| First Author | Yuan L | Year | 2013 |
| Journal | Blood | Volume | 121 |
| Issue | 21 | Pages | 4404-12 |
| PubMed ID | 23529929 | Mgi Jnum | J:198222 |
| Mgi Id | MGI:5495873 | Doi | 10.1182/blood-2012-12-473785 |
| Citation | Yuan L, et al. (2013) Role of RNA splicing in mediating lineage-specific expression of the von Willebrand factor gene in the endothelium. Blood 121(21):4404-12 |
| abstractText | We previously demonstrated that the first intron of the human von Willebrand factor (vWF) is required for gene expression in the endothelium of transgenic mice. Based on this finding, we hypothesized that RNA splicing plays a role in mediating vWF expression in the vasculature. To address this question, we used transient transfection assays in human endothelial cells and megakaryocytes with intron-containing and intronless human vWF promoter-luciferase constructs. Next, we generated knockin mice in which LacZ was targeted to the endogenous mouse vWF locus in the absence or presence of the native first intron or heterologous introns from the human beta-globin, mouse Down syndrome critical region 1, or hagfish coagulation factor X genes. In both the in vitro assays and the knockin mice, the loss of the first intron of vWF resulted in a significant reduction of reporter gene expression in endothelial cells but not megakaryocytes. This effect was rescued to varying degrees by the introduction of a heterologous intron. Intron-mediated enhancement of expression was mediated at a posttranscriptional level. Together, these findings implicate a role for intronic splicing in mediating lineage-specific expression of vWF in the endothelium. |
