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* These authors contributed equally
Here, we describe in detail the protocol for quantifying telomere length using non-radioactive chemiluminescent detection, with a focus on the optimization of various performance parameters of the TAGGG telomere length assay kit, such as buffer quantities and probe concentrations.
Telomeres are repetitive sequences which are present at chromosomal ends; their shortening is a characteristic feature of human somatic cells. Shortening occurs due to a problem with end replication and the absence of the telomerase enzyme, which is responsible for maintaining telomere length. Interestingly, telomeres also shorten in response to various internal physiological processes, like oxidative stress and inflammation, which may be impacted due to extracellular agents like pollutants, infectious agents, nutrients, or radiation. Thus, telomere length serves as an excellent biomarker of aging and various physiological health parameters. The TAGGG telomere length assay kit is used to quantify average telomere lengths using the telomere restriction fragment (TRF) assay and is highly reproducible. However, it is an expensive method, and because of this, it is not employed routinely for large sample numbers. Here, we describe a detailed protocol for an optimized and cost-effective measurement of telomere length using Southern blots or TRF analysis and non-radioactive chemiluminescence-based detection.
Telomeres are the repetitive DNA sequences present at the end of chromosomes. They have tandem repeats of TTAGGG and maintain genome integrity by protecting the chromosome from both fraying and the end replication problem, which means that part of the 3' overhang is unable to be replicated by DNA polymerase1,2. Short telomeres lead to chromosomal abnormalities in cells, due to which cells become permanently arrested in a stage called replicative senescence3. Short telomeres also cause a host of other problems, such as mitochondria dysfunction4,
NOTE: See the Table of Materials for details about all reagents used in the protocol below. Table 1 enlists lab-made reagents along with optimized volumes and Table 2 shows working concentrations of commercially available reagents.
1. Cell culture
The extracted genomic DNA (gDNA), which was run on a 1% agarose gel, showed good integrity, as shown in Figure 1B, indicating that the sample could be used for further downstream processing of TRFs. The TRF assay was then carried out by the modifying the volumes of solutions required at each step (see Table 1 and Table 2). The TRF signal was clearly visible (Figure 3). Thus, by modifying the solution volumes and concentrations, .......
We describe a detailed procedure for a non-radioactive, chemiluminescence-based method for telomere length measurement using Southern blotting. The protocol has been tested to allow the judicious use of several reagents with no compromise on the quality of results. The prehybridization and hybridization buffer can be reused up to five times. Enzyme concentration can vary between 10-20 U per 1.5-2 µg of genomic DNA without affecting the results. Several other kit components, such as the DIG-labeled molecular weight m.......
We would like to acknowledge Ms. Prachi Shah for helping us initially with the protocol optimization. We would like to thank Dr. Manoj Garg for providing the A2780 ovarian cancer cell line. EK is supported by a Research Grant from the Department of Biotechnology (No. BT/RLF/Re-entry/06/2015), Department of Science and Technology (ECR/2018/002117), and NMIMS Seed Grant (IO 401405).
....Name | Company | Catalog Number | Comments |
Cell Line | |||
A2780 (Ovarian adenocarcinoma cell line) | Received as a gift | ||
Equipment | |||
ChemiDoc XRS+ (for imaging and UV cross linking) | Biorad | Universal hood II (721BR14277) | |
Nanodrop (Epoch 2) | Biotek | EPOCH2 | |
Software | |||
TeloTool | Version 1.3 | ||
Materials | |||
Acetic Acid | Molychem | 64-19-7 | |
Agarose | MP | 180720 | |
Amphotericin B | Gibco, ThermoFisher Scientific, USA | 15240062 | |
DMEMÂ | HyClone, Cytiva, USA | SH30243.01 | |
Ethylenediamine tetraacetic acid | Molychem | 6381-92-6 | |
HI FBS | Gibco, ThermoFisher Scientific, USA | 10270106 | |
HCl | Molychem | 76-47-01-0 | |
NaCl | Molychem | 7647-14-5 | |
NaOH | Molychem | 1310-73-2 | |
Nylon membrane | Sigma | 11209299001 | |
Penicillin | Gibco, ThermoFisher Scientific, USA | 15240062 | |
Sodium dodecyl sulfate | Affymetrix | 151-21-3 | |
Streptomycin | Gibco, ThermoFisher Scientific, USA | 15240062 | |
Tris | BIORAD | 77-86-1 | |
Tris HCl | Sigma Aldrich | 1185-53-1 | |
Whatman paper | GE healthcare lifesciences | 1001-917 | |
Reagents | |||
1 kb ladder | NEB | N3232S | |
20x SSC | Invitrogen | 15557-036 | |
Anti DIG AP | Telo TAGGG Telomere Length Assay kit | 12209136001 | |
Blocking solution 10x | Telo TAGGG Telomere Length Assay kit | 12209136001 | |
Cutsmart Buffer | NEB | B6004 | |
Detection buffer 10x | Telo TAGGG Telomere Length Assay kit | 12209136001 | |
Dig easy hyb | Telo TAGGG Telomere Length Assay kit | 12209136001 | |
Digestion Buffer | Telo TAGGG Telomere Length Assay kit | 12209136001 | |
Hinf 1 | Telo TAGGG Telomere Length Assay kit | 12209136001 | |
Hinf 1 (alternative to kit) | NEB | R0155T | |
Loading Dye | BIOLABS | N3231S | |
Maleic acid buffer 10x | Telo TAGGG Telomere Length Assay kit | 12209136001 | |
Molecular marker | Telo TAGGG Telomere Length Assay kit | 12209136001 | |
Probe | Telo TAGGG Telomere Length Assay kit | 12209136001 | |
Rsa 1 | Telo TAGGG Telomere Length Assay kit | 12209136001 | |
Rsa 1 (alternative to kit) | NEB | R0167L | |
Substrate | Telo TAGGG Telomere Length Assay kit | 12209136001 | |
Wash buffer | Telo TAGGG Telomere Length Assay kit | 12209136001 |
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