Kurachi K, Kurachi S, Furukawa M, Yao S N
Department of Human Genetics, University of Michigan Medical Center, Ann Arbor 48109-0618.
Blood Coagul Fibrinolysis. 1993 Dec;4(6):953-73.
Within the past 20 years or so, factor IX has been at the centre of particularly intensive studies of its physiology, pathology and biochemistry as well as its molecular genetics and biology. With the complete nucleotide sequence of its human gene determined in 1985 and the molecular defects of over 600 abnormal human factor IX genes analysed to date, factor IX is among the few mammalian proteins which have been exhaustively studied in almost every aspect. The enormous amount of information we now have on this medium-sized plasma protein sheds light on how a gene and its protein evolve, how the protein carries out a highly regulated, specific and pivotal role in the delicately balanced blood coagulation reaction, and the correlation between clinical presentations and its highly diverse molecular mechanism of defects. This wealth of knowledge makes factor IX an excellent model for deeper study, such as truly quantitative analysis of its structure-function relationship and in vivo function and regulation. It will also provide a sound foundation which may lead to improved treatment of haemophilia B and perhaps to its cure. This paper attempts to review the recent progress in research on factor IX.
在过去约20年里,凝血因子IX一直是对其生理学、病理学、生物化学以及分子遗传学和生物学进行特别深入研究的核心对象。随着1985年确定了其人类基因的完整核苷酸序列,以及迄今已分析了600多个异常人类凝血因子IX基因的分子缺陷,凝血因子IX是少数在几乎各个方面都得到详尽研究的哺乳动物蛋白质之一。我们现在所掌握的关于这种中等大小血浆蛋白的大量信息,揭示了一个基因及其蛋白质是如何进化的,该蛋白质如何在微妙平衡的血液凝固反应中发挥高度调控、特定且关键的作用,以及临床表现与其高度多样的分子缺陷机制之间的关联。这些丰富的知识使凝血因子IX成为深入研究的优秀模型,例如对其结构 - 功能关系以及体内功能和调节进行真正的定量分析。它还将提供坚实的基础,可能带来对乙型血友病治疗的改进,甚至可能实现治愈。本文试图综述凝血因子IX的最新研究进展。