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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

Maha Othman

Yvette Chirinian

Christine Brown

Colleen Notley

Nicholas Hickson

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