Thromb Haemost 2002; 87(05): 846-853
DOI: 10.1055/s-0037-1613095
Review Article
Schattauer GmbH

Prothrombin G20210A is a Bifunctional Gene Polymorphism

Angela M. Carter
1   Academic Unit of Molecular Vascular Medicine, University of Leeds, United Kingdom
,
Mythily Sachchithananthan
2   Monash Department of Medicine, Box Hill, Victoria, Australia
,
Stan Stasinopoulos
2   Monash Department of Medicine, Box Hill, Victoria, Australia
,
Fabienne Maurer
3   Department of Medical Genetics, Central Hospital of the University of Vaud, Lausanne, Switzerland
,
Robert L. Medcalf
2   Monash Department of Medicine, Box Hill, Victoria, Australia
› Author Affiliations
Further Information

Publication History

Received 29 September 2001

Accepted 16 January 2002

Publication Date:
11 December 2017 (online)

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Summary

The G20210A polymorphism has been shown to alter the efficiency of prothrombin mRNA processing. Here we show that the G20210A mutation also alters prothrombin mRNA stability. Three-fold more prothrombin protein and mRNA were produced in NIH-3T3 cells transfected with the prothrombin cDNAs containing the 20210A variant compared to cells expressing the 20210G variant. mRNA stability assays using chimeric globin transcripts harboring the G or A variant of the 97 nt prothrombin 3’-UTR indicated that the 20210G variant conferred greater instability to the globin reporter transcript than the A variant in transfected HepG2 cells. Both variants of the prothrombin 3’-UTR were shown to provide binding sites for a number of cellular proteins including HuR, an RNA binding protein associated with mRNA stability. Our results indicate that the G20210A is a bifunctional polymorphism, as it not only alters the efficiency of mRNA processing, but also the decay rate of prothrombin mRNA.