Age-specific regulation of clotting factor IX gene expression in normal and transgenic mice

Author:

Boland EJ1,Liu YC1,Walter CA1,Herbert DC1,Weaker FJ1,Odom MW1,Jagadeeswaran P1

Affiliation:

1. Department of Cellular and Structural Biology, University of Texas Health Science Center at San Antonio 78284–7762, USA.

Abstract

Factor IX (FIX), a circulating serine protease that serves as an essential component of the blood coagulation pathway, has been shown to increase with age in humans. We show here that murine FIX mRNA and activity levels also increase with age. Furthermore, one form of hemophilia B, hemophilia B Leyden, which is caused by mutations within the promoter region of the FIX gene, has a distinct age-dependent phenotype. To determine the source of the age-related increases in FIX gene expression, we have analyzed the regulation of the normal FIX gene promoter and FIX Leyden gene promoter with the +13 mutation during aging by generating transgenic mice that contain the -189 to +21 bp promoter segment ligated to a chloramphenicol acetyltransferase reporter gene. We have established that the normal FIX promoter and the Leyden promoter transgenes are expressed in a tissue-specific manner in vivo. The normal FIX promoter transgene does not show any differences in the pattern of expression with age or sex of the organism, whereas the Leyden promoter transgene showed age-dependent male-specific expression. This is the first demonstration of the FIX Leyden phenotype in a transgenic mouse model.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Cited by 21 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Identification of zebrafish ortholog for human coagulation factor IX and its age‐dependent expression;Journal of Thrombosis and Haemostasis;2021-06-06

2. Diagnosis and phenotypic assessment of Pakistani Haemophilia B carriers;Pakistan Journal of Medical Sciences;2017-06-02

3. The modulation of coagulation by aptamers;Blood Coagulation & Fibrinolysis;2015-01

4. A CpG Mutational Hotspot in a ONECUT Binding Site Accounts for the Prevalent Variant of Hemophilia B Leyden;The American Journal of Human Genetics;2013-03

5. Animal Models of Hemophilia;Progress in Molecular Biology and Translational Science;2012

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