A novel piggyBac transposon inducible expression system identifies a role for AKT signalling in primordial germ cell migration.

In this work, we describe a single piggyBac transposon system containing both a tet-activator and a doxycycline-inducible expression cassette. We demonstrate that a gene product can be conditionally expressed from the integrated transposon and a second gene can be simultaneously targeted by a short...

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Main Authors: James D Glover, Lorna Taylor, Adrian Sherman, Caroline Zeiger-Poli, Helen M Sang, Michael J McGrew
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24223709/?tool=EBI
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spelling doaj-0eb05673365341ecaf68a58a5c7dffb92021-03-04T12:36:00ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-01811e7722210.1371/journal.pone.0077222A novel piggyBac transposon inducible expression system identifies a role for AKT signalling in primordial germ cell migration.James D GloverLorna TaylorAdrian ShermanCaroline Zeiger-PoliHelen M SangMichael J McGrewIn this work, we describe a single piggyBac transposon system containing both a tet-activator and a doxycycline-inducible expression cassette. We demonstrate that a gene product can be conditionally expressed from the integrated transposon and a second gene can be simultaneously targeted by a short hairpin RNA contained within the transposon, both in vivo and in mammalian and avian cell lines. We applied this system to stably modify chicken primordial germ cell (PGC) lines in vitro and induce a reporter gene at specific developmental stages after injection of the transposon-modified germ cells into chicken embryos. We used this vector to express a constitutively-active AKT molecule during PGC migration to the forming gonad. We found that PGC migration was retarded and cells could not colonise the forming gonad. Correct levels of AKT activation are thus essential for germ cell migration during early embryonic development.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24223709/?tool=EBI
collection DOAJ
language English
format Article
sources DOAJ
author James D Glover
Lorna Taylor
Adrian Sherman
Caroline Zeiger-Poli
Helen M Sang
Michael J McGrew
spellingShingle James D Glover
Lorna Taylor
Adrian Sherman
Caroline Zeiger-Poli
Helen M Sang
Michael J McGrew
A novel piggyBac transposon inducible expression system identifies a role for AKT signalling in primordial germ cell migration.
PLoS ONE
author_facet James D Glover
Lorna Taylor
Adrian Sherman
Caroline Zeiger-Poli
Helen M Sang
Michael J McGrew
author_sort James D Glover
title A novel piggyBac transposon inducible expression system identifies a role for AKT signalling in primordial germ cell migration.
title_short A novel piggyBac transposon inducible expression system identifies a role for AKT signalling in primordial germ cell migration.
title_full A novel piggyBac transposon inducible expression system identifies a role for AKT signalling in primordial germ cell migration.
title_fullStr A novel piggyBac transposon inducible expression system identifies a role for AKT signalling in primordial germ cell migration.
title_full_unstemmed A novel piggyBac transposon inducible expression system identifies a role for AKT signalling in primordial germ cell migration.
title_sort novel piggybac transposon inducible expression system identifies a role for akt signalling in primordial germ cell migration.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description In this work, we describe a single piggyBac transposon system containing both a tet-activator and a doxycycline-inducible expression cassette. We demonstrate that a gene product can be conditionally expressed from the integrated transposon and a second gene can be simultaneously targeted by a short hairpin RNA contained within the transposon, both in vivo and in mammalian and avian cell lines. We applied this system to stably modify chicken primordial germ cell (PGC) lines in vitro and induce a reporter gene at specific developmental stages after injection of the transposon-modified germ cells into chicken embryos. We used this vector to express a constitutively-active AKT molecule during PGC migration to the forming gonad. We found that PGC migration was retarded and cells could not colonise the forming gonad. Correct levels of AKT activation are thus essential for germ cell migration during early embryonic development.
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24223709/?tool=EBI
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