Literature DB >> 17638017

Post-integration behavior of a Minos transposon in the malaria mosquito Anopheles stephensi.

Christina Scali1, Tony Nolan, Igor Sharakhov, Maria Sharakhova, Andrea Crisanti, Flaminia Catteruccia.   

Abstract

Transposable elements represent important tools to perform functional studies in insects. In Drosophila melanogaster, the remobilization properties of transposable elements have been utilized for enhancer-trapping and insertional mutagenesis experiments, which have considerably helped in the functional characterization of the fruitfly genome. In Anopheles mosquitoes, the sole vectors of human malaria, as well as in other mosquito vectors of disease, the use of transposons has also been advocated to achieve the spread of anti-parasitic genes throughout field populations. Here we report on the post-integration behavior of the Minos transposon in both the germ-line and somatic tissues of Anopheles mosquitoes. Transgenic An. stephensi lines developed using the piggyBac transposon and expressing the Minos transposase were tested for their ability to remobilize an X-linked Minos element. Germ-line remobilization events were not detected, while somatic excisions and transpositions were consistently recovered. The analysis of these events showed that Minos activity in Anopheles cells is characterized by unconventional functionality of the transposon. In the two cases analyzed, re-integration of the transposon occurred onto the same X chromosome, suggesting a tendency for local hopping of Minos in the mosquito genome. This is the first report of the post-integration behavior of a transposable element in a human malaria vector.

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Year:  2007        PMID: 17638017     DOI: 10.1007/s00438-007-0274-5

Source DB:  PubMed          Journal:  Mol Genet Genomics        ISSN: 1617-4623            Impact factor:   3.291


  41 in total

1.  piggyBac-based insertional mutagenesis in the presence of stably integrated P elements in Drosophila.

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2.  Minos, a new transposable element from Drosophila hydei, is a member of the Tc1-like family of transposons.

Authors:  G Franz; C Savakis
Journal:  Nucleic Acids Res       Date:  1991-12-11       Impact factor: 16.971

3.  piggyBac-mediated germline transformation of the malaria mosquito Anopheles stephensi using the red fluorescent protein dsRED as a selectable marker.

Authors:  Tony Nolan; Tom M Bower; Anthony E Brown; Andrea Crisanti; Flaminia Catteruccia
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Review 4.  Methods for replacement of malaria vector populations.

Authors:  C F Curtis; P M Graves
Journal:  J Trop Med Hyg       Date:  1988-04

5.  Crucial role for DNA supercoiling in Mu transposition: a kinetic study.

Authors:  Z Wang; R M Harshey
Journal:  Proc Natl Acad Sci U S A       Date:  1994-01-18       Impact factor: 11.205

6.  Regulated transposition of a fish transposon in the mouse germ line.

Authors:  S E Fischer; E Wienholds; R H Plasterk
Journal:  Proc Natl Acad Sci U S A       Date:  2001-05-29       Impact factor: 11.205

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9.  The Berkeley Drosophila Genome Project gene disruption project: Single P-element insertions mutating 25% of vital Drosophila genes.

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  11 in total

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Journal:  Genetica       Date:  2010-07-03       Impact factor: 1.082

5.  A new powerful method for site-specific transgene stabilization based on chromosomal double-strand break repair.

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7.  Functional characterization of the active Mutator-like transposable element, Muta1 from the mosquito Aedes aegypti.

Authors:  Kun Liu; Susan R Wessler
Journal:  Mob DNA       Date:  2017-01-11

8.  Gal4-based enhancer-trapping in the malaria mosquito Anopheles stephensi.

Authors:  David A O'Brochta; Kristina L Pilitt; Robert A Harrell; Channa Aluvihare; Robert T Alford
Journal:  G3 (Bethesda)       Date:  2012-11-01       Impact factor: 3.154

9.  PiggyBac transposon-based polyadenylation-signal trap for genome-wide mutagenesis in mice.

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10.  nanos-Driven expression of piggyBac transposase induces mobilization of a synthetic autonomous transposon in the malaria vector mosquito, Anopheles stephensi.

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