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Updated: Aug 4, 2026

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Examination of the Telomere G-overhang Structure in Trypanosoma brucei
Published on: January 26, 2011
Normal human chromosomes have long G-rich telomeric overhangs at one end
W E Wright1, V M Tesmer, K E Huffman
1Department of Cell Biology and Neuroscience, The University of Texas Southwestern Medical Center, Dallas, Texas 75235-9039 USA. wright@utsw.swmed.edu
Genes & Development
|November 14, 1997
Summary
Human telomeres have different terminal overhangs after replication. Lagging-strand synthesis may create a long 3' overhang, influencing telomere shortening rates in normal cells.
Area of Science:
- Molecular Biology
- Genetics
- Cell Biology
Background:
- Telomeres protect chromosome ends and are implicated in aging and cancer.
- The precise structure of human telomeres, particularly their termini, remains largely uncharacterized.
Purpose of the Study:
- To investigate the structure of human telomere termini after replication.
- To analyze the terminal DNA overhangs in normal diploid telomerase-negative human fibroblasts.
Main Methods:
- Purification of telomeres from human fibroblasts.
- Analysis of telomere termini using electron microscopy.
Main Results:
- Daughter telomeres exhibit distinct terminal overhangs post-replication.
- Telomeres with long overhangs revealed approximately 200 +/- 75 nucleotides of single-stranded DNA.
- The observed overhang length is significantly greater than the telomere shortening rate per cell division.
Conclusions:
- Results support models where lagging-strand synthesis generates a G-rich 3' overhang.
- Variations in lagging-strand synthesis may regulate telomere shortening in human cells.
- Nuclease processing could also contribute to varied overhang lengths.
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Replication in Eukaryotes
Overview
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A functional eukaryotic chromosome must contain three elements: a centromere, telomeres, and numerous origins of replication.
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Telomeres consist of non-coding repetitive nucleotide...
The centromere is a DNA sequence that links sister chromatids. This is also where kinetochores, protein complexes to which spindle microtubules attach, are constructed after the chromosome is replicated. The kinetochores allow the spindle microtubules to move the chromosomes within the cell during cell division.
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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.
Chromosome Structure
A functional eukaryotic chromosome must contain three elements: a centromere, telomeres, and numerous origins of replication.
The centromere is a DNA sequence that links sister chromatids. This is also where kinetochores, protein complexes to which spindle microtubules attach, are constructed after the chromosome is replicated. The kinetochores allow the spindle microtubules to move the chromosomes within the cell during cell division.
Telomeres consist of non-coding repetitive nucleotide...
The centromere is a DNA sequence that links sister chromatids. This is also where kinetochores, protein complexes to which spindle microtubules attach, are constructed after the chromosome is replicated. The kinetochores allow the spindle microtubules to move the chromosomes within the cell during cell division.
Telomeres consist of non-coding repetitive nucleotide...
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.
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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.

