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CpG-island fragments from the HNRPA2B1/CBX3 genomic locus reduce silencing and enhance transgene expression from the hCMV promoter/enhancer in mammalian cells

BACKGROUND: The hCMV promoter is very commonly used for high level expression of transgenes in mammalian cells, but its utility is hindered by transcriptional silencing. Large genomic fragments incorporating the CpG island region of the HNRPA2B1 locus are resistant to transcriptional silencing. RESU...

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Detalles Bibliográficos
Autores principales: Williams, Steven, Mustoe, Tracey, Mulcahy, Tony, Griffiths, Mark, Simpson, David, Antoniou, Michael, Irvine, Alistair, Mountain, Andrew, Crombie, Robert
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1175082/
https://www.ncbi.nlm.nih.gov/pubmed/15935093
http://dx.doi.org/10.1186/1472-6750-5-17
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author Williams, Steven
Mustoe, Tracey
Mulcahy, Tony
Griffiths, Mark
Simpson, David
Antoniou, Michael
Irvine, Alistair
Mountain, Andrew
Crombie, Robert
author_facet Williams, Steven
Mustoe, Tracey
Mulcahy, Tony
Griffiths, Mark
Simpson, David
Antoniou, Michael
Irvine, Alistair
Mountain, Andrew
Crombie, Robert
author_sort Williams, Steven
collection PubMed
description BACKGROUND: The hCMV promoter is very commonly used for high level expression of transgenes in mammalian cells, but its utility is hindered by transcriptional silencing. Large genomic fragments incorporating the CpG island region of the HNRPA2B1 locus are resistant to transcriptional silencing. RESULTS: In this report we describe studies on the use of a novel series of vectors combining the HNRPA2B1 CpG island with the hCMV promoter for expression of transgenes in CHO-K1 cells. We show that the CpG island gives at least twenty-fold increases in the levels of EGFP and EPO observed in pools of transfectants, and that transgene expression levels remain high in such pools for more than 100 generations. These novel vectors also allow facile isolation of clonal CHO-K1 cell lines showing stable, high-level transgene expression. CONCLUSION: Vectors incorporating the hnRPA2B1 CpG island give major benefits in transgene expression from the hCMV promoter, including substantial improvements in the level and stability of expression. The utility of these vectors for the improved production of recombinant proteins in CHO cells has been demonstrated.
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spelling pubmed-11750822005-07-14 CpG-island fragments from the HNRPA2B1/CBX3 genomic locus reduce silencing and enhance transgene expression from the hCMV promoter/enhancer in mammalian cells Williams, Steven Mustoe, Tracey Mulcahy, Tony Griffiths, Mark Simpson, David Antoniou, Michael Irvine, Alistair Mountain, Andrew Crombie, Robert BMC Biotechnol Research Article BACKGROUND: The hCMV promoter is very commonly used for high level expression of transgenes in mammalian cells, but its utility is hindered by transcriptional silencing. Large genomic fragments incorporating the CpG island region of the HNRPA2B1 locus are resistant to transcriptional silencing. RESULTS: In this report we describe studies on the use of a novel series of vectors combining the HNRPA2B1 CpG island with the hCMV promoter for expression of transgenes in CHO-K1 cells. We show that the CpG island gives at least twenty-fold increases in the levels of EGFP and EPO observed in pools of transfectants, and that transgene expression levels remain high in such pools for more than 100 generations. These novel vectors also allow facile isolation of clonal CHO-K1 cell lines showing stable, high-level transgene expression. CONCLUSION: Vectors incorporating the hnRPA2B1 CpG island give major benefits in transgene expression from the hCMV promoter, including substantial improvements in the level and stability of expression. The utility of these vectors for the improved production of recombinant proteins in CHO cells has been demonstrated. BioMed Central 2005-06-03 /pmc/articles/PMC1175082/ /pubmed/15935093 http://dx.doi.org/10.1186/1472-6750-5-17 Text en Copyright © 2005 Williams et al; licensee BioMed Central Ltd.
spellingShingle Research Article
Williams, Steven
Mustoe, Tracey
Mulcahy, Tony
Griffiths, Mark
Simpson, David
Antoniou, Michael
Irvine, Alistair
Mountain, Andrew
Crombie, Robert
CpG-island fragments from the HNRPA2B1/CBX3 genomic locus reduce silencing and enhance transgene expression from the hCMV promoter/enhancer in mammalian cells
title CpG-island fragments from the HNRPA2B1/CBX3 genomic locus reduce silencing and enhance transgene expression from the hCMV promoter/enhancer in mammalian cells
title_full CpG-island fragments from the HNRPA2B1/CBX3 genomic locus reduce silencing and enhance transgene expression from the hCMV promoter/enhancer in mammalian cells
title_fullStr CpG-island fragments from the HNRPA2B1/CBX3 genomic locus reduce silencing and enhance transgene expression from the hCMV promoter/enhancer in mammalian cells
title_full_unstemmed CpG-island fragments from the HNRPA2B1/CBX3 genomic locus reduce silencing and enhance transgene expression from the hCMV promoter/enhancer in mammalian cells
title_short CpG-island fragments from the HNRPA2B1/CBX3 genomic locus reduce silencing and enhance transgene expression from the hCMV promoter/enhancer in mammalian cells
title_sort cpg-island fragments from the hnrpa2b1/cbx3 genomic locus reduce silencing and enhance transgene expression from the hcmv promoter/enhancer in mammalian cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1175082/
https://www.ncbi.nlm.nih.gov/pubmed/15935093
http://dx.doi.org/10.1186/1472-6750-5-17
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