Maha Othman
Functional characterization of a 13-bp deletion (c.-1522--1510del13) in the promoter of the von Willebrand factor gene in type 1 von Willebrand disease
Othman, Maha; Chirinian, Yvette; Brown, Christine; Notley, Colleen; Hickson, Nicholas; Hampshire, Daniel; Buckley, Suzanne; Waddington, Simon; Parker, Alan L.; Baker, Andrew; James, Paula; Lillicrap, David
Authors
Yvette Chirinian
Christine Brown
Colleen Notley
Nicholas Hickson
Dr Dan Hampshire D.Hampshire@hull.ac.uk
Lecturer in Genetics
Suzanne Buckley
Simon Waddington
Alan L. Parker
Andrew Baker
Paula James
David Lillicrap
Abstract
We have studied the effect of a 13-bp deletion in the promoter of the von Willebrand factor (VWF) gene in a patient with type 1 von Willebrand disease. The index case has a VWF:Ag of 0.49 IU/mL and is heterozygous for the deletion. The deletion is located 48 bp 5′ of the transcription start site, and in silico analysis, electrophoretic mobility shift assays, and chromatin immunoprecipitation studies all predict aberrant binding of Ets transcription factors to the site of the deletion. Transduction of reporter gene constructs into blood outgrowth endothelial cells showed a 50.5% reduction in expression with the mutant promoter (n = 16, P < .001). A similar 40% loss of transactivation was documented in transduced HepG2 cells. A similar marked reduction of transgene expression was shown in the livers of mice injected with the mutant promoter construct (n = 8, P = .003). Finally, in studies of BOEC mRNA, the index case showed a 4.6-fold reduction of expression of the VWF transcript associated with the deletion mutation. These studies show that the 13-bp deletion mutation alters the binding of Ets (and possibly GATA) proteins to the VWF promoter and significantly reduces VWF expression, thus playing a central pathogenic role in the type 1 von Willebrand disease phenotype in the index case. © 2010 by The American Society of Hematology.
Citation
Othman, M., Chirinian, Y., Brown, C., Notley, C., Hickson, N., Hampshire, D., Buckley, S., Waddington, S., Parker, A. L., Baker, A., James, P., & Lillicrap, D. (2010). Functional characterization of a 13-bp deletion (c.-1522--1510del13) in the promoter of the von Willebrand factor gene in type 1 von Willebrand disease. Blood, 116(18), 3645-3652. https://doi.org/10.1182/blood-2009-12-261131
Journal Article Type | Article |
---|---|
Publication Date | Nov 4, 2010 |
Deposit Date | May 24, 2022 |
Journal | Blood |
Print ISSN | 0006-4971 |
Publisher | American Society of Hematology |
Peer Reviewed | Peer Reviewed |
Volume | 116 |
Issue | 18 |
Pages | 3645-3652 |
DOI | https://doi.org/10.1182/blood-2009-12-261131 |
Keywords | Chromatin; Endothelial cells; Genes; Immunoprecipitation; Mice; Mutation; rna; Messenger; Spatial vectors; Transcription factor; Transgenes |
Public URL | https://hull-repository.worktribe.com/output/3602042 |
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