Telomere Length and Telomerase Activity; A Yin and Yang of Cell Senescence

Summary

An accurate, short, sophisticated and cheap method is described that assesses telomere length in multiple tissues and species using qRT-PCR. In addition, we will describe a simple assay to assess telomerase activity as a complementary backbone test for telomere length.

Abstract

Telomeres are repeating DNA sequences at the tip ends of the chromosomes that are diverse in length and in humans can reach a length of 15,000 base pairs. The telomere serves as a bioprotective mechanism of chromosome attrition at each cell division. At a certain length, telomeres become too short to allow replication, a process that may lead to chromosome instability or cell death. Telomere length is regulated by two opposing mechanisms: attrition and elongation. Attrition occurs as each cell divides. In contrast, elongation is partially modulated by the enzyme telomerase, which adds repeating sequences to the ends of the chromosomes. In this way, telomerase could possibly reverse an aging mechanism and rejuvenates cell viability. These are crucial elements in maintaining cell life and are used to assess cellular aging. In this manuscript we will describe an accurate, short, sophisticated and cheap method to assess telomere length in multiple tissues and species. This method takes advantage of two key elements, the tandem repeat of the telomere sequence and the sensitivity of the qRT-PCR to detect differential copy numbers of tested samples. In addition, we will describe a simple assay to assess telomerase activity as a complementary backbone test for telomere length.

Introduction

Telomeres are repeating DNA hexamer (TTAGGG) sequences found at the ends of chromosomes. In each cell replication, these chromosome ends are shortened. If they become too short, chromosomes can undergo telomere end fusions, aberrant recombination, and degradation. Thus sufficient telomere length maintenance plays a major role in chromosome stability and cell protection ³⁸. Telomere length maintenance is also crucial for genes found near the ends of chromosomes, since DNA replication cannot continue to the very end of chromosomes ^1-2. Consequently, prevention of telomere shortening may improve cell stability.

Numerous studies have reported that telomere length is correlated with an organism's longevity and diseased state, such as in cancer ^3-4, diabetes ⁵, and cardiovascular disease ^6,7. Additionally, shortened telomeres have been associated with excessive stress or an unhealthy lifestyle ⁸, perhaps by promoting premature cell aging and death ⁹. On the other hand, some studies have found that there is no significant difference between telomere length and longevity and age related disease ^{39, 40, 41}.

One of the cell's innate mechanisms of protection from telomere shortening is by activating its own enzyme telomerase reverse transcriptase (TERT). This enzyme and its subunit, telomerase RNA (TERC), a non-coding RNA, use the telomere as a template to add telomere repeats to chromosome ends ¹⁰. Although telomerase activity is absent from several types of cells and other mechanisms are involved in telomere length maintenance, increased telomerase activity is correlated with increased telomere length. Telomerase activation has been established as one of the mechanisms by which cells respond to damage and stress and avoid premature senescence and death. For example, longer telomeres were demonstrated in a population of Ashkenazi Jews with exceptional lifespan ¹¹, mutations in TERC or TERT have been shown to contribute to fatal disease ¹², and epigenetic regulation of telomerase has been shown to have an effect on age-related disease ¹³. Since its discovery, telomere length has been proposed as a biomarker for health status in various animal models as well as in humans, but these early studies were difficult to widely replicate because the method used was tedious, long and expensive. In 2002 and further tuned in 2009, Cawthon proposed and demonstrated a new, accurate, fast and simple PCR based protocol to assess telomere length and further investigate its role in various aspects of cell biology, aging and disease ¹⁹.

Choosing the correct telomere measuring method for a study is essential. Currently, there are various methods used to measure telomere length, each with its own advantages and disadvantages. Traditionally, telomere length is measured using Southern Blot analysis of terminal restriction fragments (TRFs), which involves: a. digesting the DNA with restriction enzymes that do not cut in telomere repeats in order to obtain TRFs, b. Southern Blot of these TRFs is done by determining the mean TRF length using a telomeric probe ^{14, 37}. Although this method is highly accurate with a small coefficient of variation, is a direct measure, and can be advantageous for measuring length distribution, TRF analysis is costly, labor intensive and requires at least 3 μg of DNA. This method is also insensitive to short telomeres and length determination can be confounded by subtelomeric DNA, which can be detected by the probe due the (TTAGGG)n like sequences they contain ^{15, 42}.

