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Related Concept Videos

Telomeres and Telomerase02:41

Telomeres and Telomerase

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 DNA.
Telomeres and Telomerase02:41

Telomeres and Telomerase

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 DNA.
Replicative Cell Senescence02:15

Replicative Cell Senescence

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 the telomeric...
Replication in Eukaryotes01:29

Replication in Eukaryotes

In eukaryotic cells, DNA replication is highly conserved and tightly regulated. Multiple linear chromosomes must be duplicated with high fidelity before cell division, so there are many proteins that fulfill specialized roles in the replication process. Replication occurs in three phases: initiation, elongation, and termination, and ends with two complete sets of chromosomes in the nucleus.
Many Proteins Orchestrate Replication at the Origin
Eukaryotic replication follows many of the same...
Replication in Eukaryotes02:31

Replication in Eukaryotes

Overview
Longitudinal Studies01:26

Longitudinal Studies

Longitudinal studies are also widely used in other medical and social science fields. For instance, in cardiovascular research, they can monitor patients' health over decades to identify risk factors for heart disease, such as high cholesterol or smoking, and evaluate the long-term effectiveness of preventive measures. Similarly, in mental health studies, researchers might follow individuals from adolescence into adulthood to understand the development and progression of conditions like...

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Updated: May 21, 2026

Telomere Length and Telomerase Activity; A Yin and Yang of Cell Senescence
12:08

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

Published on: May 22, 2013

Telomere length and cardiovascular aging.

Frej Fyhrquist1, Outi Saijonmaa

  • 1Minerva Institute for Medical Research and Department of Internal Medicine, Helsinki University Central Hospital, Helsinki, Finland. frej.fyhrquist@helsinki.fi

Annals of Medicine
|June 21, 2012
PubMed
Summary
This summary is machine-generated.

Telomeres, the protective caps on chromosomes, shorten with cell division, acting as a biological clock. Leukocyte telomere length (LTL) shortening is linked to cardiovascular aging and risk factors.

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Telomere Length and Telomerase Activity; A Yin and Yang of Cell Senescence
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Published on: May 22, 2013

Monochrome Multiplex Quantitative PCR Telomere Length Measurement
11:44

Monochrome Multiplex Quantitative PCR Telomere Length Measurement

Published on: March 22, 2024

Area of Science:

  • Genetics
  • Cell Biology
  • Aging Research

Background:

  • Telomeres are repetitive DNA sequences at chromosome ends, crucial for genomic stability.
  • Telomere shortening with cell division acts as a cellular clock, leading to senescence.
  • Telomerase counteracts telomere shortening, maintaining cellular functions and proliferative capacity.

Purpose of the Study:

  • To explore the role of telomeres and telomere length in cellular aging.
  • To investigate the association between telomere attrition and cardiovascular aging.
  • To determine if leukocyte telomere length (LTL) serves as a biomarker for cardiovascular aging.

Main Methods:

  • Review of telomere biology, including composition and function.
  • Analysis of factors influencing telomere shortening (e.g., aging, oxidative stress).
  • Examination of the correlation between LTL and cardiovascular risk factors and diseases.

Main Results:

  • Accelerated telomere attrition is observed in certain genetic disorders (progeria).
  • Factors like aging, inflammation, and oxidative stress contribute to telomere shortening.
  • Shorter LTL is frequently associated with cardiovascular risk factors and cardiovascular aging.

Conclusions:

  • Leukocyte telomere length (LTL) is a potential biomarker of cardiovascular aging.
  • LTL reflects the cumulative impact of detrimental endogenous and exogenous factors.
  • The causal relationship between telomere shortening and cardiovascular disease remains undetermined.