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Pathological mechanism and antisense oligonucleotide-mediated rescue of a non-coding variant suppressing factor 9 RNA biogenesis leading to hemophilia B.
Krooss, Simon Werwitzke, Sonja Kopp, Johannes Rovai, Alice Varnholt, Dirk Wachs, Amelie S Goyenvalle, Aurelie Aarstma-Rus, Annemieke Ott, Michael Tiede, Andreas
Krooss, Simon
Werwitzke, Sonja
Kopp, Johannes
Rovai, Alice
Varnholt, Dirk
Wachs, Amelie S
Goyenvalle, Aurelie
Aarstma-Rus, Annemieke
Ott, Michael
Tiede, Andreas
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2020-04-08
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Abstract
Loss-of-function mutations in the human coagulation factor 9 (F9) gene lead to hemophilia B. Here, we dissected the consequences and the pathomechanism of a non-coding mutation (c.2545A>G) in the F9 3' untranslated region. Using wild type and mutant factor IX (FIX) minigenes we revealed that the mutation leads to reduced F9 mRNA and FIX protein levels and to lower coagulation activity of cell culture supernatants. The phenotype could not be compensated by increased transcription. The pathomechanism comprises the de novo creation of a binding site for the spliceosomal component U1snRNP, which is able to suppress the nearby F9 poly(A) site. This second, splicing-independent function of U1snRNP was discovered previously and blockade of U1snRNP restored mutant F9 mRNA expression. In addition, we explored the vice versa approach and masked the mutation by antisense oligonucleotides resulting in significantly increased F9 mRNA expression and coagulation activity. This treatment may transform the moderate/severe hemophilia B into a mild or subclinical form in the patients. This antisense based strategy is applicable to other mutations in untranslated regions creating deleterious binding sites for cellular proteins.
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PLoS Genet. 2020;16(4):e1008690. Published 2020 Apr 8. doi:10.1371/journal.pgen.1008690.
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en
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1553-7404
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Attribution-NonCommercial-ShareAlike 4.0 International