Activation of EGFP expression by Cre-mediated excision in a new ROSA26 reporter mouse strain

Citation
Xh. Mao et al., Activation of EGFP expression by Cre-mediated excision in a new ROSA26 reporter mouse strain, BLOOD, 97(1), 2001, pp. 324-326
Citations number
10
Categorie Soggetti
Hematology,"Cardiovascular & Hematology Research
Journal title
BLOOD
ISSN journal
00064971 → ACNP
Volume
97
Issue
1
Year of publication
2001
Pages
324 - 326
Database
ISI
SICI code
0006-4971(20010101)97:1<324:AOEEBC>2.0.ZU;2-J
Abstract
Reporter mouse strains are important tools for monitoring Cre recombinase-m ediated excision in vivo. In practice, excision may be incomplete in a give n population due to threshold level or variegated expression of Cre, Hence, it is desirable in many experimental contexts to isolate cells that have u ndergone excision to assess the consequences of gene ablation, To generate alternative reporter mice, an enhanced green fluorescent protein (EGFP) gen e was targeted to the retroviral-trapped ROSA26 locus, Upon Cre-mediated ex cision of "Stop" sequences, EGFP was expressed ubiquitously during embryoge nesis and in adult tissues (including T cells, B cells, and myeloid cells). Using this new reporter strain, separation of excised from nonexcised cell s in vitro was achieved in thymocytes in a noninvasive manner based on acti vated EGFP expression. This new EGFP reporter strain should facilitate a va riety of conditional gene-targeting experiments, including the functional s tudies of hematopoietic cells in lineage-specific knockout mice. (C) 2001 b y The American Society of Hematology.