Transgenic mice with hematopoietic and lymphoid specific expression of Cre
Open accessAbstract
Bacteriophage P1 Cre/loxP based systems can be used to manipulate the genomes of mice in vivo and in vitro, allowing the generation of tissue‐specific conditional mutants. Wehave generated mouse lines expressing Cre recombinase in hematopoietic tissues using the vav regulatory elements, or in lymphoid cells using the hCD2 promoter and locus control region (LCR). The R26R‐EYFP Cre reporter mouse line was used to determine the pattern of Cre expression in each line and enabled the assessment of Cre activity at a single‐cell level. Analysis showed that the vav promoter elements were able to direct Cre‐mediated recombination in all cells of the hematopoietic system. The hCD2 promoter and LCR on the other hand were able to drive Cre‐mediated recombination only in T cells and B cells, but not in other hematopoietic cell types. Furthermore, in the appropriate tissues, deletion of the floxed target was complete in all cells, thereby excluding the possibility of variegated expression of the Cre transgene. Both of these Cre‐transgenic lines will be useful in generating tissue‐specific gene deletions within all the cells of hematopoietic or lymphoid tissues.
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The Commd10Tg(Vav1-icre)A2Kio mouse line has been previously described.
“Trp53tm2Tyj (ref. 88), Commd10Tg(Vav1-icre)A2Kio (ref. 89; Jackson Laboratory, 008610) and Tg(Tal1-cre/ERT)42-056Jrg (ref. 90) have been previously described.”
From Single-cell multi-omics identifies chronic inflammation as a driver of TP53-mutant leukemic evolution (2023) · cites this paper as [89]
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- Authors
- de Boer, J., Williams, A., Skavdis, G., Harker, N., Coles, M., Tolaini, M., Norton, T., Williams, K., Roderick, K., Potocnik, A. J., & Kioussis, D.
- Corresponding author
- Kioussis, Dimitris
- Venue
- European Journal of Immunology
- Publisher
- Wiley
- Published
- 2003-01-20
- Volume
- 33
- Issue
- 2
- Pages
- 314-325
- ISSN
- 0014-2980 (ISSN-L)
- 1521-4141
- OpenAlex
- W2002817805
- Cited by
- 739
- References
- 2
- Citations by year
- 2026: 23 · 2025: 44 · 2024: 41 · 2023: 32 · 2022: 55 · 2021: 56 · 2020: 35 · 2019: 44 · 2018: 45 · 2017: 38 · 2016: 35 · 2015: 42 · 2014: 51 · 2013: 39 · 2012: 36
- FWCI
- 3.68
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- European Journal of Immunology (publishedVersion)
- PubMed (publishedVersion)
- UCL Discovery (University College London) (submittedVersion)
- Funders
- Medical Research Council
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Animal Genetics and Reproduction
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › CRISPR and Genetic Engineering
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Keywords
- Cre recombinase, Cre-loxP system, tissue-specific gene deletion, hematopoietic cells, lymphoid cells, locus control region, conditional mutants, T cells, B cells
- MeSH terms
- Animals, B-Lymphocytes, Bacterial Proteins, Hematopoietic Stem Cells, Humans, Luminescent Proteins, Lymphoid Tissue, Male, Mice, Transgenic, Microscopy, Fluorescence, Organ Specificity, Recombinant Fusion Proteins, T-Lymphocytes, Testis, Viral Proteins, Oncogene Proteins, Bacteriophage P1, Genes, Reporter, Gene Targeting, CD2 Antigens, Cell Lineage, Integrases, Locus Control Region, Mice, Proto-Oncogene Proteins c-vav
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