Telomerase Repeated Amplification Protocol (TRAP).
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Journal: 2017/February - Bio-protocol
ISSN: 2331-8325
PUBMED: 27182535
Abstract:
Telomeres are found at the end of eukaryotic linear chromosomes, and proteins that bind to telomeres protect DNA from being recognized as double-strand breaks thus preventing end-to-end fusions (Griffith et al., 1999). However, due to the end replication problem and other factors such as oxidative damage, the limited life span of cultured cells (Hayflick limit) results in progressive shortening of these protective structures (Hayflick and Moorhead, 1961; Olovnikov, 1973). The ribonucleoprotein enzyme complex telomerase-consisting of a protein catalytic component hTERT and a functional RNA component hTR or hTERC- counteracts telomere shortening by adding telomeric repeats to the end of chromosomes in ~90% of primary human tumors and in some transiently proliferating stem-like cells (Shay and Wright, 1996; Shay and Wright, 2001). This results in continuous proliferation of cells which is a hallmark of cancer. Therefore, telomere biology has a central role in aging, cancer progression/metastasis as well as targeted cancer therapies. There are commonly used methods in telomere biology such as Telomere Restriction Fragment (TRF) (Mender and Shay, 2015b), Telomere Repeat Amplification Protocol (TRAP) and Telomere dysfunction Induced Foci (TIF) analysis (Mender and Shay, 2015a). In this detailed protocol we describe Telomere Repeat Amplification Protocol (TRAP). The TRAP assay is a popular method to determine telomerase activity in mammalian cells and tissue samples (Kim et al., 1994). The TRAP assay includes three steps: extension, amplification, and detection of telomerase products. In the extension step, telomeric repeats are added to the telomerase substrate (which is actually a non telomeric oligonucleotide, TS) by telomerase. In the amplification step, the extension products are amplified by the polymerase chain reaction (PCR) using specific primers (TS upstream primer and ACX downstream primer) and in the detection step, the presence or absence of telomerase is analyzed by electrophoresis. TSNT is, an internal standard control, amplified by TS primer. NT is its own reverse primer, which is not a substrate for telomerase. These primers are used to identify false-negative results by if the gel lacks internal control bands.
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Bio Protoc 5(22): e1657
PMID: 27182535

Telomerase Repeated Amplification Protocol (TRAP)

Materials and Reagents

  1. Cancer cells (H1299 non-small cell lung, A549 non-small cell lung cancer cells)

  2. Tris-HCl (pH 8.3 and pH 8.0)

  3. Magnesium Chloride (MgCl2) (Thermo Fisher Scientific, catalog number: BP241)

  4. Potassium chloride (KCl) (Sigma-Aldrich, catalog number: P9541)

  5. Tween™ 20 (Thermo Fisher Scientific, catalog number: BP337)

  6. Ethylene glycol-bis(2-aminoethylether)-N, N, N′, N′-tetraacetic acid EGTA (Sigma-Aldrich, catalog number: E3889)

  7. Ethylenediaminetetraacetic Acid (EDTA) (Thermo Fisher Scientific, catalog number: BP-120)

  8. Nonidet-P40 (Fluka BioChemika, catalog number: 74385)

    Note: Currently, it is “Sigma-Aldrich, catalog number: 74385”.

  9. Glycerol (Sigma-Aldrich, catalog number: G5516)

  10. 2-mercaptoethanol (Sigma-Aldrich, catalog number: M3148)

  11. 4-(2-Aminoethyl) benzenesulfonyl fluoride hydrochloride (AEBSF) (Sigma-Aldrich, catalog number: A8456)

  12. dNTP (Invitrogen)

  13. Cy5-TS primer (Sigma-Aldrich)

  14. ACX (reverse primer) (Sigma-Aldrich)

  15. TSNT (36-bp internal standard control) (Integrated DNA Technologies)

  16. NT (reverse primer for internal standard) (Sigma-Aldrich)

  17. Takara Taq DNA polymerase, hot start version (Takara Bio Company, ClonTech, catalog number: R007A)

  18. 40% acrylamide and bis-acrylamide solution (19:1) (Bio-Rad Laboratories, catalog number: 161-0144)

  19. Ammonium persulfate (APS) (Bio-Rad Laboratories, catalog number: 161-0700)

  20. N, N, N’, N’-Tetramethylethylenediamine (TEMED) (Sigma-Aldrich, catalog number: T9281)

  21. Primer mix (see Recipes)

  22. Cy5-TS primer (see Recipes)

  23. 10x TRAP reaction buffer (see Recipes)

  24. 50x dNTP (see Recipes)

  25. NP-40 lysis buffer (see Recipes)

Equipment

  1. Polymerase Chain Reaction (PCR) Thermo Cycler (Bio-Rad Laboratories, model: PTC-1148)

  2. Typhoon PhosphorImager scanner system (Amersham Biosciences, GE Healthcare, model: Typhoon TRIO)

Software

  1. ImageQuant Software (Molecular Dynamics)

Procedure

A. Prepare cell lysates

  1. Collect 100,000 cells into a DNase/RNase -free microfuge tube.

  2. Centrifuge cells at 3,000 × g for 5 min.

  3. Remove the supernatant.

    Note: The pellet doesn't need to be washed. If samples are to be used at a later time point, put in −80 °C.

