From Academic Kids

Transposons are sequences of DNA that can move around to different positions within the genome of a single cell, a process called Transposition. In the process, they can cause mutations and change the amount of DNA in the genome. Transposons are also called "jumping genes" or "mobile genetic elements". There are a variety of mobile genetic elements, they can be grouped based on their mechanism of transposition. Class I mobile genetic elements, or retrotransposons, move in the genome by being transcribed to RNA and then back to DNA by reverse transcriptase, while class II moble genetic elements move directly from one position to another within the genome using a transposase to "cut and paste" them within the genome. Transposons are very useful to researchers as a means to alter DNA inside of a living organism.


Types of transposons

Transposons are classified into two classes based on their mechanism of transposition.

Class I: Retrotransposons

See main article on Retrotransposons

Retrotransposons (sometimes Retroposons) work by copying themselves and pasting copies back into the genome in multiple places. Initially retrotransposons copy themselves to RNA (transcription) but, instead of being translated, the RNA is copied into DNA by a reverse transcriptase (often coded by the transposon itself) and inserted back into the genome.

Retrotransposons behave very similarly to retroviruses, such as HIV, giving a clue to their evolutionary origins.

Class II transposons

Class II transposons move by cut and paste, rather than copy and paste, using the transposase enzyme. Different types of transposase work in different ways. Some can bind to any part of the DNA molecule, and the target site can therefore be anywhere, while others bind to specific sequences. The transposase then cuts the target site to produce sticky ends, cuts out the transposon and ligases it into the target site, and then fills in the sticky ends with their base pairs.

Both classes of transposon may lose their ability to synthesise reverse transcriptase or transposase through mutation, yet continue to jump through the genome because other transposons are still producing the necessary enzyme.


  • The first transposons were discovered in maize (Zea mays), (aka corn) by Barbara McClintock in 1940, for which she was awarded a Nobel Prize in 1983. She noticed insertions, deletions, and translocations, caused by these transposons. These changes in the genome could, for example, lead to a change in the colour of corn kernels. About 50% of the total genome of maize consists of transposons. The Ac/Ds system McClintok described are class II transposons.
  • Transposons in the fruit fly Drosophila melanogaster are called P elements. They seem to have first appeared in the species only about 50 years ago. Since then, they have spread through every population of the species. Artificial P elements can be used to insert genes into Drosophila by injecting the embryo.
  • Transposons in bacteria usually carry an additional gene for a function other than transposase, often an antibiotic resistance. In bacteria, transposons can jump from the "regular" DNA to plasmids and back, allowing the transfer and permanent addition of, for example, antibiotic resistance, leading to multiresistant strains. Bacterial transposons of this type belong to the Tn family.

Transposons causing diseases

Transposons are mutagens. They can damage the genome of their host cell in different ways:

  • A transposon/retroposon that inserts itself into a functional gene will most likely disable that gene.
  • After a transposon leaves a gene, the resulting gap will probably not be repaired correctly.
  • Multiple copies of the same sequence (e.g., Alu) can hinder precise chromosomal pairing during mitosis, resulting in unequal crossovers, one of the main reasons for chromosome duplication.

Diseases that are often caused by transposons include Hemophilia A and B, SCID, porphyria, predisposition to cancer, and Duchenne muscular dystrophy.

Evolution of transposons

The evolution of transposons and their effect on genome evolution is currently a dynamic field of study.

Since transposons are found in all major branches of life, they must have either existed in the last universal common ancestor or have arisen independently multiple times. While transposons may confer some benefits on their hosts, they are generally considered to be selfish DNA parasites that live within the genome of cellular organisms. In this way, they are similar to viruses. Viruses and transposons also share features in their genome structure and biochemical abilities, leading to speculation that they share a common ancestor.

Since excessive transposon activity can destroy a genome, many organisms seem to have developed mechanisms to reduce transposition to a manageable level. Bacteria may undergo high rates of gene deletion as part of a mechanism to remove transposons and viruses from their genomes while eukaryotic organisms may have developed the RNA interference (RNAi) mechanism as a way of reducing transposon activity. In the roundworm Caenorhabditis elegans, some genes required for RNAi also reduce transposon activity.

Transposons may have been co-opted by the vertebrate immune system as a means of producing antibody diversity. The V(D)J recombination system operates by a mechanism of similar to that of transposons. [1] (

Evidence exists that transposable elements may act as mutators in bacteria and other asexual organisms.

Transposons in science

Transposons were first discovered in plants. Likewise, the first transposon to be molecularly isolated was from a plant (Snapdragon). [2] ( Appropriately, transposons have been an especially useful tool in plant molecular biology. Researchers use transposons as a means of mutagenesis. In this context, a transposon jumps into a gene and produces an interesting mutation. The presence of the transposon provides a straightforward means of identifying the locus that has been mutated, relative to chemical mutagenesis methods. Sometimes the insertion of a transposon into a gene can disrupt that gene's function in a reversible manner; transposase mediated excision of the transposon restores gene function. This produces plants in which neighboring cells have different genotypes. This feature allows researchers to distinguish between genes that must be present inside of a cell in order to function (cell-autonomous) and genes that produce observable effects in cells other than those where the gene is expressed.

Transposons are also a widely used tool for mutagenesis in Drosophila melanogaster, and in a wide variety of bacteria to study gene function.

External link

fr:Élément transposable nl:Springend gen pl:Transpozon


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