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维生素K环氧化物还原酶基因的鉴定。

Identification of the gene for vitamin K epoxide reductase.

作者信息

Li Tao, Chang Chun-Yun, Jin Da-Yun, Lin Pen-Jen, Khvorova Anastasia, Stafford Darrel W

机构信息

Department of Biology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599, USA.

出版信息

Nature. 2004 Feb 5;427(6974):541-4. doi: 10.1038/nature02254.

Abstract

Vitamin K epoxide reductase (VKOR) is the target of warfarin, the most widely prescribed anticoagulant for thromboembolic disorders. Although estimated to prevent twenty strokes per induced bleeding episode, warfarin is under-used because of the difficulty of controlling dosage and the fear of inducing bleeding. Although identified in 1974 (ref. 2), the enzyme has yet to be purified or its gene identified. A positional cloning approach has become possible after the mapping of warfarin resistance to rat chromosome 1 (ref. 3) and of vitamin K-dependent protein deficiencies to the syntenic region of human chromosome 16 (ref. 4). Localization of VKOR to 190 genes within human chromosome 16p12-q21 narrowed the search to 13 genes encoding candidate transmembrane proteins, and we used short interfering RNA (siRNA) pools against individual genes to test their ability to inhibit VKOR activity in human cells. Here, we report the identification of the gene for VKOR based on specific inhibition of VKOR activity by a single siRNA pool. We confirmed that MGC11276 messenger RNA encodes VKOR through its expression in insect cells and sensitivity to warfarin. The expressed enzyme is 163 amino acids long, with at least one transmembrane domain. Identification of the VKOR gene extends our understanding of blood clotting, and should facilitate development of new anticoagulant drugs.

摘要

维生素K环氧化物还原酶(VKOR)是华法林的作用靶点,华法林是治疗血栓栓塞性疾病最常用的抗凝剂。尽管据估计,每发生一次因用药导致的出血事件,华法林可预防20次中风,但由于难以控制剂量以及担心引发出血,华法林的使用并不充分。尽管该酶于1974年被发现(参考文献2),但至今尚未得到纯化,其基因也未被鉴定。在将华法林抗性定位到大鼠1号染色体(参考文献3)以及将维生素K依赖性蛋白缺乏症定位到人类16号染色体的同区域(参考文献4)之后,采用定位克隆方法成为可能。将VKOR定位到人类16号染色体p12-q21区域内的190个基因,使得搜索范围缩小到13个编码候选跨膜蛋白的基因,我们利用针对各个基因的短干扰RNA(siRNA)池来测试它们抑制人类细胞中VKOR活性的能力。在此,我们报告基于单个siRNA池对VKOR活性的特异性抑制鉴定出了VKOR基因。我们通过其在昆虫细胞中的表达以及对华法林的敏感性,证实MGC11276信使核糖核酸编码VKOR。所表达的酶有163个氨基酸长,至少有一个跨膜结构域。VKOR基因的鉴定扩展了我们对血液凝固的理解,应该会促进新型抗凝药物的研发。

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