Related Experiment Video
Updated: Mar 21, 2026

06:44
Assessment of Global DNA Double-Strand End Resection using BrdU-DNA Labeling coupled with Cell Cycle Discrimination Imaging
Published on: April 28, 2021
4.7K
Summary
This review details how Alternative Lengthening of Telomeres (ALT) and telomerase mechanisms can coexist in mammalian cells, challenging previous assumptions about their exclusivity in maintaining telomere length.
Area of Science:
- Cellular Biology
- Genetics
- Molecular Biology
Context:
- Two primary mechanisms maintain telomere length: telomerase and Alternative Lengthening of Telomeres (ALT).
- ALT, a homologous recombination-based process, was previously thought to function independently of telomerase in specific tumor types.
- Reactivation of telomerase or ALT are key to overcoming replicative senescence in mammalian cells.
Purpose:
- To review morphological and functional telomere changes associated with ALT activation.
- To present recent, documented evidence of combined ALT and telomerase mechanisms in mammalian cells.
- To explore the potential role of telomere recombination in telomerase-dependent cells.
Summary:
- This review synthesizes recent findings on the co-occurrence of ALT and telomerase-dependent telomere maintenance mechanisms.
- It highlights documented cases of these combined mechanisms in mammalian cells, challenging the long-held view of their mutual exclusivity.
- The review also discusses telomere recombination's potential role within telomerase-proficient cells.
Impact:
- Challenges the established paradigm of mutually exclusive telomere maintenance pathways.
- Provides a foundation for understanding complex telomere regulation in cancer and aging.
- Opens new avenues for investigating therapeutic strategies targeting telomere maintenance.
Related Concept Videos
Telomeres and Telomerase
28.3K
In eukaryotic DNA replication, a single-stranded DNA fragment remains at the end of a chromosome after the removal of the final primer. This section of DNA cannot be replicated in the same manner as the rest of the strand because there is no 3’ end to which the newly synthesized DNA can attach. This non-replicated fragment results in gradual loss of the chromosomal DNA during each cell duplication. Additionally, it can induce a DNA damage response by enzymes that recognize single-stranded...
28.3K
Telomeres and Telomerase
7.9K
7.9K
Replicative Cell Senescence
4.6K
Replicative cell senescence is a property of cells that allows them to divide a finite number of times throughout the organism's lifespan while preventing excessive proliferation. Replicative senescence is associated with the gradual loss of the telomere — short, repetitive DNA sequences found at the end of the chromosomes. Telomeres are bound by a group of proteins to form a protective cap on the ends of chromosomes. Embryonic stem cells express telomerase — an enzyme that adds...
4.6K
Homologous Recombination
65.1K
The basic reaction of homologous recombination (HR) involves two chromatids that contain DNA sequences sharing a significant stretch of identity. One of these sequences uses a strand from another as a template to synthesize DNA in an enzyme-catalyzed reaction. The final product is a novel amalgamation of the two substrates. To ensure an accurate recombination of sequences, HR is restricted to the S and G2 phases of the cell cycle. At these stages, the DNA has been replicated already and the...
65.1K
Homologous Recombination
7.2K
7.2K
Fixing Double-strand Breaks
16.0K
The double-stranded structure of DNA has two major advantages. First, it serves as a safe repository of genetic information where one strand serves as the back-up in case the other strand is damaged. Second, the double-helical structure can be wrapped around proteins called histones to form nucleosomes, which can then be tightly wound to form chromosomes. This way, DNA chains up to 2 inches long can be contained within microscopic structures in a cell. A double-stranded break not only damages...
16.0K