Another highly accurate method in measuring telomere length is Single Telomere Elongation Length Analysis (STELA), a single molecule PCR based method that only requires a small amount of DNA. In this method, primers are made to recognize the G-rich overhang at the end of chromosomes and to bind to a unique subtelomeric sequence on one chromosome, which amplifies the telomere of a specific chromosome. The resulting amplification is then visualized by Southern Blot. This method has the advantage of being highly accurate and is able to detect short outlier telomeres ¹⁶. Unfortunately, since not all chromosomes have G-rich ends and a usable subtelomeric sequence, telomere length can only be measured on specific chromosomes and these measurements may not represent the length of all the telomeres in the cell ¹⁵.

Another method that has been practiced is the use of Peptide Nucleic Acid (PNA) probes to detect telomere length. Quantitative Florescence in situ Hybridization (Q-FISH) allows us to visualize telomeres during metaphase, where the staining of telomeres with a PNA probe in proportion to their size permits the comparison of telomeres between specific chromosomes. Although this method can also be used for cells in interphase, here the telomere length for distinct chromosomes cannot be detected, which introduces a limitation when measuring telomere length in senescent or infrequently dividing cells ¹⁷. Flow FISH instead uses flow cytometry and is currently the most sensitive method for measuring telomere length of blood cells in the clinical setting, but requires highly skilled technicians ¹⁸.

Currently, the standard method for measuring average telomere length in our lab takes advantage of the precision, sensitivity, and ease of quantitative real-time PCR. This method was made possible for measuring telomere length by the development of novel primers that avoid the synthesis of primer dimer-derived products, which would have otherwise been produced in a standard assay due to the repeating nature of telomeres. For this assay, the measurement of telomere length is represented by the T/S ratio, the telomere repeat copy number to single-copy gene number. Since there is a direct proportional relationship between the telomere length and the number of labeled telomere primers binding to the DNA during the beginning stages of PCR, the T/S ratio is directly proportional to telomere length. The T/S ratio is measured by comparing the difference in Ct, the fractional cycle number at which the sample's accumulated florescence crosses a threshold that is several standard deviations above the baseline florescence, between samples with telomere primers and SCG primers ¹⁹. This method has been criticized for its indirect measurement of telomere length, which can lead to inaccurate measurements, for example, in the case of chromosome duplications or copy number variations ¹⁵. Also, comparison between studies is often difficult, but standard oligomers have been developed to measure absolute telomere length ²⁰. This method was furthered improved upon by Cawthon, using a monochrome multiplex qPCR assay. In this assay, the PCR was run at lower temperatures for the first few cycles to avoid primer-dimer binding and the telomere and control gene were analyzed in the same PCR tube to further avoid error. The resulting telomere length measurements strongly correlated with telomere length measured by Southern blot analysis of TRFs and had higher accuracy ^{15, 19, 36}. At the moment, qRT-PCR is the only convenient method available for testing large sample sizes and only requires a small amount of DNA to carry out. A crucial part of this method is comprehensive quality control measures, so that when it's done properly, this method can provide valuable comparative information about telomere length. Additionally, this method had been adapted for use beyond leukocytes for measuring telomere length in a variety of different tissues ⁴².

Additionally, in order to further understand the biology behind telomere length maintenance and interactions between the two opposing effects (i.e. telomere shortening during replication and elongation by the telomerase enzyme), we accompanied the telomere length method with an additional assay that measures telomerase activity.

