The autoregulation of a eukaryotic DNA transposon

Author:

Claeys Bouuaert Corentin1,Lipkow Karen23,Andrews Steven S4,Liu Danxu1,Chalmers Ronald1

Affiliation:

1. School of Biomedical Sciences, University of Nottingham, Nottingham, United Kingdom

2. The Babraham Institute, Cambridge, United Kingdom

3. Department of Biochemistry and Cambridge Systems Biology Centre, University of Cambridge, Cambridge, United Kingdom

4. Basic Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, United States

Abstract

How do DNA transposons live in harmony with their hosts? Bacteria provide the only documented mechanisms for autoregulation, but these are incompatible with eukaryotic cell biology. Here we show that autoregulation of Hsmar1 operates during assembly of the transpososome and arises from the multimeric state of the transposase, mediated by a competition for binding sites. We explore the dynamics of a genomic invasion using a computer model, supported by in vitro and in vivo experiments, and show that amplification accelerates at first but then achieves a constant rate. The rate is proportional to the genome size and inversely proportional to transposase expression and its affinity for the transposon ends. Mariner transposons may therefore resist post-transcriptional silencing. Because regulation is an emergent property of the reaction it is resistant to selfish exploitation. The behavior of distantly related eukaryotic transposons is consistent with the same mechanism, which may therefore be widely applicable.

Funder

Wellcome Trust

Royal Society

National Institute of General Medical Sciences

National Institutes of Health

Microsoft Research Faculty Fellowship

Apple Research & Technology Support

EU-IndiaGrid2

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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