Healing the wounds inflicted by Sleeping Beauty transposition by double-strand break repair in mammalian somatic cells

Izsvak, Z., Stuwe, E. E., Fiedler, D., Katzer, A., Jeggo, Penny and Ivics, Z. (2004) Healing the wounds inflicted by Sleeping Beauty transposition by double-strand break repair in mammalian somatic cells. Molecular Cell, 13. pp. 279-290. ISSN 1097-2765

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Abstract

The Sleeping Beauty (SB) element is a useful tool to probe transposon-host interactions in vertebrates. We investigated requirements of DNA repair factors for SB transposition in mammalian cells. Factors of nonhomologous end joining (NHEJ), including Ku, DNA-PKcs, and Xrcc4 as well as Xrcc3/Rad51C, a complex that functions during homologous recombination, are required for efficient transposition. NHEJ plays a dominant role in repair of transposon excision sites in somatic cells. Artemis is dispensable for transposition, consistent with the lack of a hairpin structure at excision sites. Ku physically interacts with the SB transposase. DNA-PKcs is a limiting factor for transposition and, in addition to repair, has a function in transposition that is independent from its kinase activity. ATM is involved in excision site repair and affects transposition rates. The overlapping but distinct roles of repair factors in transposition and in V(D)J recombination might influence the outcomes of these mechanistically similar processes.

Item Type: Article
Depositing User: Gee Wheatley
Date Deposited: 20 Mar 2007
Last Modified: 10 Sep 2019 11:08
URI: http://sro.sussex.ac.uk/id/eprint/983
Google Scholar:74 Citations
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