Thromb Haemost 2001; 86(02): 596-603
DOI: 10.1055/s-0037-1616092
Review Article
Schattauer GmbH

A Factor VIII Minigene Comprising the Truncated Intron I of Factor IX Highly Improves the In Vitro Production of Factor VIII

Jean-Luc Plantier
1   INSERM U331, Laboratoire d’Hémobiologie-Faculté de Médecine RTH Laënnec, Lyon, France
,
Marie-Hélène Rodriguez
1   INSERM U331, Laboratoire d’Hémobiologie-Faculté de Médecine RTH Laënnec, Lyon, France
,
Nathalie Enjolras
1   INSERM U331, Laboratoire d’Hémobiologie-Faculté de Médecine RTH Laënnec, Lyon, France
,
Olivier Attali
1   INSERM U331, Laboratoire d’Hémobiologie-Faculté de Médecine RTH Laënnec, Lyon, France
,
Claude Négrier
1   INSERM U331, Laboratoire d’Hémobiologie-Faculté de Médecine RTH Laënnec, Lyon, France
› Author Affiliations
Further Information

Publication History

Received 17 August 2000

Accepted after resubmission 15 February 2001

Publication Date:
12 December 2017 (online)

Preview

Summary

The biosynthesis of coagulation factor VIII (FVIII) is hampered by successive controls that limit its production. To improve this production, a truncated intron I sequence of factor IX (TFIXI1) was inserted in FVIII cDNA in place of FVIII introns 1, 12 and 13 and also as a combination between introns 1 and 12, and introns 1 and 13. The intron 12 and 13 locations were targeted because this region was previously shown to contain a transcriptional silencer. The expression of FVIII in CHO and HepG2 cells revealed important variations in the properties of the minigenes depending on the TFIXI1 insertion sites. In FVIII intron 13 location the TFIXI1 seemed to diminish the transcriptional silencer activity, whereas it was poorly spliced in intron 12 position. Among the five constructs, FVIII I1+13 leaded to a significant improvement in FVIII secretion (13 times) that was associated with a dramatic intracellular accumulation in cells. Therefore, the FVIII I1+13 minigene could represent a particular interest to produce recombinant FVIII in vitro as well as in the aim of gene therapy of haemophilia A.