Boccia L M, Lillicrap D, Newcombe K, Mueller C R
Department of Pathology, Queen's University, Kingston, Ontario, Canada.
Mol Cell Biol. 1996 May;16(5):1929-35. doi: 10.1128/MCB.16.5.1929.
Factor IX is an essential vitamin K-dependent serine protease that participates in the intrinsic pathway of coagulation. The protein is expressed exclusively in the liver. The rare Leyden form of hemophilia B (inherited factor IX deficiency) results from point mutations in three proximal promoter elements that decrease factor IX expression. Recovery of expression occurs following puberty, with factor IX protein levels rising into the normal range. We have previously implicated the PAR domain D-site-binding protein (DBP) as well as an upstream element, site 5, as playing important roles in the phenotypic recovery of hemophilia B Leyden. Here we demonstrate that site 5 binds both the CCAAT/enhancer-binding protein (C/EBPalpha) and the ubiquitous Ets factor GA-binding protein (GABPalpha/beta). Transactivation of the factor IX promoter by the PAR proteins DBP and hepatic leukemia factor (HLF) is dependent on the binding of GABPalpha/beta to site 5, and coexpression of these two factors is required for optimal activation of this promoter. The binding of C/EBPalpha to site 5 also augments the activity of GABPalpha/beta. Analysis of the developmental regulation of site 5-binding proteins in rat liver has shown that C/EBPalpha and the GABPbeta subunit increase markedly in the 2 weeks after birth. These observations establish a functional association between the Ets factor GABPalpha/beta and C/EBPalpha and indicate that the two PAR proteins, DBP and HLF, may play complementary roles in factor IX activation. Given the developmental changes exhibited by these proteins, it is likely that they play a role in regulation of the normal factor IX promoter as well as promoters carrying hemophilia B Leyden mutations.
凝血因子IX是一种必需的维生素K依赖性丝氨酸蛋白酶,参与内源性凝血途径。该蛋白仅在肝脏中表达。罕见的莱顿型B型血友病(遗传性凝血因子IX缺乏症)是由三个近端启动子元件中的点突变导致凝血因子IX表达降低引起的。青春期后表达恢复,凝血因子IX蛋白水平升至正常范围。我们之前认为PAR结构域D位点结合蛋白(DBP)以及上游元件位点5在莱顿型B型血友病的表型恢复中起重要作用。在此我们证明位点5结合CCAAT/增强子结合蛋白(C/EBPα)和普遍存在的Ets因子GA结合蛋白(GABPα/β)。PAR蛋白DBP和肝白血病因子(HLF)对凝血因子IX启动子的反式激活依赖于GABPα/β与位点5的结合,并且这两个因子的共表达是该启动子最佳激活所必需的。C/EBPα与位点5的结合也增强了GABPα/β的活性。对大鼠肝脏中位点5结合蛋白的发育调控分析表明,C/EBPα和GABPβ亚基在出生后2周内显著增加。这些观察结果建立了Ets因子GABPα/β与C/EBPα之间的功能关联,并表明两个PAR蛋白DBP和HLF可能在凝血因子IX激活中发挥互补作用。鉴于这些蛋白表现出的发育变化,它们很可能在正常凝血因子IX启动子以及携带莱顿型B型血友病突变的启动子的调控中发挥作用。