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Evolution of Immune Systems From Viruses and Transposable Elements.

Felix Broecker1, Karin Moelling2,3

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Frontiers in Microbiology
|February 15, 2019
PubMed
Summary

Mobile genetic elements, including viruses and transposable elements, have profoundly shaped cellular immunity. These elements evolved from basic virus defense to complex systems like CRISPR-Cas and RAG1/2, highlighting their crucial role in immune system evolution.

Keywords:
CRISPR-CasRNase Hantibodiesimmune systemmobile genetic elementssuperinfection exclusiontransposable elementsviruses

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Area of Science:

  • Evolutionary biology
  • Immunology
  • Genomics

Background:

  • Virus-derived sequences and transposable elements are significant components of cellular genomes.
  • Recent research highlights the deep evolutionary links between these mobile genetic elements and host immune systems.

Purpose of the Study:

  • To review the current understanding of how mobile genetic elements have contributed to the evolution of cellular immune pathways.
  • To illustrate the origin and spread of immune systems from viruses and transposable elements.

Main Methods:

  • Literature review of studies on mobile genetic elements and cellular immunity.
  • Analysis of evolutionary relationships between viral/transposable elements and immune mechanisms.
  • Synthesis of current knowledge on immune system origins.

Main Results:

  • Superinfection exclusion in prokaryotes and eukaryotes is an early virus-mediated immune system.
  • Prokaryotic CRISPR-Cas and vertebrate RAG1/2 systems are complex immune mechanisms derived from mobile genetic elements.
  • Mobile genetic elements are integral to the origin and diversification of cellular immunity.

Conclusions:

  • Cellular immune systems have evolved from simple virus exclusion to sophisticated defense strategies.
  • Viruses and transposable elements are fundamental drivers in the evolutionary trajectory of host immunity.
  • A comprehensive view reveals that mobile genetic elements are key architects of cellular immune pathways.