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正常和转基因小鼠中凝血因子IX基因表达的年龄特异性调控。

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

作者信息

Boland E J, Liu Y C, Walter C A, Herbert D C, Weaker F J, Odom M W, Jagadeeswaran P

机构信息

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

出版信息

Blood. 1995 Sep 15;86(6):2198-205.

PMID:7662969
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.

摘要

凝血因子IX(FIX)是一种循环丝氨酸蛋白酶,是血液凝固途径的重要组成部分,在人类中已显示其水平会随年龄增长而升高。我们在此表明,小鼠FIX的mRNA和活性水平也随年龄增长而升高。此外,B型血友病的一种形式,即莱顿B型血友病,由FIX基因启动子区域的突变引起,具有明显的年龄依赖性表型。为了确定FIX基因表达随年龄增长增加的来源,我们通过构建转基因小鼠来分析衰老过程中正常FIX基因启动子和具有+13突变的莱顿FIX基因启动子的调控情况,该转基因小鼠包含与氯霉素乙酰转移酶报告基因连接的-189至+21 bp启动子片段。我们已经确定正常FIX启动子和莱顿启动子转基因在体内以组织特异性方式表达。正常FIX启动子转基因在生物体的年龄或性别方面,表达模式没有任何差异,而莱顿启动子转基因则表现出年龄依赖性的雄性雄性男性特异性表达。这是在转基因小鼠模型中首次证明莱顿FIX表型。

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