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Transmission pattern of hobo transposable element in transgenic lines of Drosophila melanogaster

Published online by Cambridge University Press:  01 April 1998

VERONIQUE LADEVEZE
Affiliation:
IBMIG, Université de Poitiers, ESA 6031, 40 Avenue du Recteur Pineau, 86022 Poitiers cedex, France
IBO GALINDO
Affiliation:
Departemento de Genetica, Universidad de Valencia, 46100 Burjassot (Valencia), Spain
NICOLE CHAMINADE
Affiliation:
CNRS, Laboratoire Populations, Génétique et Evolution, 91198 Gif-sur-Yvette cedex, France
LUIS PASCUAL
Affiliation:
Departemento de Genetica, Universidad de Valencia, 46100 Burjassot (Valencia), Spain
GEORGES PERIQUET
Affiliation:
IRBI, Université François Rabelais, Parc Grandmont, 37200 Tours, France
FRANCOISE LEMEUNIER
Affiliation:
CNRS, Laboratoire Populations, Génétique et Evolution, 91198 Gif-sur-Yvette cedex, France
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Abstract

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This study is an attempt to trace the fate of hobo elements in the genomes of E strains of Drosophila melanogaster that have been transfected with pHFL1, a plasmid containing an autonomous hobo. Such long-term population studies (over 105 generations) could be very useful for better understanding the population and genomic dynamics of transposable elements and their pattern of insertions. Molecular analyses of hobo elements in the transfected lines were performed using Southern blots of XhoI-digested genomic DNAs. The complete element was observed in all six injected lines. In two lines we observed, at generation 100, two deleted elements, which did not correspond to Th1 and Th2. The results obtained by the in situ method show that the number of hybridization sites increases in each line and prove that the hobo element may be amplified in an RM genome. The hobo activity does not seem to be systematically correlated with the number of hobo elements. After generation 85, the evolution of the hobo element's insertion site number depends on the injected line. In all lines, the total number of insertions remains quite small, between 0 and 11. Hobo elements are located on each of the chromosomal arms. We describe ‘hotspots’ – insertion sites present in all lines and in all generations. On the 3R arm, a short inversion appeared once at generation 85.

Type
Research Article
Copyright
© 1998 Cambridge University Press