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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
Cell Signaling Feedback Loops01:07

Cell Signaling Feedback Loops

Positive and negative feedback loops are crucial for regulating biological signaling systems. These feedback loops are processes that connect output signals to their inputs.
Negative feedback loops
Most signaling systems have negative feedback loops that can perform different functions such as output limiter, and adaptation.
Output limiter
Upon receiving an input signal, the cellular response rapidly increases until a threshold is reached. Beyond this threshold, a negative feedback loop...

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Related Experiment Video

Updated: Jun 25, 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

Closing the feedback loop: how cells "count" telomere-bound proteins.

Neal F Lue1

  • 1Department of Microbiology and Immunology, W.R. Hearst Microbiology Research Center, Weill Medical College of Cornell University, New York, NY 10065, USA. nflue@med.cornell.edu

Molecular Cell
|March 3, 2009
PubMed
Summary
This summary is machine-generated.

Telomere length is regulated by protein counting, where abundant telomere-bound proteins limit telomerase activity. Hirano et al. reveal the specific molecular interactions governing this protein-counting mechanism in budding yeast.

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Area of Science:

  • Molecular Biology
  • Genetics
  • Cell Biology

Background:

  • Telomere length homeostasis is crucial for cellular stability and is regulated by complex mechanisms.
  • The prevailing model suggests a "protein-counting" system where excessive telomere-bound proteins inhibit telomerase, the enzyme responsible for telomere maintenance.

Discussion:

  • Hirano et al. investigated the protein-counting machinery in budding yeast (Saccharomyces cerevisiae) to understand telomere length regulation.
  • The study focused on elucidating the specific molecular interactions involved in this feedback loop.
  • Understanding these interactions provides insight into how cells control telomere length and prevent uncontrolled proliferation.

Key Insights:

  • The research successfully delineated the molecular interactions underlying the budding yeast protein-counting mechanism.
  • This work provides a detailed molecular basis for how telomere-bound proteins regulate telomerase activity.
  • Identification of key protein players and their binding dynamics offers a clearer picture of telomere length control.

Outlook:

  • Further research can explore the conservation of this mechanism in other organisms, including humans.
  • Investigating potential therapeutic targets related to telomere length regulation could emerge from these findings.
  • This study lays the groundwork for future investigations into the intricate processes of genome stability and aging.