Mobile genetic elements

• Transposons (also called transposable elements) are DNA sequences that can move locations within a genome, which includes retrotransposons and DNA transposons.
  • Retrotransposons are the most widespread class of transposons in mammals.[3] An RNA transcript of MGEs is copied by reverse transcriptase. Then, the DNA sequence can be inserted back to a random location of the genome.[4]
  • DNA transposons are a DNA segment that can move to a new location by a "cut-and-paste" strategy.
• Plasmids of bacteria are a transferable genetic element through bacterial conjugation. This is a mechanism of horizontal gene transfer that allows bacteria to share virulence factors and antibiotic resistance genes.
• Bacteriophage elements, like Mu, which integrates randomly into the genome by transduction.[5]
• Group I and Group II introns are a product from self-splicing in the host transcripts, and they act as ribozymes that can invade tRNA, rRNA, and protein coding genes in bacteria.[6]

CRISPR-Cas systems in bacteria and archaea are adaptive immune systems to protect against deadly consequences from MGEs. Using comparative genomic and phylogenetic analysis, researchers found that CRISPR-Cas variants are associated with distinct types of MGEs such as transposable elements. In addition, CRISPR-Cas controls transposable elements for their propagation.[7]

MGEs such as plasmids by a horizontal transmission are generally beneficial to an organism. The ability of transferring plasmids (sharing) is important in an evolutionary perspective. Tazzyman and Bonhoeffer found that fixation (receiving) of the transferred plasmids in a new organism is just as important as the ability to transfer them.[8] Beneficial rare and transferable plasmids have a higher fixation probability, whereas deleterious transferable genetic elements have a lower fixation probability to avoid lethality to the host organisms.

Transposition by transposable elements is mutagenic. Thus, organisms have evolved to repress the transposition events, and failure to repress the events causes cancers in somatic cells. Cecco et al. found that during early age transcription of retrotransposable elements are minimal in mice, but in advanced age the transcription level increases.[9] This age-dependent expression level of transposable elements is reduced by calorie restriction diet.

The consequence of mobile genetic elements can alter the transcriptional patterns, which frequently leads to genetic disorders such as immune disorders, breast cancer, multiple sclerosis, and amyotrophic lateral sclerosis. In humans, stress can lead to transactional activation of MGEs such as endogenous retroviruses, and this activation has been linked to neurodegeneration.[10]

The total of all mobile genetic elements in a genome may be referred to as the mobilome.

Barbara McClintock was awarded the 1983 Nobel Prize in Physiology or Medicine "for her discovery of mobile genetic elements" (transposable elements).[11]

Mobile genetic elements play a critical role in the spread of virulence factors, such as exotoxins and exoenzymes, among bacteria. Strategies to combat certain bacterial infections by targeting these specific virulence factors and mobile genetic elements have been proposed.[12]

• ACLAME (The CLAssification of Mobile genetic Elements) database
• Horizontal gene transfer
• Virulence factors

• Miller, W. J.; Capy, P., eds. (2004), Mobile genetic elements: protocols and genomic applications, Humana Press, ISBN 978-1-58829-007-6
• Shapiro, J.A., ed. (1983), Mobile genetic elements, Academic Press, ISBN 978-0-12-638680-6