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A comparison of exogenous promoter activity at the ROSA26 locus using a (Phi)iC31 integrase mediated cassette exchange approach in mouse ES cells.

Abstract:
The activities of nine ubiquitous promoters (ROSA26, CAG, CMV, CMVd1, UbC, EF1(Alpha), PGK, chicken (Beta)-actin and MC1) have been quantified and compared in mouse embryonic stem cells. To avoid the high variation in transgene expression which results from uncontrolled copy number and chromosomal position effects when using random insertion based transgenic approaches, we have adopted a PhiC31 integrase mediated cassette exchange method for the efficient insertion of transgenes at single copy within a defined and well characterized chromosomal position, ROSA26. This has enabled the direct comparison of constructs from within the same genomic context and allows a systematic and quantitative assessment of the strengths of the promoters in comparison with the endogenous ROSA26 promoter. The behavior of these exogenous promoters, when integrated at ROSA26 in both sense and antisense orientations, reveals a large variation in their levels of activity. In addition, a subset of promoters, EF1(Alpha), UbC and CAG, show an increased activity in the sense orientation as a consequence of integration. Transient transfection experiments confirmed these observations to reflect integration dependent effects and also revealed significant differences in the behaviour of these promoters when delivered transiently or stably. As well as providing an important reference which will facilitate the choice of an appropriate promoter to achieve the desired level of expression for a specific research question, this study also demonstrates the suitability of the cassette exchange methodology for the robust and reliable expression of multiple variant transgenes in ES cells.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1371/journal.pone.0023376

Authors


More by this author
Institution:
University of Oxford
Division:
MSD
Department:
RDM
Sub department:
RDM Cardiovascular Medicine
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
NDM
Sub department:
Human Genetics Wt Centre
Role:
Author


More from this funder
Funding agency for:
Bhattacharya, S
Grant:
083228


Publisher:
Public Library of Science
Journal:
PloS one More from this journal
Volume:
6
Issue:
8
Article number:
e23376
Publication date:
2011-01-01
DOI:
EISSN:
1932-6203
ISSN:
1932-6203


Language:
English
Keywords:
UUID:
uuid:258b7e13-1951-47f7-b4e7-2128706992e1
Local pid:
pubs:172055
Source identifiers:
172055
Deposit date:
2012-12-19

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