Mobility assays confirm the broad host-range activity of the Minos transposable element and validate new transformation tools.

Abstract:

:Fast and reliable methods for assessing the mobility of the transposable element Minos have been developed. These methods are based on the detection of excision and insertion of Minos transposons from and into plasmids which are co-introduced into cells. Excision is detected by polymerase chain reaction (PCR) with appropriate primers. Transposition is assayed by marker rescue in Escherichia coli, using a transposon plasmid that carries a tetracycline resistance gene and a target plasmid carrying a gene that can be selected against in E. coli. Using both assays, Minos was shown to transpose in Drosophila melanogaster cells and embryos, and in cultured cells of a mosquito, Aedes aegypti, and a lepidopteran, Spodoptera frugiperda. In all cases, mobility was dependent on the presence of exogenously supplied transposase, and both excision and transposition were precise. The results indicate that Minos can transpose in heterologous insect species with comparable efficiencies and therefore has the potential to be used as a transgenesis vector for diverse species.

journal_name

Insect Mol Biol

journal_title

Insect molecular biology

authors

Klinakis AG,Loukeris TG,Pavlopoulos A,Savakis C

doi

10.1046/j.1365-2583.2000.00183.x

subject

Has Abstract

pub_date

2000-06-01 00:00:00

pages

269-75

issue

3

eissn

0962-1075

issn

1365-2583

pii

imb183

journal_volume

9

pub_type

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