  4. Resuspend cell pellet on ice-cold NP-40 lysis buffer at a concentration of 2,500 cells per μl (40 μl lysis buffer for 100,000 cells).

  5. Leave on ice for 30 min or snap-freeze cell lysates in liquid nitrogen and then place at −80 °C.

B. Preparation for PCR-Cy5 fluorescent gel-based TRAP

  1. Keep samples on ice.

  2. Choose a positive control (i.e. HCT116, H1299) and prepare three different serial dilutions (1:10) in NP-40.

  3. Prepare the TRAP master mix. Final volume of the PCR reaction is 50 μl. Master mix for one sample:

    H2O40.2 μl
    Trap buffer5 μl
    dNTP1 μl
    Cy5-TS primer1 μl
    Primer mix1 μl
    BSA0.4 μl
    Taq polymerase0.4 μl

  4. Add 1 μl of sample to 49 μl of the master mix.

    Note: For negative control, 1 μl NP-40 to 49 μl of the master mix.

C. Amplification of the extension products by PCR

  1. 25 °C for 40 min for extension.

  2. 95 °C for 5 min to deactivate telomerase.

  3. 24 to 29 cycles at:

    • 95 °C for 30 sec

    • 52 °C for 30 sec

    • 72 °C for 45 sec

  4. 72 °C for 10 min

  5. 4 °C for up to five days

    Note: Samples can be stored at −20 °C for 1 month.

D. Running acrylamide gel

  1. Add 5 μl of loading dye to each sample.

  2. Making the 10% nondenaturing acrylamide gel.

    • 32.5 ml H2O (MilliQ water)

    • 12.5 ml 40% acrylamide (19:1 acrylamide:bisacrylamide)

    • 5 ml 5XTBE

    • 250 μl 10% APS

    • 50 μl TEMED

  3. 0.5x TBE running buffer

  4. Running time is about 2.5 h at 200/220 volts.

  5. Load 25 μl of the sample to each well.

  6. Visualize using Typhoon that can read Cy5 fluorescein.

A. Prepare cell lysates

  1. Collect 100,000 cells into a DNase/RNase -free microfuge tube.

  2. Centrifuge cells at 3,000 × g for 5 min.

  3. Remove the supernatant.

    Note: The pellet doesn't need to be washed. If samples are to be used at a later time point, put in −80 °C.

  4. Resuspend cell pellet on ice-cold NP-40 lysis buffer at a concentration of 2,500 cells per μl (40 μl lysis buffer for 100,000 cells).

  5. Leave on ice for 30 min or snap-freeze cell lysates in liquid nitrogen and then place at −80 °C.

B. Preparation for PCR-Cy5 fluorescent gel-based TRAP

  1. Keep samples on ice.

  2. Choose a positive control (i.e. HCT116, H1299) and prepare three different serial dilutions (1:10) in NP-40.

  3. Prepare the TRAP master mix. Final volume of the PCR reaction is 50 μl. Master mix for one sample:

    H2O40.2 μl
    Trap buffer5 μl
    dNTP1 μl
    Cy5-TS primer1 μl
    Primer mix1 μl
    BSA0.4 μl
    Taq polymerase0.4 μl

  4. Add 1 μl of sample to 49 μl of the master mix.

    Note: For negative control, 1 μl NP-40 to 49 μl of the master mix.

C. Amplification of the extension products by PCR

  1. 25 °C for 40 min for extension.

  2. 95 °C for 5 min to deactivate telomerase.

  3. 24 to 29 cycles at:

    • 95 °C for 30 sec

    • 52 °C for 30 sec

    • 72 °C for 45 sec

  4. 72 °C for 10 min

  5. 4 °C for up to five days

    Note: Samples can be stored at −20 °C for 1 month.

D. Running acrylamide gel

  1. Add 5 μl of loading dye to each sample.

  2. Making the 10% nondenaturing acrylamide gel.

    • 32.5 ml H2O (MilliQ water)

    • 12.5 ml 40% acrylamide (19:1 acrylamide:bisacrylamide)

    • 5 ml 5XTBE

    • 250 μl 10% APS

    • 50 μl TEMED

  3. 0.5x TBE running buffer

  4. Running time is about 2.5 h at 200/220 volts.

  5. Load 25 μl of the sample to each well.

  6. Visualize using Typhoon that can read Cy5 fluorescein.

Recipes

  1. Primer mix

    • Primer mix (50X) includes the reverse primer (ACX), the substrate for 36-bp internal standard control (TSNT), and the reverse primer for the internal standard (NT) or ITAS (internal telomerase activity standard).

    • Sequences:

      An external file that holds a picture, illustration, etc. Object name is nihms-769956-t0002.jpg
      StockFinal concentration
      ACX1.0 μg/μl100 ng/μl
      NT1.0 μg/μl100 ng/μl
      TSNT1.0 attomol/μl0.01 attomol/μl

Notes:

  1. It is highly recommended to purchase TSNT oligo from a company other than where the ACX and NT primers are bought. This helps prevention of the contamination of TSNT with ACX and NT.

