VavCre transgenic mice: a tool for mutagenesis in hematopoietic and endothelial lineages

Autor: Georgiades, Pantelis, Ogilvy, S., Duval, H., Licence, D. R., Charnock-Jones, D. S., Smith, S. K., Print, C. G.
Přispěvatelé: Georgiades, Pantelis [0000-0002-5538-3163]
Rok vydání: 2002
Předmět:
Somatic cell
genotype
polymerase chain reaction
beta galactosidase
complementary DNA
animal cell
fluorescence activated cell sorting
Mice
Endocrinology
immunocytochemistry
Genes
Reporter

Leukocytes
endothelium cell
Transgenes
Hematopoietic
Regulation of gene expression
Oncogene Proteins
Recombination
Genetic

genetic recombination
article
vav
Cre
gene expression regulation
Flow Cytometry
reporter gene
medicine.anatomical_structure
priority journal
histochemistry
mutagenesis
Genetically modified mouse
Cell type
Transgene
Mutagenesis (molecular biology technique)
Cre recombinase
Mice
Transgenic

Biology
hematopoietic cell
Endothelial
Viral Proteins
Genetics
medicine
Animalia
Mus musculus
Animals
Cell Lineage
Endothelium
cre recombinase
Proto-Oncogene Proteins c-vav
mouse
nonhuman
Integrases
nucleotide sequence
Cell Biology
Hematopoietic Stem Cells
Molecular biology
transgenic mouse
Gene Expression Regulation
Mutagenesis
Bone marrow
Murinae
Zdroj: Genesis
ISSN: 1526-954X
Popis: Cre transgenic mice can be used to delete gene sequences flanked by loxP sites in specific somatic tissues. We have generated vavCre transgenic mice, which can be used to inactivate genes specifically in adult hematopoietic and endothelial cells. In these animals, a Cre transgene is expressed under control of murine vav gene regulatory elements. To assess their usefulness, vavCre transgenic mice were bred with R26R mice, which express a lacZ reporter gene only in cells where Cre-mediated recombination has occurred. VavCre/R26R double-heterozygous offspring were analyzed by β-galactosidase histochemistry and flow cytometry. VavCre-mediated recombination occurred in most hematopoietic cells of all hematopoietic organs, including the hematopoietic progenitor-rich bone marrow. Recombination also occurred In most endothelial and germ cells, but only rarely in other cell types. The recombination in both hematopoietic and endothelial lineages may partly reflect their putative shared ontogeny and provides a unique tool for simultaneous pan-hematopoietic and endothelial mutagenesis. © 2002 Wiley-Liss, Inc. 34 251 256 Cited By :74
Databáze: OpenAIRE