For this purpose, we used a Telomeric Repeat Amplification Protocol, an in vitro assay. Briefly, lysed, preserved, enzymatically active cells synthesized telomeric repeats onto an oligonucleotide substrate using telomerase, and the products were amplified using PCR in the presence of SYBR Green. The results were then analyzed by comparing sample and control Ct threshold values. Since telomerase is a heat-sensitive enzyme, an additional heat treated control is run alongside each sample ²¹.

While measuring telomere length can provide valuable insight into the possible role of telomere length in the pathophysiology of aging and disease, telomere length is not a static property and more information is needed to understand telomere function. Telomerase activity studies can add information about telomere length regulation mechanisms. For example, the controlled activation of telomerase can maintain telomere length and cell proliferation, but the uncontrolled activation of telomerase can result in cancer. These two inexpensive and straight forward methods combined provided us not only with stronger evidence towards a relationship between telomere length and cell stability, but also further insight into the possible mechanisms of telomere shortening and recovery. With these methods we hope to further elucidate the cell's response to aging and various states of cell proliferation with the ultimate goal of a better understanding of the central mechanisms of cell biology.

Protocol

1. Telomere Length Protocol¹⁹

1. DNA isolation

Most DNA isolation methods may be used. Our Lab prefers Qiagen DNeasy Kit (#69506) for blood sources. Depending on the source of DNA, such as buccal or other sources, a different isolation method may be used.

2. Primers

All primers are diluted to a stock concentration of 100pmoles/μl in PCR grade water and stored at -20 °C until required. Working stocks of primers are made fresh and are stored at 20 °C for a short period of time (A few months.) Standard primers were used for telomeres and β-Globin, the SCG, as described in O'Callaghan et al. ²⁰.

Primer sequences:
Telo 1: 5'-CGGTTTGTTTGGGTTTGGGTTTGGGTT-TGGGTTTGGGTT-3'

Telo 2: 5'-GGCTTGCCTTACCCTTACCCTTACCCTTACCCTT-ACCCT-3'
SCG 1: 5'-GCTTCTGACACAACTGTGTTCACTAGC-3'
SCG 2: 5'-CACCAACTTCATCCACGTTC-ACC-3'

Note: Primers are diluted to a working concentration of 10pmoles/μl, prior to adding to reaction mix.

3. Serial Dilution of Genomic DNA

Serial dilutions of genomic DNA for Telo and Single Copy Gene (SCG) are created to generate a standard Ct value curve for the assay. The genomic DNA used was extracted from lymphocytes from blood samples. These dilutions are created by diluting DNA with PCR grade H₂0 to each concentration by a factor of 1.68 to yield the two sets of serial dilutions using the same genomic DNA. The starting concentrations have been optimized based on trial and error and may need to be adjusted when using different reagents, instruments, DNA from other species, cell types, and SCG used.

Note: Serial dilution using genomic DNA are made by mixing gently and waiting at least 15 min to one hour before taking DNA for the next dilution. Each dilution requires time for genomic DNA to dissociate. For long term storage, aliquot serial dilutions into PCR strips for storage at -80 °C. Each PCR strip is thawed and used once to avoid freeze thaw cycles that may damage DNA.

4. Reaction setup for RT-PCR

Instrument used: Roche480 Light Cycler

Reagent: Roche Light cycler sybr-green

Dilute test DNA samples to a final concentration of 10 ng/μl. We test concentration using Nanodrop or Qubit. We further dilute the DNA from 10ng/μl to final 5ng/μl. We do not test concentration again.

Reaction components:

TELO	1x		SCG	1x
H20	6 μl		H20	6 μl
Telo 1	0.2 μl		SCG 1	0.6 μl
Telo 2	1.8 μl		SCG 2	1.4 μl
Rxn mix	10 μl		Rxn mix	10 μl
DNA or serial dilution	2 μl		DNA or serial dilution	2 μl

Note: Master Mix is made without DNA and with an excess of 5% to 10%.

Both Telo and SCG are run together on the same plate using the following program. To test for precision, at least three replicates of each sample and control should be run. Variations in the primers used may affect the results. Our protocol has been optimized to work as follows on the Roche480 Light Cycler and our primers.

