| First Author | Ogilvy S | Year | 1999 |
| Journal | Blood | Volume | 94 |
| Issue | 6 | Pages | 1855-63 |
| PubMed ID | 10477714 | Mgi Jnum | J:140234 |
| Mgi Id | MGI:3812427 | Doi | 10.1182/blood.v94.6.1855 |
| Citation | Ogilvy S, et al. (1999) Promoter elements of vav drive transgene expression in vivo throughout the hematopoietic compartment. Blood 94(6):1855-63 |
| abstractText | To develop a method for targeting expression of genes to the full hematopoietic system, we have used transgenic mice to explore the transcriptional regulation of the vav gene, which is expressed throughout this compartment but rarely outside it. Previously, we showed that a cluster of elements surrounding its promoter could drive hematopoietic-specific expression of a bacterial lacZ reporter gene, but the expression was confined to lymphocytes and was sporadically silenced. Those limitations are ascribed here to the prokaryotic reporter gene. With a human CD4 (hCD4) cell surface reporter, the vav promoter elements drove expression efficiently and stably in virtually all nucleated cells of adult hematopoietic tissues but not notably in nonhematopoietic cell types. In multiple lines, hCD4 appeared on most, if not all, B and T lymphocytes, granulocytes, monocytes, megakaryocytes, eosinophils, and nucleated erythroid cells. Moreover, high levels appeared on both lineage-committed progenitors and the more primitive preprogenitors. In the fetus, expression was evident in erythroid cells of the definitive but not the primitive type. These results indicate that a prokaryotic sequence can inactivate a transcription unit and that the vav promoter region constitutes a potent transgenic vector for the entire definitive hematopoietic compartment. |
