Please use this identifier to cite or link to this item: https://doi.org/10.1534/genetics.106.061184
Title: Trans-kingdom transposition of the maize Dissociation element
Authors: Emelyanov, A.
Gao, Y.
Naqvi, N.I. 
Parinov, S.
Issue Date: 2006
Citation: Emelyanov, A., Gao, Y., Naqvi, N.I., Parinov, S. (2006). Trans-kingdom transposition of the maize Dissociation element. Genetics 174 (3) : 1095-1104. ScholarBank@NUS Repository. https://doi.org/10.1534/genetics.106.061184
Abstract: Transposons are very valuable tools for genetic manipulation. However, the number of transposable elements that have been suitably adapted for experimental use is insufficient and the spectrum of heterologous hosts in which they have been deployed is restricted. To date, only transposons from animal hosts have been utilized in heterologous animal species and transposons of plant origin have been used in plant genetics. There has been no experimental evidence that any of the known elements could transpose in hosts belonging to both kingdoms. Here we demonstrate that the maize Dissociation (Ds) element is capable of effective Activator (Ac) transposase-mediated transposition in the zebrafish Danio rerio, yielding remarkable germline transmission rates. In addition, mammalian cells were also found to be conducive to Ds transposition. Furthermore, we demonstrate that nuclear localization of Ac transposase is essential for genomic Ds transposition. Our results support the hypothesis that Ac/Ds elements do not rely on hostspecific factors for transposition and that host factors involved in their mobility mechanism are widely conserved. Finally, even in vertebrate cells, the Ac/Ds system displays accurate transposition, largefragment carrying capacity, high transposition frequencies, efficient germline transmission, and reporter gene expression, all of which are advantageous for various genetic applications and animal biotechnology. Copyright © 2006 by the Genetics Society of America.
Source Title: Genetics
URI: http://scholarbank.nus.edu.sg/handle/10635/130427
ISSN: 00166731
DOI: 10.1534/genetics.106.061184
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