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Related Concept Videos

Overview of Transposition and Recombination02:13

Overview of Transposition and Recombination

Transposons make up a significant part of genomes of various organisms. Therefore, it is believed that transposition played a major evolutionary role in speciation by changing genome sizes and modifying gene expression patterns. For example, in bacteria, transposition can lead to conferring antibiotic resistance. Movement of transposable elements within the genetic pool of pathogenic bacteria can aid in transfer of antibiotic-resistant genetic elements. In eukaryotes, transposons can carry out...
DNA-only Transposons02:57

DNA-only Transposons

DNA-only transposons are called autonomous transposons since they code for the enzyme transposase that is required for the transposition mechanism. Insertion of transposons can alter gene functions in multiple ways. They can mutate the gene, alter gene expression by introducing a novel promoter or insulator sequence, introduce new splice sites, and change the mRNA transcripts produced, or remodel chromatin structure.
The donor site from where the transposon is excised is either degraded or...
Retroviruses02:33

Retroviruses

Retroviruses and retrotransposons both insert copies of their genetic elements into the genome of the host cell. Thus, the viral genes are passed on when the host genome is replicated or translated. A typical retroviral DNA sequence contains 3-4 genes that encode the different proteins required for its structural assembly and function as a molecular parasite. This DNA is transcribed into a single mRNA, which is very similar in structure to conventional mRNAs, i.e., it is capped at the 5’...
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...
Non-LTR Retrotransposons03:18

Non-LTR Retrotransposons

As the name suggests, non-LTR retrotransposons lack the long terminal repeats characteristic of the LTR retrotransposons. Additionally, both LTR and non-LTR retrotransposons use distinct mechanisms of mobilization. Non-LTR retrotransposons are further divided into two classes - Long interspersed nuclear elements (LINEs) and short interspersed nuclear elements (SINEs), both of which occur abundantly in most mammals, including humans. Some of the active non-LTR retrotransposons in humans are L1...
Transposons01:24

Transposons

Transposons, or "jumping genes," are small mobile genetic elements (MGEs) that range from 700 to 40,000 base pairs in length. They are found in all organisms and can move within the same chromosome or transfer to different chromosomes. In some cases, transposons can also jump between different host DNA molecules, such as plasmids or viruses, contributing to genetic variability.Barbara McClintock first discovered these mobile genetic elements in the 1940s while studying maize genetics, and she...

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Related Experiment Video

Updated: Jul 10, 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 recent evolution of human L1 retrotransposons.

S Boissinot1, A V Furano

  • 1Department of Biology, Queens College, CUNY, Flushing, NY 11367-1597, USA. sboissin@qcl.qc.edu

Cytogenetic and Genome Research
|August 12, 2005
PubMed
Summary

Long interspersed nuclear elements (L1) are active retrotransposons in mammals, significantly impacting human DNA evolution. These elements show rapid adaptive evolution in response to host genetic load.

Area of Science:

  • Genomics
  • Evolutionary Biology
  • Molecular Biology

Background:

  • Long interspersed nuclear elements (L1) are abundant retrotransposons in mammalian genomes, comprising a substantial portion of human DNA.
  • L1 elements have demonstrated significant activity and rapid evolution, particularly within the last 25 million years.
  • The emergence of distinct L1 families and their amplification highlight their dynamic role in genome evolution.

Purpose of the Study:

  • To investigate the evolutionary dynamics of L1 elements during human evolution.
  • To understand the adaptive evolution of L1 elements in response to host selection pressures.
  • To elucidate the molecular interactions between L1 elements and their mammalian hosts.

Main Methods:

  • Comparative genomics analysis of L1 element families across mammalian species.

More Related Videos

RNA Next-Generation Sequencing and a Bioinformatics Pipeline to Identify Expressed LINE-1s at the Locus-Specific Level
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RNA Next-Generation Sequencing and a Bioinformatics Pipeline to Identify Expressed LINE-1s at the Locus-Specific Level

Published on: May 19, 2019

Detection of Retrotransposition Activity of Hot LINE-1s by Long-Distance Inverse PCR
10:54

Detection of Retrotransposition Activity of Hot LINE-1s by Long-Distance Inverse PCR

Published on: July 27, 2019

Related Experiment Videos

Last Updated: Jul 10, 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

RNA Next-Generation Sequencing and a Bioinformatics Pipeline to Identify Expressed LINE-1s at the Locus-Specific Level
11:04

RNA Next-Generation Sequencing and a Bioinformatics Pipeline to Identify Expressed LINE-1s at the Locus-Specific Level

Published on: May 19, 2019

Detection of Retrotransposition Activity of Hot LINE-1s by Long-Distance Inverse PCR
10:54

Detection of Retrotransposition Activity of Hot LINE-1s by Long-Distance Inverse PCR

Published on: July 27, 2019

  • Phylogenetic analysis to trace the evolutionary history and diversification of L1 elements.
  • Population genetics approaches to assess selection pressures on L1 activity.
  • Main Results:

    • Five distinct L1 families have emerged and amplified significantly in the last 25 million years.
    • A human-specific L1 family is currently active, accumulating copies at a rate comparable to rodent L1s.
    • Evidence of negative selection on L1 activity at certain evolutionary periods, indicating adaptive evolution.

    Conclusions:

    • L1 elements are not static parasites but actively evolving entities that engage in a dynamic interplay with their hosts.
    • Understanding L1-host interactions is crucial for comprehending genome evolution and the impact of mobile genetic elements.
    • The adaptive evolution of L1 elements suggests a co-evolutionary arms race between retrotransposons and host genomes.