Literature DB >> 17855631

Effect of single nucleotide polymorphisms on expression of the gene encoding thrombin-activatable fibrinolysis inhibitor: a functional analysis.

Michael B Boffa1, Deborah Maret, Jeffrey D Hamill, Nazareth Bastajian, Paul Crainich, Nancy S Jenny, Zhonghua Tang, Elizabeth M Macy, Russell P Tracy, Rendrik F Franco, Michael E Nesheim, Marlys L Koschinsky.   

Abstract

Thrombin-activable fibrinolysis inhibitor (TAFI) is a plasma zymogen that acts as a molecular link between coagulation and fibrinolysis. Numerous single nucleotide polymorphisms (SNPs) have been identified in CPB2, the gene encoding TAFI, and are located in the 5'-flanking region, in the coding sequences, and in the 3'-untranslated region (UTR) of the CPB2 mRNA transcript. Associations between CPB2 SNPs and variation in plasma TAFI antigen concentrations have been described, but the identity of SNPs that are causally linked to this variation is not known. In the current study, we investigated the effect of the SNPs in the 5'-flanking region on CPB2 promoter activity and SNPs in the 3'-UTR on CPB2 mRNA stability. Whereas the 5'-flanking region SNPs (with 2 exceptions) did not have a significant effect on promoter activity, either alone or in haplotypic combinations seen in the human population, all of the 3'-UTR SNPs substantially affected mRNA stability. We speculate that these SNPs, in part, contribute to variation in plasma TAFI concentrations via modulation of CPB2 gene expression through an effect on mRNA stability.

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Year:  2007        PMID: 17855631     DOI: 10.1182/blood-2007-03-078543

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


  15 in total

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Authors:  Matthew Halvorsen; Joshua S Martin; Sam Broadaway; Alain Laederach
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5.  Low thrombin activatable fibrinolysis inhibitor activity levels are associated with an increased risk of a first myocardial infarction in men.

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9.  MicroRNA regulation and the variability of human cortical gene expression.

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10.  Whole-genome sequences of DA and F344 rats with different susceptibilities to arthritis, autoimmunity, inflammation and cancer.

Authors:  Xiaosen Guo; Max Brenner; Xuemei Zhang; Teresina Laragione; Shuaishuai Tai; Yanhong Li; Junjie Bu; Ye Yin; Anish A Shah; Kevin Kwan; Yingrui Li; Wang Jun; Pércio S Gulko
Journal:  Genetics       Date:  2013-05-20       Impact factor: 4.562

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