The molecular clock regulates circadian transcription of tissue factor gene

被引:2
作者
Oishi, Katsutaka [1 ,2 ]
Koyanagi, Satoru [3 ]
Ohkura, Naoki [4 ]
机构
[1] Natl Inst Adv Ind Sci & Technol, Biomed Res Inst, Biol Clock Res Grp, Tsukuba, Ibaraki 3058566, Japan
[2] Univ Tokyo, Dept Med Genome Sci, Grad Sch Frontier Sci, Kashiwa, Chiba, Japan
[3] Kyushu Univ, Grad Sch Pharmaceut Sci, Dept Pharmaceut, Fukuoka 812, Japan
[4] Teikyo Univ, Sch Pharmasci, Dept Mol Physiol & Pathol, Tokyo, Tokyo, Japan
关键词
Circadian rhythm; Tissue factor; Transcription; Inflammation; Thromboembolic events; PLASMINOGEN-ACTIVATOR INHIBITOR-1; FIBRINOLYTIC FACTORS; MICE; EXPRESSION; COAGULATION;
D O I
10.1016/j.bbrc.2012.12.098
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Tissue factor (TF) is involved in endotoxin-induced inflammation and mortality. We found that the circadian expression of TF mRNA, which peaked at the day to night transition (activity onset), was damped in the liver of Clock mutant mice. Luciferase reporter and chromatin immunoprecipitation analyses using embryonic fibroblasts derived from wild-type or Clock mutant mice showed that CLOCK is involved in transcription of the TF gene. Furthermore, the results of real-time luciferase reporter experiments revealed that the circadian expression of TF mRNA is regulated by clock molecules through a cell-autonomous mechanism via an E-box element located in the promoter region. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:332 / 335
页数:4
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