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Molecular and Cellular Biology, June 2007, p. 4589-4600, Vol. 27, No. 12
0270-7306/07/$08.00+0     doi:10.1128/MCB.02027-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

The Ancient mariner Sails Again: Transposition of the Human Hsmar1 Element by a Reconstructed Transposase and Activities of the SETMAR Protein on Transposon Ends{triangledown} ,{dagger}

Csaba Miskey,1 Balázs Papp,2 Lajos Mátés,1 Ludivine Sinzelle,1 Heiko Keller,1 Zsuzsanna Izsvák,1,3 and Zoltán Ivics1*

Max Delbrück Center for Molecular Medicine, 13092 Berlin, Germany,1 Faculty of Life Sciences, The University of Manchester, Manchester M13 9PT, United Kingdom,2 Institute of Biochemistry, Biological Research Center of the Hungarian Academy of Sciences, 6726 Szeged, Hungary3

Received 30 October 2006/ Returned for modification 15 November 2006/ Accepted 26 March 2007

Hsmar1, one of the two subfamilies of mariner transposons in humans, is an ancient element that entered the primate genome lineage ~50 million years ago. Although Hsmar1 elements are inactive due to mutational damage, one particular copy of the transposase gene has apparently been under selection. This transposase coding region is part of the SETMAR gene, in which a histone methylatransferase SET domain is fused to an Hsmar1 transposase domain. A phylogenetic approach was taken to reconstruct the ancestral Hsmar1 transposase gene, which we named Hsmar1-Ra. The Hsmar1-Ra transposase efficiently mobilizes Hsmar1 transposons by a cut-and-paste mechanism in human cells and zebra fish embryos. Hsmar1-Ra can also mobilize short inverted-repeat transposable elements (MITEs) related to Hsmar1 (MiHsmar1), thereby establishing a functional relationship between an Hsmar1 transposase source and these MITEs. MiHsmar1 excision is 2 orders of magnitude more efficient than that of long elements, thus providing an explanation for their high copy numbers. We show that the SETMAR protein binds and introduces single-strand nicks into Hsmar1 inverted-repeat sequences in vitro. Pathway choices for DNA break repair were found to be characteristically different in response to transposon cleavage mediated by Hsmar1-Ra and SETMAR in vivo. Whereas nonhomologous end joining plays a dominant role in repairing excision sites generated by the Hsmar1-Ra transposase, DNA repair following cleavage by SETMAR predominantly follows a homology-dependent pathway. The novel transposon system can be a useful tool for genome manipulations in vertebrates and for investigations into the transpositional dynamics and the contributions of these elements to primate genome evolution.

* Corresponding author. Mailing address: Max Delbruck Center for Molecular Medicine, Robert Rössle Str. 10, D-13092 Berlin, Germany. Phone: (49) 30 9406-2546. Fax: (49) 30 9406-2547. E-mail: zivics{at}mdc-berlin.de

{triangledown} Published ahead of print on 2 April 2007.

{dagger} Supplemental material for this article may be found at http://mcb.asm.org/.

Molecular and Cellular Biology, June 2007, p. 4589-4600, Vol. 27, No. 12
0270-7306/07/$08.00+0     doi:10.1128/MCB.02027-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.



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