Double conditional human embryonic kidney cell line based on FLP and ΦC31 mediated transgene integration

<p>Abstract</p> <p>Background</p> <p>FLP recombinase mediated integration into a pre-integrated FRT site is routinely used to generate highly reproducible stable transgenic cell lines. In this study, we broaden the system of site specific integration by introducing ΦC31...

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Main Authors: Solomentsew Natalie, Yanik Mert, Schütte Fabian, Rempel Olga, Waldner Christoph, Ryffel Gerhart U
Format: Article
Language:English
Published: BMC 2011-10-01
Series:BMC Research Notes
Online Access:http://www.biomedcentral.com/1756-0500/4/420
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spelling doaj-a8fbf9512bac407b8be6c8f6d89123012020-11-25T01:28:32ZengBMCBMC Research Notes1756-05002011-10-014142010.1186/1756-0500-4-420Double conditional human embryonic kidney cell line based on FLP and ΦC31 mediated transgene integrationSolomentsew NatalieYanik MertSchütte FabianRempel OlgaWaldner ChristophRyffel Gerhart U<p>Abstract</p> <p>Background</p> <p>FLP recombinase mediated integration into a pre-integrated FRT site is routinely used to generate highly reproducible stable transgenic cell lines. In this study, we broaden the system of site specific integration by introducing ΦC31 integrase mediated integration into attP sites.</p> <p>Results</p> <p>We generated a HEK293 host cell line with a single copy FRT as well as an attP site allowing site specific integration of two distinct transgenes. To achieve conditional control, we used the tetracycline and Shld1 inducible systems. By introducing fluorescent reporters we show that integration and induction of two transgenes are completely independent. We applied this new technique to investigate the effect of HNF4α on proliferation of HEK293 cells by introducing HNF4α into each integration site. We obtained in two independent cell lines highly reproducible results that prove the usefulness of this novel HEK-attP/FRT cell line.</p> <p>Conclusions</p> <p>In this study we have established and applied a HEK-attP/FRT cell line that allows site specific integration of two conditional transgenes using the FLP recombinase as well as the ΦC31 integrase.</p> http://www.biomedcentral.com/1756-0500/4/420
collection DOAJ
language English
format Article
sources DOAJ
author Solomentsew Natalie
Yanik Mert
Schütte Fabian
Rempel Olga
Waldner Christoph
Ryffel Gerhart U
spellingShingle Solomentsew Natalie
Yanik Mert
Schütte Fabian
Rempel Olga
Waldner Christoph
Ryffel Gerhart U
Double conditional human embryonic kidney cell line based on FLP and ΦC31 mediated transgene integration
BMC Research Notes
author_facet Solomentsew Natalie
Yanik Mert
Schütte Fabian
Rempel Olga
Waldner Christoph
Ryffel Gerhart U
author_sort Solomentsew Natalie
title Double conditional human embryonic kidney cell line based on FLP and ΦC31 mediated transgene integration
title_short Double conditional human embryonic kidney cell line based on FLP and ΦC31 mediated transgene integration
title_full Double conditional human embryonic kidney cell line based on FLP and ΦC31 mediated transgene integration
title_fullStr Double conditional human embryonic kidney cell line based on FLP and ΦC31 mediated transgene integration
title_full_unstemmed Double conditional human embryonic kidney cell line based on FLP and ΦC31 mediated transgene integration
title_sort double conditional human embryonic kidney cell line based on flp and φc31 mediated transgene integration
publisher BMC
series BMC Research Notes
issn 1756-0500
publishDate 2011-10-01
description <p>Abstract</p> <p>Background</p> <p>FLP recombinase mediated integration into a pre-integrated FRT site is routinely used to generate highly reproducible stable transgenic cell lines. In this study, we broaden the system of site specific integration by introducing ΦC31 integrase mediated integration into attP sites.</p> <p>Results</p> <p>We generated a HEK293 host cell line with a single copy FRT as well as an attP site allowing site specific integration of two distinct transgenes. To achieve conditional control, we used the tetracycline and Shld1 inducible systems. By introducing fluorescent reporters we show that integration and induction of two transgenes are completely independent. We applied this new technique to investigate the effect of HNF4α on proliferation of HEK293 cells by introducing HNF4α into each integration site. We obtained in two independent cell lines highly reproducible results that prove the usefulness of this novel HEK-attP/FRT cell line.</p> <p>Conclusions</p> <p>In this study we have established and applied a HEK-attP/FRT cell line that allows site specific integration of two conditional transgenes using the FLP recombinase as well as the ΦC31 integrase.</p>
url http://www.biomedcentral.com/1756-0500/4/420
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AT yanikmert doubleconditionalhumanembryonickidneycelllinebasedonflpandphc31mediatedtransgeneintegration
AT schuttefabian doubleconditionalhumanembryonickidneycelllinebasedonflpandphc31mediatedtransgeneintegration
AT rempelolga doubleconditionalhumanembryonickidneycelllinebasedonflpandphc31mediatedtransgeneintegration
AT waldnerchristoph doubleconditionalhumanembryonickidneycelllinebasedonflpandphc31mediatedtransgeneintegration
AT ryffelgerhartu doubleconditionalhumanembryonickidneycelllinebasedonflpandphc31mediatedtransgeneintegration
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