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Hum Mutat. 2012 Sep;33(9):1373-6. doi: 10.1002/humu.22120. Epub 2012 Jun 11.

Ribosome readthrough accounts for secreted full-length factor IX in hemophilia B patients with nonsense mutations.

Author information

1
Dipartimento di Biochimica e Biologia Molecolare and LTTA Centre, Università di Ferrara, Italy. pnm@unife.it

Abstract

We investigated the spontaneous ribosome readthrough, virtually unexplored in genes encoding secreted proteins, over coagulation F9 nonsense mutations. Expression of recombinant factor IX (FIX) in eukaryotic cells demonstrated appreciable levels of secreted FIX molecules for the mutations p.R162* (5 ± 0.3% of rFIX-wt antigen levels), p.R294* (3.1 ± 1.1%) and p.R298* (2.5 ± 0.7%), but not for the p.L103*. Western blotting revealed a large proportion of truncated molecules, which correlated with small amounts of full-length FIX (rFIX-162*, ∼0.5%; rFIX-294*; and rFIX-298*, ∼0.2%). Western blotting of plasma from FIX deficient (Hemophilia B) patients revealed traces of full-length FIX for the p.R294* and p.R298* mutations, but not for the p.L103* mutation that triggered major FIX mRNA decay. The detection of full-length proteins has clinical implication, particularly for post-therapeutic immunological complications in Hemophilia. Data in patients' plasma and in vitro, obtained in the proper protein context, support a ribosome readthrough gradient, consistent with its predicted determinants of efficiency.

PMID:
22618954
DOI:
10.1002/humu.22120
[Indexed for MEDLINE]

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