Initial denature
10 min denature 95 °C
Cycling
95 °C 10 sec hold
60 °C 5 sec hold
72 °C 11 sec hold and single acquisition
Repeat 45 to 55 times as required

2. Quantitative Telomerase Detection (QTD) Protocol (Based on QTD Kit by Allied Biotech, Inc. Cat. No. MT3012)

Extract Preparation

1. Pellet cells or tissue.
2. Wash once with 1x PBS.
3. Repellet and remove 1x PBS.*
4. Resuspend the cell pellet in 200 μl of 1 x Lysis Buffer for every 10⁵-10⁶ cells or 40-100 mg of tissue.
5. Incubate on ice for 30 min.
6. Spin down the sample at 12,000 x g for 30 min at 4 °C.
7. Transfer 160 μl of the supernatant into a fresh tube and determine protein concentration.
8. Aliquot and quick-freeze the remaining extract on dry ice/ethanol, store at -80 °C.

*In this condition, telomerase in frozen cells or tissues is stable for at least a year. When thawed for use, resuspend the cells immediately in 1 x Lysis Buffer.

2.1. Assay Controls

Heat inactivation control: For each sample, heat treat an additional control extract by incubating at 85 °C for 10 min prior to telomerase activity assay.

Standard curve for TSR control template: Perform Quantitative Real-Time PCR using dilutions of TSR, an oligonucleotide with a similar sequence to telomere primers included with the kit to generate a standard curve.

1. Prepare 1:5 serial dilutions of the stock TSR concentration (0.5 amoles/μl) with Lysis Buffer
2. Perform the telomerase detection standard assay using 1 μl of each TSR dilution, including the stock concentration. These dilutions can be stored at 4 °C for at least 2 weeks.

2.2. Telomerase Activity Assay using QTD Real-Time PCR

1. For each sample, add the following to a PCR tube or thin-wall PCR plate (total volume 25.0 μl):
   • 12.5 μl of 2 x QTD Premix
   • 1.0 μl of Cell or Tissue Extract
   • 11.5 μl of PCR Qualified Water
2. Mix thoroughly
3. Program Real-Time PCR Detection Systems according to the below program:
   - 25 °C for 20 min (telomerase reaction)
   - 95 °C for 10 min (PCR initial activation step)
   35-40 cycles of:
   - 95 °C for 30 sec (denaturation)
   - 60 °C for 30 sec (annealing)
   - 72 °C for 30 sec (extension)
4. Place PCR tubes in the thermal cycler and start the cycling program.
5. Collect the threshold cycle or C_T value after cycles finish. The threshold cycle is the cycle at which a statistically significant increase of ΔRn is first detected.

2.3. Data Analysis

1. Generate a standard curve using the C_T readings and compare telomerase activity.

Results

An example of a telomere length qRT-PCR assay is shown in Figure 1. On the top left panel, samples labeled in red and green represent the location of the tested subjects on the 96-well plate. On the top right panel, the amplification curve is demonstrated. Each subject is tested by two assays (Telomere and Single Copy Gene), which is done in triplicates. Due to different DNA copy numbers produced in the two assays of selected individuals, the number of cycles until the florescence detection reache...

Discussion

Telomere length provides a unique cellular marker to study the stressed and aging cell and offers insights into the mechanisms of aging. Since its role in aging had first been suggested, a multitude of studies have been done relating telomere length to age, longevity, age-related disease, cancers, and stress. For decades, the gold standard of telomere length measurements was terminal restriction fragment analysis using Southern hybridization. However, recently an affordable, quick, and easy to perform method by Ca...

Materials

List of materials used in this article

Name	Company	Catalog Number	Comments
Quantitative Telomerase Detection	Allied Biotech	MT3012
Qiagen DNeasy Kit	Qiagen	69506
LightCycler 480 SYBR Green I Master, Ready-to-use hot start reaction mix for SYBR Green I-based real-time PCR using the LightCycler 480 Instrument	Roche Diagnostics	4707516