Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2011 Aug;19(6):777-86.
doi: 10.1007/s10577-011-9229-0.

Co-evolution between transposable elements and their hosts: a major factor in genome size evolution?

Affiliations
Review

Co-evolution between transposable elements and their hosts: a major factor in genome size evolution?

J Arvid Ågren et al. Chromosome Res. 2011 Aug.

Abstract

Most models of genome size evolution emphasize changes in relative rates of and/or the efficacy of selection on insertions and deletions. However, transposable elements (TEs) are a major contributor to genome size evolution, and since they experience their own selective pressures for expansion, genome size changes may in part be driven by the dynamics of co-evolution between TEs and their hosts. Under this perspective, predictions about the conditions that allow for genome expansion may be altered. In this review, we outline the evidence for TE-host co-evolution, discuss the conditions under which these dynamics can change, and explore the possible contribution to the evolution of genome size. Aided partly by advances in our understanding of the mechanisms of TE silencing via small RNAs, there is growing evidence that the evolution of transposition rates can be important in driving genome expansion and contraction. Shifts in genome size and transposon abundance associated with interspecific hybridization and changes in mating system are consistent with an important role for transposition rate evolution, although other possible explanations persist. More understanding of the potential for the breakdown of host silencing mechanisms and/or the potential for TEs to evade host immune responses will improve our understanding of the importance of changes in TE activity in driving genome size evolution.

PubMed Disclaimer

References

    1. Proc Biol Sci. 1992 Aug 22;249(1325):119-24 - PubMed
    1. Plant J. 2005 Jan;41(2):184-94 - PubMed
    1. Bioessays. 2005 Apr;27(4):353-5 - PubMed
    1. Cell. 2009 Feb 6;136(3):461-72 - PubMed
    1. Science. 2009 Sep 11;325(5946):1391-4 - PubMed

Substances

LinkOut - more resources