Identification of the gene for vitamin K epoxide reductase

被引:538
作者
Li, T
Chang, CY
Jin, DY
Lin, PJ
Khvorova, A
Stafford, DW
机构
[1] Univ N Carolina, Dept Biol, Chapel Hill, NC 27599 USA
[2] Dharmacon Inc, Lafayette, CO 80026 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1038/nature02254
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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(1), 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.
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页码:541 / 544
页数:4
相关论文
共 30 条
[1]   WARFARIN-ASSOCIATED EMBRYOPATHY IN A 17-WEEK-OLD ABORTUS [J].
BARR, M ;
BURDI, AR .
TERATOLOGY, 1976, 14 (02) :129-134
[2]  
Bohley P, 1996, BIOL CHEM, V377, P425
[3]   Silencing of the novel p53 target gene Snk/Plk2 leads to mitotic catastrophe in paclitaxel (Taxol)-exposed cells [J].
Burns, TF ;
Fei, PW ;
Scata, KA ;
Dicker, DT ;
El-Deiry, WS .
MOLECULAR AND CELLULAR BIOLOGY, 2003, 23 (16) :5556-5571
[4]   VITAMIN-K DEPENDENT CARBOXYLASE - SUBCELLULAR LOCATION OF THE CARBOXYLASE AND ENZYMES INVOLVED IN VITAMIN-K METABOLISM IN RAT-LIVER [J].
CARLISLE, TL ;
SUTTIE, JW .
BIOCHEMISTRY, 1980, 19 (06) :1161-1167
[5]   RELATIONSHIP BETWEEN INVIVO DEGRADATIVE RATES AND ISOELECTRIC POINTS OF PROTEINS [J].
DICE, JF ;
GOLDBERG, AL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1975, 72 (10) :3893-3897
[6]   Homozygosity mapping of a second gene locus for hereditary combined deficiency of vitamin K-dependent clotting factors to the centromeric region of chromosome 16 [J].
Fregin, A ;
Rost, S ;
Wolz, W ;
Krebsova, A ;
Muller, CR ;
Oldenburg, J .
BLOOD, 2002, 100 (09) :3229-3232
[7]   Raptor, a binding partner of target of rapamycin (TOR), mediates TOR action [J].
Hara, K ;
Maruki, Y ;
Long, XM ;
Yoshino, K ;
Oshiro, N ;
Hidayat, S ;
Tokunaga, C ;
Avruch, J ;
Yonezawa, K .
CELL, 2002, 110 (02) :177-189
[8]  
Harborth J, 2001, J CELL SCI, V114, P4557
[9]   Similar behaviour of single-strand and double-strand siRNAs suggests they act through a common RNAi pathway [J].
Holen, T ;
Amarzguioui, M ;
Babaie, E ;
Prydz, H .
NUCLEIC ACIDS RESEARCH, 2003, 31 (09) :2401-2407
[10]  
Horton JD, 1999, AM FAM PHYSICIAN, V59, P635