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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...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2005
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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. |
format | Text |
id | pubmed-1175082 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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