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Related Concept Videos

Chromosome Structure02:40

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...
Polytene Chromosomes02:04

Polytene Chromosomes

Polytene chromosomes are giant interphase chromosomes with several DNA strands placed side by side. They were discovered in the year 1881 by Balbiani in salivary glands, intestine, muscles, malpighian tubules, and hypoderm of larvae Chironomus plumosus. Hence, these are also called "Salivary gland chromosomes." These are found in insects of the order Diptera and Collembola; in certain organs of mammals; and synergids, antipodes of flowering plants. Polytene chromosomes are also regularly...
LTR Retrotransposons03:08

LTR Retrotransposons

LTR retrotransposons are class I transposable elements with long terminal repeats flanking an internal coding region. These elements are less abundant in mammals compared to other class I transposable elements. About 8 percent of human genomic DNA comprises LTR retrotransposons. Some of the common examples of LTR retrotransposons are Ty elements in yeast and Copia elements in Drosophila.
The internal coding region of LTR retrotransposons and their mechanism of transposition closely resembles a...
Chromosome Structure02:40

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...
Polytene Chromosomes02:04

Polytene Chromosomes

Polytene chromosomes are giant interphase chromosomes with several DNA strands placed side by side. They were discovered in the year 1881 by Balbiani in salivary glands, intestine, muscles, malpighian tubules, and hypoderm of larvae Chironomus plumosus. Hence, these are also called "Salivary gland chromosomes." These are found in insects of the order Diptera and Collembola; in certain organs of mammals; and synergids, antipodes of flowering plants. Polytene chromosomes are also regularly...
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...

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Activation of the Ty1-copia group retrotransposons of potato (Solatium tuberosum) during protoplast isolation.

Plant cell reports·2013
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Genetic diversity in European Pisum germplasm collections.

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Analysis of plant diversity with retrotransposon-based molecular markers.

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Effects of ascertainment bias and marker number on estimations of barley diversity from high-throughput SNP genotype data.

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Updated: Jul 7, 2026

Analysis of LINE-1 Retrotransposition at the Single Nucleus Level
11:52

Analysis of LINE-1 Retrotransposition at the Single Nucleus Level

Published on: April 23, 2016

The origin of extrachromosomal circular copia elements.

A J Flavell, D Ish-Horowicz

    Cell
    |September 1, 1983
    PubMed
    Summary

    Circular copia elements, studied via nucleotide sequence and restriction enzyme analysis, show potential roles in copia transposition. Rearranged circles suggest integration into their own sequences, similar to retroviruses.

    Area of Science:

    • Molecular Biology
    • Genetics
    • Retrovirology

    Background:

    • Copia elements are retrotransposons found in Drosophila.
    • Extrachromosomal circular forms of copia elements (copia circles) are found in cells.
    • The formation and function of copia circles remain incompletely understood.

    Purpose of the Study:

    • To investigate the formation mechanisms of cloned extrachromosomal circular copia elements.
    • To explore the potential roles of copia circles in copia transposition.
    • To elucidate the relationship between copia elements and retroviruses.

    Main Methods:

    • Nucleotide sequence analysis of cloned copia circles.
    • Restriction enzyme analysis of copia circles.
    • Comparative sequence analysis with retroviral circular forms.

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    High-throughput Identification of Gene Regulatory Sequences Using Next-generation Sequencing of Circular Chromosome Conformation Capture (4C-seq)
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    High-throughput Identification of Gene Regulatory Sequences Using Next-generation Sequencing of Circular Chromosome Conformation Capture (4C-seq)

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    Analysis of LINE-1 Retrotransposition at the Single Nucleus Level
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    Genome-wide Purification of Extrachromosomal Circular DNA from Eukaryotic Cells
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    High-throughput Identification of Gene Regulatory Sequences Using Next-generation Sequencing of Circular Chromosome Conformation Capture (4C-seq)
    09:06

    High-throughput Identification of Gene Regulatory Sequences Using Next-generation Sequencing of Circular Chromosome Conformation Capture (4C-seq)

    Published on: October 5, 2018

    Main Results:

    • Rearranged copia circles with inverted segments and flanking sequence duplications were identified.
    • Sequence heterogeneity, including 0-15 bp inserts, was observed at the junctions of fused terminal direct repeats in seven copia circles.
    • The observed junctional sequences were inconsistent with formation via reverse transcription.

    Conclusions:

    • Circular copia elements can integrate into their own sequences, forming rearranged molecules.
    • The structural similarity between rearranged copia circles and retroviral circles supports a relationship between copia-like elements and retroviruses.
    • The formation of these specific circular copia molecules likely involves mechanisms other than standard reverse transcription.