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Cooperation is Fleeting in the World of Transposable Elements

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  • Andreas Wagner

Abstract

Composite transposons are key vehicles for the worldwide spreading of genes that allow bacteria to survive toxic compounds. Composite transposons consist of two smaller transposable elements called insertion sequences (ISs), which flank the genes that permit such survival. Each IS in a composite transposon can either transpose alone, selfishly, or it can transpose cooperatively, jointly with the other IS. Cooperative transposition can enhance an IS's chance of survival, but it also carries the risk of transposon destruction. I use game theory to show that the conditions under which cooperative transposition is an evolutionarily stable strategy (ESS) are not biologically realistic. I then analyze the distribution of thousands of ISs in more than 200 bacterial genomes to test the following prediction of the game-theoretical model: if cooperative transposition was an ESS, then the closely spaced ISs that characterize composite transposons should be more abundant in genomes than expected by chance. The data show that this is not the case. Cooperativity can only be maintained in a transitional, far-from-equilibrium state shortly after a selection pressure first arises. This is the case in the spreading of antibiotic resistance, where we are witnessing a fleeting moment in evolution, a moment in which cooperation among selfish DNA molecules has provided a means of survival. Because such cooperation does not pay in the long run, the vehicles of such survival will eventually disappear again. My analysis demonstrates that game theory can help explain behavioral strategies even for mobile DNA. Synopsis: Molecules can display cooperation and selfish behavior. Wagner investigates cooperative behavior in mobile DNA molecules called transposable elements, which can “hop” among cells, which aids the worldwide spreading of antibiotic resistance genes. A composite transposon consists of two smaller mobile DNA molecules, M, that flank another gene, G, M-G-M. The molecules M are able to change location alone and selfishly. They are also able to change location jointly and cooperatively, thus taking the gene G with them. Cooperation facilitates the spreading of the gene G and of M itself. Cooperativity is advantageous to M. However, Wagner's paper shows that cooperativity is short-lived and not stable on evolutionary time scales. Cooperativity can only be maintained in a transitional, far-from-equilibrium state shortly after a selection pressure first arises. This is the case in the spreading of antibiotic resistance, where we are witnessing a fleeting moment in evolution, a moment in which cooperation among selfish DNA molecules has provided a means of survival. Because such cooperation does not pay in the long run, the vehicles of such survival will eventually disappear again.

Suggested Citation

  • Andreas Wagner, 2006. "Cooperation is Fleeting in the World of Transposable Elements," PLOS Computational Biology, Public Library of Science, vol. 2(12), pages 1-8, December.
  • Handle: RePEc:plo:pcbi00:0020162
    DOI: 10.1371/journal.pcbi.0020162
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    References listed on IDEAS

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    1. Ashleigh S. Griffin & Stuart A. West & Angus Buckling, 2004. "Cooperation and competition in pathogenic bacteria," Nature, Nature, vol. 430(7003), pages 1024-1027, August.
    2. Gregory J. Velicer & Yuen-tsu N. Yu, 2003. "Evolution of novel cooperative swarming in the bacterium Myxococcus xanthus," Nature, Nature, vol. 425(6953), pages 75-78, September.
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    1. Drakos, Nicole E. & Wahl, Lindi M., 2015. "Extinction probabilities and stationary distributions of mobile genetic elements in prokaryotes: The birth–death-diversification model," Theoretical Population Biology, Elsevier, vol. 106(C), pages 22-31.
    2. Startek, Michał & Le Rouzic, Arnaud & Capy, Pierre & Grzebelus, Dariusz & Gambin, Anna, 2013. "Genomic parasites or symbionts? Modeling the effects of environmental pressure on transposition activity in asexual populations," Theoretical Population Biology, Elsevier, vol. 90(C), pages 145-151.

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