNA Shearing. Genome Res.. 8(8):848-855. https://doi.org/10.1101/gr.8.8.848

Troubleshooting Guide

Observation	Cause	Recommended Solution
Low yield after cycling	Sample contains salt or inhibitors.	The sorting process may carry over inhibitors or salts that disrupt the process.
	Poor quality template	The DNA in the single cell was degraded during the isolation process.  The single cell was improperly stored. Performing WGA on more than one sample helps rule out quality issues that are random in nature, but will not help if the sorting process damages the sample.
	The post reaction purification was inappropriate.	We recommend GenElute™ PCR Cleanup Kit, Catalog Number NA1020. The method must retain single and double stranded DNA.
	A single cell was not captured.	Ensure you have a single cell present in your PCR-ready tube.  In addition, make certain to thoroughly vortex after adding in the single cell lysis/fragmentation buffer.
qPCR shows significant bias in WGA representation for my gene of interest.	The DNA sample is limited or degraded.	See low yield comments.
	Inappropriate controls	Genomic DNA can only be compared to GenomePlex® WGA once the control DNA has been sheared. We recommend using several pooled samples that have been subjected to the fragmentation protocol above (steps 1–5), or comparing against DNA subjected to hydroshearing.3
Negative (no template) control affords product.	Reagents have been contaminated by outside source.	One or more reagents have been contaminated with DNA. While this may not affect your results, a clean no template control can be re-achieved only by replacing the affected component.

Frequently Asked Questions

1. How does GenomePlex^® work?
Genomic DNA is randomly fragmented and the resulting product is manipulated to attach a common sequence at each DNA end. This library of fragments is amplified using twenty-five rounds of PCR.

2. What if fragmentation (99 °C step) is allowed to proceed for less or more than four minutes?
The four-minute fragmentation time was found to give optimal results over a wide variety of DNA samples. Too little or no fragmentation will afford low yields and poor gene representation in the resulting WGA product. A ten-minute fragmentation step will also give poor WGA yields in almost all cases because a significant fraction of the DNA is now too small or degraded to allow efficient library production.

3. What is the average size of fragmented DNA?
The mean size after the fragmentation step is ~0.4kb.

4. Will the GenomePlex^® process afford product with a negative control (no input DNA)?
No product will be generated without input of DNA if the procedure is performed correctly.

5. How should WGA DNA be purified? Is there a preferred way to quantify GenomePlex^® DNA?
We recommend purifying GenomePlex^® DNA using the PCR cleanup kit (Catalog Number NA1020) before it is used in any downstream process. Once purified, the DNA can be quantified by measuring absorbance, assuming that 1 A₂₆₀ unit is equivalent to 50 ng/µL DNA. Measurement techniques such as PicoGreen^® will often underestimate the actual WGA DNA yield, since single stranded DNA might be generated during amplification.

6. How can I store GenomePlex^® DNA? Where can I stop during the GenomePlex^® process? The WGA process can be divided into single cell lysis/fragmentation, generation of the OmniPlex^® library, and PCR amplification. Fragmented DNA should be processed immediately, as the ends of this DNA can degrade and will affect subsequent steps. OmniPlex library DNA, generated in the stepped isothermal reactions, can be stored up to three days at –20 °C without any detectable differences to the process. The final WGA DNA should be stored at –20 °C and is as stable as any comparably stored genomic DNA sample.

7. I have analyzed my sample for gene representation and have observed allelic dropout.
Studies have shown that allelic dropout is inherent in single cell amplification. The Single Cell WGA Kit minimizes allelic dropout. Our WGA methodology has been tested via quantitative PCR on multiple single cell WGA samples resulting in 30% allelic dropout.

This product is for research use only. Use of this product for human or animal therapeutic or diagnostic purposes requires licensing from Rubicon Genomics, Inc. Unauthorized use violates proprietary rights of Rubicon Genomics, Inc (www.rubicongenomics.com).

NOTICE TO PURCHASER: LIMITED LICENSE

Use of this product is covered by one or more of the following US patents and corresponding patent claims outside the US:  5,789,224, 5,618,711, 6,127,155 and claims outside the US corresponding to expired US Patent No. 5,079,352.  The purchase of this product includes a limited, non-transferable immunity from suit under the foregoing patent claims for using only this amount of product for the purchaser’s own internal research. No right under any other patent claim, no right to perform any patented method, and no right to perform commercial services of any kind, including without limitation reporting the results of purchaser's activities for a fee or other commercial consideration, is conveyed expressly, by implication, or by estoppel. This product is for research use only. Diagnostic uses under Roche patents require a separate license from Roche. Further information on purchasing licenses may be obtained by contacting the Director of Licensing, Applied Biosystems, 850 Lincoln Centre Drive, Foster City, California 94404, USA. 

GenomePlex and OmniPlex are Registered Trademarks of Rubicon Genomics.
GenElute is a trademark of Sigma-Aldrich Co. LLC
PicoGreen is a registered trademark of Molecular Probes, Inc.
TaqMan is a registered trademark of Roche Molecular Systems

Posters and Publications

• Single Cell Whole Genome Amplification: Unleashing a World within a Cell
• Novel Whole Genome Amplification for Difficult and Limited Templates
• Single Cell Whole Genome Amplification Method
• Single Cell Aneuploidy Analysis by High Resolution Comparative Genomic Hybridization (CGH) after Whole Genome Amplification reveals Maternal Cell Contamination in the Original Products of Conception Cultures.
  

Downstream Applications

• Gel Electrophoresis & qPCR
• Short Tandem Repeats Analysis
• Single Nucleotide Ploymorphism (SNP)