  2. Preparation of stock TSNT should be done in a separate room from the TRAP bench and use a pipetman that is not used in the TRAP area.

  3. An attomol is 10 mol.

Preparation of stock TSNT:

Dilute the dry TSNT oligonucleotide to 100 μM concentration with DEPC treated water. Then prepare the serial dilutions (1:1,000, 1:1,000, 1:100); 100 nM, 100 pM and 1 pM. So, the final concentration of the TSNT stock will contain a 100x stock of TSNT (1.0 attomol/μl).

Note: To get the correct ITAS signal, you can adjust the amount of 100x stock of TSNT. For example, try a variety of dilutions of 100x stock of TSNT such as 1,000x, 300x, 100x, and 30x and see how the ITAS looks on TRAP ladder.

Preparation of primer mix:

  1. Mix ACX and NT primers together with water.

  2. Move to the area where the TSNT was prepared and add the TSNT to the mix.

  3. Clean the outside of the tubes and rack with diluted bleach (spray 10% bleach on the tubes, then dry them with paper towel or spray 10% bleach on paper towel and clean the outside of the tubes).

  4. Return to the TRAP area with the tube and prepare aliquots to store at −20 °C up to 1 year.

  • 2.

    Cy5-TS primer

    • TS oligo is purchased modified with Cy5 on the 5’end (HPLC or PAGE purified). Final concentration of TS primer is 100 ng/μl (diluted in DEPC water).

    • Sequence: 5’-AAT CCG TCG AGC AGA GTT-3’

  • 3.

    10x TRAP reaction buffer

    Final concentration
    Tris-HCl (pH 8.3)200 mM
    MgCl215 mM
    KCl630 mM
    Tween 200.5% (v/v)
    EGTA10 mM

  • 4.

    50x dNTP

    • Use a mix containing all for DNA nucleotides (dTTP, dATP, dCTP, dGTP) at an equivalent and final concentration of 2.5 mM

  • 5.

    NP-40 lysis buffer

    Final concentration
    Tris-HCl (pH 8.0)10 mM
    MgCl21 mM
    EDTA1 mM
    NP-401% (v/v)
    Sodium deoxycholate0.25 mM
    Glycerol10% (v/v)
    NaCl150 mM
    2-mercaptoethanol5 mM
    AEBSF0.1 mM

Acknowledgement

Some of these protocols were adapted from previously published studies. Some of TRAP protocols are referenced here (Herbert et al., 2003; Norton et al., 1998; Wright et al., 1995). We thank Zeliha Gunnur Dikmen for her help in acquisition of TRAP gel and Abhijit Bugde from the Live Cell Imaging Facility at UT Southwestern for his assistance with the imaging and analysis part of Telomere dysfunction Induced Foci (TIF) analysis.

Department of Cell Biology, University of Texas Southwestern Medical Center, Dallas, USA;
Center for Excellence in Genomics Medicine Research, King Abdulaziz University, Jeddah, Saudi Arabia
For correspondence: ude.nretsewhtuostu@yahS.yrreJ
Copyright notice

Abstract

Telomeres are found at the end of eukaryotic linear chromosomes, and proteins that bind to telomeres protect DNA from being recognized as double-strand breaks thus preventing end-to-end fusions (Griffith et al., 1999). However, due to the end replication problem and other factors such as oxidative damage, the limited life span of cultured cells (Hayflick limit) results in progressive shortening of these protective structures (Hayflick and Moorhead, 1961; Olovnikov, 1973). The ribonucleoprotein enzyme complex telomerase-consisting of a protein catalytic component hTERT and a functional RNA component hTR or hTERC- counteracts telomere shortening by adding telomeric repeats to the end of chromosomes in ~90% of primary human tumors and in some transiently proliferating stem-like cells (Shay and Wright, 1996; Shay and Wright, 2001). This results in continuous proliferation of cells which is a hallmark of cancer. Therefore, telomere biology has a central role in aging, cancer progression/metastasis as well as targeted cancer therapies. There are commonly used methods in telomere biology such as Telomere Restriction Fragment (TRF) (Mender and Shay, 2015b), Telomere Repeat Amplification Protocol (TRAP) and Telomere dysfunction Induced Foci (TIF) analysis (Mender and Shay, 2015a). In this detailed protocol we describe Telomere Repeat Amplification Protocol (TRAP).

The TRAP assay is a popular method to determine telomerase activity in mammalian cells and tissue samples (Kim et al., 1994). The TRAP assay includes three steps: extension, amplification, and detection of telomerase products. In the extension step, telomeric repeats are added to the telomerase substrate (which is actually a non telomeric oligonucleotide, TS) by telomerase. In the amplification step, the extension products are amplified by the polymerase chain reaction (PCR) using specific primers (TS upstream primer and ACX downstream primer) and in the detection step, the presence or absence of telomerase is analyzed by electrophoresis. TSNT is, an internal standard control, amplified by TS primer. NT is its own reverse primer, which is not a substrate for telomerase. These primers are used to identify false-negative results by if the gel lacks internal control bands.

Abstract

References

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